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肥胖 Zucker 大鼠异常交感神经功能起源的研究

Studies of origins of abnormal sympathetic function in obese Zucker rats.

作者信息

Levin B E, Triscari J, Sullivan A C

出版信息

Am J Physiol. 1983 Jul;245(1):E87-93. doi: 10.1152/ajpendo.1983.245.1.E87.

Abstract

To explain previously described abnormalities of sympathetic function in the genetically obese Zucker rat, the kinetics of norepinephrine (NE) metabolism were examined. Lower stress-induced levels of plasma NE in the obese rat were shown to be due to decreased release of NE because uptake of [3H]NE tracer from plasma was 45% slower in the obese compared with the lean rat. NE levels were 15, 20, and 34% lower in heart, pancreas, and interscapular brown adipose tissue (IBAT), and NE turnover rates (determined by two independent methods) were 39-48 and 43-69% lower in the pancreas and IBAT of obese compared with lean rats. In vivo synthesis of [3H]NE from [3H]dopamine by the enzyme dopamine beta-hydroxylase was 60% lower in IBAT but was equal in hearts of obese compared with lean rats. These results suggest an organ-specific decrease of NE synthesis in the obese Zucker rat, possibly due to decreased dopamine beta-hydroxylase activity in IBAT.

摘要

为了解释先前描述的遗传性肥胖Zucker大鼠交感神经功能异常,研究了去甲肾上腺素(NE)代谢动力学。肥胖大鼠应激诱导的血浆NE水平较低,这是由于NE释放减少所致,因为肥胖大鼠从血浆中摄取[3H]NE示踪剂的速度比瘦大鼠慢45%。肥胖大鼠心脏、胰腺和肩胛间棕色脂肪组织(IBAT)中的NE水平分别低15%、20%和34%,与瘦大鼠相比,肥胖大鼠胰腺和IBAT中的NE周转率(通过两种独立方法测定)分别低39 - 48%和43 - 69%。肥胖大鼠IBAT中由多巴胺β-羟化酶将[3H]多巴胺体内合成[3H]NE的量比瘦大鼠低60%,但肥胖大鼠心脏中的合成量与瘦大鼠相当。这些结果表明肥胖Zucker大鼠中NE合成存在器官特异性降低,可能是由于IBAT中多巴胺β-羟化酶活性降低所致。

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