Recent findings indicate that different Endocrine Disrupting Chemicals (EDCs) interfere with lipid metabolic pathways in mammals and promote fat accumulation, a previously unknown site of action for these compounds. The antifoulant and environmental pollutant tributyltin (TBT), which causes imposex in gastropod snails, induces an “obesogenic” phenotype in mammals, through the activation of the nuclear receptors retinoid X receptor (RXR) and peroxisome proliferator-activated receptor gamma (PPARγ). In teleosts, the effects of TBT on the lipid metabolism are poorly understood, particularly following exposure to low, environmental concentrations. In this context, the present work shows that exposure of zebrafish to 10 and 50 ng/L of TBT (as Sn) from pre-hatch to 9 months of age alters the body weight, condition factor, hepatosomatic index and hepatic triglycerides in a gender and dose related manner. Furthermore, TBT modulated the transcription of key lipid regulating factors and enzymes involved in adipogenesis, lipogenesis, glucocorticoid metabolism, growth and development in the brain and liver of exposed fish, revealing sexual dimorphic effects in the latter. Overall, the present study shows that the model mammalian obesogen TBT interferes with triglyceride accumulation and the transcriptional regulation of lipid metabolism in zebrafish and indentifies the brain lipogenic transcription profile of fish as a new target of this compound.
Citation: Lyssimachou A, Santos JG, André A, Soares J, Lima D, Guimarães L, et al. (2015) The Mammalian “Obesogen” Tributyltin Targets Hepatic Triglyceride Accumulation and the Transcriptional Regulation of Lipid Metabolism in the Liver and Brain of Zebrafish. PLoS ONE 10(12): e0143911. https://doi.org/10.1371/journal.pone.0143911
Editor: Nicholas S. Foulkes, Karlsruhe Institute of Technology, GERMANY
Received: August 28, 2014; Accepted: November 11, 2015; Published: December 3, 2015
Copyright: © 2015 Lyssimachou et al. This is an open access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited
Data Availability: All relevant data are within the paper and its Supporting Information files.
Funding: This work was supported by FCT-Fundação para a Ciência e a Tecnologia (Portugal), through project PTDC/MAR/115199/2009, the European Regional Development Fund (ERDF) through the COMPETE—Operational Competitiveness Programme and national funds through FCT – Fundação para a Ciência e a Tecnologia, under the project “PEst-C/MAR/LA0015/2013” and pos-doctoral fellowship SFRH/BPD/74231/2010. The funders had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript.
Competing interests: The authors have declared that no competing interests exist.
“Obesogens” are a class of Endocrine Disrupting Chemicals (EDCs) present in the environment, named after their potential to induce obesity in mammals [1, 2]. Some of these chemicals, such as organotins, bisphenol A and phthalates, with very diverse chemical structures, were initially characterized as “androgenic” or “estrogenic” due to their ability to mimic or alter the endogenous role of androgens or estrogens, leading to reproductive dysfunction [3–5]. However, recent evidence suggest that these compounds also interfere with nuclear receptors that play a key role in adipogenesis, sometimes at concentrations much lower than the ones reported to alter the hormone synthesis and metabolism, resulting in fat accumulation [1, 2, 6].
Tributyltin (TBT) is an organotin compound that was used globally as a biocide in ships’ antifouling paints. Continuous evidence on its high toxicity towards a wide range of aquatic organisms resulted in its ban and total prohibition of use in antifouling paints in 2008 [4, 7, 8]. Organotins are also used in wood preservation, as antifungal agents in breweries, textiles, wood pulp, paper mill and industrial water systems, as well as a heat and light stabilizers for PVC material . Due to their low solubility, high octanol-water partition coefficient and persistence in sediments, their release into the aquatic environment has resulted in worldwide aquatic contamination [7, 9]. Despite its ban in antifouling paints, TBT is still detected in water samples near harbours at concentrations up to 200–400 ng/L [9, 10] and in sediments up to 1–10 μg/ L [10, 11].
Several studies have identified endocrine system abnormalities related to TBT exposure in a wide range of organisms including molluscs [4, 12, 13], fish [14–16] and mammals [17–19]. One of the most studied cases in endocrine disruption research is the imposition of male secondary sexual characteristics in female gastropods (imposex), an irreversible condition that develops following exposure to TBT at concentrations as low as 1 ng/L (as Sn) . TBT binds to and activates the molluscan retinoid X receptor (RXR) [21, 22] and the human RXR ligand 9-cis retinoic acid (9-cis RA) induces imposex to female gastropods at nanomolar concentrations . These data strongly suggest that RXR modulation is the primary mechanism of TBT imposex induction in gastropods .
In mammals, TBT is a nanomolar affinity ligand of RXRα and peroxisome proliferator-activated receptor gamma (PPARγ) [17, 24, 25]. PPARγ, which forms an obligatory permissive heterodimer with RXR, is considered a “master” regulator of adipogenesis since its activation enhances cellular processes involved in adipocyte maturation by inducing the expression of genes mediating fatty acid uptake, metabolism and storage . Indeed, in vitro studies show that exposure of rodent or human undifferentiated adipocyte cell lines (3T3-L1) and bone marrow multipotent mesenchymal stromal cells (MSCs) to TBT or RXRα- and PPARγ-specific ligands results in adipocyte differentiation and triglyceride accumulation with a parallel induction of the expression of adipogenic marker genes [17, 24, 27, 28]. TBT also stimulates mammalian adipogenesis in vivo when exposure occurs during the pre-natal and early post-natal stages. Exposed mice show increased adipose mass and liver lipid accumulation [17, 18], accompanied by alterations in the expression of key factors and enzymes of the lipid metabolism in liver and adipose tissue . The common pattern of TBT on PPARγ:RXR heterodimer target genes, both in vitro and in vivo, strongly indicate that TBT perturbs lipid metabolism favouring obesity through the activation of nuclear receptors [17, 24, 29].
Fish are continually exposed to endocrine disruptors in their natural environment and are sensitive to TBT exposure. TBT effects upon fish include altered sex ratio, suppressed fertility, inhibition of neural aromatase gene expression and alterations in the signalling of hepatic key regulatory steroidogenic enzymes [14, 15, 30, 31]. Despite the evidence on the adverse action of TBT in fish, there are limited data on the effects of this compound on fat accumulation and on the transcription network that regulates lipid metabolism. Lipid absorption, transport, storage and metabolism in fish are achieved through biological and molecular processes that resemble that of mammalian species [32, 33]. Furthermore, fish may develop human-like metabolic diseases such as the obesity-related non-alcoholic fatty liver disease (NAFLD) and hepatic steatosis [34–36]. Additionally, the mammalian targets of TBT, RXRα and PPARγ, have clear orthologues in fish, with their expression detected since early development [37, 38]. Thus, TBT and other chemicals, may act on the transcriptional regulation of lipogenesis in fish and induce either “obesogenic” or overall lipid deregulation responses, posing a yet unidentified threat to fish populations.
Following the above observations, the present study was constructed to investigate the TBT-induced disorders on the lipid metabolism of males and females of the model teleost zebrafish (Danio rerio), following chronic exposures (9 months) to low environmentally relevant concentrations (10 and 50 ng/L as Sn). Zebrafish are recommended as test species in a number of ecotoxicological test protocols . As end-points we screened the effects of TBT on the whole-body morphological parameters, the liver size and triglyceride content, as well as on the expression pattern of transcription factors and metabolizing enzymes that play a key role in the regulation of lipids (Fig 1).
Adipogenesis is characterized by the expression of PPARγ, C/EBP-family members and SREBP. Insulin, glucocorticoids or IGF stimulate the expression of C/EBPβ, which in turn stimulates the expression of EBPα and PPARγ. Upon stimulation, PPARγ forms a heterodimer with RXR and together with EBPα regulate the expression of genes involved in adipogenesis and lipogenesis . C/EBPα and C/EBPβ also regulate the expression of 11β-HSD1 and 11β-HSD2 (which catalyse the activation and deactivation, respectively, of cortisol and regulate glucocorticoid metabolism)  and of IGF-I and IGF-II (which regulate growth, cell proliferation and development) [41, 42]. SREBP1 and ChREBP, are stimulated upon insulin and glucose secretion, respectively, and regulate synergistically the expression of the de novo lipogenesis enzymes FASn and ACCα  that catalyse fatty acid synthesis. SREBP1 also regulates the expression of PPARγ . Fatty acid catabolism through β-oxidation in peroxisomes is catalysed by ACOX1 . Excess fatty acids derived from food, break-down from stored fat or synthesized through de novo lipogenesis are converted to triglycerides through a pathway the last step of which is catalysed by the DGAT2 enzyme. The transcriptional regulation of DGAT2 is also regulated by EBPβ and to a lesser extent by EBPα .
