Expression of Concern
After this article [1] was published, concerns were raised about western blot results. Specifically,
- Fig 1D, AKT blot: Similarities were noted between data shown in lanes 7 and 9, between lanes 1 and 3, and between lanes 2 and 6 (flipped horizontally).
- Fig 4F: There appear to be vertical discontinuities between lanes 1/2 and lanes 2/3 of each western blot panel.
- Figs 1C, 1D, 1I, 4B, 4D, 4F and 4G: The image quality and/or brightness-contrast levels in the western blot panels do not allow a clear assessment as to the integrity or background information within the images as the background signal across each of the blots is quite uniform.
(A), Representative semi-thin liver sections stained with toluidine blue from N, L and F rats showing the presence and the relative abundance of lipid droplets in HF-fed rats. (B), Immunohistochemical reaction and (C), immunoblot for PPARα. The intensities of the bands were normalised to that of β-actin. (D), Basal and insulin-induced AKT phosphorylation. N, L, F = sham; and Ni, Li, Fi = insulin-injected. (E) and (F), Kinetics of basal and palmitate-induced proton leaks in isolated liver mitochondria. (G) and (H), Respiration rates measured by interpolation at 170 mV or 129 mV for basal and palmitate-induced proton leaks, respectively. Data are means ± SE for 8 rats in each group. *P<0.05 vs. N rats. #P<0.05 vs. L rats. (I), Immunoblot for UCP2. Thin immunoreactive bands were evident only for F groups. The intensities of the bands were normalised to that of Cox IV.
(A), Immunohistochemical reaction and (B), immunoblot for Mfn2. (C), Immunohistochemical reaction and (D), immunoblot for OPA1. (E), Immunohistochemical reaction and (F), immunoblot for Drp1. (G), Immunoblot for Fis1. (B), (D), (F) and (G), Densitometric analysis data shown as means ± SE. *P<0.05 vs. N rats. #P<0.05 vs. L rats. For all immunoblots, representative blots are shown for each protein of interest. The intensities of the bands were normalised to that of Cox IV.
The corresponding author stated that the original data underlying results reported in this article are no longer available.
The corresponding author further explained that densitometric analysis was performed on scans of the original western blot films/plates, after which representative blot images were selected for the figures. In preparing figures, images were adjusted for brightness/contrast, and in some cases image fragments were rotated or re-ordered to present bands at a consistent orientation and layout across the panel. The corresponding author stated that all data in each panel originated from the same blot, and adjustments to brightness and contrast were applied to all data consistently in the assembled figures.
In regard to the concerns in Fig 1D, the corresponding author confirmed there are similarities across lanes in the AKT panel, but asserted that the data in the indicated lanes are different. Without the original blot image this issue remains unresolved. The corresponding author provides here another version of Fig 1 that includes more background area for the western blot panels in Fig 1C and 1D compared to the published version, and in which image splicing in panel D is visible. The corresponding author stated that image splicing occurred between lanes 3 and 4 and between lanes 6 and 7 in the AKT blot shown in panel D to present samples in an order matching the presentation in other figures. The corresponding author also provided replication data in support of Fig 1D (S1 and S2 Files). A member of PLOS ONE’s Editorial Board assessed S1 and S2 and stated that the methods are appropriate and the data support the findings of Fig 1D.
The corresponding author provides here an alternative version of Fig 4 which they stated includes all experimental lanes from the original blots without splicing, rearrangement or brightness/contrast adjustments. Although only cropped images are available, the blots presented in this alternative version clarify where lanes were rearranged in preparing the published versions of Fig 4D, 4F and 4G.
The corresponding author provides results of real-time quantitative PCR (RT-qPCR) for UCP2 mRNA (S3 and S4 Files) to support the results of the western blot for UCP2 protein levels in Fig 1I. The author stated that the mRNA used for RT-qPCR was collected under the same experimental conditions as those described in Fig 1I. The corresponding author acknowledges Vincenzo Migliaccio (Department of Chemistry and Biology “Adolfo Zambelli”, University of Salerno, Italy) who is not a listed author on [1] for generating these data. A member of PLOS ONE’s Editorial Board assessed S3 and S4, and stated that assessment of mRNA expression by RT-qPCR are not sufficient to reproduce the findings shown in the western blot in Fig 1I as a change in mRNA expression does not necessarily correspond to a change in protein expression.
In light of the unresolved concerns in Fig 1D and the unavailability of data to support results reported in this article, the PLOS ONE Editors issue this Expression of Concern to notify readers of the above concerns and relay the supporting data and updated figures provided by the corresponding author.
Supporting information
S1 File. Replication of the western blot experiment presented in Fig 1D.
pAKT/AKT western blotting analysis was performed following the protocol for gel electrophoresis and transfer described in [1] and using 12% SDS-PAGE gel. For each sample, 50 μg of proteins from total liver homogenate were loaded, and the following antibodies and conditions were used: AKT, Cell signalling (cat. #9272), rabbit, 1:500 in 5% milk-TBS-Tween (incubation O.N. 4°C); pAKT (S473), Cell signalling (cat. #9271S), rabbit, 1:500 in 2% BSA-TBS-Tween (incubation O.N. 4°C); Anti-rabbit secondary antibody, Santa Cruz (sc-2004), 1:2000 in 5% milk 1X TBS-Tween 1% (incubation 1h, RT). N, treated with the standard laboratory diet; L, treated with the High-Lard diet; F, High-Fish oil diet; Ni, Li and Fi, treated with the previously-mentioned diets and stimulated with insulin.
https://doi.org/10.1371/journal.pone.0265521.s001
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S2 File. Raw data and quantification of western blot data presented in S1 File.
https://doi.org/10.1371/journal.pone.0265521.s002
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S3 File. Real-time quantitative PCR assessment of UCP2 mRNA.
RT-q-PCR for UCP2 was performed using samples from 4 different animals for each experimental group (N, L and F). Total RNA was extracted from liver fragments processed according to the Tri-Reagent (Sigma-Aldrich) protocol. After extraction, 1μg of total RNA was processed with QuantiTect Reverse Transcription Kit (Qiagen) according to the manufacturer’s protocol to remove genomic DNA contamination and for the subsequent cDNA synthesis. The analyses were carried out on an Applied Biosystem 7500 Real-Time PCR System, using SYBR Green method (Life Technologies), following the procedures recommended by the manufacturer. Reactions were performed using forward and reverse primers designed using Primer Express software (Applied Biosystems). Each amplification mixture of 20 μl final volume contained 12 μl of real-time PCR Master Mix, 1 μl each of UCP2 or β-actin forward and reverse primers (10 μM), 2 μl of cDNA diluted 1:1 and 4 μl of nuclease-free water. Amplifications were performed with an initial step at 95°C for 1 min, followed by 40 cycles at 95°C for 15 s and 60°C for 40 s. A melting curve analysis of PCR products was performed from 60°C to 95°C in order to ensure gene specific amplification. UCP2 gene amplification was associated with β-actin as standard control. Changes in the UCP2 gene expression in the different samples were obtained in according to standard 2−ΔΔCt method [2]. UCP2 primer sequences: forward primer, 5’-AGCAGTTCTACACCAAGGGC-3’; reverse primer, 5’-AGAGGTCCCTTTCCAGAGGC-3.’ β-actin primer sequences: forward primer, 5’-ACCCGCCACCAGTTCGCCAT-3’; reverse primer, 5’-CGGCCCACGATGGAGGGGAA -3’. Specificity of UCP2 and B-actin primers was tested with conventional PCR that retrieved a single cDNA fragment of 230 bp and 128bp, respectively. The UCP2 cDNA fragment was also sequenced using automated methods on an ABI PRISM Genetic Analyzer (PE Biosystems). The results showed 100% homology with the Rattus norvegicus UCP2 gene.
https://doi.org/10.1371/journal.pone.0265521.s003
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S4 File. Raw data and quantification of RT-qPCR data presented in S2 File.
https://doi.org/10.1371/journal.pone.0265521.s004
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16 Mar 2022: The PLOS ONE Editors (2022) Expression of Concern: High-Lard and High-Fish-Oil Diets Differ in Their Effects on Function and Dynamic Behaviour of Rat Hepatic Mitochondria. PLOS ONE 17(3): e0265521. https://doi.org/10.1371/journal.pone.0265521 View expression of concern
Figures
Abstract
Background
Mitochondria are dynamic organelles that frequently undergo fission and fusion processes, and imbalances in these processes may be involved in obesity and insulin resistance.
