Figures
Abstract
In mammals, inter- and intraspecies differences in consumption of sweeteners largely depend on allelic variation of the Tas1r3 gene (locus Sac) encoding the T1R3 protein, a sweet taste receptor subunit. To assess the influence of Tas1r3 polymorphisms on feeding behavior and metabolism, we examined the phenotype of F1 male hybrids obtained from crosses between the following inbred mouse strains: females from 129SvPasCrl (129S2) bearing the recessive Tas1r3 allele and males from either C57BL/6J (B6), carrying the dominant allele, or the Tas1r3-gene knockout strain C57BL/6J-Tas1r3tm1Rfm (B6-Tas1r3-/-). The hybrids 129S2B6F1 and 129S2B6-Tas1r3-/-F1 had identical background genotypes and different sets of Tas1r3 alleles. The effect of Tas1r3 hemizygosity was analyzed by comparing the parental strain B6 (Tas1r3 homozygote) and hemizygous F1 hybrids B6 × B6-Tas1r3-/-. Data showed that, in 129S2B6-Tas1r3-/-F1 hybrids, the reduction of glucose tolerance, along with lower consumption of and lower preference for sweeteners during the initial licking responses, is due to expression of the recessive Tas1r3 allele. Hemizygosity of Tas1r3 did not influence these behavioral and metabolic traits. However, the loss of the functional Tas1r3 allele was associated with a small decline in the long-term intake and preference for sweeteners and reduction of plasma insulin and body, liver, and fat mass.
Citation: Murovets VO, Lukina EA, Sozontov EA, Andreeva JV, Khropycheva RP, Zolotarev VA (2020) Allelic variation of the Tas1r3 taste receptor gene affects sweet taste responsiveness and metabolism of glucose in F1 mouse hybrids. PLoS ONE 15(7): e0235913. https://doi.org/10.1371/journal.pone.0235913
Editor: Keiko Abe, The University of Tokyo, JAPAN
Received: February 24, 2020; Accepted: June 25, 2020; Published: July 16, 2020
Copyright: © 2020 Murovets 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.
Funding: Supported by the Russian Foundation for Basic Research, grant 19-015-00121.
Competing interests: The authors have declared that no competing interests exist.
Introduction
Perception of sweet taste of natural sugars, certain amino acids, and artificial sweeteners acts as a major determinant for strong preference and overconsumption of sweet [1], leading to risks for obesity, type 2 diabetes, nonalcoholic fatty liver disease, and cardiovascular complications [2, 3]. Investigations of the last decade suggest an involvement of the sweet taste receptor in the hormonal regulation of metabolism, in addition to its role in sweet taste sensing for detection of calorie-rich products.
There is good evidence that the sweet taste receptor proteins, along with several signal-transducing molecules, are expressed not only in taste buds on the tongue but also in organs regulating metabolism [4]. Sweet taste receptor subunits T1R2 and T1R3 are coexpressed in enteroendocrine cells of the small intestine [5, 6]. Their activation by natural sugars and artificial sweeteners leads to secretion of gut hormones such as glucagon-like peptide-1 (GLP-1), GLP-2, and the gastric inhibitory peptide (GIP), acting as incretins to enhance insulin secretion [5, 7]. In the intestine, T1R3 upregulates through GLP-1 and GIP expression of sodium-dependent glucose transporter isoform 1 (SGLT1) important for the provision of glucose to the body and avoidance of intestinal malabsorption [6]. Coupling of T1R3 with T1R1 produces a heterodimer that serves as an intestinal L-amino acid sensor modulating cholecystokinin release [8].
The T1R3 protein is detected in mouse pancreatic β-cells, where its expression level is greater than that of T1R2, suggesting that most likely T1R3 is present in homodimeric form or in more sensitive to glucose heteromers when coupled with a calcium-sensing receptor [9–11]. In pancreatic β-cells, stimulation of the sweet taste receptor elicits insulin release by elevating intracellular Ca2+ and/or cAMP [12] synergetic to the major universal mechanism of metabolic detection of glucose, which includes the glucose transporter GLUT2, glucokinase, and the ATP-sensitive K+ (KATP) channel [13]. In β-cells, T1R3 can be also dimerized with the T1R1 subunit, forming the receptor detecting amino acids, which stimulates insulin synthesis and reduces cell apoptosis, affecting the mechanistic target of rapamycin complex 1 (mTORC1) through activation of phospholipase C and extracellular signal-regulated protein kinase 1 (ERK1) and ERK2 [14]. Importantly, the knockout of T1R3 in mice resulted in substantial impairment of metabolism and cell proliferation. The Tas1r3-/- deletion decreased glucose tolerance [15, 16] and increased insulin resistance [17]. T1R3-knockout animals are resistant to sucrose-induced obesity and have smaller fat depots when fed a high-sucrose diet [15]. Deletion of Tas1r3-/- reduces activation of mTORC1 [14] and decreases density of pancreatic islets and expression of caspase 3 [18].
The considerable variation in perception and consumption of sweet taste compounds within mammalian species is mainly genetically determined. The analysis of heritable differences in sweet taste responses revealed that inbred strains of mice with higher preference for a large number of chemically diverse sweeteners had the so-called taster allele and that strains with relatively lower sensitivity had the nontaster allele [19, 20]. These differences are associated mainly with the autosomal locus named Sac (saccharin preference). The dominant allele of this locus (Sacb) found in the C57BL/6 strain is associated with higher saccharin preference, while the recessive allele (Sacd) is linked to lower saccharin preference [21, 22]. Positional cloning of the Sac locus in the subtelomeric region of mouse chromosome 4 has shown its correspondence to the Tas1r3 gene, which encodes the T1R3 receptor protein [19].