Out of the four major organs involved in energy homeostasis (Fig 2), we selected the liver and the brain since whole-body metabolic disorders may be reflected in the metabolism in these tissues. The liver is a particularly good indicator of disease as it has a limited capacity to store fat and therefore excess synthesis and storage may lead to hepatomegaly, NAFLD, hepatocyte apoptosis and hepatic steatosis . On the contrary, there is very little information on the role of the brain in the lipid metabolism of teleosts and therefore the expression of the selected lipogenic genes in the liver was also studied in the brain.
The liver has a central role in the synthesis, metabolism and distribution of glucose and fatty acids. The adipose tissue is the principal site of excess energy storage in the form of fat (triglycerides) and liberates fatty acids upon demand. The muscle is the major site of lipid oxidation and energy expenditure. The brain acts as a lipid sensor; it receives signals from the other organs to adjust energy homeostasis by changing behaviour (e.g. food intake and expenditure). When energy consumption exceeds expenditure excess triglycerides are stored not only in adipose tissue but in muscle and liver as well, leading to metabolic disorders [48, 49].
Our data show that TBT alters the body and hepatic metabolic reserves, induces the liver triglyceride content in males and perturbs the expression profile of lipogenic genes in both liver and the brain of zebrafish. We observed a clear sexual dimorphism in morphological parameters and transcriptional regulation in the liver following TBT exposure. Finally, we identified the brain lipogenic transcription profile of fish as a novel target of TBT in both males and females, which has not been investigated in mammals yet.
Material and Methods
Infinity Triglycerides Liquid Stable Reagent was purchased from ThermoScientific. Tributyltin Chloride (TBTCl; 96% purity) and all other reagents were obtained from Sigma-Aldrich unless stated otherwise in the text.
Experimental animals- breeding
All experiments conducted in this study were carried out at Biotério de Organismos Aquáticos (BOGA, CIIMAR) aquatic animal facilities and have been approved by the CIIMAR ethical committee and by CIIMAR Managing Animal Welfare Body (ORBEA) according to the European Union Directive 2010/63/EU “on the protection of animals used for scientific purposes”. The breeding stock of adult wild-type zebrafish (Danio rerio; Singapore) was kept in 250 L aquaria with dechlorinated aerated water from a recirculation system equipped with mechanical and biological filters at temperature of 28 ± 1°C under a photoperiod of 14:10 h (light:dark). The fish were fed ad libitum twice a day with a commercial fish diet Tetramin (Tetra, Melle, Germany) and supplemented with live brine shrimp (Artemia spp.). In the afternoon before breeding, two random groups of 4–6 males and 10–12 females were transferred in net cages bottom-covered with glass marbles, placed within 30 L aquaria and fed just with live brine shrimp (Artemia spp.). The next morning (1.5 hour after sunlight) breeding fish were removed, the eggs were collected from the bottom of the tank by siphoning, cleaned in egg water and randomly allocated to experimental aquaria.
Solutions preparation and exposure experiments
TBT stock solutions were prepared in acetone and four waterborne exposure conditions were set, in duplicates, in experimental aquaria: an experimental control, a solvent control (acetone at 0.0002%) and two environmentally relevant TBT concentrations (nominal concentration: 10 and 50 ng/L as Sn).
Results from our previous experiments show that continuous supply of TBT in a flow-through system fails to result in fish exposure due to adsorption of TBT to the walls of the tubes that supply the water. Hence, based on preliminary tests, we decided to dose the tanks directly, twice daily, at 0h and 8h to guarantee exposure of fish to TBT. The TBT concentration in the water was tested in the control groups and in the tanks of 50 ng/L TBT, at 20 dpf (days post fertilization) (S1 Table). In the control groups, TBT and their metabolites were below the detection limit. The analysis of organotin compounds in water was carried out according to Carvalho et al. (2007) .
The duration of the experiment was 9 months. Initially, 300 eggs were randomly allocated in 5 L aquaria situated within 30 L aquaria in a semi-static system with 7-hours water renewal with the exposure conditions as explained before. The number of eggs was selected considering 80% rate of viability . At 15 dpf, larva fish were placed in the 30 L aquaria. Throughout the experiment, larvae fish were given the same food as their parents but adjusted according to fish development, number and size. At 40 dpf the fish density was reduced to 100 fish/aquaria and at 60 dpf to 25 fish/aquaria. The handling of fish was kept to a minimum to avoid suffering and distress and their health was monitored closely twice on a daily basis by examining spinal deformities and body wasting. Throughout the experimental period the temperature was checked daily (28 ± 1°C of temperature) and the water physicochemical parameters weekly (pH 7.7 ± 0.2; 6 ± 1 mg/L of dissolved oxygen; 376 μS/cm of conductivity; 0.08 ± 0.06 mg/L of ammonium and 0.01 ± 0.01 mg/L of nitrite). During the initial developmental period, unhatched eggs/dead larvae were detected by their opaque appearance and lack of movement and were immediately removed. Mortality was higher during the metamorphosis stage (approx. 10–18 dpf), when larvae are most vulnerable as the yolk sac is gradually depleted and the larvae must adapt to exogenous feeding. After 24 dpf mortality was practically zero and fish did not demonstrate signs of poor health. At 60 dpf the overall mortality rate along the exposure groups was between 34 and 41% (S2 Table), which is within the normal range observed in previous studies [31, 51].
At the end of the experiment, 15 male and female zebrafish were randomly selected from each of the duplicate exposure conditions and sacrificed with anaesthetic overdose using 300 mg/L 3-amino-benzoic acid ethyl ester (MS-222) to guarantee minimum pain and alleviation from discomfort, according to Annex IV of the EU Directive 2010/63/EU. After recording the morphological parameters, the liver and brain tissues of individual zebrafish were dissected and placed either in RNAlater for RNA extraction or, in the case of liver samples designated for triglyceride content analysis, at -80°C. All samples were assessed in a random order. To confirm the uptake and accumulation of TBT in fish, the remaining liver samples were processed for TBT and its degradation products dibutyltin (DBT) and monobutyltin (MBT), following lyophilisation, as described in Carvalho et al. (2007)  (S1 Appendix).
RNA purification and cDNA synthesis
Total RNA was purified from either 5 mg of liver tissue or whole brain tissue using the illustra RNAspin Mini RNA Isolation Kit (GE Healthcare) and quantification was performed using the Quant-iTTM RiboGreen® RNA Reagent and Kit (Invitrogen). RNA quality was verified by electrophoresis in 1% agarose gels. Total cDNA was generated either from 0.5 μg or 0.15 μg of total RNA extracted from the liver or brain tissue, respectively, using the iScriptTM cDNA Synthesis Kit (Bio-Rad). All assays were carried out following the manufacture’s protocol.
Fluorescence-base quantitative (real-time) PCR was used to evaluate gene expression profiles. For each treatment and tissue, the expression of individual target genes was performed with the Mastercycle ep realplex system (Eppendorf). Each sample was amplified in duplicate using 96-well PCR plates in a 10 μL reaction volume containing 2.5 μL of cDNA (1:5 dilution), 2 μL HOT FIREPol Evagreen qPCR Mix Plus (no ROX; Solis BioDyne) and 200 nM of each forward and reverse primer (S3 Table). Primers were designed using the Primer-Blast-NCBI tool and synthesized by STABVIDA (Portugal). In each plate, a ‘‘no template control” was included to determine the specificity of target cDNA amplification. The three-step real-time PCR program consisted of an enzyme activation step at 95°C (10 min), a 40-cycles amplification step of denaturation at 95°C (10 s), annealing at 60–64°C depending on target gene (30 s) and extension at 72°C (30 s), and a melting curve step generated at the end of every run to confirm specificity of the assays. The PCR products were analyzed by agarose gel electrophoresis to confirm the presence of single bands. Reference genes [ribosomal protein l8 (rpl8) for liver samples and β-actin for brain samples] were selected according to their stability across the exposure groups and controls in each tissue, following validation by one-way ANOVA. The PCR efficiency for target genes of interest and the reference genes was determined through a standard curve, using serial dilutions of cDNA pools from each tissue. Only genes with efficiencies between 88–109% were used. The expression of all genes was measured from cDNAs belonging to the same fish, allowing for comparisons among genes in the same individual.
