Steviol glycosides (SGs), such as stevioside and rebaudioside A, are natural, non-caloric sweet-tasting organic molecules, present in extracts of the scrub plant Stevia rebaudiana, which are widely used as sweeteners in consumer foods and beverages. TRPM5 is a Ca2+-activated cation channel expressed in type II taste receptor cells and pancreatic β-cells. Here we show that stevioside, rebaudioside A and their aglycon steviol potentiate the activity of TRPM5. We find that SGs potentiate perception of bitter, sweet and umami taste, and enhance glucose-induced insulin secretion in a Trpm5-dependent manner. Daily consumption of stevioside prevents development of high-fat-diet-induced diabetic hyperglycaemia in wild-type mice, but not in Trpm5−/− mice. These results elucidate a molecular mechanism of action of SGs and identify TRPM5 as a potential target to prevent and treat type 2 diabetes.
Steviol glycosides (SGs) are found in the leaves of a scrub plant native to the subtropical regions of South America, Stevia rebaudiana Bertoni sp. Stevia extract has been used for centuries as a sweetening food additive in South America1, and was recently approved for this purpose also in the European Union and the United States. These molecules have a common aglycone core structure steviol (ent-13-hydroxykaur-16-en-18-oic acid), and differ in their glycosylation pattern. The two major glycosides found in the leaves are stevioside and rebaudioside A2. Both taste ∼200–300 times sweeter than sucrose. Non-caloric sweeteners are increasingly introduced into common foods such as diet sodas, cereals and desserts, as sugar replacement, and are for this reason recommended for weight loss and for individuals suffering from glucose intolerance and diabetes3. However, stevia extracts might have direct insulinotropic and anti-hyperglycaemic effects in type 2 diabetic animal models4. Mechanistic insight into the biological and health effects of Stevia extract and SGs is lacking.
Taste perception in type II taste receptor cells relies on the activity of transient receptor potential cation channel subfamily melastatin member 5 (TRPM5), a monovalent cation channel, activated by a rise in intracellular calcium5. In short, type II taste receptor cells detect sweet, bitter and umami tastants on the tongue. Taste specificity of the cell is accomplished by expression of a specific G-protein-coupled receptor. Sweet, bitter and umami taste receptors have a common downstream signal transduction cascade, which consists of the activation of phospholipase C, release of Ca2+ from IP3-sensitive Ca2+ stores and activation of TRPM5 (ref. 6). TRPM5 activity depolarizes the cell, which triggers the voltage-gated channel calcium homeostasis modulator 1 that mediates the release of ATP neurotransmitter, which in turn activates afferent signalling to the brain7. TRPM5 is also present in insulin-producing β-cells in the pancreas and in peripheral enteroendocrine cells in the gut5,8,9,10,11,12. We showed recently that TRPM5 determines the frequency of glucose-induced calcium oscillations of insulin-releasing pancreatic β-cells10. Consistent with the cellular expression and action of TRPM5, the systemic phenotype of Trpm5-deficient mice includes loss of sweet, bitter and umami taste responsiveness13, and decreased glucose tolerance due to impaired glucose-induced insulin release10,14. It is also interesting to note that Trpm5 expression in the small intestine from diabetic patients is negatively correlated with blood glucose concentrations15. Likewise, WFS-1 diabetic pancreatic islets show a reduced Trpm5 expression16. Moreover, TRPM5 variants are associated with a prediabetic phenotype in humans. TRPM5 single-nucleotide polymorphisms occurred more often in patients with disturbed insulin secretion, elevated plasma glucose, lower glucagon-like peptide 1 (GLP-1) levels and decreased insulin sensitivity17. Specific TRPM5 polymorphisms showed increased prevalence in patients with obesity-related metabolic syndrome18. On the basis of these observations, the hypothesis was developed that TRPM5 might be a pharmacological target for the development of a novel type of insulin secretagogue19,20,21. However, since pharmacology for TRPM5 is currently limited to fairly non-selective-blocking agents, this hypothesis remained untested22,23,24,25.
Our current results indicate that SGs potentiate TRPM5 ion channel activity. In this way, they potentiate the glucose-induced insulin secretion (GIIS) from pancreatic islets and enhance peripheral taste responsiveness in type II taste receptor cells. Chronic stevioside consumption effectively prevents development of high-fat-diet (HFD)-induced diabetes in mice, in a TRPM5-dependent manner.
Steviol and its glycosides potentiate TRPM5
To test whether SGs affect TRPM5-mediated signal transduction pathways, TRPM5 currents were measured in HEK293T cells using the whole-cell patch-clamp technique. TRPM5 currents are readily activated upon break-in with 1 μM free Ca2+ in the pipette solution and inactivate quickly with a variable time course25. Instead, when cells were perfused with stevioside during the inactivating phase, a strong increase of the inward and outward current was observed, which disappeared upon washout (Fig. 1a–d). With strongly buffered [Ca2+]int, stevioside does not activate TRPM5 (Fig. 1d). Similar results were obtained with rebaudioside A, another SG that differs from stevioside by one additional glycosylation (Fig. 1e–h). We also tested steviol, the chemical core group of steviol compounds and the circulating metabolite in blood plasma after oral consumption of SGs1 (Fig. 1i). As shown in Fig. 1j–l, steviol yielded similar results compared to its glycosylated derivatives, indicating that the steviol group is sufficient for the interaction between SGs and TRPM5.
In cell-free inside-out patches, TRPM5 can be activated by direct application of Ca2+ to the intracellular side of the membrane25. In this setting, TRPM5 currents quickly and irreversibly inactivate25. Stevioside and steviol delay inactivation of Ca2+-activated TRPM5 currents, both when applied on the intra- and extracellular side of the membrane (Supplementary Fig. 1). These data strongly indicate that steviol interacts directly with the TRPM5 protein.
We have shown before that TRPM5 is weakly voltage-dependent25,26. As shown in Supplementary Fig. 2a,b, stevioside induces a shift of the voltage-dependent activation of TRPM5 towards more negative membrane potentials. The voltage for half maximal activation (V1/2) shifted from +145.9±33.9 to +42.8±30.6 mV in the presence of stevioside (P=5.1 × 10−4, n=8, paired t-test, Supplementary Fig. 2c). Finally, stevioside has no effect on untransfected cells (Supplementary Fig. 2d,e), and stevioside and steviol have no effect on cells expressing TRPM4 and other, more distantly related, TRP channels (TRPA1, TRPV1, TRPM3 and TRPM8; Supplementary Fig. 2f–h).
