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腺苷、5'-三磷酸腺苷及相关嘌呤对离体兔胃腺胃酸分泌影响的特性研究

Characterization of the effects of adenosine, adenosine 5'-triphosphate and related purines on acid secretion in isolated rabbit gastric glands.

作者信息

Gil-Rodrigo C E, Galdiz B, Gandarias J M, Gomez R, Ainz L F

机构信息

Department of Physiology, Biochemistry and Biophysics, Faculty of Medicine, University of the Basque Country (UPV-EHU), Bilbao, Spain.

出版信息

Pharmacol Res. 1990 Mar-Apr;22(2):103-13. doi: 10.1016/1043-6618(90)90706-j.

Abstract

The influence of adenosine, AMP, ADP, ATP, the adenosine analogue L-PIA and the ATP analogue beta,gamma-methylene ATP, on gastric acid secretion, as measured by the aminopyrine accumulation method, in resting and histamine-stimulated glands isolated from rabbit gastric mucosa was studied. In resting glands, adenosine and its analogue L-PIA (10 microM-1 mM) caused significant concentration-related increases of the basal H+ secretion, whereas no changes were obtained in response to the other purines tested. In histamine-stimulated glands, adenosine, L-PIA and AMP (10 microM-1 mM) induced concentration-related increases of the H+ secretory rate, whereas ATP, beta,gamma-methylene ATP and ADP (10 microM-1 mM) produced concentration-related decreases of the H+ raised rate. The rank order of potency of the purine compounds in increasing the stimulated H+ secretion was: adenosine greater than L-PIA much greater than AMP, and in decreasing it was: ATP much greater than ADP greater than beta,gamma-methylene ATP. The stimulatory responses to adenosine were inhibited by theophylline (10 microM-100 microM) and caffeine (10 microM-1 mM); whereas, the inhibitory responses to ATP were significantly reduced by the well known prostaglandin synthesis inhibitor indomethacin (1 microM-100 microM). From the results it is concluded that in isolated rabbit gastric glands, purine compounds are effective modulators of the gastric H+ secretory process. The pattern of purine activity obtained suggests that the stimulatory responses, inhibited by methylxanthines, may be mediated via P1-purinoceptors, while the inhibitory responses, reduced by indomethacin, may be mediated via P2-purinoceptors.

摘要

采用氨基比林蓄积法,研究了腺苷、AMP、ADP、ATP、腺苷类似物L-PIA以及ATP类似物β,γ-亚甲基ATP对从兔胃黏膜分离出的静息和组胺刺激的腺体胃酸分泌的影响。在静息腺体中,腺苷及其类似物L-PIA(10微摩尔/升-1毫摩尔/升)引起基础H⁺分泌显著的浓度依赖性增加,而对其他测试嘌呤无反应。在组胺刺激的腺体中,腺苷、L-PIA和AMP(10微摩尔/升-1毫摩尔/升)诱导H⁺分泌速率的浓度依赖性增加,而ATP、β,γ-亚甲基ATP和ADP(10微摩尔/升-1毫摩尔/升)使升高的H⁺分泌速率呈浓度依赖性降低。嘌呤化合物在增加刺激的H⁺分泌方面的效力顺序为:腺苷>L-PIA>>AMP,在降低刺激的H⁺分泌方面的顺序为:ATP>>ADP>β,γ-亚甲基ATP。茶碱(10微摩尔/升-100微摩尔/升)和咖啡因(10微摩尔/升-1毫摩尔/升)抑制对腺苷的刺激反应;而众所周知的前列腺素合成抑制剂吲哚美辛(1微摩尔/升-100微摩尔/升)显著降低对ATP的抑制反应。从结果得出结论,在分离的兔胃腺体中,嘌呤化合物是胃酸H⁺分泌过程的有效调节剂。所获得的嘌呤活性模式表明,被甲基黄嘌呤抑制的刺激反应可能通过P1嘌呤受体介导,而被吲哚美辛降低的抑制反应可能通过P2嘌呤受体介导。

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