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利血平对镁离子诱导的大鼠主动脉钙通量及反应性的影响。

Effect of reserpine on Mg++-induced calcium fluxes and reactivity of the rat aorta.

作者信息

Krishnamurty V S, Mukherjee A

出版信息

Arch Int Pharmacodyn Ther. 1981 Jun;251(2):180-91.

PMID:6792999
Abstract

The effect of reserpine on 45Ca++ fluxes and reactivity of the rat aorta in Mg++-free and Mg++ (1.2 or 3.6 mM) media to various agonists was examined to gain further insight into mechanism(s) responsible for the altered sensitivities in vascular smooth muscle. Incubation of rat aorta in Mg++-free and high Mg++ (3.6 mM) media containing ethylene diamine tetra-acetic acid (EDTA 0.03 mM), respectively, increased and decreased the sensitivity to noradrenaline (NA), 5-hydroxytryptamine (5-HT) and KCl. Mg++-free medium significantly enhanced maximal response to 5-HT whereas high Mg++ (3.6 mM) medium reduced the maximal responses to KCl and 5-HT but not to NA. Mg++-free medium had no effect on 45Ca++ uptake, while it enhanced 45Ca++ efflux from the aorta. Reserpine treatment induced supersensitivity in the aorta to KCl, but not to either NA or 5-HT in normal medium, whereas in Mg++-free medium, it induced partial contraction and inhibited both maximal responses and sensitivity to NA and 5-HT but not to KCl. Reserpine in high Mg++ (3.6 mM) medium had no effect on sensitivity and maximal responsiveness to all these agents. Reserpine reduced 45Ca++ uptake by aorta in either Mg++-free or normal Mg++ medium and it reduced 45Ca++ efflux for aorta in Mg++-free but not in normal Mg++ medium. These observations suggest that reserpine may promote membrane permeability rather nonspecifically to divalent ions. However, the presence of EDTA in the media may have partially reduced the antagonistic effects of Mg++ due to reserpine treatment in this tissue.

摘要

研究了利血平对大鼠主动脉在无镁和含镁(1.2或3.6 mM)培养基中45Ca++通量以及对各种激动剂反应性的影响,以进一步深入了解血管平滑肌敏感性改变的机制。分别在含乙二胺四乙酸(EDTA 0.03 mM)的无镁和高镁(3.6 mM)培养基中孵育大鼠主动脉,可分别增加和降低对去甲肾上腺素(NA)、5-羟色胺(5-HT)和氯化钾的敏感性。无镁培养基显著增强了对5-HT的最大反应,而高镁(3.6 mM)培养基降低了对氯化钾和5-HT的最大反应,但对NA无影响。无镁培养基对45Ca++摄取无影响,但增强了主动脉的45Ca++流出。在正常培养基中,利血平处理可使主动脉对氯化钾产生超敏反应,但对NA或5-HT无此作用;而在无镁培养基中,它可引起部分收缩,并抑制对NA和5-HT的最大反应及敏感性,但对氯化钾无此作用。在高镁(3.6 mM)培养基中,利血平对所有这些药物的敏感性和最大反应性均无影响。在无镁或正常镁培养基中,利血平均可降低主动脉对45Ca++的摄取;在无镁培养基中,利血平可降低主动脉的45Ca++流出,但在正常镁培养基中则无此作用。这些观察结果表明,利血平可能非特异性地促进膜对二价离子的通透性。然而,培养基中EDTA的存在可能部分降低了利血平处理对该组织中镁的拮抗作用。

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