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二乙基二硫代氨基甲酸盐会损害胃泌素的α-酰胺化作用。

Alpha-amidation of gastrin is impaired by diethyldithiocarbamate.

作者信息

Hilsted L

机构信息

University Department of Clinical Chemistry, Rigshospitalet, Copenhagen, Denmark.

出版信息

Regul Pept. 1990 Jul 30;29(2-3):179-87. doi: 10.1016/0167-0115(90)90081-7.

Abstract

The influence of gastrin alpha-amidation of the heavy-metal chelator diethyldithiocarbamate and disulfiram, its disulfide dimer, was studied in rat gastric antrum. Sensitive, sequence-specific immunoassays for glycine-extended and amidated gastrin were used to monitor extractions and chromatography. The results showed that intraperitoneal diethyldithiocarbamate administration (1000 mg/kg body weight) for two days caused a decrease in amidated gastrin from 2.6 +/- 0.4 to 1.4 +/- 0.3 nmol/g tissue (n = 11) with a simultaneous increase in glycine-extended gastrin from 0.84 +/- 0.15 to 2.4 +/- 0.3 nmol/g. Peroral administration of disulfiram (4 mg/kg body weight) for nine days did not change alpha-amidation significantly. The results of the present study demonstrate that the heavy-metal chelating agent diethyldithiocarbamate inhibits alpha-amidation of gastrin in vivo, in agreement with the inhibition of amidating activity observed in vitro. These results are in accordance with the previous observations that the presence of copper ions is necessary for the alpha-amidation to take place.

摘要

在大鼠胃窦中研究了重金属螯合剂二乙基二硫代氨基甲酸盐及其二硫化物二聚体双硫仑对胃泌素α-酰胺化的影响。使用针对甘氨酸延伸型和酰胺化胃泌素的灵敏、序列特异性免疫测定法来监测提取物和色谱分析。结果显示,连续两天腹腔注射二乙基二硫代氨基甲酸盐(1000 mg/kg体重)导致酰胺化胃泌素从2.6±0.4降至1.4±0.3 nmol/g组织(n = 11),同时甘氨酸延伸型胃泌素从0.84±0.15增至2.4±0.3 nmol/g。连续九天口服双硫仑(4 mg/kg体重)对α-酰胺化没有显著影响。本研究结果表明,重金属螯合剂二乙基二硫代氨基甲酸盐在体内抑制胃泌素的α-酰胺化,这与体外观察到的酰胺化活性抑制一致。这些结果与先前的观察结果相符,即α-酰胺化发生需要铜离子的存在。

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