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大鼠中通过钙离子内流和细胞内钙离子蓄积激活神经垂体血管加压素释放

Activation of neurohypophysial vasopressin release by Ca2+ influx and intracellular Ca2+ accumulation in the rat.

作者信息

Shibuki K

机构信息

Department of Physiology, Jichi Medical School, Tochigi-ken, Japan.

出版信息

J Physiol. 1990 Mar;422:321-31. doi: 10.1113/jphysiol.1990.sp017986.

Abstract
  1. Isolated rat neurohypophyses were stimulated electrically in an in vitro perifusion system. A Ca2(+)-sensitive microelectrode was placed in the centre of each neurohypophysis and [Ca2+]o decrease evoked by the stimulation were determined. 2. In neurohypophyses injected with Fura-2 AM (acetoxymethyl ester), increases and decreases in fluorescence excited at 340 and 380 nm, respectively, were evoked by stimulation. The time course of the fluorescence changes was similar to that of [Ca2+]o decreases, suggesting that the [Ca2+]o changes mirrored [Ca2+]i increases. 3. Calcium influx into neurosecretory axons and terminals was estimated as the difference in [Ca2+]o decrease rates immediately before and after train pulse stimulation. 4. Vasopressin release from the neurohypophysis, measured by specific radioimmunoassay, was facilitated by stimulation in parallel with a parameter of [Ca2+]o decrease multiplied by Ca2+ influx. 5. The O2 consumption rate, estimated as rate of PO2 decrease in the tissue, was facilitated by stimulation in parallel with [Ca2+]o decreases. 6. Possible calcium-dependent mechanisms of vasopressin release, and the energy-dependent step of the release by Ca2+, are discussed.
摘要
  1. 在体外灌流系统中对分离的大鼠神经垂体进行电刺激。将一个Ca2+敏感微电极置于每个神经垂体的中心,并测定刺激引起的[Ca2+]o降低。2. 在注射了Fura-2 AM(乙酰氧基甲酯)的神经垂体中,刺激分别引起在340和380 nm激发的荧光增加和降低。荧光变化的时间进程与[Ca2+]o降低的时间进程相似,表明[Ca2+]o变化反映了[Ca2+]i增加。3. 钙流入神经分泌轴突和终末的量通过串刺激前后[Ca2+]o降低速率的差值来估算。4. 通过特异性放射免疫测定法测量,神经垂体中血管加压素的释放因刺激而增加,且与[Ca2+]o降低参数乘以钙流入量平行。5. 以组织中PO2降低速率估算的耗氧率因刺激而增加,且与[Ca2+]o降低平行。6. 讨论了血管加压素释放可能的钙依赖机制以及Ca2+释放的能量依赖步骤。

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