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人参多糖对降低肝糖原的作用

[Effects of the ginseng polysaccharides on reducing liver glycogen].

作者信息

Yang M, Wang B X

机构信息

Academy of Traditional Medicine and Materia Medica of Jilin Province, Changchun, China.

出版信息

Zhongguo Yao Li Xue Bao. 1991 May;12(3):272-5.

PMID:1664170
Abstract

The ginseng polysaccharides GH1 (100, 200 mg.kg-1) iv reduced liver glycogen and increased adenosine-3',5'-cyclic monophosphate (cAMP) level and adenyl cyclase (AC) activity in mice. The action of GH1 was completely antagonized by propranolol, inhibitor of adrenergic beta receptor. The stimulating effect of GH1 on AC activity was significant 2 and 4 h after iv GH1. However, GH1 at concentration of 20-120 mumol.L-1 in vitro showed no manifest effect on AC activity. GH1 stimulated the activities of 3',5'-cyclic-GMP phosphodiesterases (PDE) and calmodulin (CaM) in a dose-dependent manner. It is suggested that the reduction of liver glycogen induced by GH1 resulted from its obvious increase of cAMP which promoted glycogenolysis and decreased glycogenesis.

摘要

人参多糖 GH1(100、200 毫克·千克-1,静脉注射)可降低小鼠肝脏糖原含量,提高腺苷 3',5'-环磷酸(cAMP)水平及腺苷酸环化酶(AC)活性。GH1 的作用被肾上腺素能β受体抑制剂普萘洛尔完全拮抗。静脉注射 GH1 后 2 小时和 4 小时,GH1 对 AC 活性的刺激作用显著。然而,体外浓度为 20 - 120 微摩尔·升-1 的 GH1 对 AC 活性无明显影响。GH1 以剂量依赖方式刺激 3',5'-环鸟苷酸磷酸二酯酶(PDE)和钙调蛋白(CaM)的活性。提示 GH1 诱导肝脏糖原减少是由于其明显增加 cAMP,促进糖原分解并减少糖原合成所致。

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