Aims
The present work had the following aims: (a) to evaluate whether the mitochondrial dysfunction present in the hepatic steatosis induced by a high-fat diet is associated with changes in mitochondrial dynamics and morphology; (b) to evaluate whether effects on the above parameters differ between high-lard and high-fish-oil diets, as it has been suggested that fish oil may have anti-obesity and anti-steatotic effects by stimulating fatty acids utilisation.
Methods
The development of hepatic steatosis and insulin resistance was monitored in rats fed a high-lard or high-fish-oil diet. Immunohistochemical and electronic microscopic observations were performed on liver sections. In isolated liver mitochondria, assessments of fatty acids oxidation rate, proton conductance and oxidative stress (by measuring H2O2 release and aconitase activity) were performed. Western blot and immunohistochemical analyses were performed to evaluate the presence of proteins involved in mitochondrial dynamics (i.e., fusion and fission processes). To investigate the fusion process, mitofusin 2 and autosomal dominant optic atrophy-1 (OPA1) were analysed. To investigate the fission process, the presence of dynamin-related protein 1 (Drp1) and fission 1 protein (Fis1) was assessed.
Results
High-lard feeding elicited greater hepatic lipid accumulation, insulin resistance with associated mitochondrial dysfunction, greater oxidative stress and a shift towards mitochondrial fission processes (versus high-fish-oil feeding, which had an anti-steatotic effect associated with increased mitochondrial fusion processes).
Citation: Lionetti L, Mollica MP, Donizzetti I, Gifuni G, Sica R, Pignalosa A, et al. (2014) High-Lard and High-Fish-Oil Diets Differ in Their Effects on Function and Dynamic Behaviour of Rat Hepatic Mitochondria. PLoS ONE 9(3): e92753. https://doi.org/10.1371/journal.pone.0092753
Editor: Mika Jekabsons, University of Mississippi, United States of America
Received: May 6, 2013; Accepted: February 25, 2014; Published: March 24, 2014
Copyright: © 2014 Lionetti 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.
Funding: The authors have no support or funding to report.
Competing interests: The authors have declared that no competing interests exist.
Introduction
Mitochondrial dysfunction is characteristic of both insulin resistance (IR) and non-alcoholic fatty liver disease (NAFLD) [1], [2]. In conditions involving IR, impaired lipid oxidation in the liver has been reported [2], and in NAFLD, an elevated lipid flux stimulates hepatic fat oxidation, which is associated with electron chain impairment and results in excessive formation of reactive oxygen species (ROS) [3]–[5]. Mitochondrial respiratory chain impairment may be associated with ultrastructural damage, as found in individuals with non-alcoholic steatohepatitis (NASH) [6]. Indeed, the functions of mitochondria correlate well with their structure and morphology. Mitochondria may exhibit a tubular or fragmented morphotype, or they may be assembled into networks, with their distribution and morphology frequently altered by recurrent fission and fusion events in response to both cellular energy demands and environmental challenges [7]–[9]. Several proteins regulate these dynamic processes. Fusion is coordinated by mitofusin 1 and 2 (Mfn1 and Mfn2, respectively) and by autosomal dominant optic atrophy-1 (OPA1) [9]–[11], and these proteins are associated with the mitochondrial outer and inner membranes, respectively. With regard to fission, dynamin-related protein 1 (Drp1) is recruited to mitochondria to mediate fission activities, and fission 1 protein (Fis1), an integral outer mitochondrial membrane protein, plays an essential role in completing the fission process [8]–[9]. Maintaining normal mitochondrial morphology by tilting the balance between fusion and fission may be important in the regulation of mitochondrial energetics [7]–[9]. Moreover, a reduction in mitochondrial fusion may be involved in the development of obesity and IR [12]. Furthermore, fission inhibition and/or fusion activation have been found to counteract many of the disease phenotypes related to IR and diabetes [13], whereas enhanced fission machinery has been found in skeletal muscle in genetically obese and diet-induced obese mice [14] as well as in the db/db mouse liver alongside decreased mitochondrial respiratory capacity [15].
The present study aimed to determine whether mitochondrial dysfunction in the rat liver induced by a high-fat diet is associated with changes in the mitochondrial fusion/fission balance. In particular, we compared the effect of different dietary fat sources on the above parameters, as fish oil feeding (in contrast to saturated fatty acids feeding) has anti-obesity and anti-steatotic effects [16], [17] as well as potential benefits for IR [18]. In rodents, fish oil feeding prevents lipid accumulation in white adipose tissue (WAT) [16], [19] by limiting the triglyceride supply to WAT through increased PPAR alpha-mediated fatty acids oxidation in the liver. In fact, it has been suggested that PPARα activation in the liver might be related to the anti-obesity and anti-steatotic effects of fish oil feeding [16].
The aim of the present study was to compare the effects on hepatic mitochondrial function and dynamic behaviour between a high-lard (HL) diet (mainly saturated fatty acids) and a high-fish-oil (HFO) diet (mainly omega-3 polyunsaturated fatty acids; PUFAs). Our results suggested that these two high fat diets elicited different degrees of hepatic steatosis in treated rats with different behaviours in the mitochondrial dynamics and bioenergetics, indicating that a HFO diet may lead to a lower degree of hepatic steatosis through mitochondrial fusion and the amelioration of mitochondrial fatty acids utilisation.
Materials and Methods
Ethics statement
This study was performed in strict accordance with the criteria established by the National Institutes of Health. The protocol was approved by the Committee on the Ethics of Animal Experiments of the University of Naples “Federico II” (Permit Number: 2010/0149862). All surgeries were performed under chloral hydrate anaesthesia, and all efforts were made to minimise suffering.
Materials
The analytical-grade chemicals used were purchased from Sigma (St. Louis, MO, USA). The fish oil used in this study was cod liver oil (New.Fa.Dem. srl, Giugliano, Naples, Italy).
Animals and diets
Male Wistar rats aged 60 days (Charles River Italia, Calco, Como, Italy) were caged singly in a temperature-controlled room at 24°C with a 12 h light–dark cycle. The rats were divided into 3 groups (8 rats each), and in each group, the mean body weight was approximately 400 g. For 6 weeks, the groups were fed the following diets: the first group (N) received a standard diet (10.6% fat J/J); the second group (L) received the HL diet (40% fat J/J); and the third group (F) received the HFO diet (40% fat J/J). Diet compositions are shown in Table 1. The two high-fat diets were formulated to differ from the standard low-fat diet with regard to the contributions of fat and carbohydrate to the energy value but to be identical in terms of proteins, vitamins, minerals and fibres. The body weights and food intake were monitored daily to enable calculations of gain in body weight and energy intake. The energy contents of the standard, HL and HFO diets were determined by bomb calorimetry.
The experimental design was repeated three times (using different rats each time) for all the required measurements to be made. In particular, groups of rats were fasted overnight to determine basal glucose and serum insulin levels. For the measurements of insulin-dependent AKT phosphorylation, rats that had fasted for five h were euthanised 15 min after an i.p. injection of insulin (homologue rapid-acting, 10 units/kg body wt; Novartis, Basel, Switzerland).
At the end of the dietary treatment, the rats were anaesthetised by injection of the abovementioned chloral hydrate (40 mg/100 g body weight, i.p.), and blood was taken via the inferior vena cava. The livers were removed, weighed and either immediately processed for isolation, processed for the morphological analysis of mitochondria or frozen in liquid nitrogen and stored at −80°C for later processing.
Determination of serum parameters
Serum levels of triglycerides (TGs) and alanine aminotransferase (ALT) were determined using standard procedures [4]. Serum glucose and insulin values were determined by means of a glucose monitor (BRIO, Ascensia, NY) calibrated for use with rats and with ELISA (Mercodia rat insulin; Mercodia, Uppsala, Sweden), respectively.
Hepatic lipid content
Lipid content was determined gravimetrically after extraction in chloroform–methanol and evaporation to constant weight with a rotating evaporator (Heidolh, Germany) according to the method described by Folch [20].
