首页> 外文期刊>European Journal of Pharmacology: An International Journal >Long-term oral nicotine administration reduces insulin resistance in obese rats.
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Long-term oral nicotine administration reduces insulin resistance in obese rats.

机译:长期口服尼古丁可以降低肥胖大鼠的胰岛素抵抗。

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摘要

This study aimed to investigate the effect of long-term oral nicotine administration on insulin resistance in an animal model of obesity. Eight-week-old male Zucker fatty rats (ZFRs) were administered nicotine tartrate dihydrate (4.6 mg/kg/day) in the drinking water. The control group was pair-fed. The body weights and food intake over 8 weeks were similar in both groups. Plasma glucose levels at 3, 6, 9, 12, and 15 min after insulin administration (0.5 U/kg) in the nicotine group were significantly lower than those in the control group. The calculated K(ITT) value for the nicotine group was significantly higher than that for the control group. Wet weight of the liver in the nicotine group was significantly lower than that in the control group. Transaminases and histological examination of the liver revealed no alteration by nicotine administration. Glycogen, glycogen synthetase activity and gluconeogenesis in the liver in the nicotine group were significantly lower than those in the control group. Phosphorylase-a activity of the liver in the nicotine group was significantly higher than that in the control group. Glycogen, glycogen synthetase, and phosphorylase-a activity of skeletal muscle were similar in both groups. These results suggest that long-term oral nicotine administration may reduce insulin resistance in obese diabetic rats through a reduced hepatic glucose release and, in part, contribute to lowering blood glucose levels.
机译:这项研究旨在研究长期口服尼古丁对肥胖动物模型胰岛素抵抗的影响。对八周大的雄性Zucker脂肪大鼠(ZFR)在饮用水中给予酒石酸尼古丁二水合物(4.6 mg / kg /天)。对照组为配对喂养。两组在8周内的体重和食物摄入量相似。尼古丁组在胰岛素注射后第3、6、9、12和15分钟的血浆葡萄糖水平(0.5 U / kg)显着低于对照组。尼古丁组的计算K(ITT)值明显高于对照组。尼古丁组的肝脏湿重显着低于对照组。转氨酶和肝脏组织学检查显示尼古丁给药未引起改变。尼古丁组肝脏中的糖原,糖原合成酶活性和糖异生显着低于对照组。尼古丁组肝脏的磷酸化酶-a活性显着高于对照组。两组的糖原,糖原合成酶和磷酸化酶-a骨骼肌活性相似。这些结果表明,长期口服尼古丁可以通过减少肝葡萄糖的释放来降低肥胖糖尿病大鼠的胰岛素抵抗,并且部分地有助于降低血糖水平。

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