Stevioside increases action potential frequency in β-cells
In pancreatic β-cells, TRPM5 mediates a depolarizing current, which tunes [Ca2+]int and Vm oscillation frequency after glucose stimulation10. Consistent with this, a glucose-induced cation current is potentiated by stevioside in pancreatic β-cells. This current shares some properties of TRPM5, including an outwardly rectifying I–V relation and a reversal potential around 0 mV (Fig. 2a,b). We analysed the effects of stevioside on the frequency of action potential firing, stimulated by high glucose (20 mM) or tolbutamide (100 μM). Stevioside increased the frequency of action potentials in wild-type (WT) β-cells, as demonstrated by a reduction in the number of longer intervals between action potentials (Wilcoxon sign-rank test, Fig. 2c,d, n=5 cells each). In contrast, in Trpm5−/− β-cells, the frequency of (tolbutamide-induced) action potential firing was not significantly affected by stevioside (Fig. 2e).
Steviol and stevioside increase calcium activity in islets
When stimulated with 10 mM glucose, pancreatic islets respond with oscillations of [Ca2+]int (Fig. 3). Application of stevioside resulted in a dose-dependent increase of the frequency of glucose-induced Ca2+ oscillations in WT islets, but not in Trpm5−/− islets (Fig. 3a–f). Stevioside exerts this effect with an effector concentration for half-maximum response of 690 nM. Similar results were obtained with steviol (Fig. 3h–j). Note that stevioside did not induce any changes in [Ca2+]int in low-glucose conditions (3 mM; Supplementary Fig. 3a). The frequency of glucose-induced Ca2+ oscillations is stable for up to 1 h in the continuous presence of glucose (Supplementary Fig. 3b,c). From these experiments it can be also derived that the size of pancreatic islets, reflecting the β-cell mass, is not statistically different between WT and Trpm5−/− mice (Fig. 3d,e,g).
Using Fourier analysis, the effect of steviol and stevioside on WT islets can be clearly distinguished from the effect on Trpm5−/− islets (Supplementary Fig. 3g–k). The Fourier-transformed (FT) frequency spectrum from WT islets highlights a shift of the frequency count towards higher frequencies, in response to stevioside unlike in Trpm5−/− islets (Kolmogorov–Smirnov test, P=2.96 × 10-4, Supplementary Fig. 3g). Allocation of the islets to slow-, fast- or mixed-oscillating populations (as described in ref. 10) resulted in a significant increase of the proportion of fast-oscillating islets in the presence of stevioside (Fisher’s exact test, P=0.009, Supplementary Fig. 3h) or steviol (Supplementary Fig. 3i). In the Trpm5−/− mice, stevioside or steviol did not change the proportion of fast-oscillating islets (Fisher’s exact test, P=0.16, Supplementary Fig. 3g,j,k). These findings demonstrate that SGs increase the frequency of glucose-induced calcium oscillations in pancreatic islets in a TRPM5-dependent manner.
When ingested by humans or mice, stevioside is metabolized in the intestine to its aglycon steviol. Once taken up in the blood, steviol circulates in the blood plasma and is finally metabolized by the liver to steviol glucuronide, which is excreted via the urine27. To increase the physiological relevance of our results, we measured the concentration of free steviol circulating in the plasma of mice that received 100 mg l−1 (124 μM) stevioside in their drinking water for 2 weeks. Circulating plasma steviol levels amounted to 391±58.6 nM in these animals (Fig. 3k)28. Application of this physiological concentration of steviol evoked a significant increase of glucose-induced calcium oscillation frequency, similar to stevioside (Fig. 3l,m).
It has been suggested previously that stevioside activates the sweet taste receptor, TAS1R2,TAS1R3 (refs 29, 30). Since pancreatic β-cells functionally express these receptors31, we tested the effect of stevioside in sweet receptor knockout mice (Tas1r2,Tas1r3(−/−)2). Qualitatively similar results were obtained compared to WT islets upon perfusion with stevioside or steviol (Supplementary Fig. 3d–f), that is, a significant increase (+29%) in the glucose-induced Ca2+ oscillation frequency (Supplementary Fig. 3f) such as WT islets (+31%, Fig. 3c). As in WT islets, the distribution of dominant oscillation frequencies of the islets from Tas1r2,Tas1r3(−/−)2 mice was significantly shifted towards faster frequencies in the presence of stevioside (P=1.07 × 10−8, Supplementary Fig. 3g, blue). Subdivision of the islets in slow, mixed or fast islets showed that the fast sub-population appears or increases in the presence of stevioside or steviol (Supplementary Fig. 3l,m).
TRPM5 was previously shown to play a role in GLP-1-mediated insulin secretion32. The observed effects of stevioside are however independent from GLP-1 receptor (GLP-1R)-mediated signalling. Stevioside has an additive potentiating effect on the GLP-1 potentiated calcium oscillation frequency (Supplementary Fig. 4a,d). As anticipated from Shigeto et al.32, the GLP-1 potentiation of glucose-induced calcium oscillations was significantly lower in Trpm5−/− islets, and no additional stevioside-mediated potentiation was observed (Supplementary Fig. 4b,e). The GLP-1R antagonist exendin-3 (100 nM) inhibited the GLP-1-mediated increase in glucose-induced calcium oscillations in WT mice, but did not interfere with the stevioside-induced potentiation of calcium oscillations (Supplementary Fig. 4c,f).
Stevioside stimulates insulin secretion in vitro and in vivo
Considering the effect of SGs on glucose-induced Ca2+ oscillations, and the observation that Ca2+ oscillation frequency correlates with insulin release10, we aimed to test the effect of these compounds on GIIS. As shown in Fig. 4a,b, stevioside potentiated GIIS in WT islets, but not in Trpm5−/− islets (WT: P=0.001, Trpm5−/−: P=0.35; two-sample t-test). Both in WT and Trpm5−/− islets, stevioside treatment was without effect on insulin release in low-glucose conditions (3 mM). During supraphysiological saturating conditions (30 mM KCl or 20 mM glucose), the effect of steviol supplementation on insulin secretion was no longer apparent (Supplementary Table 1). Also in vivo, after intraperitoneal (i.p.) injection of glucose alone or glucose plus stevioside in fasted anaesthetized mice, there is a significantly higher plasma insulin level 30 min post injection of stevioside in the WT mice. This effect was equally absent in Trpm5−/− mice (Fig. 4c).
In perifusion experiments, we analysed the effect of steviol on the dynamics of GIIS (Fig. 4d,e; Supplementary Fig. 5). Steviol supplementation has no effect in low glucose. The 10 mM GIIS displays a rapid peak phase (phase 1), and a more sustained level of insulin release (phase 2). Insulin secretion during both phases is increased in the continuous presence of steviol (Fig. 4d,e). Secretion was normalized to the secretion during maximal stimulation by K30, which was not different between control and steviol perfused conditions (control: 0.12±0.06 versus steviol: 0.15±0.04 pg per islet per minute, P=0.46; two-sample t-test). These effects were not observed in Trpm5−/− islets (Supplementary Fig. 5a,b). Also, in moderately high-glucose conditions (15 mM), supplementation of 10 μM steviol reversibly potentiated the GIIS (Supplementary Fig. 5c,d).