Light microscopy and immunohistochemistry
Small pieces of liver were fixed in Bouin's fluid, embedded in Paraplast and cut into 4–5 μm sections. Immunohistochemical reactions were performed by the polymer Envision dual-link technique as previously described [21]. After antigen retrieval and quenching of endogenous peroxidase, sections were incubated overnight at 4°C with the following primary antisera (diluted 1∶300–1∶400): Mfn2, peroxisome proliferator-activated receptor-α (PPARα, Abcam, Cambridge, UK), Drp1 (Santa Cruz, CA, USA) and OPA1 (Novus Biologicals, Cambridge, UK). The sections were then incubated in Envision at RT, and immunostaining was performed using 3,3′-diaminobenzidine (DAB) as the chromogen. To test the specificity of the reagents, the following controls were performed: (a) omission of the primary antiserum and incubation of the sections with either non-immune serum (1∶10 and 1∶20) or bovine serum albumin (BSA; Sigma); (b) absorption of the optimally diluted primary antiserum with its specific peptide (10 nmol/ml of optimally diluted antiserum) for 24 h at 4°C. When specific peptides were used, the staining was abolished.
Images of sections were acquired using a Zeiss Axioskop microscope fitted with a TV camera.
Electron microscopy (EM)
A conventional EM technique was used as previously described [22]. Briefly, small liver slices were fixed for 2 h at 4°C in 1% glutaraldehyde in Millonig buffer (pH 7.3). The slices were post-fixed in 1% osmium tetroxide, embedded in Epon 812 and cut using an ultra-microtome. Ultra-thin sections were mounted on copper grids and contrasted with uranyl acetate and lead citrate. In addition to ultra-thin sections, sections of 1–3 μm (semi-thin sections) were collected on glass slides and stained with toluidine blue. All the sections were examined using a CM 12 Philips electron microscope at the interdepartmental centre for electron microscopy (CISME).
Morphometric analysis
For each liver, seventeen adjacent sections were acquired at 20,000× magnification. For each micrograph, we selected three different non-superimposed areas that were analysed for morphometric analysis, with care taken to ensure that areas of the analysed livers were the same size. The diameter of each mitochondrion (the long diameter for tubular mitochondria) was drawn interactively using Zeiss Axiovision image analysis software. The numbers of tubular, round and total mitochondria were determined. Data are expressed as the mean ± SE.
Preparation of isolated mitochondria
Mitochondria were isolated from the liver as previously described [23]. Briefly, tissue fragments were gently homogenised with a medium (pH 7.4) containing 220 mM mannitol, 70 mM sucrose, 20 mM HEPES, 1 mM EDTA and 0.1% (w/v) fatty-acid-free BSA in a Potter Elvehjem homogeniser set at 500 rpm (4 strokes/min). The homogenate was then centrifuged at 1000 gav for 10 min, and the resulting supernatant was again centrifuged at 3000 gav for 10 min. The mitochondrial pellet was washed twice and finally resuspended in a medium (pH 7.0) containing 80 mM LiCl, 50 mM HEPES, 5 mM Tris-PO4, 1 mM EGTA and 0.1% (w/v) fatty-acid-free BSA. Enzymatic and electron microscopy characterisation has shown that this isolation procedure (centrifugation at 3000 gav for 10 min) results in a cellular fraction, which is constituted essentially by mitochondria [24]. The protein content of the mitochondrial suspension was determined by the method of Hartree [25] using BSA as the protein standard.
Mitochondrial parameters
Mitochondrial oxygen consumption was measured polarographically using a Clark-type electrode (Yellow Springs Instruments, Yellow Springs, Ohio) at a temperature of 30°C. Isolated mitochondria were incubated in a medium (pH 7.0) containing 80 mM KCl, 50 mM HEPES, 5 mM KH2PO4, 1 mM EGTA and 0.1% (w/v) fatty-acid-free BSA to oxidise their endogenous substrates for a few minutes. Substrates were then added at the following concentrations: 10 mM succinate plus 3.75 μM rotenone; 10 mM pyruvate plus 2.5 mM malate; or 40 mM palmitoyl-CoA plus 2 mM carnitine and 2.5 mM malate. State 4 oxygen consumption was obtained in the absence of ADP, and State 3 oxygen consumption was measured in the presence of 0.3 mM ADP. The respiratory control ratio (RCR) was calculated as the ratio between states 3 and 4 according to Estabrook [26]. Oxygen consumption rates (OCRs) in the presence of oligomycin (2 μg/ml) or FCCP (1 μM) were also measured to evaluate the ratio of the maximum OCR in the presence of FCCP to the OCR with oligomycin (OCR FCCP/OCR oligomycin).
The activity of the carnitine palmitoyltransferase (CPT) system (CPT1 plus CPT2) was measured spectrophotometrically at 412 nm [27].
Measurement of basal proton leak
Mitochondrial oxygen consumption was measured polarographically with a Clark-type electrode, and membrane potential recordings were performed in parallel with safranin O using a JASCO dual-wavelength spectrophotometer [23], [28]. Safranin is a positively charged dye that undergoes spectral shifts upon its potential-dependent distribution between the external medium and the intramitochondrial compartment and on its staking to inner mitochondrial membrane anionic sites [29]–[30]. As previously described [23], [28], the quenching of the colour was measured at 511–533 nm, yielding an upward deflection for increased quenching. The absorbance readings were transferred to mV membrane potential using the Nernst equation as follows: Δψ = 61 mV×log ([K+]in/[K+]out). Independent calibration curves constructed for each mitochondrial preparation were obtained as previously described [28], [29], [31]–[33] from traces in which the extramitochondrial K+ level ([K+]out) was altered in the 0.1–20 mM range. The change in absorbance caused by the addition of 3 μM valinomycin was plotted against [K+]out. [K+]in was then estimated by extrapolation of the line to the zero-uptake point [32], and the extrapolated concentration of matrix K+ was 130 mM, which was in close agreement with earlier observations [28]. Measurements were performed at 30°C and in a medium (pH 7.0) containing 80 mM LiCl, 50 mM HEPES, 5 mM TrisPO4, 1 mM EGTA and 0.1% (w/v) fatty-acid-free BSA in the presence of succinate (10 mM), rotenone (3.75 μM), oligomycin (2 μg/ml), safranin O (9.6 μM; 83.3 nmol/mg) and nigericin (80 ng/ml). Oxygen consumption and membrane potential determinations were performed by sequential additions of malonate up to 5 mM.
Measurement of inducible leak
Mitochondrial oxygen consumption and membrane potential were measured as above in the presence of succinate (10 mM), rotenone (3.75 μM), oligomycin (2 μg/ml), safranin O (9.6 μM; 83.3 nmol/mg) and 85 μM palmitate. Due to the presence of 0.1% BSA in the incubation medium, the above concentration of palmitate corresponds to 98 nM free (not bound) fatty acid, calculated using the equation described by Richieri et al. [34]. Oxygen consumption and membrane potential determinations were performed by sequential additions of malonate up to 600 μM.
Oxidative stress parameters: mitochondrial aconitase, H2O2 release and hepatic nitrotyrosine content
To determine the aconitase-specific activity, mitochondrial aliquots were immediately frozen in liquid nitrogen and stored at −80°C. On the day of the assay, the mitochondria were sonicated and centrifuged to obtain a mitochondrial extract. The mitochondria were solubilised in 1% Triton X-100. Aconitase-specific activity was measured in a medium (pH 7.4) containing 30 mM sodium citrate, 0.6 mM MnCl2, 0.2 mM NADP, 50 mM Tris-HCl and 2 U of isocitrate dehydrogenase. The formation of NADPH was followed spectrophotometrically (340 nm) at 25°C. [35], [36]. The level of aconitase activity measured equals the level of active aconitase (basal level). Aconitase inhibited by ROS in vivo was reactivated so that total activity could be measured by incubating mitochondrial extracts in a medium containing 50 mM dithiothreitol, 0.2 mM Na2S and 0.2 mM ferrous ammonium sulphate [37].
