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  4. Comparison of the metabolic effects of metformin and troglitazone on fructose-induced insulin resistance in male sprague-dawley rats
 
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Comparison of the metabolic effects of metformin and troglitazone on fructose-induced insulin resistance in male sprague-dawley rats

Journal
Journal of the Formosan Medical Association
Journal Volume
100
Journal Issue
3
Pages
176-180
Date Issued
2001
Author(s)
Chen C.-C.
Wang H.-J.
Shih H.-C.
Sheen L.-Y.  
Chang C.-T.
Chen R.-H.
Wang T.-Y.
URI
https://scholars.lib.ntu.edu.tw/handle/123456789/413592
URL
https://www.scopus.com/inward/record.uri?eid=2-s2.0-0035025176&partnerID=40&md5=4cac32c5ac28502a04da574ed06d5899
Abstract
Background and purpose: Insulin resistance is a hallmark of the development of type 2 diabetes. Metformin and troglitazone are oral antidiabetic agents used to reduce insulin resistance. The aim of this study was to compare the metabolic effects of these two drugs in fructose-induced insulin-resistant rodents. Methods: Male Sprague-Dawley rats were allocated to receive one of the following four treatments for 6 weeks: normal rat chow (control group, n = 7), high-fructose diet (fructose group, n = 7), high-fructose diet plus metformin (metformin group, n = 8), or high-fructose diet plus troglitazone (troglitazone group, n = 8). Systolic blood pressure (SBP), insulin, free fatty acid (FFA), and triglyceride concentrations were measured as parameters of insulin resistance. Leptin concentration was also measured in the four groups. Results: The fructose group developed significantly elevated SBP, hyperinsulinemia, and hypertriglyceridemia without significant change in body weight or leptin concentration compared with the control group. The metformin group had significantly reduced body weight (397.9 ¡? 40.9 vs 470.1 ¡? 59.6 g, p < 0.05), insulin concentration (14.8 ¡? 10.5 vs 48.4 ¡? 15.2 £gU/mL, p < 0.05), triglyceride concentration (75.3 ¡? 65.5 vs 250.1 ¡? 95.7 mg/dL, p < 0.05), and leptin concentration (3.1 ¡? 1.5 vs 6.9 ¡? 2.0 ng/mL, p < 0.05) without significant change in SBP (147.8 ¡? 5.8 vs 152.4 ¡? 13.0 mm Hg, p > 0.05) compared with the fructose group. The troglitazone group had significantly reduced SBP (137.8 ¡? 9.2 vs 15.24 ¡? 13.0 mm Hg, p < 0.05), insulin concentration (15.0 ¡? 13.6 vs 48.4 ¡? 15.2 £gU/mL, p < 0.05), FFA concentration (38.9 ¡? 22.7 vs 78.7 ¡? 24.6 mg/dL, p < 0.05), triglyceride concentration (67.6 ¡? 32.4 vs 250.1 ¡? 95.7 mg/dL, p < 0.05), and leptin concentration (4.4 ¡? 2.0 vs 6.9 ¡? 2.0 ng/mL, p < 0.05) without significant change in body weight (452.5 ¡? 32.8 vs 470.1 ¡? 59.6 g, p > 0.05) compared with the fructose group. The metabolic effects of metformin and troglitazone on insulin, FFA, triglyceride, and leptin concentrations were not significantly different. However, metformin treatment resulted in significantly lower body weight (397.9 ¡? 40.9 vs 452.5 ¡? 32.8 g) and troglitazone treatment in significantly lower SBP (137.8 ¡? 9.2 vs 147.8 ¡? 5.8 mm Hg) compared to the fructose group, after adjusting for basal values (p < 0.05). Conclusions: Both metformin and troglitazone were comparably effective in reducing insulin resistance. Metformin treatment caused body weight reduction but was not effective in reducing SBP. Troglitazone treatment lowered SBP but did not reduce body weight.
Subjects
Hyperinsulinemia
Insulin resistance
Leptin
Metformin
Rat
Troglitazone
SDGs

[SDGs]SDG3

Type
journal article

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