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大脑中的肽能传递。III. 杏仁核对海马体的抑制作用。

Peptidergic transmission in the brain. III. Hippocampal inhibition by the amygdala.

作者信息

Smock T, Albeck D, McMechen P

机构信息

Department of Psychology, University of Colorado, Boulder 80309.

出版信息

Peptides. 1991 Jan-Feb;12(1):47-51. doi: 10.1016/0196-9781(91)90165-l.

Abstract

The mechanism of arginine vasopressin (AVP) action in the rat hippocampus has been determined. The peptide activates inhibitory interneurons and constricts cerebral microvessels. In the whole animal, each of these direct actions has secondary consequences for the excitability of pyramidal cells. Recent studies have shown that a peptide similar to AVP mediates endogenous neurotransmission in the hippocampus. Here we report experiments showing that the endogenous peptide activates the same mechanisms as exogenously applied AVP. The endogenous AVP-like peptide has no effect on the presynaptic fiber volley, or on pure somatic and dendritic postsynaptic potentials. These results are taken to exclude presynaptic mechanisms as explanations for the peptide's action. The endogenously released peptide inhibits individual pyramidal cells in single unit recording and excites presumed interneurons, just as AVP itself is known to act. The endogenous peptide is released only by stimuli applied to a nucleus that contains immunoreactive AVP and projects to the hippocampus.

摘要

精氨酸加压素(AVP)在大鼠海马体中的作用机制已被确定。该肽激活抑制性中间神经元并收缩脑微血管。在完整动物中,这些直接作用中的每一个都会对锥体细胞的兴奋性产生继发性影响。最近的研究表明,一种与AVP相似的肽介导海马体中的内源性神经传递。在此,我们报告实验表明内源性肽激活与外源性应用的AVP相同的机制。内源性AVP样肽对突触前纤维群或纯躯体和树突状突触后电位没有影响。这些结果被认为排除了突触前机制作为该肽作用的解释。内源性释放的肽在单单位记录中抑制单个锥体细胞并兴奋假定的中间神经元,正如已知AVP本身的作用一样。内源性肽仅由施加到含有免疫反应性AVP并投射到海马体的核的刺激释放。

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