Loss of T1R genes or their pseudogenization in several vertebrate species, as well as artificial gene deletion, results in sharp decreases in perception and intake of sweeteners [23]. One analysis found that about 78% of differences among mouse strains in preference for saccharin are explained by amino acid sequence variation in the T1R3 protein. Allelic variants of the Tas1r3 gene correspond mainly to three nonsynonymous single nucleotide polymorphisms (SNPs) which do not act by blocking gene expression, changing alternative splicing, or interfering with protein translation in taste tissue. Among the polymorphisms, T179C, which causes a substitution of isoleucine to threonine at position 60 in the extracellular N domain of the T1R3 protein, influence the ability of the protein to form dimers or bind sweeteners [24]. This substitution reduces in vitro binding of T1R3 to caloric or noncaloric sweeteners, increasing, for instance, effective dose for sucrose up to 1000% [25]. Synonymous or nonsynonymous SNPs were also found in human TAS1R genes, as well as haplotypes of separate populations [26, 27]. These polymorphisms may be associated with sweet taste sensitivity and carbohydrate consumption [28, 29].
Evidence for interactions of Tas1r3 polymorphisms with preference and consumption of nutritive or nonnutritive sweeteners was obtained using a congenic 129.B6-Tas1r3 strain [30] or sequencing Tas1r3-containing fragments of DNA in strains with marked differences in sweetener preference [24]. The genetic architecture of postoral detection of glucose and artificial sweeteners is more complicated than inborn determinants affecting oral taste responses; thus, contributions of Tas1r3 polymorphisms likely are masked by background genotype variability. For example, in F2 crosses between C57BL/6 and 129P3 strains, variation in sweetener intake depended less on Tas1r3 genotype (10–35%) than did variation in preference (64–96%) [31, 32].
The goal of the current study was to define in vivo influences of Tas1r3/Sac allelic variation, against the mixed 129S2B6F1 genetic background, on carbohydrate metabolism and body composition, which to our knowledge has not yet been assessed. For this purpose, we undertook the investigation using mouse F1 hybrids between 129SvPasCrl (129S2) and C57BL/6J (B6) inbred strains, or between 129S2 and Tas1r3-knockout C57BL/6J-Tas1r3tm1Rfm (B6-Tas1r3-/-) strains. The inbred B6 strain is homozygous for the Sacb “taster” (T) allele associated with high avidity for sweeteners [23], while the 129S was among the first strains described as sweet “nontasters” (NT) [22, 33] carrying the recessive Sacd allele with nucleotide sequence identical to other nontaster strains [34].
Studies have shown that plasma glucose level was considerably higher in the B6 strain (phenome.jax.org/projects/Eumorphia3/strains) than in 129 [35, 36]. Mice from the B6 strain show mild glucose intolerance and impaired insulin secretion despite normal insulin sensitivity [37]. In contrast, the 129 substrains (phenome.jax.org/projects/Eumorphia3/strains) exhibited higher glucose tolerance [35]. Likewise, the B6 mice were more insulin resistant during the insulin tolerance test, whereas 129SVE mice were relatively insulin sensitive [35]. Unexpectedly, we found no reliable data on glucose tolerance for the 129P3/J strain, which is why we selected 129S2 mice as the parental strain. The Tas1r3-knockout (B6-Tas1r3-/-) strain lacking the entire T1R3 coding region does not demonstrate behavioral or nerve responses to sweet substances [11, 22, 38]. Furthermore, the B6-Tas1r3-/- mice have decreased glucose tolerance compared to the parental strain [15, 16].
By mating females from the 129S2 strain with males from B6 or B6-Tas1r3-/- strain, we obtained F1 hybrids with identical background genotypes but carrying different Tas1r3 alleles: either both recessive NT and dominant T alleles, Sacb and Sacd (129S2B6F1), or the single recessive NT allele Sacd (129S2B6-Tas1r3-/-F1). Taking into account dominance of the Sacb allele [21], we hypothesized differences between hybrids in oral and postoral detection of sweet compounds leading to variations in carbohydrate metabolism. Additionally, we examined the effect of Sac hemizygosity, comparing phenotypes of the B6 parental strain (Sacb homozygote) with the crosses B6 × B6-Tas1r3-/-. Earlier it was shown that T1R3-mediated increase in insulin secretion from pancreatic islets required an optimal concentration of glucose in the media matching the postprandial level in blood [9, 39]. Therefore, in our experiments we used nonfasted animals having free access to the normocaloric lab chow during the light period.
Materials and methods
All experimental procedures have been approved by the Animal Care and Use Committee at the Pavlov Institute of Physiology (Animal Welfare Assurance #A5952-01). The protocols were designed in accordance with the National Institutes of Health Guidelines for the Care and Use of Laboratory Animals.
Animals, housing, and diet
Subjects were adult mice of inbred strains and their intercrosses. C57BL/6J (B6) and 129SvPasCrl (129S2) mice were derived from the parental stocks obtained from the Jackson Laboratory (Bar Harbor, ME, USA) and Charles River Laboratory (Sulzfeld, Germany), respectively. The C57BL/6J-Tas1r3tm1Rfm Tas1r3-knockout mice were offspring of the breeding group kindly provided by Dr. R. F. Margolskee (Monell Chemical Senses Center, Philadelphia, PA, USA). Insulin and triglyceride measurements were made in hybrids between C57BL/6ByJ (B6By) and 129P3/J (129P) mice.
Experiments were performed with male mice at 3–7 months of age maintained at the vivarium of the Pavlov Institute. Animals were housed individually during taste tests, or otherwise in groups of 4–5 in standard polycarbonate cages in a temperature- and humidity-controlled room on a 12/12-h light/dark cycle. Laboratory chow (PK-120, MEST Ltd., Moscow, Russia) containing 67% carbohydrate, 5% lipids, and 19% protein, with an energy value of 13000 kJ/kg, and tap water were available ad libitum, unless otherwise specified.
