The effect of long-term taurine supplementation and fructose feeding on glucose and lipid homeostasis in Wistar rats
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The effect of long-term taurine supplementation and fructose feeding on glucose and lipid homeostasis in Wistar rats. / Larsen, Lea Hüche; Orstrup, Laura Kofoed Hvidsten; Hansen, Svend Høime; Grunnet, Niels; Quistorff, Bjørn; Mortensen, Ole Hartvig.
In: Advances in Experimental Medicine and Biology, Vol. 776, 2013, p. 39-50.Research output: Contribution to journal › Journal article › Research › peer-review
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TY - JOUR
T1 - The effect of long-term taurine supplementation and fructose feeding on glucose and lipid homeostasis in Wistar rats
AU - Larsen, Lea Hüche
AU - Orstrup, Laura Kofoed Hvidsten
AU - Hansen, Svend Høime
AU - Grunnet, Niels
AU - Quistorff, Bjørn
AU - Mortensen, Ole Hartvig
PY - 2013
Y1 - 2013
N2 - The nonprotein amino acid taurine has been shown to counteract the negative effects of a high-fructose diet in rats with regard to insulin resistance and dyslipidemia. Here we examined the long-term (26 weeks) effects of oral taurine supplementation (2% in the drinking water) in fructose-fed Wistar rats.The combination of fructose and taurine caused a significant increase in fasting glucose compared to the control diet without changing hepatic phosphoenol pyruvate carboxykinase mRNA levels. The combination of fructose and taurine also improved glucose tolerance compared to control. Neither a high-fructose diet nor taurine supplementation induced significant changes in body weight, body fat or total calorie intake, fasting insulin levels, HOMA-IR, or insulin-induced Akt phosphorylation in skeletal muscle.Fructose alone caused a decrease in liver triglyceride content, with taurine supplementation preventing this. There was no effect of long-term fructose diet and/or taurine supplementation on plasma triglycerides, plasma nonesterified fatty acids, as well as plasma HDL, LDL, and total cholesterol.In conclusion, the study suggests that long-term taurine supplementation improves glucose tolerance and normalize hepatic triglyceride content following long-term fructose feeding. However, as the combination of taurine and fructose also increased fasting glucose levels, the beneficial effect of taurine supplementation towards amelioration of glucose intolerance and insulin resistance may be questionable.
AB - The nonprotein amino acid taurine has been shown to counteract the negative effects of a high-fructose diet in rats with regard to insulin resistance and dyslipidemia. Here we examined the long-term (26 weeks) effects of oral taurine supplementation (2% in the drinking water) in fructose-fed Wistar rats.The combination of fructose and taurine caused a significant increase in fasting glucose compared to the control diet without changing hepatic phosphoenol pyruvate carboxykinase mRNA levels. The combination of fructose and taurine also improved glucose tolerance compared to control. Neither a high-fructose diet nor taurine supplementation induced significant changes in body weight, body fat or total calorie intake, fasting insulin levels, HOMA-IR, or insulin-induced Akt phosphorylation in skeletal muscle.Fructose alone caused a decrease in liver triglyceride content, with taurine supplementation preventing this. There was no effect of long-term fructose diet and/or taurine supplementation on plasma triglycerides, plasma nonesterified fatty acids, as well as plasma HDL, LDL, and total cholesterol.In conclusion, the study suggests that long-term taurine supplementation improves glucose tolerance and normalize hepatic triglyceride content following long-term fructose feeding. However, as the combination of taurine and fructose also increased fasting glucose levels, the beneficial effect of taurine supplementation towards amelioration of glucose intolerance and insulin resistance may be questionable.
KW - Animals
KW - Body Weight
KW - Dietary Supplements
KW - Drinking Behavior
KW - Feeding Behavior
KW - Fructose
KW - Glucose
KW - Glucose Tolerance Test
KW - Homeostasis
KW - Insulin
KW - Lipid Metabolism
KW - Male
KW - Rats
KW - Rats, Wistar
KW - Signal Transduction
KW - Taurine
KW - Time Factors
U2 - 10.1007/978-1-4614-6093-0_5
DO - 10.1007/978-1-4614-6093-0_5
M3 - Journal article
C2 - 23392869
VL - 776
SP - 39
EP - 50
JO - Advances in Experimental Medicine and Biology
JF - Advances in Experimental Medicine and Biology
SN - 0065-2598
ER -
ID: 49787701