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首页> 外文期刊>Hormone and Metabolic Research >Unacylated Ghrelin Regulates Glucose-Sensitive Neurons Activity and Glycolipid Metabolism via Orexin-A Neurons in the Lateral Hypothalamic Area
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Unacylated Ghrelin Regulates Glucose-Sensitive Neurons Activity and Glycolipid Metabolism via Orexin-A Neurons in the Lateral Hypothalamic Area

机译:未通过侧面下丘脑区域的神经元调节葡萄糖敏感的Ghrelin调节葡萄糖敏感性神经元活性和糖脂代谢

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The objective of the study was to investigate the regulatory actions of unacylated ghrelin (UAG) on glucose-sensitive (GS) neurons and glycolipid metabolism in the lateral hypothalamus area (LHA) and its involvement with orexin-A-immunopositive neurons. The effects of UAG administered into the LHA on GS neurons discharges and glycolipid metabolism were detected by single neuron discharge recording, biochemical index analysis and quantitative real-time PCR; the level of c-fos protein in orexin-A-immunopositive neurons was observed using immunofluorescence staining. UAG microinjected into the LHA activated glucose-inhibited neurons, which were partially blocked by pre-administration of anti-orexin-A antibody in the LHA. Furthermore, UAG microinjected into the LHA significantly reduced serum triglycerides (TG), total cholesterol, low-density lipoprotein cholesterol, blood glucose, insulin and hepatic TG levels, while elevated serum high-density lipoprotein cholesterol levels. UAG elevated the mRNA expression of carnitine palmitoyltransferase-1 and reduced the mRNA expression of acetyl-CoA carboxylase-1 in the liver. The above-mentioned effects of UAG were partially blocked by pre-administration of anti-orexin-A antibody. The expressions of orexin-A and c-fos were observed in the LHA. After UAG injection into the LHA, some neurons showed double labeling, and the percentage of double-labeled orexin-A/c-fos neurons in orexin-A-immunopositive neurons increased significantly. UAG in the LHA regulates glycolipid metabolism by activating orexin-A-immunopositive neurons in the LHA.
机译:本研究的目的是探讨未酰化ghrelin(UAG)对下丘脑外侧区(LHA)葡萄糖敏感(GS)神经元和糖脂代谢的调节作用及其与orexin-A免疫阳性神经元的关系。通过单神经元放电记录、生化指标分析和实时定量PCR检测UAG对LHA内GS神经元放电和糖脂代谢的影响;免疫荧光染色观察orexin-A免疫阳性神经元c-fos蛋白水平。将UAG微量注射到LHA激活的葡萄糖抑制神经元中,在LHA中预给药抗食欲素A抗体可部分阻断该神经元。此外,向LHA微量注射UAG可显著降低血清甘油三酯(TG)、总胆固醇、低密度脂蛋白胆固醇、血糖、胰岛素和肝脏TG水平,同时升高血清高密度脂蛋白胆固醇水平。UAG提高了肉碱棕榈酰转移酶-1的mRNA表达,降低了肝脏中乙酰辅酶A羧化酶-1的mRNA表达。UAG的上述作用部分被抗食欲素A抗体预给药阻断。在LHA中观察到orexin-A和c-fos的表达。将UAG注入LHA后,部分神经元出现双标记,orexin-A免疫阳性神经元中双标记orexin-A/c-fos神经元的百分比显著增加。LHA中的UAG通过激活LHA中的食欲素A免疫阳性神经元来调节糖脂代谢。

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