Taste tests
Behavioral taste responses to sucrose or noncaloric sweeteners were examined in separate groups of mice using the brief-access licking test (Group 1: 129S2B6F1, n = 6; 129S2B6-Tas1r3-/-F1, n = 5; B6, n = 19; B6-Tas1r3+/-, n = 29) or the long-term two-bottle choice test (Group 2: 129S2B6F1, n = 11; 129S2B6-Tas1 r3-/-F1, n = 13; B6, n = 22; B6-Tas1r3+/-, n = 23). The brief-access licking test (BALT) was conducted in the middle of the light period (1–3 p.m.) using procedures described by J. Glendinning et al. [40], with minor modifications. During the experimental session, an animal was exposed in a Davis MS-160 gustometer (DiLog Instruments, Tallahassee, FL, USA), in which a sipper tube containing test solution was presented for 5 s, with 20-s interpresentation interval. Animals first had two training sessions with water at 1-day intervals. On training day 1, the animal could drink water freely for 30 min from a single spout. On training day 2, the mouse had 24 trials with water, each lasting for 5 seconds. After each training day, animals had free access to water for 60 min in their home cages. To motivate licking from the sipper tube, animals were deprived of water for 22–23 h before training. To encourage drinking of sweet solutions, we limited the mice to 1.5 mL of water for 22–23 h prior the test session.
In the BALT, animals had access to solutions of sucrose (0.5–4%; Vecton Ltd., St. Petersburg, Russia), sodium saccharinate (0.2–60 mmol/L; Tiaujin Chaugjie Chem. Co., Ltd., China), sucralose or potassium acesulfame (both 0.3–10 mmol/L; Sigma Aldrich Corp., St. Louis, MO, USA) dissolved in deionized water and presented at room temperature. Sweet taste substances were tested at day intervals. The sequence of testing of substances was the same for all animals.
In the 48-h two-bottle choice test (2-BT), individually housed mice from Group 2 had unlimited access to two tubes, one containing solution of sucrose (1–16%) or saccharin (0.2–60 mmol/L), and the other filled with deionized water [41]. Each concentration of solution was given for 48 h. Every 24 h tubes were weighed to the nearest 0.02 g and their position in the cage was changed. Average daily intakes were calculated for each concentration. Preference score was determined as the ratio (in percent) of daily intake of test solution to daily intake of fluid (solution + water). Solutions of sucrose and saccharin were tested in separate groups in ascending order of concentrations.
Glucose and insulin tolerance tests
Glucose and insulin tolerance tests were performed in the middle of the light period in a separate group of nonfasted awake male mice, including 129S2B6F1 (n = 21), 129S2B6-Tas1r3-/-F1 (n = 22), B6 (n = 42), and B6-Tas1r3+/- (n = 36). These animals were kept in their home cages. In the glucose tolerance test (GTT), matching specific recommendations of the National Institutes of Health Mouse Metabolic Phenotyping Center [42], 2 g/kg glucose (Sigma Aldrich Corp.) was administered in aqueous solution either by intragastric gavage (IG) or intraperitoneally (IP). In the insulin tolerance test (ITT), animals were injected IP with 2 U/kg insulin (insulin aspart, Novo Nordisk A/S, Bagsvaerd, Denmark). Blood was sampled by tail cut, and two measurements of glucose concentration were made at 0, 10, 15, 30, 60, 90, and 120 minutes after injection of glucose or at 0, 15, 60, and 120 minutes after administration of insulin, using the OneTouch® UltraEasy® glucometer (LifeScan Europe Ltd., Division of the Cilag Gmbh Int., Zug, Switzerland) and OneTouch® Ultra® test strips (LifeScan Scotland Ltd., Inverness, Great Britain).
Biochemical assay and morphometry
Blood sampling for estimation of hormone and metabolite levels was done immediately after sedation with gas mixture of CO2 and O2 (50/50 volume %) in a separate group of nonfasted awake male mice, including 129PB6ByF1 (n = 18), 129PB6-Tas1r3-/-F1 (n = 17), B6 (n = 19), and B6-Tas1r3+/- (n = 21). These animals were kept in their home cages. Blood was withdrawn from the orbital sinus into tubes containing EDTA and then centrifuged for plasma separation. Concentrations of triglycerides and glycerol were assessed in fresh plasma using the TR0100 assay kit (Sigma Aldrich Corp.); other samples were kept at -30°C. Plasma insulin level was measured with Elisa kit EZRMI-13K (Millipore Corp., Burlington, MA, USA).
Body composition was assessed in a group of naïve mice, as well as mice used in the BALT 3 weeks earlier. After euthanasia by decapitation, liver and fat were removed and weighed to the nearest 0.001 g. The anterior subcutaneous (interscapular), posterior subcutaneous (dorsolumbar, inguinal, and gluteal), visceral perirenal visceral mesenteric, and retroperitoneal visceral epididymal (gonadal) bilateral depots were excised.
Data analysis
Plasma glucose area under the curve (AUC) was calculated using the trapezoidal rule. Data from behavioral taste tests and glucose levels in GTT and ITT were compared using two-way ANOVA (Statistica, version 7.0). Concentration (for taste tests) and time (for GTT or ITT) were considered as within-subject factors, and genotype as a between-subject factor. Post hoc paired comparisons were made using Fisher’s least significant difference (LSD) test. Differences between AUCs or water consumption in training sessions for the BALT were determined with one-way ANOVA. Other comparisons were made with unpaired two-tailed Student’s t-test. All data are presented as mean ± SEM; p-values < 0.05 are considered significant. ANOVA results are listed in Table 2.
Results
Licking response
In the training sessions of the BALT, we found no differences in water intake between 129S2B6F1 and 129S2B6-Tas1r3-/-F1 hybrids. Interestingly, mice from the 129S2 parental strain showed water consumption similar to hybrid groups. The B6-Tas1r3+/- hemizygotes drank less water during the first training session than animals from the B6 strain, but both genotypes showed a similar lick rate the next day (Table 1). These results justify the following comparison of raw lick rates between 129S2B6F1 and 129S2B6-Tas1r3-/-F1 or between B6 and B6-Tas1r3+/-mice without converting licking number per trial into a standardized lick ratio [43].