Steviol and stevioside intensify taste perception
To establish the in vivo relevance of TRPM5 modulation by SGs, we first considered taste perception. TRPM5 is an essential component of the intracellular signal transduction cascade elicited by sweet, bitter and umami tastants in type II taste receptor cells6. The two-bottle preference test is a well-established method to detect preferences in mice33, and can be combined with lick detection (lick-o-meter). We used this assay to assess the effect of steviol and SGs in WT, Trpm5−/− and Tas1r2,Tas1r3(−/−)2 mice at various time scales. Considering that SGs are ≈ × 300 sweeter than sucrose (in humans), we used a concentration of 124 μM (equimolar to 300 times <1% sucrose) for each of the SGs and steviol. At this concentration, WT mice show a significant preference for stevioside and rebaudioside A in a 48 h two-bottle preference test (versus water; Fig. 5a, blue bars), which can be attributed to the sweet taste of the SGs. Steviol, on the other hand, does not evoke a specific preference or avoidance in WT mice (Fig. 5a,b). However, when combined with a sweet (1% sucrose), umami (150 mM monopotassium glutamate (MKG)) or bitter (100 μM quinine) tastant, steviol significantly increases the preference for sucrose and umami, and avoidance of quinine (Fig. 5a). Importantly, the increased taste preference or avoidance is apparent within 5 min, in a lick-o-meter test (Fig. 5b–g) and persistent after 60 min (Supplementary Figs 6 and 7). Steviol has no effect on the avoidance of 10 mM citric acid both in short- or long-term exposure tests. Trpm5−/− mice are deficient in the signalling pathway downstream of the taste receptor. This is reflected in the lack of preference or avoidance for sweet, bitter or umami tastants (Fig. 5a, orange bars; Supplementary Figs 6 and 8). Likewise, there is no preference for SGs in Trpm5−/− mice. Neither could we observe an increase in peripheral taste responsiveness upon addition of steviol to the test solution, but avoidance of citric acid was unaffected.
To test whether the taste-enhancing effect of stevioside and steviol is dependent on the sweet taste receptor, we used Tas1r2,Tas1r3(−/−)2 mice. It should be noted that these mice also do not detect umami tastants, as TAS1R3 is an essential subunit of the umami receptor13. Bitter perception is preserved in this mouse line. Interestingly, we found that both steviol and stevioside increase the avoidance of quinine in Tas1r2,Tas1r3(−/−)2 mice (Fig. 5a, green bars; Supplementary Figs 6 and 9). The avoidance of sour taste is conserved and not changed with steviol addition also in this mouse line.
Oral stevioside administration decreases hyperglycaemia
To analyse the effects of stevioside on glucose metabolism in conscious mice, we performed two i.p. glucose tolerance tests (GTTs) in the same mice, combined with stevioside or vehicle treatment, 2 weeks apart. Blood glucose values were significantly reduced after stevioside treatment in WT, but not Trpm5−/− mice (Fig. 6a,b,g). This effect was even more pronounced in obese WT mice, after 20 weeks of HFD, and equally absent in Trpm5−/− animals on HFD (Fig. 6c,d,g). Notably, both in WT and Trpm5−/− animals, we observed no acute effect of stevioside administration on the glucose level in the fasting state (Supplementary Fig. 10a). Even at very high dosage levels of intravenous (i.v.) administration, stevioside and steviol do not induce hypoglycaemia (Supplementary Fig. 10b,c).
To investigate whether the glucose-lowering effect of stevioside is dependent on TRPM5 expression in pancreatic islets, we transplanted pancreatic islets from Trpm5−/− mice or WT mice underneath the kidney capsule of WT-recipient mice that were selectively depleted of their endogenous pancreatic β-cells by alloxan injection34 (Supplementary Fig. 11a). Hyperglycaemia in recipient mice was confirmed before implantation (day 0). After transplantation, normoglycaemia was re-established (Supplementary Fig. 11c,e, day 1). After recovery, acceptor mice showed normal glycaemic profiles and body mass (Fig. 6e,f, solid lines; Supplementary Fig. 11b–e). Only mice transplanted with WT islets showed a reduction in the glycaemia after stevioside treatment (Fig. 6e–g). This effect was like the effect in WT mice.
Stevioside prevents glucose intolerance in mice on HFD
To test the effect of chronic stevioside treatment on the development of diet-induced diabetes, we randomly divided WT littermate mice in two groups: one group receiving HFD (control), and another group receiving HFD and stevioside. Their age, weight and glycaemic profile at the start of the experiment were not different (Fig. 7; Supplementary Fig. 12; Supplementary Table 2). Subsequent i.p. GTTs showed a time-dependent development of glucose intolerance in control mice on HFD (Fig. 7a,c). After 20 weeks on HFD blood glucose levels at 2 h after the glucose challenge, were as high as 300±53 mg dl−1, which is indicative for type 2 diabetes35. We observed a strong protective effect of stevioside against the development of HFD-induced glucose intolerance in WT mice (Fig. 7b,c). In comparison to control mice, animals after 20 weeks of HFD+stevioside had plasma levels of 220±70 mg dl−1 at 2 h after the glucose challenge (P=0.04, two-sample t-test compared to untreated animals). These mice maintained a normal glycaemic profile over the course of 20 weeks of HFD (Fig. 7b). In Trpm5−/− animals, we observed no difference between the control and the stevioside-treated group (Fig. 7d-f). WT and Trpm5−/− mice, both the control group and the stevioside-treated group, had a similar body weight and weekly caloric intake (Supplementary Fig. 12a,b,f,g). Notably, WT mice on HFD showed a significant lower resting glycaemia when treated with stevioside, which was not the case in Trpm5−/− mice (Supplementary Fig. 12c,h).
The increased glucose tolerance in stevioside-treated WT animals is not due to increased islet size (Supplementary Fig. 12e). Of note, islets from stevioside-treated mice did not display the hypertrophy, which is apparent in WT HFD mice (compare Supplementary Fig. 12e (HFD and HFD+stevioside) with Fig. 3g, black (control diet)). We also tested functional responses of isolated pancreatic islets from these mice. Glucose-induced Ca2+ oscillations measured in islets from stevioside-treated WT mice displayed the same sensitivity to stevioside application as described above for untreated mice, while in islets from Trpm5−/− mice these effects were equally absent (Supplementary Fig. 12d,i). Weight gain during 20 weeks of HFD was essentially the same between the control mice and stevioside-treated mice (Supplementary Fig. 12a,f). To study this in more detail, 20 WT mice were placed on HFD without regular GTT and associated fasting, which reduces fluctuations in the body weight. Start weight (20.7±0.2 g (control) and 20.9±0.4 g (stevioside); P=0.69, n=10 mice per group, two-sample t-test) and weight after 10 weeks of HFD (35.9±0.9 g (control) and 34.3±0.8 g (stevioside) P=0.20, two-sample t-test) was not different.