To determine the H2O2 release, the final mitochondrial suspensions were maintained on ice and immediately used for the oxygen consumption and H2O2 production measurements, which were completed in less than 2 h. The rate of mitochondrial H2O2 production was assayed as previously reported [38] by measuring the increase in fluorescence (excitation at 312 nm and emission at 420 nm) caused by the oxidation of homovanillic acid by H2O2 in the presence of horseradish peroxidase. The reaction conditions were as follows: 0.25 mg of mitochondrial protein per ml, 6 U of horseradish peroxidase per ml, 0.1 mM homovanillic acid and 50 U of SOD per ml; and 5 mM succinate +0.2 μM rotenone were added as substrates at the end to initiate the reaction in the incubation buffer (pH 7.4; 145 mM KCl, 30 mM HEPES, 5 mM KH2PO4, 3 mM MgCl2, 0.1 mM EGTA and 0.1% albumin) at 37°C. All the assays with succinate as a substrate were performed in the presence of rotenone to avoid the backward flow of electrons to complex I [38].
To determine the hepatic nitrotyrosine content, frozen liver samples (300 mg) were homogenised in 2 ml of 25 mM HEPES (pH 7.5), 150 mM NaCl, 1% NP40, 10 mM MgCl2, 1 mM EDTA and 2% glycerol, followed by centrifugation. Supernatants were used for measurements of nitrotyrosine concentrations with the OxiSelect Nitrotyrosine ELISA kit (Cell Biolabs, San Diego, CA). Nitrotyrosine concentrations were normalised per mg of protein.
Immunoblotting
Immunoblot analysis was performed as described previously [39]. The following primary antibodies were used: PPARα and β-actin (Abcam); OPA-1 (Novus Biologicals); Mfn2, DRP and Fis1 (Santa Cruz); AKT, phospho-AKT (Ser473) and UCP2 (Santa Cruz); and COX-IV (Cell Signalling Technology, Beverly, MA).
Data analysis.
Data are expressed as the mean ± SE. Respiration rates at the highest membrane potential common to all three curves were used to test for differences in proton leak. Differences between groups were compared by ANOVA followed by the Newman-Keuls test to correct for multiple comparisons. Differences were considered statistically significant at P<0.05. All analyses were performed using GraphPad Prism 4 (GraphPad Software, San Diego, CA).
Results
Body weight gain and serum metabolite levels
We first analysed whether the different source of fat (lard or fish oil) in high-fat diets differentially affected obesity development and serum levels of metabolites related to obesity-linked diseases. In particular, we assessed TG, ALT, insulin and glucose levels as markers of dyslipidaemia, liver injury and insulin resistance, respectively. For obesity development, rats fed high-lard (L rats) and high-fish-oil (F rats) diets displayed similar increases in energy intake compared to the intake of rats fed standard diets (N rats), and L rats gained significantly more body weight than F rats (Table 2). Serum TG and ALT levels were each significantly higher in L rats than in N rats (Table 2), and both parameters were lower in F rats than in L rats, with TG levels not differing between F and N rats.
L and F rats displayed significantly higher serum glucose levels than N rats, whereas both the serum insulin level and the HOMA index value were highest in L rats (Table 2). Taken together, these first results showed the high fish oil feeding was associated with a lower degree of obesity development, dyslipidaemia, insulin resistance and hepatic injury compared to high lard feeding.
Hepatic parameters
We next focused our attention on hepatic parameters to further investigate the effects of both high-fat diets on hepatic steatosis and insulin-resistance development. The liver weight was higher in both L and F rats compared to control rats, and the highest value was observed in L rats (Table 2). To investigate hepatic lipid accumulation, we used both histologic observations and lipid extraction according to the method of Folch [20]. Semi-thin sections of L and F livers revealed hepatocytes moderately well-filled with lipid droplets, whereas these sections of N livers displayed little or no fat accumulation. Group L livers had both the largest lipid droplets (Figure 1A) and the highest lipid content, as determined by the Folch method (Table 2), among the three groups.
(A), Representative semi-thin liver sections stained with toluidine blue from N, L and F rats showing the presence and the relative abundance of lipid droplets in HF-fed rats. (B), Immunohistochemical reaction and (C), immunoblot for PPARα. The intensities of the bands were normalised to that of β-actin. (D), Basal and insulin-induced AKT phosphorylation. N, L, F = sham; and Ni, Li, Fi = insulin-injected. (E) and (F), Kinetics of basal and palmitate-induced proton leaks in isolated liver mitochondria. (G) and (H), Respiration rates measured by interpolation at 170 mV or 129 mV for basal and palmitate-induced proton leaks, respectively. Data are means ± SE for 8 rats in each group. *P<0.05 vs. N rats. #P<0.05 vs. L rats. I, Immunoblot for UCP2. Thin immunoreactive bands were evident only for F groups. The intensities of the bands were normalised to that of Cox IV.
To verify whether the different degree of lipid accumulation was associated with a different degree of lipid oxidation, we analysed the presence of PPARα, a nuclear receptor implicated in the regulation of CPT, and other genes involved in mitochondrial fatty acid β-oxidation, by immunohistochemistry and western blot analysis. The results showed that PPARα immunostaining labelled the cytosol in all rat groups, whereas nuclear staining of PPARα following its activation and translocation into nuclei was more evident in F and L rats than in N rats (Figure 1B). Moreover, the PPARα content was higher in F rats than in N rats (Figure 1C).
Because the HOMA index values suggested a systemic insulin resistance in L rats, we analysed the presence and activation of AKT, a key enzyme involved in the insulin-signalling pathway, to assess the onset of insulin resistance in the liver. Basal AKT content did not differ among the three groups, but L rats exhibited the lowest value for insulin-stimulated AKT phosphorylation (at Ser473) (Figure 1D).
Taken together, these results suggested that the HFO diet did not elicit hepatic insulin resistance but that it induced a lower degree of hepatic steatosis compared to the HL diet, possibly through an ameliorated utilisation of lipid substrates mediated by PPARα.
Liver mitochondrial function
Because mitochondria are the main site of the substrate oxidative process, we analysed respiratory rates in isolated liver mitochondria. Oxidative mitochondrial respiratory activity was determined by using both NADH- and FADH2-linked substrates (pyruvate plus malate and succinate plus rotenone, respectively) to involve different dehydrogenases, carriers and entry sites of reducing equivalents. We also used palmitoyl-CoA as a substrate to assess the capacity of lipid substrate oxidation.
Table 3 shows that no difference among the groups was found in the respiratory rates when pyruvate plus malate was used as a substrate both in State 3 (maximal oxidative capacity in the presence of ADP) and State 4 (in absence of ADP).
In contrast, when succinate plus rotenone was used as a substrate, both states 3 and 4 were significantly lower in L rats than in N and F rats. In addition, the fatty acid State 3 oxidation rate, which was measured using palmitoyl-CoA as a substrate, and CPT system activity were each increased (vs. N) in the L group and further increased in the F group (Table 3).
To test mitochondrial efficiency, we measured the OCR FCCP/OCR oligomycin ratio as well as basal and fatty-acid-induced proton leak kinetics. The OCR FCCP/OCR oligomycin ratio was lower in F rats than in N and L rats, suggesting reduced mitochondrial efficiency in F rats. Concerning proton leak kinetics, Figure 1E shows that under basal conditions (in the absence of free FAs), the F rats exhibited increased basal proton leak kinetics (F rat mitochondria had to consume more oxygen than either N or L rat mitochondria to maintain a given membrane potential), with N and L rats displaying superimposable kinetic curves. Moreover, at the highest membrane potential common to all three curves (170 mV), the respiration rate for F rats was significantly higher (P<0.05) than that for either N or L rats (Figure 1G).
With regard to the fatty-acid-induced proton leak (measured using physiological amounts of palmitate), L rats had the lowest proton leak among the three groups, and F rats had the highest proton leak among the three groups analysed (Figure 1F). Moreover, the respiration rates measured at the highest membrane potential common to all three curves (129 mV) were significantly different (P<0.05) among the groups (Figure 1H).