Mice from all groups exhibited robust concentration-dependent increases in licking rate for all four tested sweet compounds (ANOVA results are shown in the Table 2). Compared with the 129S2B6-Tas1r3-/-F1 hybrids, mice from 129S2B6F1 group showed enhanced lick responsiveness to certain concentrations (Fig 1A–1D). The 129S2B6F1 hybrids licked 2–4% sucrose solutions more vigorously than did 129S2B6-Tas1r3-/-F1 mice (Fig 1A; p<0.01, Fisher’s LSD test). When animals were offered solutions of saccharin, sucralose, or acesulfame, 129S2B6F1 mice displayed more active licking of higher concentrations than did 129S2B6-Tas1r3-/-F1 mice (Fig 1B–1D). An influence of Tas1r3 hemizygosity was assessed by matching reactions of the B6 strain (Tas1r3 homozygote) and B6-Tas1r3+/- mice, carrying a single Tas1r3 allele. We did not detect significant signs of haplo-insufficiency at any tested concentration of either caloric (sucrose) or noncaloric (saccharin and sucralose) sweeteners (Fig 1E–1G).
Initial licking responses to solutions with a range of concentrations of sucrose and artificial sweeteners in the brief-access testing of 4- to 7-month-old male mice with different Tas1r3 genotypes: 129S2B6F1 and 129S2B6-Tas1r3-/-F1 (a–d), or B6 and B6-Tas1r3+/- (e–g). Post hoc comparisons with Fisher’s LSD test: *p<0.05, **p<0.01.
Long-term two-bottle sweetener preference
The 2-BT was used to examine preference and intake of sucrose and saccharin. For both sweeteners, the 129S2B6F1 hybrids demonstrated overall higher intakes and preference scores than did 129S2B6-Tas1r3-/-F1 mice (Fig 2A–2D; Table 2). Paired post hoc comparisons confirmed that 129S2B6F1 mice consumed larger amounts of intermediate and high concentrations of sucrose (4–8%) and showed higher preference for sucrose solutions at a relatively lower (1–4%) concentration range (Fig 2A and 2B; p<0.05). 129S2B6-Tas1r3-/-F1 hybrids sharply increased consumption of sucrose when they were given 8–16% solutions (p<0.01) and did not differ from 129S2B6F1 mice in preference for 8–16% solutions (Fig 2A and 2B). The 129S2B6F1 hybrids preferred and consumed saccharin more vigorously than did 129S2B6-Tas1r3-/-F1 at higher tested concentrations (6–60 mM; Fig 2C and 2D). Assessment of the effect of the Tas1r3 hemizygosity revealed that the loss of a Tas1r3 allele led to reduced intake of 4–8% sucrose solution and slightly reduced preference score for the lowest tested concentrations (1–2%; Fig 2E and 2F). Additionally, Tas1r3 hemizygosity was associated with a decrease in preference for lower concentrations of saccharin in the range of 0.2–2 mmol/L but did not affect saccharin consumption (Fig 2G and 2H).
Sucrose and noncaloric sweetener intakes and preferences in the two-bottle preference test in 2- to 7-month-old male mice with different Tas1r3 genotypes: 129S2B6F1 and 129S2B6-Tas1r3-/-F1 (a–d), or B6 and B6-Tas1r3+/- (e–h). Post hoc comparisons with Fisher’s LSD test: *p<0.05, **p<0.01.
Together, these findings indicate that initial lick responses to nutritive and nonnutritive sweeteners depend mainly on polymorphisms of the Tas1r3 gene and that the effect of haplo-insufficiency of Tas1r3 is negligible. Presence of the dominant Tas1r3 allele confers higher lick responsiveness to lower concentrations of sucrose and higher concentrations of saccharin, sucralose, and acesulfame. The preference for sucrose in the 2-BT is also affected by the Tas1r3 polymorphisms; however, between-genotype differences in long-term consumption of sucrose may partially depend on Tas1r3 hemizygosity.
The relationship between Sac genotype and glucose and insulin tolerance
Initial analysis of IP glucose tolerance was performed in parental strains: 129P, 129S2, B6, B6By, and B6-Tas1r3-/-. In the nonfasting state, parental strains differed in baseline glucose level, which was higher in the B6 strain, including the knockout substrain, than in 129 (Fig 3; p<0.05). However, there was significant overlap between responses of B6 and B6By, as well as between 129P and 129S2. The IP glucose tolerance was substantially reduced in the B6 strain compared to 129 (p<0.005), but no significant differences were found within strains excluding B6-Tas1r3-/-. The Tas1r3 gene deficiency markedly worsens glucose tolerance (Fig 3) compared both to B6 and to B6By (p<0.01).
Plasma glucose concentrations and glucose area under the curve (AUC) were determined after intraperitoneal (IP) administration of 2 g/kg glucose. Post hoc comparisons with Fisher’s LSD test: **p<0.01.
Comparison of Figs 3 and 4A demonstrates that hybrid groups had intermediate glucose tolerance between parental strains. After both IP and IG glucose load, nonfasted 129S2B6F1 hybrids exhibited higher glucose tolerance than did 129S2B6-Tas1r3-/-F1 (Fig 4A and 4B). Interestingly, in B6 and B6-Tas1r3+/- mice, plasma glucose concentration was nearly identical after IP injection; however, after IG administration, glucose levels in B6-Tas1r3+/- were significantly reduced (Fig 4C and 4D). IP injection of insulin elicited a rapid (<15 min) fall of plasma glucose concentration, which barely recovered during the subsequent 2 h. We found no significant differences in tolerance to insulin between 129S2B6F1 and 129S2B6-Tas1r3-/-F1 hybrids or between B6 and B6-Tas1r3+/- mice (Fig 4E and 4F).
Glucose tolerance test (IP and IG GTT; a–d) in 3–4-month-old nonfasted male mice and insulin tolerance test (ITT; e, f) in 5–6-month-old nonfasted male mice with different Tas1r3 genotypes: 129S2B6F1 and 129S2B6-Tas1r3-/-F1, or B6 and B6-Tas1r3+/-. Plasma glucose concentrations and glucose area under the curve (AUC) were determined after the intraperitoneal (IP) or intragastric (IG) glucose administration of 2 g/kg glucose. Post hoc comparisons with Fisher’s LSD test: *p<0.05, **p<0.01.
