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百日咳毒素治疗可改变大鼠脑纹状体中的阿片类药物作用。

Pertussis toxin treatment modifies opiate action in the rat brain striatum.

作者信息

Abood M E, Law P Y, Loh H H

出版信息

Biochem Biophys Res Commun. 1985 Mar 15;127(2):477-83. doi: 10.1016/s0006-291x(85)80185-6.

Abstract

In this report we present evidence that a guanine nucleotide regulatory protein, Gi, mediates opiate action in the rat brain striatum. Opiates inhibit basal adenylate cyclase activity in rat brain striatum. This effect on adenylate cyclase is dose-dependently attenuated by pretreatment of membranes with pertussis toxin, which ADP-ribosylates a protein with a molecular mass of 41,000 daltons. This protein co-migrates with the GTP-binding subunit of Gi, which mediates inhibition of adenylate cyclase. Several brain regions were compared for the extent of radiolabeling and effects on adenylate cyclase activity. Although Gi was found in each region examined, opiate inhibition of adenylate cyclase is clearly seen only in the striatum.

摘要

在本报告中,我们提供证据表明,一种鸟嘌呤核苷酸调节蛋白Gi介导了阿片类药物在大鼠脑纹状体中的作用。阿片类药物抑制大鼠脑纹状体中的基础腺苷酸环化酶活性。用百日咳毒素预处理膜,可使这种对腺苷酸环化酶的作用呈剂量依赖性减弱,百日咳毒素能将一种分子量为41,000道尔顿的蛋白质进行ADP核糖基化。该蛋白质与Gi的GTP结合亚基共迁移,Gi介导对腺苷酸环化酶的抑制作用。比较了几个脑区的放射性标记程度以及对腺苷酸环化酶活性的影响。虽然在所检查的每个区域都发现了Gi,但仅在纹状体中能清楚地看到阿片类药物对腺苷酸环化酶的抑制作用。

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