Because mild uncoupling may protect against ROS damage, mitochondrial oxidative stress markers (H2O2 production and aconitase activity) were assessed. Compared to both N and F rats, L rats exhibited increased mitochondrial ROS production based on their lower basal/total aconitase activity ratio (a sensitive marker of oxidative stress) and on their significantly higher H2O2 production in isolated mitochondria (Table 3). To test hepatic oxidative stress, nitrotyrosine content was assessed in liver homogenates. The results showed that the highest nitrotyrosine was found in L rats, confirming the higher oxidative stress found in isolated mitochondria in this group of rats compared to F and N rats.
We next tested the presence of uncoupling protein 2, which might be involved both in mitochondrial uncoupling and ROS protection. Western blot analysis showed that UCP2 was undetectable in N and L rats, but a thin UCP2 band was observed in F rats (Figure 1 I).
Electron microscopy (EM)
Because changes in mitochondrial function may be associated with changes in mitochondrial morphology, EM observations were performed to evaluate ultrastructural features in the three groups of experimental rats. Mitochondria in N rats displayed a moderately electron-dense matrix, lamellar cristae and regular boundaries (Figure 2 N1-2).
(N1–N2), N mitochondria with lamellar cristae and moderately dense matrix. (L1–L6), L mitochondria exhibited a dense matrix, and a few appeared slightly swollen (white arrows). Small, round mitochondria (L1) were often observed close to others (L2, L3, black arrows). (L3), Two mitochondria coming into contact at two sites (interrupted arrow). (L1–L3), Lipid droplets (ld) close to mitochondria. (L4) Dumbbell-shaped mitochondrion, suggesting on-going fission (black arrow). (L5) Cup-shaped mitochondrion enveloping another mitochondrion (interrupted arrow), suggesting a donut formation. (L6) Asymmetric dumbbell-like mitochondrion close to another mitochondrion (arrowhead) as well as a donut-like mitochondrion (white asterisk).
Mitochondria in L rats mostly exhibited an electron-dense matrix, with the mitochondria appearing slightly swollen in some cases, and the intracristal spaces were often larger than those observed in control preparations. The presence of numerous small, round mitochondria (often in contact with lipid droplets) (Figure 2 L1-3) and mitochondria with a dumb-bell shape suggested division processes (Figure 2 L4). In contrast, we observed both the presence and the apparent formation of donut-like mitochondria by autofusion and anomalous fusion between two organelles, as suggested by comma-shaped or ring-like mitochondria in some instances enveloping other mitochondria. We inferred that when the adjacent ends of mitochondria come into contact, a hole enclosing cytoplasm may be created (Figure 2 L3, L 5–6).
Mitochondria in F rats exhibited regular cristae and a less electron-dense matrix than that of L rat mitochondria. The presence of boomerang-shaped mitochondria and several mitochondria clustered together suggested fusion and network formation in F rats (Figure 3A F1–2). The clustered mitochondria often surrounded lipid droplets (Figure 3A F3). In some mitochondria in F and L rats, dilated intracristal spaces encased ordered parallel aggregates of helical filaments, which appeared as a close hexagonal array of microcylinders in cross-section (Figure 3A F4–5). Donut-like mitochondria were also found in F livers. Figure 3A F6 depicts one such mitochondrion enveloped by a lysosomal membrane.
Mitochondrial length and tubular/round ratio. (A), F1–6, F mitochondria exhibited light matrix and numerous cristae parallel with the longitudinal axis (double-arrow). F1: Boomerang-shaped mitochondria, suggesting a previous fusion process. F2–3: Mitochondrial cluster forming a fused network. F3: Long, cup-shaped mitochondrion surrounding a lipid droplet (ld). F4–5: Paracrystalline inclusions (black arrows) in the intracristal space. Donut-shaped formation (interrupted arrow). F6: Autophagosome containing a donut-like mitochondrion with enclosed degraded cytoplasm. (B) and (C), Based on EM images, L rats had the shortest mitochondria and the lowest tubular/round ratio (%). *P<0.05 vs. N. #P<0.05 vs. L rats.
To examine the distribution of mitochondrial length, we divided liver mitochondria into three length ranges, which revealed that L and F rats exhibited the highest percentages of short and long mitochondria, respectively (Figure 3B). Furthermore, most of the mitochondria in L rats were round, whereas round and tubular mitochondria were almost equally represented in F rats (Figure 3C). Because these observations suggested a different distribution of mitochondrial length among the three groups of rats, we next assessed mitochondrial dynamic behaviour, in which an imbalance has been suggested to be involved in obesity and insulin resistance. In particular, we evaluated the presence of the proteins relevant to mitochondrial dynamics by western blot analysis and immunohistochemistry.
Proteins relevant to mitochondrial dynamics
Immunostaining of N rat liver sections for Mfn2 revealed numerous positive hepatocytes. In F rat liver sections, Mfn2 labelling was even more evident, with some strongly immunoreactive cells, but Mfn2 labelling was weak in L rat livers (Figure 4A). Moreover, L rat livers had the lowest Mfn2 content in mitochondrial extracts as measured by western blot analysis (Figure 4B).
(A), Immunohistochemical reaction and (B), immunoblot for Mfn2. (C), Immunohistochemical reaction and (D), immunoblot for OPA1. (E), Immunohistochemical reaction and (F), immunoblot for Drp1. (G), Immunoblot for Fis1. (B), (D), (F) and (G), Densitometric analysis data shown as means ± SE. *P<0.05 vs. N rats. #P<0.05 vs. L rats. For all immunoblots, representative blots are shown for each protein of interest. The intensities of the bands were normalised to that of Cox IV.
OPA1 immunostaining labelled most of the F rat liver mitochondria, but such staining in N and L rat livers was weak (Figure 4C). F rats exhibited significantly higher OPA1 content than either N or L rats (Figure 4D).
In N rat livers, Drp1 immunostaining was localised to numerous mitochondria (Figure 4E N), but in F rat livers, mitochondria in only a few cells were labelled (Figure 4E F). In L rat livers, Drp1 immunostaining heavily labelled the cytoplasm and mitochondria, which appeared fragmented to various degrees (Figure 4E L–L1). Moreover, L rats had the highest Drp1 content in their mitochondrial extracts (Figure 4F).
The Fis1 mitochondrial content was highest in L rats and lowest in F rats (Figure 4G). Together, these results suggested a shift towards fission processes in L rats and a shift towards fusion processes in F rats.
Discussion
The current study serves to focus attention on functional and structural features that could be differentially impacted by high-lard and high-fish oil feeding. The high-fish oil feeding elicited a lower degree of obesity development and IR compared to high-lard feeding, in accordance with previous studies suggesting that omega-3 fatty acids have anti-obesity effect and potential benefits for IR [16], [18]. In our results, L and F rats showed blood glucose levels higher than N rats, but within the normal range [40], [41]. It should be noted that F rats showed higher blood glucose level vs. N rats, but normal insulin level, whereas L rats exhibited both higher blood glucose and insulin values vs. N rats. It has been reported that the composition of dietary fat directly influences glucose-stimulated insulin secretion [42], in fact dietary saturated fatty acids stimulate insulin secretion in rats [43], whereas long-chain omega-3 fatty acids decrease insulin secretion leading to a ‘diabetogenic effect’ [43]. In particular, measurement of insulin release from pancreas of fasted rats perfused with glucose and a range of individual fatty acids of varying degree of saturation revealed that the fold stimulation of insulin secretion was greater for saturated vs. unsaturated fatty acids [44]. It has been suggested that omega-3 fatty acids act directly at the level of the β-cell to modify insulin responsiveness to glucose. [45]. Therefore, a reduced responsiveness of pancreatic β-cells to plasma glucose elevation and a reduced suppression of hepatic glucose output by insulin may contribute to the rise in fasting glucose observed in our F rats which exhibited normal insulin levels.
We then focused our attention on the effects of the two different fat dietary sources in liver and the results revealed that the HL diet induced fat accumulation and IR, which was parallel to impaired mitochondrial function, and a dysregulated expression profile of proteins participating in mitochondrial dynamics. In contrast, the HFO diet led to less hepatic lipid accumulation through improved mitochondrial fatty acid utilisation supported by a shift towards fusion, which counteracted oxidative stress and possibly the hepatocyte damage induced by long-term over-feeding. This study suggests an association between mitochondrial dynamic behaviour and functionality in the liver in rats fed a high-fat diet, and it also suggests that both dynamics and functions are affected differently between diets rich in lard or in fish oil.