Baseline plasma glucose, insulin, triglyceride, and glycerol levels and body composition
Baseline glucose and body composition were assessed in the B6 strain and hybrids 129S2B6F1, 129S2B6-Tas1r3-/-F1, and B6-Tas1r3+/- in the nonfasting state in the middle of the light period (Fig 5). Concentration of plasma glucose was not affected by Tas1r3 polymorphisms or hemizygosity for the Tas1r3 allele (Fig 5A and 5E). We found no differences in body, fat, or liver mass between 129S2B6F1 and 129S2B6-Tas1r3-/-F1 mice (Fig 4B–4D). However, the lack of a single functional Tas1r3 allele in B6-Tas1r3+/- was associated with significant increase of the body, fat, and liver mass (Fig 4F–4H).
**p<0.01, Student’s t-test.
Insulin and metabolite concentrations were measured in plasma of the B6 strain and hybrids 129PB6ByF1, 129PB6-Tas1r3-/-F1, and B6-Tas1r3+/- in the nonfasting state in the middle of the light period. 129PB6ByF1 hybrids exhibited substantially higher baseline insulin levels compared with 129PB6-Tas1r3-/-F1 (Fig 6A). A marked reduction of plasma insulin was found in the B6-Tas1r3+/- hemizygotes, unlike B6 homozygotes (Fig 6D). There was no significant difference between all compared genotypes in plasma triglyceride concentration (Fig 6B and 6E). In contrast, the nonfasted plasma level of glycerol depended on the Tas1r3 genotype: 129PB6-Tas1r3-/-F1 hybrids demonstrated higher concentration of glycerol compared with 129PB6ByF1 mice (Fig 6C). Hemizygous B6-Tas1r3+/- mice and Tas1r3-homozygous B6 mice showed similar plasma glycerol levels (Fig 6F).
*p<0.05, **p<0.01, Student’s t-test.
Discussion
In this study, we confirmed that our experimental model reproduces polymorphic influences of the mouse Tas1r3 genotype on the appetitive responses to sweeteners described in the earlier investigations with 129.B6-Tas1r3 congenic mice [30]. Using the F1 hybrids between C57BL/6J and 129SvPasCrl strains, which had identical background genotypes but carried different Tas1r3 alleles, we demonstrated that the presence of the dominant T allele in 129S2B6F1 hybrids is associated with the stronger preference for sweet solutions compared with 129S2B6-Tas1r3-/-F1 mice expressing only the recessive NT allele. The effect of the Tas1r3 genotype depended on concentrations of sweet taste compound that were specific to each sweetener. In the BALT, lick rate for sucrose was influenced by the Tas1r3 genotype when lower (2–4%) concentrations were tested (Fig 1A). As shown in our previous study in crosses between C57BL/6ByJ and 129P3/J strains, responses to higher concentrations of sucrose (8–32%) were not linked to the Tas1r3 polymorphisms [44]. At the same time, when animals were exposed to nonmetabolized sweeteners (saccharin, sucralose, and acesulfame), the impact of Tas1r3 polymorphisms tended to be strongest at the higher concentration range (Fig 1B–1D).
The Tas1r3 gene polymorphisms also affected long-term intake and preference scores for sweeteners in the 48-h 2-BT. 129S2B6F1 hybrids carrying the dominant Tas1r3 allele demonstrated a marked increase in consumption of low to intermediate concentrations (4–8%) and preference for lower (1–4%) concentrations of sucrose, compared with hybrids having the recessive allele. However, allelic variation of the Tas1r3 gene did not influence the preference for higher concentrations (8–16%) of sucrose (Fig 2A and 2B). The 129S2B6F1 mice consumed larger amounts and showed greater preference scores for higher concentrations of saccharin compared to 129S2B6-Tas1r3-/-F1 (Fig 2C and 2D).
These data are generally consistent with results of earlier studies of responsiveness to different concentrations of sweeteners, determined by Tas1r3 allelic variations, which were performed with inbred mouse strains bearing T or NT Tas1r3 alleles [40] or the 129.B6-Tas1r3 segregating congenic strain [30]. The lack of Tas1r3/Sac polymorphic effects on the preference of high concentrations of sucrose probably is not related to taste perception, because impulse discharge of the chorda tympani nerve to lingual application of sweeteners progressively increased across the whole range of tested concentrations of stimuli [30]. Potentially, the influence of Tas1r3 polymorphisms can be masked by responses to the calorie content of test solutions, which does not depend on T1R2/T1R3-mediated perception, such as enhancement of the cephalic phase of insulin release [45], or by conditional reflexes to nongustatory stimuli, such as smell and texture [46]. Intake of nonnutritive sweeteners likely does not induce strong responses such as these. Although excitations induced by nutritive or nonnutritive sweeteners are relayed to the brain through common primary pathways, they interact with different brain regions [47].
In the experimental model used here, an influence of Tas1r3 hemizygosity should also be considered. Hemizygosity can lead to haplo-insufficiency, wherein a single functional copy of a gene is insufficient to maintain the standard phenotype [48]. In this connection, we estimated the effect of absence of a single Tas1r3 allele. In the BALT, the impact of the Tas1r3 gene hemizygosity was not detected, as we showed comparing responses between the B6 strain and B6-Tas1r3+/- hybrids (Fig 1E–1G). Moderate signs of Tas1r3 haplo-insufficiency were found in the long-term 2-BT. Lack of the T allele in B6-Tas1r3+/- mice was associated with reduced consumption of intermediate (4–8%) and preference for lower concentrations of sucrose (1–2%) and saccharin (0.2–2 mmol/L) relative to the B6 strain. However, the difference between Tas1r3 homozygous and hemizygous mice was notably smaller than that between 129S2B6F1 and 129S2B6-Tas1r3-/-F1 hybrids (Fig 2).
