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体内给予卵巢甾体激素后大鼠脑区突触体对钙离子的摄取

Ca2+ uptake by rat brain region synaptosomes following in vivo administration of ovarian steroids.

作者信息

Nikezić G, Horvat A, Milenković L, Martinović J V

机构信息

Institute for Molecular Biology and Endocrinology, Boris Kidric Institute for Nuclear Sciences, Belgrade, Yugoslavia.

出版信息

Mol Cell Endocrinol. 1988 May;57(1-2):77-80. doi: 10.1016/0303-7207(88)90034-2.

Abstract

Effects of progesterone (P) and estradiol-17 beta benzoate (EB), applied s.c. into sexually mature, long-term ovariectomized (OVX) rats, on subsequent depolarization-induced uptake of Ca2+ were studied in synaptosomes isolated from the brain stem, mesencephalic reticular formation (MRF), nucleus caudatus putamen (NCP) and the hippocampus. In intact animals, synaptosomal Ca2+ uptake differed from region to region: it was lowest in the brain stem and highest in the hippocampus. In comparison to intact animals, ovariectomy resulted in a marked increase of the uptake regardless the structure investigated, suggesting an inhibitory action of ovaries on the uptake of Ca2+ in a considerable portion of rat brain. Single injection of 2 mg P, given to OVX rats 24 h prior to decapitation, evoked a marked decrease in Ca2+ uptake by synaptosomes of the brain stem and MRF and particularly by those of NCP and the hippocampus. Single injection of 5 micrograms EB into OVX animals 72 h prior to the experiment was as effective as P in inhibiting Ca2+ uptake by synaptosomes of the brain stem and MRF, but less effective than P in case of NCP and the hippocampus. This suggests involvement of P and EB in the modulation of synaptic transmission by affecting neuronal Ca2+ uptake.

摘要

将孕酮(P)和苯甲酸雌二醇-17β(EB)皮下注射到性成熟、长期卵巢切除(OVX)的大鼠体内,研究其对从脑干、中脑网状结构(MRF)、尾状核壳核(NCP)和海马体分离的突触体中随后去极化诱导的Ca2+摄取的影响。在完整动物中,突触体Ca2+摄取因区域而异:在脑干中最低,在海马体中最高。与完整动物相比,卵巢切除导致无论所研究的结构如何,摄取均显著增加,表明卵巢对大鼠大脑相当一部分区域的Ca2+摄取具有抑制作用。在断头前24小时给OVX大鼠单次注射2毫克P,可使脑干和MRF的突触体,特别是NCP和海马体的突触体对Ca2+的摄取显著减少。在实验前72小时给OVX动物单次注射5微克EB,在抑制脑干和MRF的突触体对Ca2+摄取方面与P一样有效,但在NCP和海马体的情况下比P效果差。这表明P和EB通过影响神经元Ca2+摄取参与突触传递的调节。

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