Hepatic mitochondrial respiratory capacity was determined by measuring State 3 and 4 respiration with various substrates to involve different dehydrogenases, carriers and entry sites of reducing equivalents into the respiratory chain. With regard to the respiration rates measured in the presence of a NADH-linked substrate, namely, pyruvate plus malate, no significant differences were found among the experimental groups. In contrast, when succinate was used as the FADH2-linked substrate, a significant decrease in State 3 respiration was observed in L rat mitochondria. In addition, when a lipid substrate (palmitoyl CoA) was used, L rat mitochondria showed significantly higher State 3 respiration compared to control mitochondria. It should be noted that a decrease in succinate State 3 respiration may be due to defects both in the activity of substrate oxidation reactions (which are complex II, complex III, complex IV and dicarboxylate carrier in this case) and/or in the activity of the phosphorylation reactions (ANT, ATP synthase and phosphate carrier). The results obtained with succinate plus FCCP (a condition in which the oxidation reactions are close to the State 3 kinetic rate but the phosphorylating reactions no longer exert control over respiration) appeared to exclude phosphorylating reactions from being the site of impairment. In fact, the data showed that the impairment in oxygen consumption remained, with a significant decrease in FCCP respiration in L rat mitochondria, suggesting that the defect resided in the substrate oxidation reactions and not in phosphorylating reactions. Many of the reactions controlling State 3 respiration with succinate also participate in State 3 respiration with pyruvate or palmitoyl-CoA. The fact that the State 3 rate with malate/pyruvate in L rat mitochondria was not different from that in N rat mitochondria and was similar to the State 4 (and oligomycin) succinate rate may indicate that the defect in the succinate State 3 rate resided within complex II (rather than complex III or IV).
However, the lower succinate State 4 respiration in L rat mitochondria may not necessarily result from a complex II defect; Figure 1E/F illustrates the lower proton leak in L rat mitochondria, which might account for the difference in State 4 respiration because proton leak is a major controller of State 4 (the difference shifts to a complex II defect as the mitochondria approach State 3).
The increased capacity of mitochondria to oxidise acyl-CoA in L rats might serve as a compensatory mechanism for the elevated hepatic fatty acids uptake that occurs during high fat feeding, which is in accordance with previous results [4], [5]. The observed increases in PPAR-α nuclear immunostaining and CPT system activity may be relevant to this enhanced β-oxidation. However, this increase in acyl-CoA oxidation capacity was not sufficient to handle the increased load of hepatic free FAs, resulting in lipid accumulation in L rat livers. With the limitation that in vitro differences may not translate to in situ differences, the fat accumulation was most likely also due to an increase in mitochondrial energy efficiency, as shown by the decrease in induced proton leak. The presence of an increase in β-oxidation rate [46], [47] might play a crucial role in enhancing ROS production, as suggested by the increased H2O2 production, inhibited aconitase activity in L rat mitochondria and increased nitrotyrosine content in L rat liver homogenates. However, it should be noted that H2O2 production measurements were performed in the presence of succinate and not in the presence of palmitoyl CoA, which is critical because different substrates can substantially affect the rates of H2O2 production. Moreover, the measured H2O2 production rates were under State 4, non–phosphorylating conditions, whereas in situ the actual rate of production can vary substantially depending on the overall rate of cellular ATP consumption.
By comparison with the HL diet, the HFO diet led to less lipid accumulation associated with greater increases in PPAR-α content, CPT system activity and β-oxidation rate. Moreover, in the HFO rats, the decreased mitochondrial energy efficiency, as evidenced by the increased basal and induced proton leaks, might also have contributed to increased fatty acid utilisation. The mild uncoupling observed in F rats may have been due to an enhanced expression of uncoupling protein 2 (UCP2). To test this hypothesis, we analysed UCP2 content, and we found a detectable amount of UCP2 protein only in F rat mitochondria, which was in accordance with previous results showing increased UCP2 expression induced by PUFAs [48]. We cannot exclude the possibility that the mild uncoupling found in this work may be mediated by anion carriers (such as ADP/ATP antiporter) or by changes in internal mitochondrial membrane fluidity [49], [50]. However, this uncoupling by preventing respiratory complex over-reduction might serve to counteract excessive ROS formation [51], which was supported by F rats exhibiting a significantly lower mitochondrial H2O2 release, higher mitochondrial basal aconitase/total aconitase ratio and lower liver homogenate nitrotyrosine content compared to L rats. This functional adaptation in mitochondria (through a mild uncoupling that reduced ROS production) may protect against the initial damage induced by a high-fat diet, which may lead to hepatosteatosis and thus may be an adaptation similar to that found in A/J mice, which are resistant to high-fat-diet-induced hepatosteatosis and obesity [52]. It should be noted that F rat mitochondria, even with a higher proton leak, did not exhibit significantly lower H2O2 production rates than N rat mitochondria because a greater supply of lipid substrates reached the liver due to hyperlipidic feeding, leading to an increase in lipid oxidation. This increase should have led to a greater ROS production, but this trend was counteracted by increasing proton leak, thereby maintaining normal H2O2 levels. However, this adaptation was not able to further reduce H2O2 levels below normal values. Further studies are needed to test this hypothesis by using more physiological substrates, such as palmitoyl CoA, in the measurements of H2O2 production.
Concerning morphological features, the EM observations revealed certain similarities but many different morphological adaptations between L and F rats. A peculiar feature observed in both L and F rats was the presence of paracrystalline inclusions. The role of paracrystalline inclusions has not yet been clarified. Paracrystalline inclusions may be a normal constituent of mitochondria, or they may reflect either mitochondrial injury (e.g., NASH patients exhibit paracrystalline inclusions in mega-mitochondria) or an adaptive process [6].
The observed mitochondrial dynamic behaviour differed between L and F rats. In L rats, the expression of mitochondrial fission proteins was enhanced and the expression of fusion proteins was reduced, suggesting an imbalance towards mitochondrial fragmentation, which agreed with the observation of smaller mitochondria, with round mitochondria being more prevalent that tubular ones in ultra-thin sections from L rats. In contrast, the expression of mitochondrial Mfn2 and Drp1 in F rats was closer to that observed in the control group. However, the Opa1 levels and Fis1 levels were significantly higher and lower, respectively, in F rats compared to N rats, supporting the shift to elongated mitochondria observed in the EM analysis.
Regarding the proteins involved in fusion/fission processes, the L group experienced a reduced expression of Mfn2 and an increase in the mitochondrial fission proteins, Drp1 and Fis1, which was consistent with the down-regulation of Mfn2 reported in skeletal muscle in obese insulin-resistant humans and in obese rodents [9], [12], [53]. Recent data have indicated that hepatic ablation of Mfn2 causes glucose intolerance and deficient hepatic insulin signalling [54]. Based on these data, we propose that the reduced Mfn2 expression upon exposure to the HL diet participates in the insulin resistance that affects the liver under these conditions.
Moreover, mitochondrial fragmentation and enhancements of fission machinery have been reported after treatment with high glucose (HG) and/or high free FAs in the following models: insulin-resistant 3T3-L1 adipocytes (which have smaller and more compact mitochondria) [55], pancreatic islet cells exposed to glucose and fatty acid [56] and skeletal muscle in genetically obese and diet-induced obese mice [14]. Interestingly, upon exposure to HG concentrations, mitochondrial fragmentation has been shown to occur in association with ROS formation in both a rat liver cell line and myoblasts [57]. These authors suggested that the small spherical mitochondria formed in HG conditions may represent condensed, metabolically active organelles with increased total surface area, which is a modification that would increase the accessibility of metabolic substrate to carrier proteins. Such fragmentation might induce alterations in electron transport and coupling, leading to an increase in ROS [10], [57]. Therefore, in L rat livers, mitochondrial fragmentation may be an adaptive cellular response to increases in the mitochondrial intake and oxidation of FAs, which would result in elevated ROS production.