The central finding of our study showed that the dominant Tas1r3 allele reduces plasma glucose concentration after enteral or parenteral glucose administration. Conversely, 129S2B6-Tas1r3-/-F1 hybrids, carrying the recessive allele, exhibited lower glucose tolerance (Fig 4A and 4B). To distinguish between effects of Tas1r3 functional polymorphisms and haplo-insufficiency, we additionally compared responses of the B6 parental strain (Tas1r3 homozygote) and B6-Tas1r3+/- hemizygote and found no difference between the groups in the IP GTT (Fig 4C). Surprisingly, after IG load with glucose, B6-Tas1r3+/- hemizygotes exhibited lower plasma glucose concentrations, which can reflect reduced expression of SGLT1 because of decreased GLP1 and GIP production in the small intestine mucosa [6, 49] rather than a consequence of impaired utilization of glucose in tissues. Altogether, the analyses we performed suggest that the reduction of glucose tolerance in 129S2B6-Tas1r3-/-F1 hybrids is due to expression of the recessive NT allele. At the same time, Tas1r3 genotype did not influence baseline glucose level in nonfasting mice (Fig 5A). As we reported earlier, insulin sensitivity was reduced in the Tas1r3-knockout mice [16]; however, in the present assay, there was no relationship between tissue sensitivity to insulin and Tas1r3 genotype (Fig 4E and 4F).
Potentiation of insulin secretion in islet cells of the pancreas and incretin secretion in the small intestine, dependent on the T1R3 receptor protein, are supposed to be important mechanisms of the influence of postoral sweet taste receptors on glucose tolerance [26, 50, 51]. In the present study, plasma insulin level was assessed in F1 crosses between 129P and B6By substrains, which did not differ in glucose tolerance from 129S2 and B6 substrains, respectively (Fig 3). Plasma insulin level declined in 129PB6-Tas1r3-/-F1 hybrids carrying the recessive allele relative to 129PB6ByF1 mice (Fig 6A), which corresponds to the attenuation of glucose tolerance in 129S2B6-Tas1r3-/-F1 hybrids. However, reduction of insulin level was due to haplo-insufficiency, as confirmed by comparison between the B6 strain and B6-Tas1r3+/- mice (Fig 6D).
Ablation of the T1R3 receptor affects anabolism, including lipid biosynthesis. Although deletion of the T1R2 or T1R3 protein did not influence body weight in B6 mice maintained on the normocaloric diet [52, 53], there was an increase in epididymal fat weight and signs of dyslipidemia, including elevation of plasma triglycerides and increased glycerol levels [53]. In contrast, when mice were fed the high-calorie diet, impaired sweet taste perception slowed down body and adipose tissue weight gain [54, 55]. This result is consistent with data obtained in experiments with adipocyte cell cultures, which have confirmed that the T1R3 protein mediates a stimulative influence of artificial sweeteners on adipogenesis [51, 56]. Comparison between 129S2B6F1 and 129S2B6-Tas1r3-/-F1 hybrids performed in this study did not reveal a relation between Tas1r3 polymorphisms and body, fat, and liver mass (Fig 5B–5D) or triglyceride levels (Fig 6B). However, Tas1r3 hemizygosity caused an increase of body, fat, and liver mass (Fig 5F–5H), allowing us to speculate that, in the experimental model used here, the recessive Tas1r3 allele confers reduction of body, liver, and fat mass, which is masked by haplo-insufficiency.
Concluding remarks
On the whole, the obtained data provide new in vivo evidence that polymorphisms of the Tas1r3 gene (Sac locus) influence carbohydrate metabolism, as well as sweetener intake and preference. In particular, presence of the dominant Tas1r3 allele (Sacb locus) on the 129S2B6F1 background genotype results in higher glucose tolerance, along with increased consumption and preference for sugars and artificial sweeteners during initial licking. Hemizygosity of Tas1r3 does not affect these behavioral and metabolic traits. However, the loss of one functional Tas1r3 allele was linked to decline in intake and preference for sweeteners in the long-term 2-BT, as well as reduction of plasma insulin, body mass, liver mass, and fat mass. Our results suggest that further investigation of postoral sweet detection with the T1R3 protein may lead to new understanding of carbohydrate homeostasis disorders.
References
- 1. Hladik CM., Pasquet P, Simmen B. 2002. New perspectives on taste and primate evolution: the dichotomy in gustatory coding for perception of beneficent versus noxious substances as supported by correlations among human thresholds. Am. J. Phys. Anthropol. 4: 342–348.
- 2. Garcia-Bailo B, Toguri C, Eny M, Sohemy (El-) A. 2009. Genetic variation in taste and its influence on food selection. OMICS J. Integr. Biol. 1: 69–80.
- 3. Liu S, Manson JE. 2001. Dietary carbohydrates, physical inactivity, obesity, and the 'metabolic syndrome' as predictors of coronary heart disease. Curr. Opin. Lipidol. 4: 395–404.
- 4. Laffitte A, Neiers F, Briand L. 2014. Functional roles of the sweet taste receptor in oral and extraoral tissues. Curr. Opin. Clin. Nutr. Metab. Care. 4: 379–385.
- 5. Jang HJ, Kokrashvili Z, Theodorakis MJ, Carlson OD, Kim BJ, Zhou J, et al. 2007. Gut-expressed gustducin and taste receptors regulate secretion of glucagon-like peptide-1. Proc. Natl. Acad. Sci. U S A 104(38):15069–74. pmid:17724330
- 6. Margolskee RF, Dyer J, Kokrashvili Z, Salmon KS, Ilegems E, Daly K, et al. 2007. T1R3 and gustducin in gut sense sugars to regulate expression of Na+-glucose cotransporter 1. PNAS. 38: 15075–15080.
- 7. Kokrashvili Z, Mosinger B, Margolskee RF. 2009. Taste signaling elements expressed in gut enteroendocrine cells regulate nutrient-responsive secretion of gut hormones. Am. J. Clin. Nutr. 3: 822–825.