Insulin resistance of peripheral tissue is an important aspect of type 2 diabetes36. To test insulin resistance, we performed an insulin tolerance test in control WT mice, and WT mice that received 124 μM steviol for 2 weeks via the drinking water (∼0.5 mg per day per mouse). The glycaemic changes after insulin injections were not different between the two groups (Supplementary Fig. 13a). The insulin sensitivity of mice chronically fed a HFD with or without supplementation of stevioside in their drinking water was assessed in a euglycaemic hyperinsulinemic clamp test. Trpm5−/− animals showed no difference in insulin sensitivity compared to WT animals (Fig. 7g,h; Supplementary Fig. 13b,c). The glucose infusion rate to reach euglycaemia in animals on a HFD was not different from the animals that were on HFD+stevioside, indicating that stevioside consumption does not alter the insulin sensitivity (Fig. 7i,j). Both groups on the HFD were, however, significantly insulin-resistant compared to normal WT animals (Fig. 7i,j versus Fig. 7g,h; Supplementary Fig. 13b,c). Note the difference in glycaemia before infusion of glucose between stevioside-treated mice and control mice (Fig. 7i). To test an acute effect of steviol on peripheral insulin sensitivity, we infused in euglycaemic conditions 0.8 nmol g−1 steviol i.v., while maintaining constant glucose infusion rate. This elicited no change in the glycaemia (Fig. 7g,i; Supplementary Fig. 13c,d).
To test whether stevioside influences the incretin pathway, we compared the glycaemic profile during an oral and an i.p. GTT. We observed a similar reduction of glucose levels in the stevioside-treated group during an oral GTT and an i.p. GTT (Supplementary Fig. 14a,b,e). The incretin effect, measured as the difference in area under the curve between the two GTTs, was the same when comparing the control and the stevioside-treated group (Supplementary Fig. 14d, left, P=0.16, n=10 mice per group, two-sample t-test). This indicates that stevioside has no impact on incretin secretion from K- and L-cells in the gut.
Finally, the gut microbiome is an important factor in the development of metabolic diseases such as diabetes37. We analysed this effect by treating mice with broad-spectrum antibiotics (ABX) in their drinking water, which leads to dysbiosis of the microbial colonies in the gut38. After 6 weeks, the effect of stevioside on the i.p. GTT was completely preserved in the ABX-treated animals. The increase of the glycaemic values after ABX treatment was the same in the stevioside-treated group as in the control group (Supplementary Fig. 14c,d,e).
Withdrawal of stevioside leads to impaired glucose tolerance
We tested the reversibility of stevioside’s effects on systemic glucose homeostasis. We assessed glucose tolerance in WT mice that received HFD in three scenarios: continuous (15 weeks) treatment with stevioside (group 1), 10 weeks of HFD+stevioside followed by 5 weeks of HFD without stevioside (group 2) and a group on HFD without stevioside for 15 weeks (control—group 3; Fig. 8a; Supplementary Table 3). Mice received 124 μM stevioside in the drinking water, as above. This experiment confirms that stevioside improves glucose tolerance in HFD-treated mice (compare group 1 and 3; Fig. 8b,d). The most striking result is discernible in group 2 where glucose tolerance deteriorates in 5 weeks after stevioside is removed from the diet to the level of the untreated group. Also, 5 weeks after stevioside treatment is stopped, resting glycaemia is significantly higher in group 2, compared to the level when stevioside was administered (Fig. 8c,e,f; Supplementary Table 3). Finally, in this experimental set-up, stevioside treatment slightly reduces HFD-induced weight gain (Fig. 8g, compare group 1, 2 and 3 at 10 weeks). Group 2 mice show an HFD-induced increase in body weight after stevioside treatment is ceased, resulting at the end of the experiment (at 15 weeks) in a similar weight as the untreated group (Fig. 8g; Supplementary Table 3).
Our results can be summarized as follows: (i) we show that TRPM5 is essential for the biological action of steviol and SGs; (ii) we show that potentiation of TRPM5 ion channel activity by SGs modulates taste responses and insulin release; and (iii) potentiation of TRPM5 activity protects mice against the development of HFD-induced hyperglycaemia. Our data indicate that stevioside, rebaudioside A and their aglycon steviol are novel leads for the further development of antidiabetic drugs targeting TRPM5. Considering the tremendous health cost of type 2 diabetes and that stevioside is a widely used natural product, we believe that stevioside might be a cost-effective compound for the global battle against diabetes.
Steviol, stevioside and rebaudioside A are not direct agonists of TRPM5, but potentiate Ca2+-dependent activity of the channel. The steviol group of SGs is sufficient for the interaction, but the interaction site on the TRPM5 protein remains unknown. Inside-out patch-clamp experiments indicate that steviol can interact with TRPM5 directly, independent of an intracellular signal transduction pathway. On the other hand, our data do not exclude other receptors for SGs, but, as outlined below, our data strongly suggest that TRPM5 is essential for the effect of SGs on taste sensation and glucose-induced insulin secretion.
Previously, it was shown that TRPM5 is essential for sweet, bitter and umami taste detection, which are type II taste receptor cell-dependent taste modalities6. Stevioside and steviol specifically enhance these modalities in WT mice: avoidance of a bitter compound (quinine) and preference for sweet (sucrose) and umami (MKG). Sour taste (which is TRPM5-independent6) is not affected. The effect of steviol and SGs on taste is divergent, in a sense that avoidance and preference are intensified depending on the tastant. The observation that taste preference is markedly affected as short as 5 min into the preference test, excludes a significant contribution of post-ingestive effects independent of acute tasting. Taken together, our data are consistent with the model that TRPM5-mediated depolarization of type II taste receptor cells serves as the link between taste receptor activation and initiation of afferent signalling via ATP release from these cells, and that SG-mediated potentiation of TRPM5 activity potentiates this signalling pathway (Fig. 9). Our data identify steviol as a novel, potent and specific modulator of bitter, sweet and umami taste, which is taste neutral on itself. It is tempting to speculate that the extreme sweetness of SGs originates likely from a dual interaction with the sweet taste receptor but also via potentiation of TRPM5 channel activity, via its steviol core.