Relative quantification of target genes was performed according to the Pfaffl method . The relative gene expression ratio (R) of a target gene was calculated based on the gene efficiency E and the ∆Ct between the sum of the control group and the unknown sample, and expressed in comparison to the reference gene: R = (Etarget)∆Ct target (∑Control-sample)/ (Eref) ∆Ct reference (∑Control-sample)
Data were then expressed as fold changes of the solvent control group (value of treatment/mean value of solvent control group).
Lipid extraction and triglyceride determination.
Lipids were extracted from the liver tissues of sacrificed animals using a low toxicity solvent protocol, as described by Schwartz and Wolins . Extracts were re-suspended in isopropanol and triglyceride content was measured using Infinity Triglycerides Liquid Stable Reagent (Thermo Scientific), according to manufacture’s protocol. Samples were measured in duplicates and absorbance was determined at 540 nm using a microplate reader (PowerWave 340, Bio-Tek). Triglycerides concentration was calculated against a standard curve generated from triolein standards. The intra-assay variability, calculated by determining the coefficient of variation (CV) for five replicates of a pooled sample was 8.7%.
Fulton’s condition factor (CF) was calculated according to the equation CF = (Body Weight × Length-3) × 100. The hepatosomatic index (HSI) was calculated as (Liver Weight / Body Weight) × 100. Results are mean values ± SEM. Control and solvent control groups were compared using Student’s t-test to verify that there were no significant differences and thereafter the latter was used for comparison against the exposure groups. Normality and homogeneity of variance was confirmed using Shapiro-Wilk and Levene’s tests, respectively.
Thereafter, all data were analyzed by one-way ANOVA followed by Dunnett's post hoc test. P-values of less than or equal to 0.05 were considered statistically significant unless stated otherwise. For morphological parameters and hepatic triglyceride levels, when parametric assumptions were not fulfilled, data was log-transformed. In the case of qPCR gene fold expressions, all data was previously log-transformed (log2) to stabilize the variance. In very few cases, transformed data did not meet the assumptions for parametric testing, thus data were analyzed using a Kruskal-Wallis followed by Mann-Whiney U test with Bonferroni adjustment.
Discrimination of gene expression profiles associated with TBT exposures in males and females was achieved by statistical analysis using Principal Component Analysis (PCA). PCA involves a mathematical procedure that transforms a number of possibly correlated variables into a smaller number of uncorrelated variables called “principal components” (PCs). PCA was applied to the log-transformed ratios (exp/cont) of all genes, within each tissue. Thereafter, we performed one-way ANOVA followed by Dunnett's comparison post hoc test with PCs as dependent variables and exposure groups as independent variables to test which treatments were discriminated significantly within each PC (p<0.05). Statistical analysis was performed using the software package SPSS/Mac version 20 and “R”.
Table 1 shows the mean weight, length, condition factor (CF) and hepatosomatic index (HSI) of zebrafish (Danio rerio), following 9-month chronic waterborne exposure to 10 and 50 ng TBT/L (as Sn). In TBT-exposed fish, the body weight increased significantly only in male fish exposed to 10 ng/L TBT by 10% compared to the control (p = 0.027) and marginally (8%) in male fish exposed to 50 ng/L TBT (p = 0.095). The CF, which could be considered the fish equivalent to the body-mass index in humans, was altered in both exposed males and females but in an opposite manner. Thus, CF showed an 11% increase in males at 10 ng/L (p = 0.001), whereas in females it showed an 11 and 12% decrease at 10 (p = 0.006) and 50 ng/L (p = 0.002) exposure, respectively. Exposed females revealed hepatomegaly as indicated by the increase in the HSI by 33 and 40% at 10 (p = 0.018) and 50 ng/L (p = 0.004) exposure, respectively. No significant differences among treatments were found in fish length.
Hepatic Triglyceride content
Next we examined whether the increase in liver size was due to an increase in triglyceride content. TBT exposure caused a significant increase in the hepatic triglyceride levels in male fish, of approximately 2.2-fold at 10 (p = 0.042) and a marginal increase of 1.8-fold at 50 ng/L (p = 0.086) exposure (Fig 3). Hepatic triglyceride levels also increased in females, however not being significantly different from the control.
The effect of TBT on hepatic triglyceride levels in male and female zebrafish following chronic exposure (9 months) to waterborne 10 and 50 ng/L of TBT (as Sn). Values as mean ± SEM (n = 4). * *p<0.05, *p<0.1 compared to control (one-way ANOVA, followed by Dunnett’s test).
Mammalian studies indicate that TBT exposure induces fat accumulation in vivo through the transcriptional regulation of lipogenic and adipogenic genes [17, 19]. Thus, we next selected to study the effects of TBT exposure on the transcription level of genes involved in adipogenesis [RXRα/a, PPARγ, CCAAT-enhancer-binding protein alpha (C/EBPα) and beta (C/EBPβ), diacylglycerol O-acyltransferase 2 (DGAT2)], lipogenesis [sterol regulatory element-binding protein 1 (SREBP1), carbohydrate-responsive element-binding protein (ChREBP), acetyl- CoA carboxylase alpha (ACCα), fatty acid synthase (FASn), acetyl-CoA oxidase 1 (ACOX1)] and also in glucocorticoid metabolism [11beta-hydroxysteroid dehydrogenase 2 (11β-HSD2) and 3 alpha (11β-HSD3α)], growth and development [insulin-like growth factor-I (IGF-I) and II alpha (IGF-IIα)] (Fig 1) in the liver and the brain of zebrafish.
In the liver, chronic exposure of male and female zebrafish to the low (10 ng/L) TBT concentration up-regulated the expression of PPARγ–the “master” regulator of adipogenesis  -by 34% in males (p = 0.012) and 25% in females (p = 0.039) and IGF-IIα—the regulator of growth and development in vertebrates  -by approximately 3-fold in males (p = 0.025) and 2-fold in females (p = 0.064) (Fig 4A and 4B). Thereafter, males, which had significantly higher hepatic triglyceride levels, showed induced de novo lipogenesis responses as indicated from the up-regulation of SREBP1 (approximately 2- and 4-fold at 10 and 50 ng/L, p = 0.001 and p<0.001, respectively) and FASn transcription (2-fold at 50 ng/L, p = 0.085), two key lipogenic genes that are also highly expressed during adipogenesis . In parallel, at 50 ng/L exposure, 11β-HSD2- the enzyme that deactivates cortisol- was down-regulated by 48% (p = 0.037) . Thereafter, TBT suppressed the mRNA levels of both the adipogenic markers C/EBPβ and DGAT2  in male livers by 43% (p = 0.002 and p<0.001, respectively). The transcription of RXRα/a, the heterodimeric partner of PPARγ, was altered in a gender- and dose-specific manner in the liver, being significantly down-regulated in males at 50 ng/L TBT exposure (by 42%, p = 0.016) and significantly up-regulated in females at 10 ng/L (by 72%, p = 0.043). In the case of females, which exhibited hepatomegaly, we only observed subtle adipogenic responses in the transcription of genes, where apart from RXRα/a, PPARγ and IGF-IIα, the expression of the adipogenic genes C/EBPβ and DGAT2 showed a tendency to increase at the low TBT exposure, however not being statistically significant (p>0.1).
qRT-PCR analysis of selected lipogenic transcription factors and metabolizing enzymes in the liver of (A) male, and (B) female zebrafish following chronic exposure (9 months) to waterborne 10 and 50 ng/L of TBT (as Sn). Values were normalized to rpl8 and expressed as the average fold changes ± SEM (n = 8) of the solvent control group. **p<0.05 and *p<0.1 compared to solvent control (one-way ANOVA, followed by Dunnett’ test).
In the brain, although the transcription of PPARγ remained unchanged following TBT exposure, RXRα/a was significantly down-regulated in both genders at the low TBT exposure (10 ng/L; by 45% in males and 43% in females; p<0.008 and 0.058 respectively) and so did the expression of the adipogenic factor DGAT2 (by 59% in males and 58% in females, p = 0.001 and p = 0.006 respectively; Fig 5A and 5B) as well as C/EBPα but the down-regulation was only significant in males (30%, p = 0.014). Overall in males, responses were dose-specific. The transcription of ChREBP, which controls synergistically with SREBP1 the expression of lipogenic enzymes FASn and ACCα , was marginally down-regulated by 20% at 10 ng/L TBT exposure (p = 0.070), and so did FASn (by 27%, p = 0.069), whereas at 50 ng/L exposure the lipogenic factor SREBP1 was up-regulated significantly by 39% (p = 0.011), and its encoding enzyme FASn showed a tendency to increase without being statistically significant (p = 0.297). At 50 ng/L exposure, DGAT2 was down-regulated by 64% (p<0.001) and so did IGF-IIα (by 45%, p = 0.078). In the brain of females, at 10 ng/L exposure TBT up-regulated the expression of the adipogenic regulating factor EBPβ but down-regulated the expression of ACCα (47%, p = 0.009) and ACOX1 (26%, p = 0.008). At 50 ng/L exposure, TBT up-regulated the cortisone synthesizing enzyme 11β-HSD2 by approximately 2-fold (p = 0.012), whereas 11β-HSD3α, the cortisol synthesizing enzyme, was marginally down-regulated (p = 0.098).
qRT-PCR analysis of selected lipogenic transcription factors and metabolizing enzymes in the brain of (A) male, and (B) female zebrafish following chronic exposure (9 months) to waterborne 10 and 50 ng/L of TBT (as Sn). Values were normalized to β-actin and expressed as the average fold changes ± SEM (n = 7) of the solvent control group. **p<0.05 and *p<0.1 compared to solvent control (one-way ANOVA, followed by Dunnett’s test).
