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硫糖铝对胃黏膜钙通道活性的调节作用。

Modulation of gastric mucosal calcium channel activity by sucralfate.

作者信息

Slomiany B L, Liu J, Slomiany A

机构信息

Research Center, New Jersey Dental School, University of Medicine and Dentistry of New Jersey, Newark 07103-2400.

出版信息

Biochem Int. 1992 Dec;28(6):1125-34.

PMID:1283940
Abstract

A gastric mucosal calcium channel complex was isolated from solubilized epithelial cell membranes by affinity chromatography on wheat germ agglutinin. The complex following reconstitution into phosphatidylcholine vesicles exhibited an active 45Ca2+ uptake and responded to calcium channel activator, BAY K8644, and the antagonist, PN200-110. The uptake of 45Ca2+ was inhibited by an antiulcer agent, sucralfate, which at 100 micrograms/ml evoked maximal inhibitory effect of 52%. The channel complex on epidermal growth factor (EGF) binding in the presence of ATP showed an increase in tyrosine phosphorylation of 55 and 170kDa proteins, and the vesicles containing the phosphorylated channels displayed a 48% greater 45Ca2+ uptake. The phosphorylation process was inhibited by sucralfate, which also interfered with the binding of EGF to calcium channel protein. The results indicate that sucralfate has the ability to protect the cellular integrity from calcium imbalance.

摘要

通过麦胚凝集素亲和层析从溶解的上皮细胞膜中分离出一种胃黏膜钙通道复合物。该复合物重构到磷脂酰胆碱囊泡后表现出活跃的45Ca2+摄取,并对钙通道激活剂BAY K8644和拮抗剂PN200-110有反应。45Ca2+的摄取受到抗溃疡药物硫糖铝的抑制,硫糖铝在100微克/毫升时引起的最大抑制作用为52%。在ATP存在下,该通道复合物与表皮生长因子(EGF)结合后,55 kDa和170 kDa蛋白的酪氨酸磷酸化增加,含有磷酸化通道的囊泡显示45Ca2+摄取增加48%。磷酸化过程受到硫糖铝的抑制,硫糖铝也干扰EGF与钙通道蛋白的结合。结果表明,硫糖铝有能力保护细胞完整性免受钙失衡的影响。

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