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组胺和钾离子对突触体中(钙 - 镁)-ATP酶活性影响的比较研究

A comparative study of histamine and K+ effects on (Ca(2+)-Mg2+)-ATPase activity in synaptosomes.

作者信息

Rodriguez R, Toledo A, Sabriá J, Rodriguez J, Blanco I

机构信息

Dpto bioquímica y Biología Molecular, Facultad de Medicina, Universidad Autónoma de Barcelona, Spain.

出版信息

Biochem Pharmacol. 1991 Jun 15;41(12):1981-6. doi: 10.1016/0006-2952(91)90139-v.

Abstract

Histamine (10(-4) M) and 60 mM K+, but not 60 mM Na+ or 60 mM choline+, increased the maximal synaptosomal (Ca(2+)-Mg2+)-ATPase activity by 15 and 36% respectively and decreased the extrasynaptosomal Ca2+ concentration necessary to reach it. Histamine and K+ enhanced the synaptosomal (Ca(2+)-Mg2+)-ATPase activity in a concentration-dependent manner. In synaptic plasma membranes histamine (10(-4) M) and 60 mM choline+ were not able to alter the enzymatic activity, however 60 mM K+ and 60 mM Na+ elevated (Ca(2+)-Mg2+)-ATPase activity by 20 and 15%, respectively, without altering the affinity for Ca2+. Histamine effects in synaptosomes were mediated by H2 receptor stimulation. 3-Isobutyl-1-methyl-xanthine (10(-4) M) potentiated (15%) the maximal histamine effect. The slow Ca2+ channel antagonists verapamil and diltiazem, both at 10(-6) M, completely inhibited K+ effects in synaptosomes, however histamine effects were only blocked by verapamil. The data suggest that K+ and histamine effects on synaptosomal (Ca(2+)-Mg2+)-ATPase activity are mediated by increases of intrasynaptosomal Ca2+ levels. Moreover, histamine effects on synaptosomal enzyme activity were mediated by cAMP.

摘要

组胺(10⁻⁴ M)和60 mM钾离子可使突触体(钙 - 镁)-ATP酶的最大活性分别增加15%和36%,但60 mM钠离子或60 mM胆碱离子则无此作用,同时降低了达到该最大活性所需的突触外钙离子浓度。组胺和钾离子以浓度依赖的方式增强突触体(钙 - 镁)-ATP酶的活性。在突触质膜中,组胺(10⁻⁴ M)和60 mM胆碱离子不能改变酶活性,然而60 mM钾离子和60 mM钠离子分别使(钙 - 镁)-ATP酶活性提高20%和15%,且不改变对钙离子的亲和力。组胺在突触体中的作用是由H₂受体刺激介导的。3 - 异丁基 - 1 - 甲基 - 黄嘌呤(10⁻⁴ M)增强(15%)组胺的最大作用。慢钙通道拮抗剂维拉帕米和地尔硫䓬,均为10⁻⁶ M,完全抑制钾离子在突触体中的作用,然而组胺的作用仅被维拉帕米阻断。数据表明,钾离子和组胺对突触体(钙 - 镁)-ATP酶活性的作用是由突触体内钙离子水平的升高介导的。此外,组胺对突触体酶活性的作用是由环磷酸腺苷介导的。

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