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首页> 外文期刊>Journal of Hepatology: The Journal of the European Association for the Study of the Liver >Impairment of metabolic hepatic nerve action by chronic but not acute ethanol intoxication studied in isolated perfused rat liver.
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Impairment of metabolic hepatic nerve action by chronic but not acute ethanol intoxication studied in isolated perfused rat liver.

机译:在单独的灌注大鼠肝脏中研究了慢性(但不是急性)乙醇中毒对代谢性肝神经功能的损害。

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摘要

BACKGROUND/AIMS: Liver carbohydrate metabolism and blood flow are regulated by hepatic nerves and hormones such as glucagon, insulin or catecholamines. Acute and chronic application of alcohol are known to depress the function of central and peripheral nerves. The extent of inhibition of the autonomic nervous system is not well characterized; thus, the possible impairment of hepatic nerve function by acute and chronic application of ethanol was investigated. METHODS: Rat livers were perfused simultaneously via both the portal vein and hepatic artery. Hepatic nerves were stimulated electrically for 2 min (20 Hz, 20 V, 2 ms). As a control, noradrenaline (1 microM) was infused into the portal vein for 2 minutes. RESULTS: During acute application of ethanol in portal concentrations of 50, 150 and 300 mM, which elevated basal glucose release, stimulation of hepatic nerves as well as portal noradrenaline infusion caused the same increase in glucose output and decrease in portal and arterial flow as in controls. Following chronic application of ethanol by feeding rats the Lieber-DeCarli liquid diet containing 5% (v/v) ethanol for 4 and 6 weeks, only nerve stimulation caused a significantly reduced enhancement of glucose output (50%, p < 0.025), whereas portal noradrenaline was as effective as in controls. Noradrenaline overflow was significantly reduced following nerve stimulation. CONCLUSION: The decrease in nerve stimulation-dependent glucose output and noradrenaline overflow in chronically ethanol fed rats indicates an impaired function of hepatic nerves.
机译:背景/目的:肝碳水化合物的代谢和血流量受肝神经和激素(例如胰高血糖素,胰岛素或儿茶酚胺)的调节。已知急性和长期使用酒精会降低中枢神经和末梢神经的功能。自主神经系统的抑制程度尚不明确。因此,研究了急性和慢性应用乙醇可能损害肝神经功能。方法:通过门静脉和肝动脉同时灌注大鼠肝脏。电刺激肝神经2分钟(20 Hz,20 V,2 ms)。作为对照,将去甲肾上腺素(1 microM)注入门静脉2分钟。结果:在急性应用门静脉浓度分别为50、150和300 mM的乙醇期间,该水平升高了基础葡萄糖的释放,对肝神经的刺激以及门静脉去甲肾上腺素的输注导致葡萄糖输出的增加与门静脉和动脉血的减少相同。控制。在通过长期给大鼠喂食含5%(v / v)乙醇的Lieber-DeCarli流质饮食4周和6周后,仅使用神经刺激即可显着降低葡萄糖输出的增强(50%,p <0.025),而门脉去甲肾上腺素与对照组一样有效。神经刺激后,去甲肾上腺素溢出明显减少。结论:长期用乙醇喂养的大鼠神经刺激依赖性葡萄糖输出减少和去甲肾上腺素上溢表明肝神经功能受损。

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