PCA analysis of the gene expression profiles of males and females in the liver or brain.
A PCA analysis was performed on the gene expression data to highlight the differences in the transcription profile of lipogenic transcription factors and energy metabolism enzymes among treatment groups in either liver or brain tissues of male and female zebrafish. For each of the liver and brain gene expression data, 5 components had eigenvalues over Kaiser’s criterion of 1, which explained together 69.7% and 70.4% of the total variance in the data for liver and brain tissue, respectively (S4 and S5 Tables).
In the liver, PC1 and PC2, which explain together 42% of the total variance, discriminated significantly the high TBT exposure group of males from the control, whereas only PC2 discriminated marginally the low TBT exposure group of females, showing an opposite response than males (Fig 6A and 6B; S4 Table). The two clusters of genes that separated the genders along PC2 (SREBP1-FASn-ACCα and RXRα/a-C/EBPβ-DGAT2) are in agreement with adipocyte studies showing that SREBP1 regulates the transcription of FASn and ACCα , and C/EBPβ of DGAT2 .
PCA applied to the gene expression data of the lipogenic transcription factors and metabolizing enzymes in the liver of male and female zebrafish exposed to waterborne 10 and 50 ng/L of TBT (as Sn) for 9 months. Data are presented against PC1 and PC2 as (A) a loading plot of the 14 studied genes and (B) a scores’ plot of each treatment group of males and females separately.
In the brain, even though the changes in the expression of the some genes were less evident, PCA analysis revealed that the transcriptional profile was very similar between sexes. Thus, PC1 and PC2, which explained together 43.3% of the total variance, separated significantly the low TBT exposure group and the high TBT exposure group from the control group, respectively, in both genders (Fig 7A and 7B; S5 Table). Here, the low TBT exposure groups showed a negative significant correlation with PC1 and thus with RXRα/a, DGAT2, FASn, C/EBPα, ACOX1, ACCα, SREBP1 and ChREBP, whereas the high TBT exposure groups showed a negative significant correlation with PC2 and consequently with PPARγ, C/EBPβ, IGF-II, 11β-HSD3α and C/EBPα and a positive correlation with SREBP1, FASn and 11β-HSD2 (Fig 7A and 7B; S5 Table).
PCA applied to the gene expression data of the lipogenic transcription factors and metabolizing enzymes in the brain of male and female zebrafish exposed to waterborne 10 and 50 ng/L of TBT (as Sn) for 9 months. Data are presented against PC1 and PC2 as (A) a loadings plot of the 14 studied genes and (B) a scores’ plot of each treatment group of males and females separately.
The lipid metabolism as a target of EDCs is a recent field in endocrine disruption research. Studies on mammalian species demonstrate that specific contaminants induce fat accumulation, particularly when exposure takes place during sensitive life-time windows, such as embryogenesis and the early stages of development [1, 2, 6]. Fish are exposed to EDCs in their natural environment throughout their life-cycle and although several lipid regulatory mechanisms are conserved between fish and mammals [32, 33], there are very few studies on the interaction of these compounds with fish lipogenesis. In this context, the present work demonstrates that the mammalian “obesogen” TBT -reported to increase adipose mass and induce NAFLD in mammals through the activation of PPARγ and RXR [17–19]- perturbs the energy reserves and transcriptional regulation of lipid metabolism in the model teleost zebrafish following chronic exposure to very low and environmentally relevant concentrations. This is of concern, taking into account that lipids have a fundamental role in metabolism, growth, reproduction and migration of fish . Therefore, any alterations on their homeostasis may result in adverse effects at individual and population level.
Exposure of zebrafish to TBT since the pre-hatch stage revealed sex-dependent differences on the somatic energy reserves of fish when adults: an increase in body weight and condition factor in males and suppressed condition factor in females. There is very limited information on the effects of TBT on the weight control mechanisms in fish. Recently, Meador and colleagues  found an increase in the body weight of juvenile salmon (Oncorhynchus tshawytscha) fed with low-doses of TBT (0.4–3.5 ng/g fish/day) for 62 days, whereas fish that received the highest TBT dose (458 ng/g fish/day) showed reduced body weight. In a different study, dietary exposure of genetically female flounder (Paralichthys olivaceus) for 65 dpf to 0.1 and 1 μg TBT/g ad libitum, daily, resulted in reduced body weight, total length and consequently condition factor . Differences in body weight between genders following exposure to TBT have been observed in mammalian studies, where reduced body weight in female rats , body weight gain in male mice [18, 19], dose-relevant alterations in body weight of male mice , or no alterations at all  have been reported. These results, in combination with those of the present study, show that TBT alters the overall weight and somatic energy reserves in vertebrates, in a species-, dose- and gender-dependent manner.
Exposure to TBT lead to an increase in HSI and hepatic triglyceride levels, with exposed males showing significant triglyceride accumulation and females of hepatomegaly, which suggest hepatic metabolic dysfunction. We also noticed an increased adipose mass in zebrafish viscera (S1 Fig). Similar to our results, an increase in lipid-containing vacuoles in fish hepatocytes following exposure to TBT has been reported before, but in fish that were exposed during adulthood either to higher TBT concentrations  or for a much smaller period of time . The capacity of TBT to induce lipid accumulation in fish is not restricted to the liver. Juvenile Chinook salmon fed TBT for 57 days showed increased whole body total lipids together with triglyceride levels at 150 ng/g exposure  and immature males and females of rockfish exposed to 100 ng/L TBT (as Sn) for 48 days showed increased total lipids and lipid droplets in the testis  or ovary . These data suggest that the mammalian obesogen TBT promotes lipid accumulation in fish and as the present study shows, even at concentrations as low as 10 ng/L. Hepatomegaly in fish usually indicates the presence of lipid-filled hepatocytes  and in some cases storage of excess glucose in the form of glycogen . Even though glycogen levels were not measured in the present study, the observation that triglycerides levels increased significantly only in males, suggests that the enlargement of female liver may be due to increased glycogen content.
At the molecular level, the metabolic regulation of lipids is controlled by the transcription of factors, which regulate the expression of genes coding for enzymes involved in the lipid synthesis and metabolism . Here we show that the observed TBT-induced somatic and hepatic effects occurred in parallel with significant alterations in the expression levels of transcription factors and enzymes in the liver and the brain, that regulate different pathways of the lipid metabolism (Fig 8A and 8B). The activation of transcription factors leads to gene transcription and synthesis of the corresponding enzymes. Thereafter the transcription of the nuclear receptor itself is controlled by phosphorylation events by specific kinases, which determine its up-regulation or down-regulation . Thus, the observed alterations in the expression of the nuclear receptors in the present study indicate that TBT interacts with these receptors. We also observed a nonlinear dose-response relationship in the expression of most of the selected lipogenic genes in female liver and in the brain of both genders, showing a U- or inverted U-shaped response, where the low TBT exposure appeared more potent than the higher exposure. This is a common pattern in endocrine studies, especially related to nuclear receptor activation during chronic exposure experiments. A low concentration exposure to an endocrine disruptor may result in the activation of a specific receptor and produce an endocrine response. However, at higher doses or prolonged exposure, the receptor gets saturated and no further responses are observed or the receptor may even be down-regulated to achieve homeostasis . At even higher exposure concentrations theses responses may be totally suppressed or compensated, a phenomenon also known as “hormesis” .
Schematic representation summary of genes that were either up- or down-regulated (p<0.1) in males (blue), females (pink), both genders (yellow) or neither (blank) in (A) the liver and (B) the brain of zebrafish following chronic waterborne exposure (9 months) to either 10 or 50 ng/L TBT (as Sn). The connectors indicate the genes that are related.