Steviol and SGs augment glucose-induced Ca2+ oscillations and insulin release in WT pancreatic islets, but not Trpm5−/− islets. These data are consistent with the idea that TRPM5 serves as a facilitator of fast glucose-induced Ca2+ oscillations, which trigger insulin release (Fig. 9). This model was originally proposed from our analysis of Trpm5−/− mice10, and SGs are the first compounds that can validate this hypothesis. It is worth noting that steviol and SGs yield a very similar effect as GLP-1 on glucose-induced Ca2+ oscillations in islets. Interestingly, Shigeto et al.32 could show that TRPM5 is directly involved in the signal transduction in the pancreatic β-cell elicited by GLP-1. This further supports the similar action of TRPM5 activators and GLP-1R agonists. Our data exclude that the GLP-1R is involved in the functional effect of steviol and SGs on pancreatic islets, as the effect of stevioside and GLP-1 is additive, and the stevioside effect is not affected by a GLP-1R blocker.
The dosage of stevioside used in the drinking water of mice in both our drinking test and during the HFD experiments was 124 μM or 100 mg l−1. This concentration is half of the maximum allowed dosage of SGs in soft drinks allowed in the European Union, and <25% of the suggested maximal dose by the World Health Organization and Food and Agriculture Organization39,40. Consumption of this dosage of stevioside in the drinking water resulted in a plasma concentration of 396 nM steviol in mice. We show that also at these physiological concentrations steviol has clear effect on glucose-induced Ca2+ signalling in pancreatic islets, indicating that the dosages of stevioside that we use are realistic and physiologically relevant.
It has been suggested that SGs interact with the mammalian sweet taste receptor, TAS1R2/TAS1R3 (refs 29, 30) and ATP-sensitive K+ channels in pancreatic β-cells41, which might explain some of the data we observe. However, our results exclude that the potentiating effect of steviol and stevioside on pancreatic islet function is mediated via the TAS1R2/TAS1R3 receptor. We observed essentially the same effect of steviol and stevioside on Ca2+ signalling in Tas1r2,Tas1r3(−/−)2, as in WT islets. Our observation that stevioside does not induce Ca2+ signals and insulin release in pancreatic islets in low-glucose conditions (3 mM) argues against the idea that stevioside would be a direct blocker of ATP-sensitive K+ channels.
Acute oral administration of stevioside reduces hyperglycaemia in a GTT in WT, but not in Trpm5−/− mice. Importantly, the same effect is present in alloxan-diabetic WT-recipient mice that received WT islets, but not in WT-recipient mice that received Trpm5−/− islets. This shows that the glucose-lowering effect of stevioside is dependent on the expression of TRPM5 in pancreatic islets, and not from a TRPM5-dependent action in peripheral tissue outside of the pancreatic islet.
Long-term oral intake of stevioside improves the development of plasma hyperglycaemia in WT mice on HFD, but not in Trpm5−/− mice. There was no difference in the development of insulin resistance in the control and stevioside-treated group. HFD-induced obesity in mice is commonly used for the development of insulin resistance and IGT. Because obesity is induced via food-intake/composition and not by genetic manipulation, this model is considered to be relevant for the human condition. Interestingly, two studies suggest that Trpm5−/− mice are resistant to diet-induced obesity; in Larsson et al.42 on a HFD and in Glendinning et al.43 on a carbohydrate-based diet. However, in both studies, Trpm5−/− mice had a significantly lower caloric intake, which could explain the apparent resistance to obesity. In our study, WT and Trpm5−/− mice had the same caloric intake and gained the same amount of weight on HFD.
Similar as GLP-1, stevioside treatment is weight neutral or even slightly limits weight gain during HFD. Furthermore, stevioside and steviol do not induce hypoglycaemia. Stevioside enhances the physiological profile of insulin secretion, instead of inducing increased plasma insulin levels independent of plasma-glucose concentrations, as sulfonylureas and exogenous insulin. In this respect, we propose that TRPM5-potentiating compounds might be functionally equivalent to GLP-1 mimetics. GLP-1R agonists are highly successful in diabetes care. The drawback of current GLP-1R agonists is the way of administration, as they are often injectables, the high price and the short time of action44. Although advances are being made in improving GLP-1R agonists, the identification of TRPM5 as a new pharmacological target with an analogous mode of action broadens the possibilities for drug development.
Considering the epidemiological development of type 2 diabetes and the financial burden on public healthcare systems worldwide, there is an eminent need to develop cost-effective pharmacological interventions for this condition. An unmet need on the anti-diabetes drug market is compounds that prevent or delay the progression of the disease. Our data show that stevioside has potent therapeutic effects for the prevention and treatment of type 2 diabetes in mice, and we show that the molecular mechanism of these effects is the potentiation of TRPM5 activity in β-cells. Thus, we anticipate that TRPM5-potentiating drugs are a bona fide target for the development of antidiabetic drugs, and that steviol and its glycosylated derivatives are interesting start compounds to develop this novel type of drugs.
Cell culture and transfection
HEK293T cells were obtained from American Type Culture Collection and split twice weekly. Cells were grown in Dulbecco’s modified Eagle’s medium containing 10% fetal calf serum, 2 U ml−l penicillin and 2 mg ml−1 streptomycin, and 2 mM L-glutamine. Cells were transfected with Trpm3, Trpm8, Trpa1 or Trpv1 using Mirius transIT-293 transfection reagent.
All animal experiments were approved by the ethical committee for animal welfare of the KU Leuven. Sample size was determined using a power analysis based on the results of preliminary experiments. Mouse strains were homozygously bred in a conventional animal facility. We used C57Bl6/J (WT) and B6;129-Trpm5tm1Csz/J (Trpm5−/−, obtained from C. Zuker, NY, USA) animals. The Trpm5− allele was backcrossed for 12 generations in C57Bl6/J background. Sweet receptor knockout (Tas1r2,Tas1r3(−/−)2) mice were derived by crossing B6;129-Tas1r2tm1Csz/J and B6;129-Tas1r3tm1Csz/J mice (obtained from Jax Labs).
Islets for Ca2+ imaging were isolated from male and female mice aged 10–18 weeks, or after the diet study. Action potential recordings, static insulin secretion, insulin secretion under dynamic perfusion and in vivo insulin secretion (Fig. 4; Supplementary Fig. 5) was assessed in age-matched male mice. For the insulin secretion experiments in supraphysiological conditions (Supplementary Table 1), we used age-matched female mice. Drinking and licking experiments were performed on male mice aged 10–20 weeks. Donor pups for the transplantation experiments were used before visual sexing is possible and were whole-litter mixed gender. Receptor animals were 6-week-old littermate WT mice. Diet experiments were started with 7-week-old male mice. Male, 8-12 week old, WT or Trpm5−/− mice or mice after the diet test were used for the euglycaemic clamp or insulin tolerance test.
