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脊髓中沿Ia类传入纤维侧支的突触前抑制的系列电子显微镜和模拟研究。

Serial E-M and simulation study of presynaptic inhibition along a group Ia collateral in the spinal cord.

作者信息

Walmsley B, Graham B, Nicol M J

机构信息

Neuroscience Group, Faculty of Medicine, University of Newcastle, Callaghan, New South Wales, Australia.

出版信息

J Neurophysiol. 1995 Aug;74(2):616-23. doi: 10.1152/jn.1995.74.2.616.

Abstract
  1. A muscle spindle primary afferent (group Ia) was physiologically identified and labeled intracellularly with the use of horseradish peroxidase (HRP) in the cat lumbar spinal cord. Serial-section electron microscopy (EM) was used to examine and reconstruct an entire axon collateral and its branches within Clarke's column. In the present study the existence and location of presynaptic contacts on Ia afferent boutons along these collateral branches were determined from examination of the serial-section electron-micrographs. 2. Of 36 Ia boutons examined in serial sections along the branches of the same collateral, 3 presynaptic contacts were found. Two of these contacts were made with Ia boutons in a complex nodal region consisting of two unmyelinated side branches exhibiting a total of six Ia boutons. The other presynaptic contact was made with a Ia bouton in a nodal region consisting of two Ia boutons connected by a thin unmyelinated bridge. 3. Computer simulations, based directly on the serial-section-reconstructions, were used to investigate the possible effects of these presynaptic contacts on membrane potential and on a propagating action potential along the Ia collateral. The effect of a presynaptic contact was modeled by a sustained gamma-aminobutyric acid-A (GABAA)-activated chloride conductance. 4. The simulation results indicated that the effect of a presynaptic contact on membrane potential and action-potential amplitude is likely to extend beyond the contacted bouton to other boutons occurring along the short unmyelinated branches arising from the same node.(ABSTRACT TRUNCATED AT 250 WORDS)
摘要
  1. 在猫的腰脊髓中,通过生理方法鉴定出肌梭初级传入纤维(Ia类),并用辣根过氧化物酶(HRP)进行细胞内标记。采用连续切片电子显微镜(EM)检查并重建了克拉克柱内的整个轴突侧支及其分支。在本研究中,通过检查连续切片电子显微照片,确定了沿这些侧支分支的Ia传入终扣上突触前接触的存在和位置。2. 在沿同一侧支分支的连续切片中检查的36个Ia终扣中,发现了3个突触前接触。其中两个接触是在一个复杂的节点区域与Ia终扣形成的,该区域由两个无髓鞘侧支组成,共有6个Ia终扣。另一个突触前接触是在一个由两个通过细无髓鞘桥连接的Ia终扣组成的节点区域与一个Ia终扣形成的。3. 基于连续切片重建直接进行计算机模拟,以研究这些突触前接触对膜电位以及沿Ia侧支传播的动作电位的可能影响。突触前接触的影响通过持续的γ-氨基丁酸-A(GABAA)激活的氯电导进行建模。4. 模拟结果表明,突触前接触对膜电位和动作电位幅度的影响可能会超出接触的终扣,延伸到同一节点产生的短无髓鞘分支上的其他终扣。(摘要截短于250字)

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