钙对猪空肠分泌反应的调节作用。

G W Forsyth, P H Wong, D D Maenz
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摘要

用体外系统研究了钙离子作为分泌介质参与猪空肠上皮的作用。从组织两侧的Ringer-HCO3洗液中剔除Ca++对猪空肠黏膜基础电活动的影响较小。游离Ca++介质仅使上皮电位差略有降低,电导略有增加。低EGTA浓度可逆地阻断了对分泌剂的电位差反应,对基础电活动的影响也很小。对A23187、茶碱和大肠杆菌热稳定型肠毒素的体外分泌反应均可通过Ca++耗尽消除,并通过替换浴液中正常Ca++浓度恢复。丹曲林可以抑制热稳定型肠毒素和A23187引起的分泌反应,但不能抑制电位差的增加,提示细胞内Ca++的储存可能是分泌信号剂的储存库。维拉帕米只阻断了对热稳定型肠毒素的分泌反应。氯丙嗪对基础条件的影响可以忽略不计,但完全阻断了A23187和热稳定型肠毒素对电位差的分泌反应和Ca++依赖性作用。氯丙嗪对茶碱的反应仅部分抑制,暗示cAMP和ca++作为茶碱的分泌信号参与其中。在调节猪空肠的分泌作用方面,细胞质钙离子浓度似乎至少与环核苷酸一样重要。
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Calcium mediation of the pig jejunal secretory response.

The involvement of Ca++ ions as secretory mediators in pig jejunal epithelia has been investigated with an in vitro system. Omission of Ca++ from the Ringer-HCO3 bathing media on both sides of the tissue had minor effects on the basal electrical activity of pig jejunal mucosa. There were only slight decreases in transepithelial potential difference and increases in conductance with Ca++ free media. Low EGTA concentrations which reversibly blocked potential difference responses to secretory agents also had minimal effects on basal electrical activity. The in vitro secretory responses to A23187, to theophylline, and to Escherichia coli heat-stable enterotoxin were all eliminated by Ca++ depletion and restored by replacing normal Ca++ concentrations in the bathing media. Dantrolene prevented the secretory response but not the potential difference increases caused by heat-stable enterotoxin and A23187, suggesting that intracellular Ca++ stores may be reservoirs of secretory signal agent. Verapamil only blocked the secretory response to heat-stable enterotoxin. Chlorpromazine had negligible effects on basal conditions, but totally blocked both the secretory response and the Ca++-dependent effects of A23187 and heat-stable enterotoxin on potential difference. The response to theophylline was only partially inhibited by chlorpromazine, implying some involvement of both cAMP and Ca++ as secretory signals for theophylline. Cytoplasmic Ca++ concentrations appear to be at least as important as cyclic nucleotides in regulating the secretory effects of pig jejunum.

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