HEK293T cells stably transfected with Trpm5 or Trpm4 were developed using the Flp-In system (Life Technologies). The cells were seeded onto poly-L-lysine-coated coverslips and incubated for 2 h. The coverslips were mounted onto an inverted microscope equipped with a multichannel perfusion system. We used the whole-cell patch-clamp configuration. A ramp protocol from −125 to +125 mV in 300 ms, from Vhold=0 mV, was applied to the cells at 1 Hz. The current at +100 and −100 mV was extracted to analyse time-dependent current changes. We measured steady-state control conditions and peak currents during the application of stevioside, rebaudioside A or steviol. Voltage dependency of TRPM5 was analysed with a voltage-step protocol, from Vhold=+25 mV, consisting of a 75 ms test-pulse from −175 to +150 mV in 25 mV increments. The membrane potential was kept at −125 mV for 50 ms before returning to holding potential. The analysed current is the steady-state current at the end of the test-pulse. This was fitted with the Boltzmann equation and V1/2 was calculated in the presence of stevioside and in control conditions, of the same cells. The standard external solution contained (mM) 150 NaCl, 6 KCl, 1.5 CaCl2, 1 MgCl2, 10 glucose and 10 HEPES titrated with 1 M NaOH to a pH of 7.4. The appropriate amount of stevioside was added to this solution. Our internal solution contained (mM) 50 NaCl, 100 N-methyl-D-glucamine, 10 HEPES, 4 K2ATP, 10 ethylene glycol tetra-acetic acid and 8.62 CaCl2 (resulting in 1 μM of free Ca2+), titrated to pH 7.2 with 1 M HCl. The internal solution for measuring in the absence of intracellular calcium contained (mM) 50 NaCl, 100 N-methyl-D-glucamine, 10 HEPES, 4 K2ATP and 10 1,2-Bis(2-aminophenoxy)-ethane-N,N,N′,N′-tetra-acetic acid, titrated to pH 7.2 with 1 M HCl.
For inside-out patch recordings, the bath and pipette solution contains in (mM) 156 NaCl, 1.5 CaCl2, 1 MgCl2 and 10 HEPES at pH 7.4, supplemented with 10 μM steviol or 10 μM stevioside in the pipette as indicated. After excision, the patch is kept in a calcium-free bath solution containing (mM) 150 NaCl, 1 MgCl2, 10 HEPES and 10 ethylene glycol tetra-acetic acid at pH 7.3. The calcium-containing solution was (mM) 150 NaCl, 1 MgCl2, 10 HEPES and 0.5 CaCl2 at pH 7.3 supplemented with 10 μM steviol in the indicated condition. The stimulation protocol consists of a 500 ms step at −100 mV immediately followed by a 250 ms step to +100 mV at 1 Hz. The analysed currents are the steady-state currents extracted at the end of the voltage step.
Membrane potential recordings in β-cells were performed using the perforated-patch whole-cell configuration. The pipette solution contained (mM) 120 K-gluconate, 10 KCl, 10 NaCl, 1 MgCl2, 5 HEPES (pH 7.2 with KOH) and 0.24 mg ml−l amphotericin B, while the bath solution contained (mM) 140 NaCl, 3.6 KCl, 0.5 MgSO4, 1.5 CaCl2 and 10 HEPES (pH 7.2 with NaOH). Action potential firing in isolated β-cells was induced by 100 μM tolbutamide or 20 mM glucose and recorded in the presence, or the absence, of 10 μM stevioside. The interval between subsequent action potentials was calculated and distribution was compared using a non-parametric Wilcoxon sign-rank test in Matlab (R2012a). To examine voltage dependency of the glucose-induced current, cells were held at −70 mV and stepped for 200 ms to voltages ranging from −80 to +50 mV.
Calcium imaging on HEK cells
Cells were incubated with 1 μM FURA2-AM for 1 h and mounted on a fluorescence microscope equipped with a multichannel perfusion system. Transfected cells were identified by green fluorescent protein expression. FURA2 fluorescence was followed at 1 Hz sampling frequency. Extracellular solutions as indicated above were used. We applied 10 μM stevioside, 10 μM steviol and used specific activators of the channels of interest as positive control, that is, 2 μM capsaicin for TRPV1, 100 μM allyl isothiocyanate for TRPA1, 500 μM (+)menthol for TRPM8 and 20 μM pregnenolone sulphate for TRPM3.
Isolation of pancreatic islets and single cells
The Krebs solution for preparation contained (in mM) 119 NaCl, 4.75 KCl, 1.2 MgSO4, 1.18 KH2PO4, 2.54 CaCl2, 5 NaHCO3, 20 HEPES and 5 glucose (pH 7.4). Collagenase P (2 mg ml−l) was injected into the pancreatic duct of C57Bl6/J WT, Trpm5−/− or Tas1r2,Tas1r3(−/−)2 mice, followed by dissection of the pancreas. Digestion of the whole pancreas was obtained by shaking for 8 min at 37 °C. After gravitational sedimentation, islets were isolated by three rounds of handpicking. Islets were cultured in advanced RPMI 1640 (Gibco) supplemented with 10% FCS, 100 U ml−1 penicillin/streptomycin and 4 mM glutamax at 37 °C and 5% CO2. Islets were dispersed into single cells by trypsin digestion. The cells were cultured at 37 °C and 5% CO2 in RPMI 1640 medium supplemented with 10% FCS, 10 U ml−1 penicillin/streptomycin, and 10 mM glucose, for 24 h prior to experimentation.
Calcium imaging on islets
Pancreatic islets were incubated with 1 μM FURA2-AM for 1 h in a humidified incubator at 37 °C and 5% CO2. They were mounted on an Olympus BX51W1 inverted fluorescence microscope equipped with an UMPLANFL × 10 objective with a Bioptech objective heater set at 37 °C. We used a Warner Instruments CL-100 temperature controlled multichannel perfusion system, kept at 37 °C. Excitation was done with a Polychrome V lichtsource and image acquisition with an Andor iXon 888 camera, pre-amplifier gain was set to 1, EM gain to 160 with the TILL Photonics Live Acquisition 22.214.171.124 software. We measured the fluorescence of whole pancreatic islets. The islets were perfused with a solution containing (mM) 120 NaCl, 4.8 KCl, 1.2 MgCl2, 2.5 CaCl2 and 10 HEPES (pH 7.4) supplemented with the indicated amount of glucose and stevioside or steviol. Depolarization of the islets with 30 mM KCl was used as positive control at the end of the measurement. Ca2+ oscillation frequency before or during the application of stevioside was analysed. The FT frequency spectrum of the first time derivative of the calcium oscillations was used in further analysis. The relevant oscillation frequencies between 0 and 0.05 Hz were determined. The highest peak represents the dominant oscillation frequency and all frequencies peaking at ≥60% of the maximum were considered relevant frequencies. The dominant oscillation frequency distribution during perfusion with 10 mM glucose was compared with the dominant oscillation frequency during perfusion with 10 mM glucose and 10 μM stevioside or steviol with the Kolmogorov–Smirnov test. On the basis of the oscillation frequency, the islets were divided into fast- (relevant frequencies only >0.015 Hz), slow- (relevant frequencies only <0.015 Hz) or mixed- (relevant frequencies in both parts of the FT spectrum) oscillating islets. The proportion of fast-oscillating islets in control and stevioside conditions was compared using Fisher’s exact test.