Compared to the HL diet, the HFO diet led to a mild uncoupling with less ROS production as well as a shift towards fusion (with concomitant increases in Mfn2 and OPA1 as well as decreases in Drp1 and Fis1) together with an improvement in insulin sensitivity and to less lipid accumulation. This result suggests that the high caloric intake per se is not the key factor involved, and the specific fatty acid composition may be relevant to consider. The different expression pattern of mitochondrial dynamic proteins when comparing the F and L groups was consistent with the observation that the inhibition of mitochondrial fission ameliorates muscle insulin signalling and systemic insulin sensitivity in obese mice [14] as well as the observation that Mfn2 deficiency impairs insulin signalling in both mouse liver and muscle [54]. Moreover, a previous study reported mitochondrial fission during in vitro hepatocyte steatosis and its reversal by omega-3 fatty acids (i.e., tubular elongation and Mfn2 upregulation) [58]. Therefore, our present results confirmed hepatic mitochondrial fusion through fish oil in vivo. The mechanism underlying fish oil/omega-3 fatty acid mitochondrial fusion stimulation may involve receptor-mediated signalling and/or lipid composition, among other factors. Further studies are needed to elucidate this mechanism.
An interesting phenomenon that may be linked to the fusion/fission balance was the presence of donut-like mitochondria in both L and F rats. Donut-like mitochondria may result from anomalous fusion activity during metabolic stress both when the fission/fusion machinery is heavily tilted towards fusion [59] and when it is tilted towards fission [60]. Such a condition may be transient and followed by recovery to linear mitochondria or, in some instances, by mitophagy, as shown in Figure 2 F6. The presence of donut-like mitochondria in both L and F rat livers suggested that they may represent a mitochondrial adaptation to the stress induced by high fat feeding [61], either leading to the elimination of impaired organelles or aiding functional recovery.
In conclusion, the results of the present work suggested that the HL diet induced hepatic fat accumulation and IR, with an associated impairment of mitochondrial function, fission-shifted dynamic behaviour and oxidative stress, and that the HFO diet led to less hepatic lipid accumulation through improved mitochondrial fatty acid utilisation, which was concomitant with a fusion phenotype similar to that of the controls, thereby counteracting oxidative stress and possibly the hepatocyte damage induced by long-term over-feeding. To support these suggestions, we are planning further experiments to analyse whether the genetic manipulation of specific proteins participating in mitochondrial dynamics rescues the phenotype observed in response to a high-lard diet.
Acknowledgments
We thank Prof. Antonio Barletta for helpful discussion. We thank Dr. Emilia De Santis for skilful management of the animal house.
Author Contributions
Conceived and designed the experiments: LL RP. Performed the experiments: LL MPM ID GG RS AP GC MG CDF RP. Analyzed the data: LL AZ RP. Contributed reagents/materials/analysis tools: LL MPM RP. Wrote the paper: LL RP.
References
- 1. Pessayre D, Fromenty B (2005) NASH: a mitochondrial disease. J Hepatol 42: 928–940.
- 2. Szendroedi J, Phielix E, Roden M (2011) The role of mitochondria in insulin resistance and type 2 diabetes mellitus. Nat Rev Endocrinol 8: 92–103.
- 3. Sanyal AJ, Campbell-Sargent C, Mirshahi F, Rizzo WB, Contos MJ, et al. (2001) Nonalcoholic steatohepatitis: association of insulin resistance and mitochondrial abnormalities. Gastroenterology 120: 1183–1192.
- 4. Mollica MP, Lionetti L, Moreno M, Lombardi A, De Lange P, et al. (2009) 3,5-diiodo-l-thyronine, by modulating mitochondrial functions, reverses hepatic fat accumulation in rats fed a high-fat diet. J Hepatol 51: 363–370.
- 5. Mantena SK, Vaughn DP, Andringa KK, Eccleston HB, King AL, et al. (2009) High fat diet induces dysregulation of hepatic oxygen gradients and mitochondrial function in vivo. Biochem J 417: 183–193.
- 6. Caldwell SH, de Freitas LAR, Park SH, Moreno MLV, Redick JA, et al. (2009) Intramitochondrial crystalline inclusions in nonalcoholic steatohepatitis. Hepatology 49: 1888–1895.
- 7. Nunnari J, Wong ED, Meeusen S, Wagner JA (2002) Studying the behavior of mitochondria. Methods Enzymol 351: 381–393.
- 8. Palmer CS, Osellame LD, Stojanovski D, Ryan MT (2011) The regulation of mitochondrial morphology: intricate mechanisms and dynamic machinery. Cell Signal 23: 1534–1545.
- 9. Liesa M, Palacin M, Zorzano A (2009) Mitochondrial dynamics in mammalian health and disease. Physiol Rev 89: 799–845.
- 10. Pellegrini L, Scorrano L (2007) A cut short to death: Parl and Opa1 in the regulation of mitochondrial morphology and apoptosis. Cell Death Differ 14: 1275–1284.
- 11. Cipolat S, Martins de Brito O, Dal Zilio B, Scorrano L (2004) OPA1 requires mitofusin 1 to promote mitochondrial fusion. Proc Natl Acad Sci USA 101: 15927–15932.
- 12. Bach D, Pich S, Soriano FX, Vega N, Baumgartner B, et al. (2003) Mitofusin-2 determines mitochondrial network architecture and mitochondrial metabolism. A novel regulatory mechanism altered in obesity. J Biol Chem 278: 17190–17197.
- 13. Civitarese AE, Ravussin E (2008) Mitochondrial energetics and insulin resistance. Endocrinology 149: 950–954.
- 14. Jheng HF, Tsai PJ, Guo SM, Kuo LH, Chang CS, et al. (2012) Mitochondrial fission contributes to mitochondrial dysfunction and insulin resistance in skeletal muscle. Mol Cell Biol 32: 309–319.
- 15. Holmström MH, Iglesias-Gutierrez E, Zierath JR, Garcia-Roves PM (2012) Tissue-specific control of mitochondrial respiration in obesity-related insulin resistance and diabetes. Am J Physiol Endocrinol Metab 302: E731–739.
- 16. Nakatani T, Kim HJ, Kaburagi Y, Yasuda K, Ezaki O (2003) A low fish oil inhibits SREBP-1 proteolytic cascade, while a high-fish-oil feeding decreases SREBP-1 mRNA in mice liver: relationship to anti-obesity. J Lipid Res 44: 369–79.
- 17. Xin YN, Xuan SY, Zhang JH, Zheng MH, Guan HS (2008) Omega-3 polyunsaturated fatty acids: a specific liver drug for non-alcoholic fatty liver disease (NAFLD). Med Hypotheses 71: 820–821.
- 18. Xin I, Goyenechea E, Zulet MA, Martínez JA (2011) Obesity and metabolic syndrome: potential benefit from specific nutritional components. Nutr Metab Cardiovasc Dis 21: B1–15.
- 19. Ikemoto S, Takahashi M, Tsunoda N, Maruyama K, Itakura H, et al. (1996) High-fat diet-induced hyperglycemia and obesity in mice. Differential effects of dietary oils. Metabolism 45: 1539–1546.
- 20. Folch J, Lees M, Stanley GHS (1957) A simple method for the isolation and purification of total lipids from animal tissues. J Biol Chem 226: 497–510.
- 21. Buono S, Cristiano L, D'Angelo B, Cimini A, Putti R (2007) PPARalpha mediates the effects of the pesticide methyl thiophanate on liver of the lizard Podarcis sicula. Comp Biochem Physiol C Toxicol Pharmacol 145: 306–314.
- 22. Putti R, Della Rossa A (1996) PeptideYY and insulin coexist in β-granules in B cells of the Madagascan lizard Zonosaurus laticaudatus. Gen Comp Endocrinol 103: 249–256.
- 23. Lionetti L, Crescenzo R, Mollica MP, Tasso R, Barletta A, et al. (2004) Modulation of hepatic mitochondrial energy efficiency with age. Cell Mol Life Sci 61: 1366–1371.
- 24. Liverini G, Iossa S, Barletta A (1991) The effect of cold exposure on rat liver mitochondrial respiratory capacity. Comp. Biochem. Physiol 98: 583–585.
- 25. Hartree EF (1972) Determination of protein: a modification of Lowry method that gives a linear photometric response. Anal Biochem 48: 422–427.