- 8. Daly K, Al-Rammahi M, Moran A, Marcello M, Ninomiya Y, Shirazi-Beechey SP. 2013. Sensing of amino acids by the gut-expressed taste receptor T1R1-T1R3 stimulates CCK secretion. Am. J. Physiol. Gastrointest Liver. Physiol. 304(3): G271–82. pmid:23203156
- 9. Kyriazis GA, Soundarapandian MM, Tyrberg B. 2012. Sweet taste receptor signaling in beta cells mediates fructose-induced potentiation of glucose-stimulated insulin secretion. PNAS. 8: E524–532.
- 10. Maitrepierre E, Sigoillot M, Le Pessot L, Briand L. 2012. Recombinant expression, in vitro refolding, and biophysical characterization of the N-terminal domain of T1R3 taste receptor. Protein Expr. Purif. 1: 75–83.
- 11. Damak S, Rong M, Yasumatsu K, Kokrashvili Z, Varadarajan V, Zou S, et al. 2003. Detection of sweet and umami taste in the absence of taste receptor T1r3. Science 5634: 850–853.
- 12. Kojima I, Nakagawa Y. 2011. The Role of the sweet taste receptor in enteroendocrine cells and pancreatic β-cells. Diabetes Metab. J. 35(5):451–7. pmid:22111035
- 13. Craig TJ, Ashcroft FM, Proks P. 2008. How ATP inhibits the open K(ATP) channel. J. Gen. Physiol. 1: 131–144.
- 14. Wauson EM, Zaganjor E, Lee AY, Guerra ML, Ghosh AB, Bookout AL, et al. 2012. The G protein-coupled taste receptor T1R1/T1R3 regulates mTORC1 and autophagy. Mol. Cell. 47(6):851–62. pmid:22959271
- 15. Simon BR, Learman BS, Parlee SD, Scheller EL, Mori H, Cawthorn WP, et al. 2014. Sweet taste receptor deficient mice have decreased adiposity and increased bone mass. PLoS One 9(1):e86454. pmid:24466105
- 16. Murovets VO, Bachmanov AA, Zolotarev VA. 2015. Impaired glucose metabolism in mice lacking the Tas1r3 taste receptor gene. PLoS One. 6: e0130997. pmid:26107521
- 17. Murovets VO, Bachmanov AA, Travnikov SV, Churikova AA, Zolotarev VA. 2014. The involvement of the T1R3 receptor protein in the control of glucose metabolism in mice at different levels of glycemia. J. Evol. Biochem. Physiol. 4: 334–344.
- 18. Murovets VO, Sozontov EA, Zachepilo TG. 2019. The effect of the taste receptor protein T1R3 on the development of islet tissue of the murine pancreas. Dokl. Biol. Sci. May;484(1):1–4. pmid:31016494
- 19. Bachmanov AA, Li X, Reed DR, Ohmen JD, Li S, Chen Z, et al, Beauchamp GK. 2001. Positional cloning of the mouse saccharin preference (Sac) locus. Chem. Senses 7: 925–933.
- 20. Frank ME, Blizard DA. 1999. Chorda tympani responses in two inbred strains of mice with different taste preferences. Physiol. Behav. 2: 287–297.
- 21. Fuller JL. 1974. Single-locus control of saccharin preference in mice. J. Hered. 1: 33–36.
- 22. Nelson G, Hoon MA, Chandrashekar J, Zhang Y, Ryba NJ, Zuker CS. 2001. Mammalian sweet taste receptors. Cell. 3: 381–390.
- 23. Bachmanov AA, Bosak NP, Floriano WB, Inoue M, Li X, Lin C, et al. 2011. Genetics of sweet taste preferences. Flavour. Fragr. J. 4: 286–294.
- 24. Reed DR, Li S, Li X, Huang L, Tordoff MG, Starling-Roney R, et al. 2004. Polymorphisms in the taste receptor gene (Tas1r3) region are associated with saccharin preference in 30 mouse strains. J. Neurosci. 4: 938–946.
- 25. Nie Y, Vigues S, Hobbs JR, Conn GL, Munger SD. 2005. Distinct contributions of T1R2 and T1R3 taste receptor subunits to the detection of sweet stimuli. Curr. Biol. 21: 1948–1952.
- 26. Kim UK, Wooding S, Riaz N, Jorde LB, Drayna D. 2006. Variation in the Human TAS1R Taste Receptor Genes. Chem. Senses 7: 599–611.
- 27. Raliou M, Grauso M, Hoffmann B, Schlegel–Le-Poupon C, Nespoulous C, Debat H, et al. 2011. Human genetic polymorphisms in T1R1 and T1R3 taste receptor subunits affect their function Chem. Senses 36: 527–537, pmid:21422378
- 28. Fushan AA, Simons CT, Slack JP, Manichaikul A, Drayna D. 2009 Allelic polymorphism within the TAS1R3 promoter is associated with human taste sensitivity to sucrose. Curr. Biol. 19(15):1288–93. pmid:19559618
- 29. Han P, Keast RSJ, Roura E. 2017 Salivary leptin and TAS1R2/TAS1R3 polymorphisms are related to sweet taste sensitivity and carbohydrate intake from a buffet meal in healthy young adults. Br. J. Nutr. Nov;118(10):763–770. pmid:29110749
- 30. Inoue M, Glendinning JI, Theodorides ML, Harkness S, Li X, Bosak N, et al. 2007. Allelic variation of the Tas1r3 taste receptor gene selectively affects taste responses to sweeteners: evidence from 129.B6-Tas1r3 congenic mice. Physiol. Genomics 1: 82–94.
- 31. Bachmanov AA, Reed DR, Ninomiya Y, Inoue M, Tordoff MG, Price RA, et al. 1997. Sucrose consumption in mice: major influence of two genetic loci affecting peripheral sensory responses. Mamm. Genome 8: 545–548. pmid:9250857
- 32. Inoue M, Reed DR, Li X, Tordoff MG, Beauchamp GK, Bachmanov AA. 2004. Allelic variation of the Tas1r3 taste receptor gene selectively affects behavioral and neural taste responses to sweeteners in the F2 hybrids between C57BL/6ByJ and 129P3/J mice. J. Neurosci. 9: 2296–2303.
