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细胞外5'-三磷酸腺苷对兔胃黏膜壁细胞的抑制作用。

Inhibitory action of extracellular adenosine 5'-triphosphate on parietal cells isolated from rabbit gastric mucosa.

作者信息

Gil-Rodrigo C E, Bergaretxe I, Carou M, Galdiz B, Salgado C, Ainz L F

机构信息

Departamento de Fisiología, Facultad de Medicina, Universidad del País Vasco (UPV-EHU), Bilbao, Spain.

出版信息

Gen Physiol Biophys. 1996 Jun;15(3):251-64.

PMID:9076507
Abstract

The effects of the purine nucleotides, adenosine 5'-triphosphate (ATP) and their analogs 2-methylthio ATP and beta, gamma-methylene ATP, as well as those of the pyrimidine nucleotide, uridine 5'-triphosphate (UTP), on acid production in isolated rabbit gastric parietal cells prepared by enzymatic dispersion and enriched by counterflow elutriation were studied. The (14C)-aminopyrine (AP) accumulation method was used as an index of acid production by the parietal cells. In histamine-stimulated parietal cells, ATP and 2-methylthio ATP, but not beta, gamma-methylene ATP or UTP, produced significant and concentration-related inhibition of the histamine-stimulated AP uptake. The rank order of potency of these nucleotides in inhibiting histamine-stimulated AP accumulation was 2-methylthio ATP > ATP > > beta, gamma-methylene ATP, UTP. In contrast to these results, the AP accumulation responses to secretagogues other than histamine such as carbachol and dibutyryl-cAMP, were not significantly modified by ATP and analogs. Pretreatment of parietal cells with indomethacin, a prostaglandin synthesis inhibitor, led to a significant reduction of the inhibitory responses elicited by ATP on histamine-stimulated AP uptake. These data suggest that ATP selectively inhibits the histamine-stimulated gastric acid secretion in rabbits by acting directly on parietal cells; that a component of this action seems to be related with a stimulation of prostaglandin production; and that the antisecretory effect of ATP on isolated rabbit parietal cells may be mediated via P2Y-purinoceptors.

摘要

研究了嘌呤核苷酸腺苷5'-三磷酸(ATP)及其类似物2-甲硫基ATP和β,γ-亚甲基ATP,以及嘧啶核苷酸尿苷5'-三磷酸(UTP)对通过酶分散制备并用逆流淘析富集的离体兔胃壁细胞产酸的影响。采用(14C)-氨基比林(AP)积累法作为壁细胞产酸的指标。在组胺刺激的壁细胞中,ATP和2-甲硫基ATP可显著且浓度依赖性地抑制组胺刺激的AP摄取,而β,γ-亚甲基ATP或UTP则无此作用。这些核苷酸抑制组胺刺激的AP积累的效力顺序为2-甲硫基ATP>ATP>>β,γ-亚甲基ATP,UTP。与这些结果相反,ATP及其类似物对组胺以外的促分泌剂如卡巴胆碱和二丁酰-cAMP引起的AP积累反应无显著影响。用前列腺素合成抑制剂吲哚美辛预处理壁细胞,可显著降低ATP对组胺刺激的AP摄取所引发的抑制反应。这些数据表明,ATP通过直接作用于壁细胞选择性抑制兔组胺刺激的胃酸分泌;这种作用的一部分似乎与前列腺素生成的刺激有关;并且ATP对离体兔壁细胞的抗分泌作用可能通过P2Y嘌呤受体介导。

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