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麻醉剂对脑微粒体钙储存及膜有序性的影响。

Effect of anesthetics on calcium stores and membrane order of brain microsomes.

作者信息

Daniell L C, Harris R A

机构信息

Department of Pharmacology, University of Colorado Health Sciences Center, Denver 80262.

出版信息

Mol Pharmacol. 1989 Sep;36(3):471-7.

PMID:2779526
Abstract

The effects of anesthetic agents from different chemical classes and a nonanesthetic membrane-disordering agent, 2-[2-methoxyethoxy]ethyl-8-[cis-2-n-octylcyclopropyl]octanoate (A2C), on calcium stores of whole brain microsomes and on order of microsomal membranes were compared. Calcium release was determined by measurement of the extramicrosomal calcium concentration and membrane order by the fluorescence polarization of diphenylhexatriene (membrane core) and trimethylammonium-diphenylhexatriene (membrane "surface"). n-Alkanols (methanol, ethanol, propanol, butanol, pentanol, and hexanol), benzyl alcohol (10-100 mM), and diethyl ether (30-300 mM) released calcium from brain microsomes and decreased the surface and interior membrane order of microsomal membranes. Pentobarbital (0.05-1 mM) did not release calcium from microsomes and did not alter the order of brain microsomal membranes. Halogenated anesthetics (halothane, methoxyflurane, and enflurane), 4-phenyl-1-butanol, and A2C decreased membrane order but failed to release calcium from brain microsomes. Comparison of the effects of these agents on microsomal calcium release and order of microsomal membranes revealed that decreases in membrane order are unrelated to the calcium-mobilizing actions of anesthetic compounds. In addition, molecular size appeared to limit ability of anesthetic compounds to release calcium from microsomes. For n-alkanols, benzyl alcohol, and diethyl ether, the ability to release microsomal calcium was correlated with anesthetic potency. Our results demonstrate, for the first time, direct effects of anesthetic agents on intracellular calcium stores of brain tissue and indicate that these stores may be target sites for anesthetics.

摘要

比较了不同化学类别的麻醉剂以及一种非麻醉性膜紊乱剂2-[2-甲氧基乙氧基]乙基-8-[顺式-2-正辛基环丙基]辛酸酯(A2C)对全脑微粒体钙储存和微粒体膜有序性的影响。通过测量微粒体外钙浓度来确定钙释放,通过二苯基己三烯(膜核心)和三甲基铵-二苯基己三烯(膜“表面”)的荧光偏振来确定膜有序性。正烷醇(甲醇、乙醇、丙醇、丁醇、戊醇和己醇)、苄醇(10 - 100 mM)和乙醚(30 - 300 mM)可从脑微粒体中释放钙,并降低微粒体膜的表面和内部膜有序性。戊巴比妥(0.05 - 1 mM)不会从微粒体中释放钙,也不会改变脑微粒体膜的有序性。卤代麻醉剂(氟烷、甲氧氟烷和恩氟烷)、4-苯基-1-丁醇和A2C可降低膜有序性,但未能从脑微粒体中释放钙。比较这些药物对微粒体钙释放和微粒体膜有序性的影响发现,膜有序性的降低与麻醉化合物的钙动员作用无关。此外,分子大小似乎限制了麻醉化合物从微粒体中释放钙的能力。对于正烷醇、苄醇和乙醚,释放微粒体钙的能力与麻醉效力相关。我们的结果首次证明了麻醉剂对脑组织细胞内钙储存的直接影响,并表明这些储存可能是麻醉剂的作用靶点。

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