The effects of such low concentrations of TBT on the transcription of lipid regulating genes in the liver of fish combined with the increased triglyceride levels or hepatomegaly, in males and females respectively, is of concern. In fish, mammalian-like liver dysfunction diseases such as NAFLD and liver steatosis may occur [35, 36], which lead to an increased oxidative damage and cell death . In our study, both TBT exposures caused a significant up-regulation of SREBP1 and FASn genes in the liver of males, who also contained high hepatic triglycerides levels. An up-regulation of the de novo lipogenesis genes SREBP1 and FASn has been observed in the liver of zebrafish larvae, either following exposure to ethanol  or by over-expression of the cannabinoid receptor . This was accompanied by the development of hepatic steatosis and fatty liver, suggesting that TBT exposed male fish in our study experience signs of NAFLD. In the case of severe hepatic metabolic conditions manifested in transgenic zebrafish either by specific expression of Hepatitis virus X protein  or over-expression of the Ying-Yang 1 transcription factor , fish develop hepatic steatosis, fatty liver and hepatocyte inflammation resulting in an increased death rate. In parallel, the transcription of lipogenic factors (e.g. PPARγ, C/EBPα, SREBP1) and enzymes (e.g. FASn, ACCα, DGAT2) in the liver is significantly up-regulated. In female zebrafish of our study, the low TBT exposure (10 ng/L) up-regulated the expression of PPARγ and RXRα/a in the liver, which showed a positive correlation with C/EBPβ and DGAT2 (S4 Table). Although the hepatic lipid accumulation in females was not significant, these gene expression responses indicate signs of adipogenesis stimulation. Moreover, in male fish exposed to 50 ng/L TBT (as Sn), the increase in the up-regulation of the de novo lipogenesis genes SREBP1 and FASn didn’t result in the production of more triglycerides. Interestingly, these adipogenic genes C/EBPβ and DGAT2, as well as RXRα/a, were down-regulated. Overall, transcriptional alterations in the liver reflect hepatic metabolic dysfunction in fish as observed in mammals, and therefore the alterations observed in the present study, although less severe, suggest that fish experience lipid deregulation, which may lead to disease.
The “obesogenic” effects of TBT have been studied in mammals, demonstrating that TBT exposure during prenatal or early postnatal stages causes an increase in adipose mass and liver lipids [17–19]. Similar to our findings, single injections of adult mice with TBT or in utero exposure regulated the transcription of both adipogenic (PPARγ and its target genes) and lipogenic genes (SREBP1, FASn, ACCα, C/EBPα,β) in the liver and bone marrow MSCs  as well as testis and adipose tissue . The results were comparable to the effects of the synthetic RXR ligand AGN195203 and PPARγ ligands troglitazone  or Rosiglitazone (Rosi) . These data, together with the observations that TBT is a high affinity ligand of RXRα and PPARγ [17, 24, 25], it induces adipocyte differentiation in vitro [17, 24, 27, 28] and that TBT-induced effects are blocked by PPARγ antagonists GW9662 or T0070907, totally  or partially  strongly suggest that TBT induces adipogenesis, both in vitro and in vivo through the transcriptional activation of RXR:PPARγ heterodimer.
In fish RXR and PPARγ show a high similarity with the human or mouse orthologues [37, 38]. In the present study, although the protein levels were not quantified, we show that TBT induced an increase in triglyceride levels or hepatomegaly and altered the transcription of RXRα/a, PPARγ and genes downstream the RXR and PPARγ pathways. Our data are in agreement with other studies, showing that TBT may interfere with the expression of RXR and/or PPARs in liver or other tissues of fish [63, 73, 74]. The interaction of TBT with either RXR or PPARγ is an ongoing research. In a recent study, TBT induced lipid accumulation in zebrafish larvae, but failed to activate zebrafish PPARγ in vitro . A different study showed that exposure of zebrafish larvae to either TBT or the PPARγ synthetic ligand Rosi for 24 hours, induced comparable lipid accumulation . Given that the RXR:PPARγ heterodimer is permissive, being activated by both PPARγ and RXR ligands, it may be hypothesized that PPARγ and lipid induction in zebrafish under chronic TBT exposure occurs through RXR .
A novel finding of the current work relates with the perturbation of the transcription profile of key genes involved in lipid homeostasis in the brain of fish following TBT exposure, an observation that has yet to be investigated in mammals. This is of concern since the central nervous system regulates the whole body lipid homeostasis: it acts as an energy sensor by detecting lipid molecules and hormones secreted from other tissues and regulates food intake and expenditure in response . Thus, triglycerides administration in the brain of rats stimulates insulin secretion and down-regulates hepatic glucose production  and induction of obesity-related hormones such as leptin and ghrelin in the brain repress or stimulate, respectively, the transcription of enzymes involved in FA de novo synthesis in the liver and adipose tissue . In relation to the genes studied here, enzymes of the fatty acid synthesis pathway such as FASn and ACC are highly expressed in the brain of rats and their regulation has been attributed to feeding behaviour. Inhibition of FASn or activation of ACCα result in reduced food intake and body weight loss [79, 80]. Fish share several signaling pathways of brain metabolism with mammals . The fish brain uses glucose and ketone bodies as fuels and has the capacity to synthesize and metabolize fatty acids . Moreover, the mammalian appetite regulating factors leptin and ghrelin, are all expressed in adult fish brain [82, 83]. Thus, the observed TBT alterations in the brain transcription profile of zebrafish are signs of a central deregulation of the lipid metabolism. Further studies should focus on the relation of these alterations to the physiological responses at the whole organism level.
Despite the obesogenic effects of TBT, very few studies have examined its interaction with glucocorticoid regulation and IGFs transcription, even though both glucocorticoids and IGF-I induce adipogenic responses and promote preadipocyte maturation . In teleosts, IGF-I and -II play a key role in growth and development  and 11β-HSDs regulate the cortisol levels, the key hormone released during stress response and controls the hypothalamus–pituitary–interrenal axis . Both the IGF system and 11β-HSDs are potential targets of environmental contaminants in fish [84, 85]. Here, the transcription of IGF-IIα and 11β-HSD2s was altered by TBT exposure in either liver or brain of zebrafish, with IGF-IIα being strongly up-regulated in both male and female livers from the low exposure group along with the induced hepatic triglyceride or HSI in males and females, respectively. In females, we hypothesize that the gene expression of 11β-HSDs in the brain at high TBT exposure (50 ng/L) was inversely regulated to suppress cortisol levels. Cortisol in fish activates glucose synthesis and glycogenolysis processes  and therefore, changes in the expression of 11β-HSDs may alter the glycogen reserves. Whether the effects of TBT on 11β-HSDs signalling induced glycogen storage in the liver of females that exhibited hepatomegaly should be further investigated. Moreover, in rainbow trout the IGF-IIα promoter region has C/EBPβ responsive elements  and C/EBPβ regulates 11β-HSD2 transcription in human cell lines . Interestingly, in our study C/EBPβ was correlated with 11β-HSD2 and ΙGF-IIα in fish liver (S4 Table), and with IGF-IIα in fish brain (S5 Table), suggesting that C/EBPβ may be a prime target of TBT. The interplay between TBT-induced changes in IGF-II and 11β-HSD2 signalling and lipid or glycogen accumulation in fish is a subject that requires further research.
The observed gender-specific differences in the transcription profile of zebrafish in the liver are not surprising. Similar to our results, the expression of lipogenic genes in mice showed a clear sexual dimorphism in the liver, which was less evident in the brain . Some modest gender-dependent effects in the transcription of lipogenic genes were also observed in mice exposed to TBT in utero, with females showing stronger signs of the NAFLD-like phenotype than males . Zebrafish also show a sexual dimorphism in the lipogenic hepatic gene transcription profiles . In the present study the regulation of most lipogenic genes in the liver was gender-specific, with males showing stronger lipid synthesis responses (SERBP1 and FASn up-regulation). Gender-specific effects on lipid metabolism were also observed in zebrafish exposed to the endocrine disruptor Perfuorononanoic acid for 3 months; males showed higher hepatic triglyceride levels and up-regulation of hepatic PPARs, C/EBPs and fatty acid binding protein (fabp) mRNA levels, whereas exactly the opposite was true for females . This sexual dimorphism suggests that genders should be evaluated separately, not only when studying EDCs’ effects on reproduction but also on lipid metabolism. The observed sex-dependent alterations do not seem to be related to differential TBT uptake and accumulation in the liver of fish. Analysis of the remaining liver samples for TBT and its break-down products DBT and MBT, showed similar organotin levels between genders (S6 Table). In fact, the liver revealed higher levels of DBT than TBT. The rapid metabolism of TBT in fish liver has been reported before and it’s not observed in the brain or other organs . The differences in the accumulation of organotins between tissues may play a role in the different molecular responses observed in the liver and brain of zebrafish. For example, a recent study revealed that DBT and not TBT acts as a potent antagonist of the glucocorticoid receptor in human cell lines  and suppresses glucocorticoid signaling in zebrafish embryo . Whether the observed differential response of 11β-HSDs expression in the liver and brain of zebrafish in the present study is attributed to the higher levels of DBT in the liver should be further investigated.
