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Acute effects of corticosterone on tissue protein synthesis and insulin-sensitivity in rats in vivo.

机译:皮质酮对大鼠体内组织蛋白合成和胰岛素敏感性的急性影响。

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摘要

The effect of corticosterone treatment on the sensitivity of muscle protein synthesis to insulin infusion was assessed in post-absorptive young rats. To select the optimal time period for corticosterone treatment, protein synthesis was measured by injection of L-[2,6-3H]phenylalanine (1.5 mmol/kg body weight) 1, 4, 12 or 24 h after injection of corticosterone (5 mg/kg body wt.). Muscle protein synthesis was significantly decreased at 4 h and the effect was maximal by 12 h; liver protein synthesis was elevated at 12 h and 24 h. The dose-response of muscle protein synthesis to a 30 min infusion with 0-150 munits of insulin/h was then compared in rats pretreated with corticosterone (10 mg/100 g body wt.) or vehicle alone. When no insulin was infused, corticosterone inhibited protein synthesis in gastrocnemius muscle. High doses of insulin stimulated protein synthesis, but the inhibition by corticosterone was similar to that in the absence of insulin. At intermediate doses of insulin there was an increased requirement for insulin to elicit an equivalent response in muscle protein synthesis. Plantaris muscle responded in a manner similar to that of gastrocnemius, but neither soleus muscle nor liver responded significantly to insulin. These data suggest that corticosterone has two modes of action; one which is independent from and opposite to that of insulin, and a second which causes insulin-resistance through a decrease in sensitivity rather than a change in responsiveness.
机译:在吸收后的年轻大鼠中评估了皮质酮治疗对肌肉蛋白合成对胰岛素输注敏感性的影响。为了选择皮质酮治疗的最佳时间,在注射皮质酮(5 mg)1、4、12或24小时后,通过注射L- [2,6-3H]苯丙氨酸(1.5 mmol / kg体重)来测量蛋白质合成/ kg体重。肌肉蛋白合成在4 h显着降低,并且在12 h达到最大;肝蛋白合成在12h和24h升高。然后在用皮质酮(10 mg / 100 g体重)或单独使用媒介物预处理的大鼠中比较了肌肉蛋白合成对30分钟输注0-150 munits胰岛素/ h的剂量反应。当不注射胰岛素时,皮质酮抑制腓肠肌的蛋白质合成。高剂量的胰岛素刺激了蛋白质的合成,但是皮质酮的抑制作用与没有胰岛素时的抑制作用相似。在中等剂量的胰岛素下,需要更多的胰岛素来引起肌肉蛋白质合成中的等效反应。肌的反应方式类似于腓肠肌,但比目鱼肌和肝脏均对胰岛素无明显反应。这些数据表明皮质酮具有两种作用方式。一种独立于胰岛素并与之相反,另一种通过降低敏感性而不是改变响应性而引起胰岛素抵抗。

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