期刊论文详细信息
Cell Structure and Function | |
Effects of Sulphydryl Reagents on Receptor-Mediated Hormonal Responses at the Cellular Level: Insulin-mimicking Characteristics of Thiol-blocking Compounds in Rat Hepatocyte Primary Cultures | |
Boot J. H.1  | |
[1]Department Veterinary Pharmacology, Pharmacy and Toxicology | |
关键词: SH; thiol-blocking compounds; endocrine test-system; rat hepatocyte primary cultures; insulin-mimicking; in vitro toxicology; | |
DOI : 10.1247/csf.21.1 | |
学科分类:分子生物学,细胞生物学和基因 | |
来源: Japan Society for Cell Biology | |
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【 摘 要 】
References(42)Cited-By(1)The interference of various SH-blocking chemicals with the insulin-controlled regulation of the hepatic carbohydrate metabolism was studied in rat hepatocyte primary cultures. The organic mercurials PCMB, PCMBS, mersalyl the disulphide agents DTP, CPDS, disulfiram and the SH-alkylating reagent NEM were used as experimental SH-blocking model compounds. All studied compounds, except for NEM, induced an increased glycogen deposition comparable with the physiological insulin-induced glycogen-deposition. PCMBS appeared to be the most effective insulin-mimicking anabolic trigger. The action of the insulin molecule itself was potentiated by PCMBS as well as demonstrated by increased glycogen deposition, induced pyruvate kinase (PK) and decreased phosphoenol-pyrnvate carboxykinase (PEP-CK) activity. However, cell-exposure to insulin and PCMBS in relatively high doses was destructive, as demonstrated by decreased glycogen levels, most probably as a result of insulin-receptor overstimulation and metabolic stress. Thus, SH-blocking compounds are able to trigger insulin-dependent metabolic processes. The relatively non-permeant organic mercurial PCMBS proved to be the most effective insulin-mimicking SH-blocking compound.【 授权许可】
Unknown
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