- 26. Estabrook RW (1967) Mitochondrial respiratory control and the polarographic measurement of ADP:O ratios. Methods Enzymol 10: 4711–4722.
- 27. Alexson SEH, Nedergaard J (1988) A novel type of short- and medium chain acyl-CoA hydrolases in brown adipose tissue mitochondria. Biol Chem 263: 13564–13571.
- 28. Nedergaard J (1983) The relationship between extramitochondrial Ca2+ concentration, respiratory rate, and membrane potential in mitochondria from brown adipose tissue of the rat. Eur J Biochem 33: 185–191.
- 29. Akerman KEO, Wikstrom MKF (1976) Safranine as a probe of the mitochondrial membrane potential. FEBS Letters 68: 191–197.
- 30. Colonna R, Massari S, Azzone GF (1973) The problem of cation-binding sites in the energized membrane of intact mitochondria. Eur J Biochem 34: 577–585.
- 31. Figueira TR, Melo DR, Vercesi AE, Castilho RF (2012) Safranin as a fluorescent probe for the evaluation of the mitochondrial membrane potential in isolated organelles and permabilized cells. Methods Mol Biol 810: 103–117.
- 32. Iossa S, Lionetti L, Mollica MP, Crescenzo R, Botta M, et al. (2001) Differences in proton leak, but not in UCP3 protein content, in subsarcolemmal and intermyofibrillar skeletal muscle mitochondria from fed and fasted rats. FEBS Lett 505: 53–56.
- 33. Nishihira T, Tanaka J, Nishikava K, Jikko A, Taki Y, et al. (1986) Biological significance of enhanced mitochondrial membrane potential in regenerating liver. Hepatology 6: 220–224.
- 34. Richieri GV, Anel A, Kleinfeld AM (1993) Interaction of long-chain fatty acids and albumin: determination of free fatty acid levels using the fluorescent probe ADIFAB. Biochemistry 32: 7574–7580.
- 35. Gardner PR (2002) Aconitase: sensitive target and measure of superoxide. Methods Enzymol 349: 9–23.
- 36. Lionetti L, Mollica MP, Crescenzo R, D'Andrea E, Ferraro M, et al. (2007) Skeletal muscle subsarcolemmal mitochondrial dysfunction in high-fat fed rats exhibiting impaired glucose homeostasis. Int J Obes 3: 1596–1604.
- 37. Hausladen A, Fridovich I (1996) Measuring nitric oxide and superoxide:rate constants for aconitase reactivity. Methods Enzymol 269: 37–41.
- 38. Gredilla R, Sanz A, Lopez-Torres M, Barja G (2001) Caloric restriction decreases mitochondrial free radical generation at complex I and lowers oxidative damage tomitochondrial DNA in the rat heart. FASEB J 15: 1589–91.
- 39. de Lange P, Cioffi F, Senese R, Moreno M, Lombardi A, et al. (2011) Nonthyrotoxic prevention of diet-induced insulin resistance by 3,5-diiodo-L-thyronine in rats. Diabetes 60: 2730–2739.
- 40.
Johnson-Delaney C (1996) Exotic Animal Companion Medicine Handbook for Veterinarians, (2 Vol. Set). Lake Worth, FL: Zoological Education Network.
- 41.
Kohn DF, Clifford CB (2002) Biology and diseases of rats. In: JG Fox, LC Anderson, FM Lowe, et al.., Laboratory Animal Medicine, 2nd ed. New York: Academic Press, 121–167.
- 42. Dobbins RL, Szczepaniak LS, Myhill J, Tamura Y, Uchino H, et al. (2002) The composition of dietary fat directly influences glucose-stimulated insulin secretion in rats. Diabetes 51: 1825–1833.
- 43. Holness MJ, Greenwood GK, Smith ND, Sugden MC (2003) Diabetogenic impact of long-chain-3 fatty acids on pancreatic β-cell function and the regulation of endogenous glucose production. Endocrinology 144(9): 3958–3968.
- 44. Stein DT, Stevenson BE, Chester MW, Basit M, Daniels MB, et al. (1997) The insulinotropic potency of fatty acids is influenced profoundly by their chain length and degree of saturation. J Clin Invest 15 (100): 398–403.
- 45. Holness MJ, Smith ND, Greenwood GK, Sugden MC (2004) Acute omega-3 fatty acid enrichment selectively reverses high-saturated fat feeding-induced insulin hypersecretion but does not improve peripheral insulin resistance. Diabetes 53 Suppl 1S166–171.
- 46. St Pierre J, Buckingham JA, Roebuck SJ, Brand MD (2002) Topology of superoxide production from different sites in the mitochondrial electron transport chain. Biol Chem 277: 44784–44790.
- 47. Schönfeld P, Wojtczak L (2008) Fatty acids as modulators of the cellular production of reactive oxygen species. Free Radic Biol Med 45: 231–241.
- 48. Armstrong MB, Towle HC (2001) Polyunsaturated fatty acids stimulate hepatic UCP-2 expression via a PPARalpha-mediated pathway. Am J Physiol Endocrinol Metab 28: E1197–204.
- 49. Stillwell W, Jenski LJ, Crump FT, Ehringer W (1997) Effect of docosahexaenoic acid on mouse mitochondrial membrane properties. Lipids 32: 497–506.
- 50. Fan YY, Ran Q, Toyokuni S, Okazaki Y, Callaway ES, et al. (2011) Dietary fish oil promotes colonic apoptosis and mitochondrial proton leak in oxidatively stressed mice. Cancer Prev Res 4: 1267–1274.
- 51. Jezek P (2002) Possible physiological roles of mitochondrial uncoupling proteins–UCPn. Int J Biochem Cell Biol 34: 1190–1206.
- 52. Poussin C, Ibberson M, Hall D, Ding J, Soto J, et al. (2011) Oxidative phosphorylation flexibility in the liver of mice resistant to high-fat diet-induced hepatic steatosis. Diabetes 60: 2216–2224.
- 53. Bach D, Naon D, Pich S, Soriano FX, Vega N, et al. (2005) Expression of Mfn2, the Charcot-Marie-Tooth neuropathy type 2A gene, in human skeletal muscle: effects of type 2 diabetes, obesity, weight loss, and the regulatory role of tumor necrosis factor alpha and interleukin-6. Diabetes 54: 2685–93.
- 54. Sebastián D, Hernández-Alvarez MI, Segalés J, Sorianello E, Muñoz JP, et al. (2012) Mitofusin 2 (Mfn2) links mitochondrial and endoplasmic reticulum function with insulin signaling and is essential for normal glucose homeostasis. Proc Natl Acad Sci USA 109: 5523–5528.
- 55. Gao CL, Zhu C, Zhao YP, Chen XH, Ji CB, et al. (2010) Mitochondrial dysfunction is induced by high levels of glucose and free fatty acids in 3T3-L1 adipocytes. Mol Cell Endocrinol 320: 25–33.
- 56. Molina AJ, Wikstrom JD, Stiles L, Las G, Mohamed H, et al. (2009) Mitochondrial networking protects beta-cells from nutrient-induced apoptosis. Diabetes 58: 2303–2315.
- 57. Yu T, Robotham JL, Yoon Y (2006) Increased production of reactive oxygen species in hyperglycemic conditions requires dynamic change of mitochondrial morphology. Proc Natl Acad Sci USA 103: 2653–2658.
- 58. Zhang Y, Jiang L, Hu W, Zheng Q, Xiang W (2011) Mitochondrial dysfunction during in vitro hepatocyte steatosis is reversed by omega-3 fatty acid-induced up-regulation of mitofusin 2. Metabolism 60: 767–775.
- 59. Cui M, Tang X, Christian WV, Yoon Y, Tieu KJ (2010) Perturbations in mitochondrial dynamics induced by human mutant PINK1 can be rescued by the mitochondrial division inhibitor mdivi-1. Biol Chem 285: 11740–1152.
- 60. Liu X, Hajnóczky G (2011) Altered fusion dynamics underlie unique morphological changes in mitochondria during hypoxia–reoxygenation stress. Cell Death Differ 18: 1561–1572.
- 61. Benard G, Bellance N, James D, Parrone P, Fernandez H, et al. (2007) Mitochondrial bioenergetics and structural network organization. J Cell Sci 120: 838–848.