- 33. Lush IE. 1989. The genetics of tasting in mice. VI. Saccharin, acesulfame, dulcin and sucrose. Genet. Res. 53(2):95–9. pmid:2744455
- 34. Max M, Shanker YG, Huang L, Rong M, Liu Z, Campagne F, et al. 2001. Tas1r3, encoding a new candidate taste receptor, is allelic to the sweet responsiveness locus Sac. Nat. Genet. 28(1):58–63. pmid:11326277
- 35. Almind K, Kahn CR. 2004. Genetic determinants of energy expenditure and insulin resistance in diet-induced obesity in mice. Diabetes 53(12):3274–85. pmid:15561960
- 36. Berglund ED, Li CY, Poffenberger G, Ayala JE, Fueger PT, Willis SE, et al. 2008. Glucose metabolism in vivo in four commonly used inbred mouse strains. Diabetes 57(7):1790–9. pmid:18398139
- 37. Toye AA, Lippiat JD, Proks P, Shimomura K, Bentley L, Hugill A, et al. 2005. A genetic and physiological study of impaired glucose homeostasis control in C57BL/6J mice. Diabetologia, 48(4), 675–686. pmid:15729571
- 38. Zhao GQ, Zhang Y, Hoon MA, Chandrashekar J, Erlenbach I, Ryba NJ, et al. 2003. The receptors for mammalian sweet and umami taste. Cell. 3: 255–266.
- 39. Nakagawa Y, Nagasawa M, Yamada S, Hara A, Mogami H, Nikolaev VO, et al. 2009. Sweet taste receptor expressed in pancreatic beta-cells activates the calcium and cyclic AMP signaling systems and stimulates insulin secretion. PLoS One. 4: e51062009.
- 40. Glendinning JI, Chyou S, Lin I, Onishi M, Patel P, Zheng KH. 2005. Initial licking responses of mice to sweeteners: effects of tas1r3 polymorphisms. Chem. Senses 7: 601–614.
- 41.
Spector A. C. 2003. Psychophysical evaluation of taste function in non-human mammals. Handbook of Olfaction and Gustation Ed. R. L. Doty. New York. 869–879.
- 42. McGuinness OP, Ayala JE, Laughlin MR, Wasserman DH. 2009. NIH experiment in centralized mouse phenotyping: the Vanderbilt experience and recommendations for evaluating glucose homeostasis in the mouse. Am. J. Physiol. Endocrinol. Metab. 4: E849–855.
- 43. Glendinning JI, Gresack J, Spector AC. 2002. A high-throughput screening procedure for identifying mice with aberrant taste and oromotor function. Chem. Senses 5: 461–474.
- 44. Murovets VO, Lukina EA, Zolotarev VA. 2018. The Effect of Tas1r3 Gene Polymorphism on Preference and Consumption of Sucrose and Low-Calorie Sweeteners in Interstrain Hybrid Mice of the First Filial Generation. J. Evol. Biochem. Phys. 54: 221–233.
- 45. Glendinning JI, Stano S, Holter M, Azenkot T, Goldman O, Margolskee RF, et al. 2015. Sugar-induced cephalic-phase insulin release is mediated by a T1r2+T1r3-independent taste transduction pathway in mice. Am. J. Physiol. Regul. Integr. Comp. Physiol. 5: R552–560.
- 46. Sclafani A. 2013. Gut-brain nutrient signaling. Appetition vs. satiation. Appetite. 71: 454–458. Epub 2012. pmid:22664300
- 47. Frank GK, Oberndorfer TA, Simmons AN, Paulus MP, Fudge JL, Yang TT, et al. 2008. Sucrose activates human taste pathways differently from artificial sweetener. Neuroimage 4: 1559–69. Epub 2007.
- 48. Huang N, Lee I, Marcotte EM., Hurles ME. 2010. Characterizing and predicting haploinsufficiency in the human genome. PLoS Genet. 10: e1001154.
- 49. Sigoillot M, Brockhoff A, Meyerhof W, Briand L. 2012. Sweet-taste-suppressing compounds: current knowledge and perspectives of application. Appl. Microbiol. Biotechnol. 3: 619–630.
- 50. Jiang P, Josue J, Li X, Glaser D, Li W, Brand JG, et al. 2012. Major taste loss in carnivorous mammals. PNAS. 13: 4956–4961.
- 51. Masubuchi Y, Nakagawa Y, Ma J, Sasaki T, Kitamura T, Yamamoto Y, et al. 2013. A novel regulatory function of sweet taste-sensing receptor in adipogenic differentiation of 3T3-L1 cells. PLoS One. 1: e54500.
- 52. Treesukosol Y, Smith KR, Spector AC. 2011. The functional role of the T1R family of receptors in sweet taste and feeding. Physiol. Behav. 1: 14–26.
- 53. Murovets VO, Sozontov EA, Andreeva JV, Khropycheva RP, Zolotarev VA. 2016. Effect of T1R3 receptor protein deletion on gluconeogenesis and lipid metabolism in mice. Ross. Fiziol. Zh. Im. IM Sechenova. 6: 668–679.
- 54. Glendinning JI, Gillman J, Zamer H, Margolskee RF, Sclafani A. 2012. The role of T1r3 and Trpm5 in carbohydrate-induced obesity in mice. Physiol. Behav. 1: 50–58.
- 55. Larsson MH., Håkansson P, Jansen FP, Magnell K, Brodin P. 2015. Ablation of TRPM5 in mice results in reduced body weight gain and improved glucose tolerance and protects from excessive consumption of sweet palatable food when wed high caloric diets. PLoS One 9: e0138373.
- 56. Masubuchi Y, Nakagawa Y, Medina J, Nagasawa M, Kojima I, Rasenick MM, et al. 2017. Correction: T1R3 homomeric sweet taste receptor regulates adipogenesis through Gαs-mediated microtubules disassembly and Rho activation in 3T3-L1 cells. PLoS One 7: e0181293.