Overall, the present study shows that the mammalian obesogen TBT disrupts the lipid metabolism in zebrafish following chronic exposure since the pre-hatched stage to low, environmentally relevant concentrations. The screening of the transcription profile of lipogenic genes revealed that not only the liver but also the brain is affected, a previously unidentified target of this compound. Further, we found a sexual dimorphism mainly in the morphological parameters and hepatic gene profile, which indicates that the effects of such chemicals should be studied in a gender-specific manner. Considering lipid metabolism similarities between fish and mammals and the disruption of energy balance mechanisms by TBT, future studies should investigate the lipid metabolism of fish as a target of environmental contaminants. Furthermore, the use of fish models to unravel the mechanisms underlying metabolic disorders should become a promising and informative approach.
S1 Appendix. Quantification of organotins in zebrafish liver.
S1 Table. TBT concentration in the water.
Evaluation of the concentration of Tributyltin (TBT), Dibutyltin (DBT) and Monobutyltin (MBT) in the water from the 50 ng/L TBT (as Sn) exposure tanks at 20 days post fertilization. The aquaria were dosed twice daily (at 0 and 8 hours).
S2 Table. Zebrafish mortality.
Mortality rate in zebrafish exposed to TBT (as Sn) at 60 days post fertilization (dpf).
S3 Table. Primer pair sequences used for RT-qPCR analysis.
S4 Table. Principal Component Analysis of the liver gene expression profile in TBT-exposed zebrafish.
S5 Table. Principal Component Analysis of the brain gene expression profile in TBT-exposed zebrafish.
This work was supported by Fundação para a Ciência e a Tecnologia (Portugal), through project PTDC/MAR/115199/2009, the European Regional Development Fund (ERDF) through the COMPETE—Operational Competitiveness Programme and national funds through FCT–Fundação para a Ciência e a Tecnologia, under the project “PEst-C/MAR/LA0015/2013” and pos-doctoral fellowship SFRH/BPD/74231/2010. The authors declare they have no actual or potential competing financial interests.
Conceived and designed the experiments: AL JS LFCC MMS. Performed the experiments: AL AA DL JS. Analyzed the data: AL JGS LG MMS. Contributed reagents/materials/analysis tools: AL JGS CMRA CT. Wrote the paper: AL LFCC MMS.
- 1. Newbold RR, Padilla-Banks E, Jefferson WN, Heindel JJ. Effects of endocrine disruptors on obesity. Int J Androl. 2008;31:201–8. pmid:18315718
- 2. Grun F, Blumberg B. Endocrine disrupters as obesogens. Mol Cell Endocrinol. 2009;304(1–2):19–29. pmid:19433244
- 3. Jobling S, Reynolds T, White R, Parker MG, Sumpter JP. A variety of environmentally persistent chemicals, including some phthalate plasticizers are weakly estrogenic. Environ Health Perspect. 1995;103:582–7. pmid:7556011
- 4. Matthiessen P, Gibbs PE. Critical appraisal for the evidence for tributyltin-mediated endocrine disruption in mollusks. Environ Toxicol Chem. 1998;17:37–43.
- 5. Welshons WV, Nagel SC, vom Saal FS. Large effects from small exposures. III. Endocrine mechanisms mediating effects of bisphenol A at levels of Human exposure. Endocrinology. 2006;147:S56–S69. pmid:16690810
- 6. Janesick A, Blumberg B. Endocrine disrupting chemicals and the developmental programming of adipogenesis and obesity. Birth Defects Res C Embryo Today. 2011;93(1):34–50. pmid:21425440
- 7. Fent K. Ecotoxicology of organotin compounds. Crit Rev Toxicol. 1996;26:1–117. pmid:8833456
- 8. Antizar-Ladislao B. Environmental levels, toxicity and human exposure to tributyltin (TBT)-contaminated marine environment. A review. Environ Int. 2008;34(2):292–308. pmid:17959247
- 9. Sousa A, Laranjeiro F, Takahashi S, Tanabe S, Barroso CM. Imposex and organotin prevalence in a European post-legislative scenario: temporal trends from 2003 to 2008. Chemosphere. 2009;77:566–73. pmid:19656548
- 10. Radke B, Wasik A, Jewell LL, Paczek U, Namiesnik J. The Speciation of Organotin Compounds in Sediment and Water Samples from the Port of Gdynia. Soil Sediment Contam. 2013;22(6):614–30.
- 11. Briant N, Bancon-Montigny C, Elbaz-Poulichet F, Freydier R, Delpoux S, Cossa D. Trace elements in the sediments of a large Mediterranean marina (Port Camargue, France): levels and contamination history. Mar Pollut Bull. 2013;73(1):78–85. pmid:23790459
- 12. Morcillo Y, Porte C. Monitoring of organotin compounds and their effects in marine molluscs. Trac-Trend Anal Chem. 1998;17(2):109–16.
- 13. Titley-O'Neal CP, Munkittrick KR, MacDonald BA. The effects of organotin on female gastropods. J Environ Monitor. 2011;13(9):2360–88.
- 14. McAllister BG, Kime DE. Early life exposure to environmental levels of the aromatase inhibitor tributyltin causes masculinisation and irreversible sperm damage in zebrafish (Danio rerio). Aquat Toxicol. 2003;65:309–16. pmid:13678849
- 15. McGinnis CL, Crivello JF. Elucidating the mechanism of action of tributyltin (TBT) in zebrafish. Aquat Toxicol. 2011;103:25–31. pmid:21388611
- 16. Fent K, Stegeman JJ. Effects of Tributyltin Invivo on Hepatic Cytochrome-P450 Forms in Marine Fish. Aquat Toxicol. 1993;24(3–4):219–40.
- 17. Grün F, Watanabe H, Zamanian Z, Maeda L, Arima K, Cubacha R, et al. Endocrine-disrupting organotin compounds are potent inducers of adipogenesis in vertebrates. Mol Endocrinol. 2006;20:2141–55. pmid:16613991
- 18. Zuo Z, Chen S, Wu T, Zhang J, Su Y, Chen Y, et al. Tributyltin causes obesity and hepatic steatosis in male mice. Environ Tox. 2009;26(1):79–85.
- 19. Chamorro-Garcia R, Sahu M, Abbey RJ, Laude J, Pham N, Blumberg B. Transgenerational inheritance of increased fat depot size, stem cell reprogramming, and hepatic steatosis elicited by prenatal exposure to the obesogen tributyltin in mice. Environ Health Perspect. 2013;121:359–66. pmid:23322813
- 20. Smith BS. Sexuality in the American mud snail, Nassarius obsoletus. Proceedings of the Malacological Society of London. 1971;39:377–8.
- 21. Nishikawa J, Mamiya S, Kanayama T, Nishikawa T, Shiraishi F, Horiguchi T. Involvement of the retinoid X receptor in the development of imposex caused by organotin gastropods. Environ Sci Technol. 2004;38:6271–6. pmid:15597881
- 22. Castro LF, Lima D, Machado A, Melo C, Hiromori Y, Nishikawa J, et al. Imposex induction is mediated through the Retinoid X Receptor signalling pathway in the neogastropod Nucella lapillus. Aquat Toxicol.
