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配体诱导的大鼠肝脏胰岛素受体亚细胞分布变化:秋水仙碱的作用

Ligand-induced changes in the subcellular distribution of insulin receptors in rat liver: effects of colchicine.

作者信息

Postel-Vinay M C, Kayser C, Desbuquois B

机构信息

INSERM Unité 30, Hôpital des Enfants-Malades, Paris, France.

出版信息

Mol Cell Endocrinol. 1987 Aug;52(3):199-204. doi: 10.1016/0303-7207(87)90044-x.

Abstract

The in vivo effects of colchicine on the subcellular distribution of insulin receptors have been studied in insulin-injected rats and in control animals. Colchicine (0.1 mg/100 g or 10 mg/100 g body weight, i.v.) did not affect the ability of plasma membranes and Golgi fractions of control rats to bind insulin. As previously reported (Desbuquois et al., 1982), the injection of native insulin (8 nmol, i.v.) caused a 50% decrease in the insulin binding activity of plasma membranes and a concomitant 50% increase in insulin binding to Golgi fractions. These changes occurred at 4 and 40 min after insulin injection but were no longer detectable at 3 h. Colchicine treatment did not affect the initial changes in the distribution of insulin receptors induced by insulin; however, in rats treated with the low dose of colchicine, insulin binding to plasma membranes at 3 h was not fully restored. Colchicine treatment did not alter the amount of acid-extractable insulin associated with Golgi fractions of insulin-injected rats. The time course of uptake of 125I-insulin was similar in plasma membranes, microsomal fraction and Golgi fractions of colchicine-treated (0.1 mg/100 g) and of untreated rats. These results suggest that colchicine does not interfere with the endocytosis of insulin receptors induced by their ligand and has little effect, if any, on the reinsertion of internalized receptors in the plasma membrane.

摘要

已在注射胰岛素的大鼠和对照动物中研究了秋水仙碱对胰岛素受体亚细胞分布的体内作用。秋水仙碱(0.1mg/100g或10mg/100g体重,静脉注射)不影响对照大鼠质膜和高尔基体组分结合胰岛素的能力。如先前报道(Desbuquois等人,1982年),注射天然胰岛素(8nmol,静脉注射)导致质膜胰岛素结合活性降低50%,同时高尔基体组分上的胰岛素结合增加50%。这些变化发生在胰岛素注射后4分钟和40分钟,但在3小时后不再可检测到。秋水仙碱处理不影响胰岛素诱导的胰岛素受体分布的初始变化;然而,在用低剂量秋水仙碱处理的大鼠中,3小时时质膜上的胰岛素结合未完全恢复。秋水仙碱处理未改变与注射胰岛素的大鼠高尔基体组分相关的酸可提取胰岛素的量。秋水仙碱处理(0.1mg/100g)和未处理大鼠的质膜、微粒体组分和高尔基体组分中125I-胰岛素的摄取时间进程相似。这些结果表明,秋水仙碱不干扰其配体诱导的胰岛素受体的内吞作用,并且对内化受体重新插入质膜几乎没有影响(如果有影响的话)。

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