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肥胖雌性 Zucker 大鼠分离的肝细胞中,与年龄相关的胰高血糖素敏感性降低以及二丁酰环磷酸腺苷对脂肪酸合成的抑制作用减弱。

Age-related decrease in sensitivity to glucagon and dibutyryl cyclic AMP inhibition of fatty acid synthesis in hepatocytes isolated from obese female Zucker rats.

作者信息

McCune S A, Durant P J, Harris R A

出版信息

Horm Metab Res. 1984 Feb;16(2):79-84. doi: 10.1055/s-2007-1014702.

Abstract

Hepatocytes were isolated from 3 and 5 month old female genetically obese Zucker rats and their lean littermate controls. An age-dependent loss in sensitivity of fatty acid synthesis to inhibition by both glucagon and dibutyryl cyclic AMP was observed with hepatocytes from the obese rats. Hepatocytes from lean animals were much more sensitive to these agents, regardless of age. Low concentrations of glucagon and dibutyryl cyclic AMP actually produced some stimulation of fatty acid synthesis with hepatocytes prepared from the older obese rats. 5-Tetradecyloxy-2-furoic acid, a compound which inhibits fatty acid synthesis, was a very effective inhibitor of fatty acid synthesis by hepatocytes isolated from all rats used in the study. An inhibition of lactate plus pyruvate accumulation and a strong stimulation of glycogenolysis occurred in response to both glucagon and dibutyryl cyclic AMP with hepatocytes from both age groups of lean and obese rats. The results suggest that with aging of the obese female Zucker rat some step of hepatic fatty acid synthesis becomes progressively less sensitive to inhibition by glucagon and dibutyryl cyclic AMP. This may play an important role in maintenance of obesity in these animals.

摘要

从3月龄和5月龄的雌性遗传性肥胖Zucker大鼠及其瘦的同窝对照大鼠中分离出肝细胞。观察到肥胖大鼠的肝细胞中,脂肪酸合成对胰高血糖素和二丁酰环磷酸腺苷抑制作用的敏感性存在年龄依赖性降低。无论年龄如何,瘦动物的肝细胞对这些药物更为敏感。低浓度的胰高血糖素和二丁酰环磷酸腺苷实际上对老年肥胖大鼠制备的肝细胞的脂肪酸合成有一定的刺激作用。5-十四烷氧基-2-呋喃甲酸是一种抑制脂肪酸合成的化合物,对本研究中所用的所有大鼠分离出的肝细胞的脂肪酸合成都是非常有效的抑制剂。胰高血糖素和二丁酰环磷酸腺苷均可使瘦大鼠和肥胖大鼠两个年龄组的肝细胞的乳酸加丙酮酸积累受到抑制,并强烈刺激糖原分解。结果表明,随着肥胖雌性Zucker大鼠的衰老,肝脏脂肪酸合成的某些步骤对胰高血糖素和二丁酰环磷酸腺苷抑制作用的敏感性逐渐降低。这可能在这些动物肥胖的维持中起重要作用。

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