- 23. Lima D, Reis-Henriques MA, Silva R, Santos AI, Castro LFC, Santos MM. Tributyltin-induced imposex in marine gastropods involves tissue-specific modulation of the retinoid X receptor. Aquat Toxicol. 2011;101(1):221–7 pmid:21036407
- 24. Kanayama T, Kobayashi N, Mamiya S, Nakanishi T, Nishikawa J. Organotin Compounds Promote Adipocyte Differentiation as Agonists of the Peroxisome Proliferator-Activated Receptor γ/Retinoid X Receptor Pathway. Mol Pharmacol. 2005;67:766–74. pmid:15611480
- 25. le Maire A, Grimaldi M, Roecklin D, Dagnino S, Vivat-Hannah V, Balaguer P, et al. Activation of RXR-PPAR heterodimers by organotin environmental endocrine disruptors. EMBO reports. 2009;10(4):367–73. pmid:19270714
- 26. Tontonoz P, Spiegelman BM. Fat and Beyond: The Diverse Biology of PPARγ. Annu Rev Biochem. 2008;77:289–312. pmid:18518822
- 27. Kirchner S, Kieu T, Chow C, Casey S, Blumberg B. Prenatal Exposure to the Environmental Obesogen Tributyltin Predisposes Multipotent Stem Cells to Become Adipocytes. Mol Endocrinol. 2010;24:526–39. pmid:20160124
- 28. Yanik SC, Baker AH, Mann KK, Schlezinger JJ. Organotins Are Potent Activators of PPAR gamma and Adipocyte Differentiation in Bone Marrow Multipotent Mesenchymal Stromal Cells. Toxicol Sci. 2011;122(2):476–88. pmid:21622945
- 29. Santos MM, Reis-Henriques MA, Castro LFC. Lipid Homeostasis Perturbation by Organotins: Effects on Vertebrates and Invertebrates. In: Pagliarani A, Trombetti F, Ventrella V, editors. Biochemical and Physiological Effects of Organotins. 1: Bentham Science Publishers; 2012. p. 83–96.
- 30. Lyssimachou A, Jenssen BM, Arukwe A. Brain cytochrome P450 aromatase gene isoforms and activity levels in Atlantic salmon after waterborne exposure to nominal environmental concentrations of the pharmaceutical ethynylestradiol and antifoulant tributyltin. Toxicol Sci. 2006;91:82–92. pmid:16484284
- 31. Santos MM, Micael J, Carvalho AP, Morabito R, Booy P, Massanisso P, et al. Estrogens counteract the masculinizing effect of tributyltin in zebrafish. Comp Biochem Physiol C Toxicol Pharmacol 2006;142:151–5. pmid:16406357
- 32. Oka T, Nishimura Y, Zang L, Hirano M, Shimada Y, Wang Z, et al. Diet-induced obesity in zebrafish shares common pathophysiological pathways with mammalian obesity. BMC Physiol. 2010;10:21. pmid:20961460
- 33. Carmona-Antonanzas G, Tocher DR, Martinez-Rubio L, Leaver MJ. Conservation of lipid metabolic gene transcriptional regulatory networks in fish and mammals. Gene. 2013;534:1–9. pmid:24177230
- 34. Amali AA, Rekha RD, Lin CJF, Wang WL, Gong HY, Her GM, et al. Thioacetamide induced liver damage in zebrafish embryo as a disease model for steatohepatitis. J Biomed Sci. 2006;13(2):225–32. pmid:16456712
- 35. Shieh YS, Chang YS, Hong JR, Chen LJ, Jou LK, Hsu CC, et al. Increase of hepatic fat accumulation by liver specific expression of Hepatitis B virus X protein in zebrafish. Biochim Biophys Acta 2010;1801:721–30. pmid:20416398
- 36. Her GM, Pai WY, Lai CY, Hsieh YW, Pang HW. Ubiquitous transcription factor YY1 promotes zebrafish liver steatosis and lipotoxicity by inhibiting CHOP-10 expression. Biochim Biophys Acta. 2013;1831(6):1037–51. pmid:23416188
- 37. Ibabe A, Bilbao E, Cajaraville MP. Expression of peroxisome proliferator activated receptors in zebrafish (Danio rerio) depending on gender and developmental stage. Histochem Cell Biol. 2005;123:75–87. pmid:15616845
- 38. Tallafuss A, Hale LA, Yan Y- L, Dudley L, Eisen JS, Postlethwait JH. Characterization of retinoid-X receptor genes rxra, rxrba, rxrbb and rxrg during zebrafish development. Gene Expr Patterns. 2006;6:556–65. pmid:16448862
- 39. Oberemm A. The use of a refined zebrafish embryo bioassay for the assessment of aquatic toxicity. Lab Animal. 2000;29(7):32–40.
- 40. Balazs Z, Schweizer RAS, Frey FJ, Rohner-Jeanrenaud F, Odermattt A. DHEA induces 11 beta-HSD2 by acting on CCAAT/enhancer-binding proteins. J Am Soc Nephrol. 2008;19(1):92–101. pmid:18032797
- 41. Moreno-Navarrete J, Fernández-Real J. Adipocyte Differentiation. In: Symonds ME, editor. Adipose Tissue Biology: Springer New York; 2012. p. 17–38.
- 42. Lo JH, Chen TT. CCAAT/Enhancer Binding Protein 2 Is Involved in Growth Hormone-Regulated Insulin-Like Growth Factor-II Gene Expression in the Liver of Rainbow Trout (Oncorhynchus mykiss). Endocrinology. 2010;151(5):2128–39. pmid:20228168
- 43. Dentin R, Girard J, Postic C. Carbohydrate responsive element binding protein (ChREBP) and sterol regulatory element binding protein-1c (SREBP-1c): two key regulators of glucose metabolism and lipid synthesis in liver. Biochimie. 2005;87(1):81–6. pmid:15733741
- 44. Kim JB, Spiegelman BM. ADD1/SREBP1 promotes adipocyte differentiation and gene expression linked to fatty acid metabolism. Genes Dev. 1996;10(9):1096–107. pmid:8654925
- 45. Reddy JK, Hashimoto T. Peroxisomal beta-oxidation and peroxisome proliferator-activated receptor alpha: an adaptive metabolic system. Annu Rev Nutr. 2001;21:193–230. pmid:11375435
- 46. Payne VA, Au WS, Gray SL, Nora ED, Rahman SM, Sanders R, et al. Sequential regulation of diacylglycerol acyltransferase 2 expression by CAAT/Enhancer-binding protein ss(C/EBP ss) and C/EBP alpha during adipogenesis. J Biol Chem. 2007;282:21005–14 pmid:17504763
- 47. Fabbrini E, Sullivan S, Klein S. Obesity and Nonalcoholic Fatty Liver Disease: Biochemical, Metabolic, and Clinical Implications. Hepatology. 2010;51(2):679–89. pmid:20041406
- 48. Luquet S, Magnan C. The central nervous system at the core of the regulation of energy homeostasis. Front Biosci. 2009;S1:448–65.
- 49. Frayn KN, Arner P, Yki-Järvinen . Fatty acid metabolism in adipose tissue, muscle and liver in health and disease. Essays in biochem. 2005;42:89–103.
- 50. Carvalho PN, Pinto LF, Basto MCP, Vasconcelos ATSD. Headspace solid-phase micro-extraction and gas chromatography-ion trap tandem mass spectrometry method for butyltin analysis in sediments: Optimization and validation. Microchem J. 2007;87(2):147–53.
- 51. Carvalho AP, Araújo L, Santos MM. Rearing zebrafish (Danio rerio) larvae without live food: evaluation of a commercial, a practical and a purified starter diet on larval performance. Aquac Res. 2006;37:1107–11.
- 52. Pfaffl MW. Quantification Strategies in real-time PCR. In: Bustin SA, editor. The Real-Time PCR Encyclopedia A–Z of Quantitative PCR. La Jolla, CA, USA: International University Line (IUL); 2004. p. 87–120.
- 53. Schwartz DM, Wolins N. A simple and rapid method to assay triacylglycerol in cells and tissues. J Lip Res. 2007;48:2514–20.
- 54. Wood AW, Duan C, Bern HA. Insulin-like growth factor signaling in fish. International review of cytology. 2005;243:215–85. pmid:15797461
- 55. Alsop D, Vijayan MM. Development of the corticosteroid stress axis and receptor expression in zebrafish. Am J Physiol Regul Integr Comp Physiol. 2008;294(3):R711–9. pmid:18077507
- 56. Tocher DR. Metabolism and functions of lipids and fatty acids in teleost fish. Rev Fish Sci. 2003;11:107–84.
- 57. Meador JP, Sommers FC, Cooper KA, Yanagida G. Tributyltin and the obesogen metabolic syndrome in a salmonid. Environ Res 2011;111:50–6. pmid:21167482
- 58. Shimasaki Y, Kitano T, Oshima Y, Inoue S, Imada N, Honjo T. Trinutyltin causes masculinization in fish. Environ Toxicol Chem. 2003;22:141–4. pmid:12503757
- 59. Cooke GM, Forsyth DS, Bondy GS, Tachon R, Tague B, Coady L. Organotin speciation and tissue distribution in rat dams, fetuses, and neonates following oral administration of tributyltin chloride. J Toxicol Env Heal A. 2008;71(6):384–95.