After isolation and overnight incubation, pancreatic islets from six mice were pooled and transferred from the culture medium to 3 mM glucose containing Krebs solution for 30 min. Individual islets were transferred to a well in a 96-well plate with the appropriate glucose and stevioside concentration45. After 60 min of incubation at 37 °C, the supernatant was collected. The experiment was repeated twice, and insulin concentration was determined on duplicate samples (Fig. 4a,b).
Insulin secretory capacity of the islets in G5, K30 and G20 was determined by comparing the released insulin from pooled islets to the total insulin content of these islets (Supplementary Table 1). The represented data are a result of five independent experiments (mice) per genotype.
For in vivo insulin release experiment, fasted WT or Trpm5−/− mice were anaesthetised through an i.p. injection with 5 μl g–1 VDF (ventranquil:dormicum:fentanyl:water 1:2:10:3). The mice received 2.5 g kg–1 glucose (30% solution in H2O) or 2.5 g kg–1 glucose with 200 mg kg–1 stevioside at time point 0 min. Blood samples were taken at 0 and 30 min. Blood was sampled by filling heparinized capillaries through tail bleeding. The blood was centrifuged for 12 min at 5,000 r.p.m. and 4 °C, and the plasma was collected for further analysis.
In all cases, the insulin concentration was determined using the Crystal Chem Inc, USA, ultra-sensitive mouse insulin ELISA kit, as per the manufacturer’s protocol.
Dynamic insulin secretion experiments
After overnight culture in RPMI 1640 containing 10% heat-inactivated fetal calf serum, batches of 40–200 islets were perifused at 37 °C at a flow rate of 1 ml min−1. The perifusion medium (pH 7.4) used for these experiments contained (in mM): 124 NaCl, 4.8 KCl, 2.5 CaCl2, 1.2 MgCl2, 20 NaHCO3, 1 mg ml−l bovine serum albumin and various test agents as indicated. It was gassed with O2:CO2 (95:5%). Effluent was collected every 2 min and insulin was measured by radioimmunoassay.
Stevioside treatment and HFD
Only male mice were used in the diet experiments. After weaning, the mice were randomly allocated to a test group per genotype and housed individual. At the age of 7 weeks, the diet was switched from normal chow (ssniff spezialdiäten, V1535-0) to pellets containing 30% (w/w) saturated fat (ssniff spezialdiäten, E15116-34), given ad libitum. There was a weekly measuring of the body mass and the blood glucose. This resting glycaemia was taken during the light cycle of the mice with a standard glucometer by a drop of blood after tail puncturing in conscious unrestrained mice. The consumed food was measured by weighting the on the grid pellets every week. There was free access to drinking water and the supplementary drinking bottle from the indicated groups was filled daily with a stevioside containing solution (25 mg stevioside per kg in a 0.1% solution in water). The mice were monitored to consequently drink the stevioside solution. In the experiments decribed in Fig. 8 and Supplementary Fig. 14, five mice were housed in one cage. Stevioside (100 mg l−1) and antibiotics (ABX—1 g l−1 metronidazole and 200 mg l−1 ciprofloxacin) were added to the drinking water of the indicated groups. No animals were excluded from the analysis, outliers in resting glycaemia or food consumption at a distinct time point were attributed to experimental error and discarded from final analysis.
Glucose tolerance test
The mice were fasted overnight in their home cage before the GTT with free access to water. Mice from different treatment groups were evenly distributed over technical replicates of the GTT. The investigator was blinded towards the treatment group the animal was allocated to. For the acute stevioside administration, the mice received either 500 mg kg−1 stevioside or the same volume of vehicle via oral gavage 2 h before the start of the GTT. At time 0 min, they receive an i.p. injection of 2.5 g kg−1 glucose in a 30% solution in water. In the case of the oral GTT, the glucose is administered through oral gavage. Glycaemia is followed at time points 0, 15, 30, 60 and 120 min using a standard glucometer (Aviva Accu-Check). The tip of the tail was punctured with a 26 G needle to initiate bleeding. After the GTT, the mice received ad libitum feeding of their appropriate diet. At individual time points, we show average±s.e.m. and the indicated significances are the result of a paired or a two-sample t-test. We excluded animals were the maximal glycaemia did not exceed 250 mg dl−1 from analysis. The results of the GTT are also presented as area under the curve of the glycaemia during the 120 min of the GTT.
Euglycaemic hyperinsulinemic clamp
Mice were fasted overnight before the experiment. To obtain anaesthesia, mice under 40 g were i.p. injected with a mixture of 3.125 mg kg−1 acepromazine, 3.125 mg kg−1 midazolam and 0.156 mg kg−1 fentanyl while mice over 40 g received half this dose. A maintenance bolus of 18.75 μg acepromazine, 18.75 μg midazolam and 0.936 μg fentanyl was subcutaneous injected every 45 min. An i.v. catheter was placed in the tail vein and initially PBS was infused at 50 μl h−1 for 40 min using syringe pumps and the basal glycaemia was determined as the average measured at −20 and −10 min, before the start of the hyperinsulinemic clamp. The mice received a bolus of 2.7 mU insulin at 0 min and continuous infusion of 6.8 mU insulin per hour. In all, 12.5% glucose in PBS was i.v. infused at a variable rate to maintain euglycaemia, determined every 5–10 min by tail bleeding. After 2 h, we infused 0.8 μmol kg−1 steviol while maintaining the insulin and glucose infusions at the euglycaemic level.
