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Increases of spinal kinin receptor binding sites in two rat models of insulin resistance.

机译:在两个胰岛素抵抗大鼠模型中脊髓激肽受体结合位点的增加。

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An autoradiographic study was conducted to determine whether kinin receptors are altered in the rat spinal cord in two experimental models of chronic hyperglycemia and insulin resistance. Sprague-Dawley rats were given 10% d-glucose in their drinking water alone or with insulin (9 mU/kg/min with osmotic pumps) for 4 weeks. Both groups and control rats were treated either with a normal chow diet or with an alpha-lipoic acid-supplemented diet as antioxidant therapy. After 4 weeks of treatment, glycemia, insulinemia, blood pressure, insulin resistance index, the production of superoxide anion in the aorta and the density of B2 receptor binding sites in the dorsal horn were significantly increased in the two models. These effects were prevented or attenuated by alpha-lipoic acid. In contrast, B2 receptor binding sites of most spinal cord laminae were increased in the glucose group only and were not affected by alpha-lipoic acid. Results show that chronic hyperglycemia associated with insulin resistance increases B1 and B2 receptor binding sites in the rat spinal cord through distinct mechanisms, including the oxidative stress for the B1 receptor.
机译:进行了一项放射自显影研究,以确定在慢性高血糖和胰岛素抵抗的两个实验模型中大鼠脊髓中激肽受体是否发生改变。 Sprague-Dawley大鼠仅在饮用水中或与胰岛素一起(在渗透泵中为9 mU / kg / min)被给予10%d-葡萄糖,持续4周。两组和对照组大鼠均接受正常食物饮食或补充α-硫辛酸的饮食作为抗氧化剂治疗。治疗4周后,两种模型的血糖,胰岛素血症,血压,胰岛素抵抗指数,主动脉中超氧阴离子的产生以及背角中B2受体结合位点的密度均显着增加。这些作用被α-硫辛酸阻止或减弱了。相反,大多数脊髓椎板的B2受体结合位点仅在葡萄糖组中增加,而不受α-硫辛酸的影响。结果表明,与胰岛素抵抗相关的慢性高血糖症通过不同的机制增加了大鼠脊髓中的B1和B2受体结合位点,包括B1受体的氧化应激。

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