- 60. Si J, Wu X, Wan C, Zeng T, Zhang M, Xie K, et al. Peripubertal exposure to low doses of tributyltin chloride affects the homeostasis of serum T, E2, LH, and body weight of male mice. Environ Toxicol 2011;26:307–14. pmid:20052771
- 61. Holm G, Norrgren L, Lindén O. Holm G, Norrgren L, Lindén O. Reproductive and histopathological effects of long-term experimental exposure to bis(tributyltin)oxide (TBTO) on the three-spined stickleback, Gasterosteus aculeatus Linnaeus. J Fish Biol 1991;38:373–86.
- 62. Oliveira Ribeiro CA, Schatzmann M, Silva de Assis HC, Silva PH, Pelletier E, Akaishi FM. Evaluation of Tributyltin Subchronic Efects in Tropical Freshwater Fish (Astyanax bimaculatus, Linnaeus,1758). Ecotoxicol Environ Saf. 2002;51:161–7. pmid:11971636
- 63. Zhang J, Zuo Z, He C, Cai J, Wang Y, Chen Y, et al. Effect of tributyltin on testicular development in Sebastiscus marmoratus and the mechanism involved. Environl Toxicol Chem. 2009;28:1528–35.
- 64. Zhang J, Zuo Z, Xiong J, Sun P, Chen Y, Wang C. Tributyltin exposure causes lipotoxicity responses in the ovaries of rockfish, Sebastiscus marmoratus. Chemosphere. 2013;90:1294–9. pmid:23153777
- 65. Passeri MJ, Cinaroglu A, Gao C, Sadler KC. Hepatic steatosis in response to acute alcohol exposure in zebrafish requires sterol regulatory element binding protein activation. Hepatology 2009;49:443–52. pmid:19127516
- 66. Enes P, Panserat S, Kaushik S, Oliva-Teles A. Hepatic glucokinase and glucose-6-phosphatase responses to dietary glucose and starch in gilthead sea bream (Sparus aurata) juveniles reared at two temperatures. Comp Biochem Physiol A Mol Integr Physiol. 2008;149(1): 80–6. pmid:18023221
- 67. Desvergne B, Michalik L, Wahli W. Transcriptional regulation of metabolism. Physiol Rev. 2006;86(2):465–514. pmid:16601267
- 68. Rochette-Egly C. Nuclear receptors: integration of multiple signalling pathways through phosphorylation. Cell Signal. 2003;15:355–66. pmid:12618210
- 69. Vandenberg LN, Colborn T, Hayes TB, Heindel JJ, Jacobs DR Jr., Lee DH, et al. Hormones and endocrine-disrupting chemicals: low-dose effects and nonmonotonic dose responses. Endocr Rev. 2012;33(3):378–455. pmid:22419778
- 70. Calabrese EJ. Toxicological awakenings: the rebirth of hormesis as a central pillar of toxicology. Toxicol Appl Pharmacol. 2005;204:1–8. pmid:15781288
- 71. Malhi H, Gores GJ. Molecular mechanisms of lipotoxicity in nonalcoholic fatty liver disease. Semin Liver Dis. 2008;28:360–9. pmid:18956292
- 72. Pai WY, Hsu CC, Lai CY, Chang TZ, Tsai YL, Her GM. Cannabinoid receptor 1 promotes hepatic lipid accumulation and lipotoxicity through the induction of SREBP-1c expression in zebrafish. Transgenic Res. 2013;22(4):823–38. pmid:23315130
- 73. Zhang J, Zuo Z, Zhu W, Sun P, Wang C. Sex-different effects of tributyltin on brain aromatase, estrogen receptor and retinoid X receptor gene expression in rockfish (Sebastiscus marmoratus). Mar Environ Res. 2013;90:113–8. pmid:23850073
- 74. Pavlikova N, Kortner TM, Arukwe A. Peroxisome proliferator-activated receptors, estrogenic responses and biotransformation system in the liver of salmon exposed to tributyltin and second messenger activator. Aquat Toxicol. 2010;99:176–85. pmid:20466441
- 75. Riu A, McCollum CW, Pinto CL, Glimaldi M, Hillenweck A, Perdu E, et al. Halogenated Bisphenol-A Analogs Act as Obesogens in Zebrafish Larvae (Danio rerio).
- 76. Tingaud-Sequeira A, Ouadah N, Babin PJ. Zebrafish obesogenic test: a tool for screening molecules that target adiposity. J Lipid Res. 2011;52:1765–72. pmid:21724975
- 77. Clement L, Cruciani-Guglielmacci C, Magnan C, Vincent M, Douared L, Orosco M, et al. Intracerebroventricular infusion of a triglyceride emulsion leads to both altered insulin secretion and hepatic glucose production in rats. Pflug Arch Eur J Phy.
- 78. Nogueiras R, Wilson H, Rohner-Jeanrenaud F, Tschop MH. Central nervous system regulation of adipocyte metabolism. Regul Pept. 2008;149:26–31. pmid:18453013
- 79. Gao S, Lane MD. Effect of the anorectic fatty acid synthase inhibitor C75 on neuronal activity in the hypothalamus and brainstem. Proc Natl Acad Sci USA. 2003;100:5628–33. pmid:12724522
- 80. Gao S, Kinzig KP, Aja S, Scott KA, Keung W, Kelly S, et al. Leptin activates hypothalamic acetyl-CoA carboxylase to inhibit food intake. Proc Natl Acad Sci USA. 2007;104(44):17358–63. pmid:17956983
- 81. Soengas JL, Aldegunde M. Energy metabolism of fish brain. Comp Biochem Physiol B Mol Biol. 2002;131:271–96.
- 82. Cruz SA, Tseng YC, Kaiya H, Hwang PP. Ghrelin affects carbohydrate-glycogen metabolism via insulin inhibition and glucagon stimulation in the zebrafish (Danio rerio) brain. Comp Biochem Physiol A Mol Integr Physiol. 2010;156(2):190–200. pmid:20138234
- 83. Liu Q, Chen Y, Copeland D, Ball H, Duff RJ, Rockich B, et al. Expression of leptin receptor gene in developing and adult zebrafish. Gen Comp Endocrinol. 2010;166:346–55. pmid:19941865
- 84. Hanson AM, Kittilson JD, McCormick SD, Sheridan MA. Effects of 17 beta-estradiol, 4-nonylphenol, and beta-sitosterol on the growth hormone-insulin-like growth factor system and seawater adaptation of rainbow trout (Oncorhynchus mykiss). Aquaculture. 2012;362:241–7
- 85. Ribeiro C, Urbatzka R, Castro LFC, Carrola J, Fontainhas-Fernandes A, Monteiro RAF, et al. In vitro exposure of Nile tilapia (Oreochromis niloticus) testis to estrogenic endocrine disrupting chemicals: mRNA expression of genes encoding steroidogenic enzymes. Toxicol Mech Method. 2012;22:47–53.
- 86. Porchas MM, Cordova MLF, Enriquez RR. Cortisol and glucose; reliable indicators of fish stress? Pan- Am JAq Sci. 2009;4(2):58–178.
- 87. Yang X, Schadt EE, Wang S, Wang H, Arnold AP, Ingram-Drake L, et al. Tissue-specific expression and regulation of sexually dimorphic genes in mice. Genome Res. 2006;16:995–1004. pmid:16825664
- 88. Zheng W, Xu H, Lam SH, Luo H, Karuturi RJM, Gong Z. Transcriptomic Analyses of Sexual Dimorphism of the Zebrafish Liver and the Effect of Sex Hormones. PLoS ONE. 2013;8:e53562. pmid:23349717
- 89. Zhang W, Zhang Y, Zhang H, Wang J, Cui R, Dai J. Sex differences in transcriptional expression of FABPs in zebrafish liver after chronic Perfuorononanoic Acid exposure. Environ Sci Technol. 2012;46:5175–82. pmid:22500729
- 90. Shimasaki Y, Oshima Y, Inoue N, Shibata K, Nakajima K, Inoue S, et al. Distribution of Tributyltin in Tissues of Mature Japanese Whiting, Sillago japonica and Their Eggs. J Fac Agr Kyushu. 2008;53(1):67–72.
- 91. Gumy C, Chandsawangbhuwana C, Dzyakanchuk AA, Kratschmar DV, Baker ME, Odermatt A. Dibutyltin Disrupts Glucocorticoid Receptor Function and Impairs Glucocorticoid-Induced Suppression of Cytokine Production. PLoS One. 2008;3(10):e3545. pmid:18958157
- 92. Weger BD, Weger M, Nusser M, Brenner-Weiss G, Dickmeis T. A chemical screening system for glucocorticoid stress hormone signaling in an intact vertebrate. ACS Chem Biol. 2012;7(7):1178–83. pmid:22545806