Islets from 2–3-week-old WT or Trpm5−/− donor mice were isolated by collagenase digestion, washed and counted. Thereafter, islets were transferred to silicon microtubing (Becton Dickinson, Erembodegem, Belgium), and centrifuged for 5 min at 1,500 r.p.m. to create a compact pellet of islets for injection46. Endogenous β-cells from 7-week-old WT-recipient mice were selectively destroyed with 90 mg kg−1 alloxan 2 days before transplantation. Severe hyperglycaemia and glucosuria were confirmed in the recipient mice shortly before transplantation. During transplantation, the mice were anaesthetized with ketamine/xylazine i.p. (80–100 mg kg−1 ketamine and 5–10 mg kg−1 xylazine) and the left kidney was exposed by a lumbar incision. Recipient mice were given 500 islets under the kidney capsule. Non-fasting blood glucose levels from the tail vein of each recipient were measured to monitor functionality of the transplanted islets, 1 day, 1 week and 4 months after transplantation. Mice recovered for 14 days after surgery before a GTT was performed.
Plasma steviol concentration determination
Ten WT mice were given 124 μM steviol in their drinking water during 21 days. Blood was collected after anaesthesia by exsanguination through puncture of the maxillary vein. The plasma was separated by 10 min centrifugation at 10,000 r.p.m. A liquid–liquid extraction was employed as follows: to 50 μl of plasma, 1 μl (1 mg ml−1 in MeOH) ibuprofen was added as an internal standard. The mixture was vortexed and protein precipitation was carried out adding 50 μl acetonitrile while vortexing. After centrifugation, the upper layer was collected and 25 μl was injected. Liquid chromatography–mass spectrometryanalysis was carried out using a UFLC Shimadzu system consisting of a LC-20ADXR pump, a SIL-20ACXR autosampler, a DGU-20A3 degasser and a CTO-20A oven (Shimadzu Prominence, Antwerpen, Belgium) in combination with a 3200 QTRAP (ABSciex, Halle, Belgium) and Analyst software (version 1.5). The instrument was operated in atmospheric pressure chemical ionization, negative-single ion mode monitor m/z 317.1 (steviol) and m/z 205.2 (ibuprofen). The corona discharge needle voltage was −4,500 V and heated nebulizer temperature was set at 500 °C for 0.5 ml min−1 flow rate. Nitrogen was set as nebulizer gas, auxiliary gas at 50 p.s.i. and curtain gas at 35 p.s.i. Other parameters were as follows: declustering potential −50 V, entrance potential −10 V. Liquid chromatography conditions: an Accucore C18 column (2.6 μm particle size, 2.1 mm × 100 mm) was used. Mobile phases were (A) 20 mM amoniumacetate at pH 4.8 and (B) acetonitrile. The used flow rate was 0.5 ml min−1. The autosampler temperature was set at 10 °C, the column oven at 30 °C. The method had following gradient conditions 0–0.01 min: 20% B; 0.01–10 min: 70% B; 10–11: 20% B. Retention times were defined as 7.07 (steviol) and 6.21 (ibuprofen). Calibration curves were constructed using linear regression of the peak area ratios of steviol against internal standard (ibuprofen). Calibration standards were prepared by spiking blank plasma at concentrations 10, 50, 100, 250, 500, 1,000, 2,500, 5,000 ng ml−1 (R2=0.9926).
WT, Trpm5−/− or Tas1r2,Tas1r3(−/−)2 mice were age-matched, individually caged and given two drinking bottles. After an adaptation period the animals drank 50% from each of the bottles containing deionized water. A test solution was placed in one of the bottles, and after 24 h, the position of the bottles was switched to control for a position preference. The bottles were weighted to measure the intake from each bottle. All tastants were given in an increasing stimulating order. The used solutions were 1% sucrose (sweet), the minimal concentration for which a preference can be detected47. A stimulatory concentration of 150 mM MKG; umami)48, 100 μM quinine (bitter) or 25 μM in the Tas1r2,Tas1r3(−/−)2 mice on the 48 h taste preference test and 10 mM citric acid (Sour). As stevioside tastes 300 times sweeter than sucrose and 3% sucrose is preferred by WT mice to a great extent, we used 0.01% or 124 μM stevioside, and similarly 124 μM rebaudioside A or steviol29,47. The same animals were used in the control condition and the condition with steviol added and the indicated significance is the result of a paired t-test from two individual experiments with 24–48 animals per group each. For the brief access drinking tests, we used a custom-build lick-o-meter49. The mice were deprived from water for 23 h before the experiment. Individual mice were placed in a cage equipped with a copper grounding platform under two metal drinking spouts connected to an analogue/digital converter. The drinking spouts were isolated except for the tip so only tongue licks are recorded as a positive step of 25–150 mV. Custom software recorded the junction potential at 200 Hz. We analysed potentials exceeding 25 mV as a licking event. Licking events were recorded for 60 min. We analysed the total number of licks and the fraction of licks from each bottle (per mouse) over the complete time course to measure the 1 h preference. The first 5 min were analysed for initial taste preference. For each mouse, the total number of licks was normalized to avoid unequal contribution of extreme individuals. These incremental licks were pooled and divided by the number of animals in the group to yield the data in Fig. 5b–g and Supplementary Figs 7–9. Statistical significance was assessed with paired or two-sample t-tests on the normalized fractions that each mouse drank at the end of 5 min (Fig. 5f) or 60 min (Supplementary Fig. 6a,b). The variance between individual mice in the same condition is displayed with the data spread and the 25–75% data-interval boxplot, indicating the mean and median of each group. The amount of licks in each condition for each mouse is represented in Supplementary Fig. 6c–e for the 60 min lick-o-meter test and in Supplementary Fig. 6f for the first 5 min.
Data analysis and statistics
We used Matlab R2012a, OriginPro 8.6, Microsoft Excel and Igor Pro 6.34 for data analysis. Values deviating>3 × s.d. of the population mean were considered outliers. Normality was confirmed with the Shapiro–Wilk test (95% confidence level). For significance testing, we used two-tailed paired or unpaired t-test, unless otherwise indicated. For equivalence testing, we used the two one-sided tests approach and withheld the largest P-value. Data represent mean±s.e.m. Significance levels are indicated in the figures as P>0.05, not significant; *P<0.05; **P<0.01; ***P<0.001.
The data that support the findings of this study are available upon request from the corresponding author.
How to cite this article: Philippaert, K. et al. Steviol glycosides enhance pancreatic beta-cell function and taste sensation by potentiation of TRPM5 channel activity. Nat. Commun. 8, 14733 doi: 10.1038/ncomms14733 (2017).
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We thank Professor Em. Bernd Nilius and the members of the Laboratory of Ion Channel Research for stimulating discussions. This work was supported by FWO Vlaanderen (G.0761.10N, G.0596.12 and G.0565.07), IUAP program from the Belgian Federal Government (IcePath, P7/13), KU Leuven ‘Bijzonder Onderzoeksfonds’ (STRT1/09/046, GOA 2009/07, EF/95/010 and TRPLe). P.G. is Research Director of the Fonds National de la Recherche Scientifique, Brussels, and has been supported by an ARC (13/18-051).
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