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均匀的橄榄小脑传导时间是大鼠小脑中浦肯野细胞复合峰同步性的基础。

Uniform olivocerebellar conduction time underlies Purkinje cell complex spike synchronicity in the rat cerebellum.

作者信息

Sugihara I, Lang E J, Llinás R

机构信息

Department of Physiology and Biophysics, New York University Medical Center, NY 10016.

出版信息

J Physiol. 1993 Oct;470:243-71. doi: 10.1113/jphysiol.1993.sp019857.

Abstract
  1. The issue of isochronicity of olivocerebellar fibre conduction time as a basis for synchronizing complex spike activity in cerebellar Purkinje cells has been addressed by latency measurement, multiple-electrode recording and Phaseolus vulgaris leucoagglutinin (PHA-L) tracing of climbing fibres in the adult rat. 2. The conduction time of the olivocerebellar fibres was measured by recording Purkinje cell complex spike (CS) responses from various areas of the cerebellum. The CSs were evoked by stimulating the olivocerebellar fibres near the inferior olive. In spite of a difference in length, as determined directly by light microscopy, the conduction times of different climbing fibres were quite uniform, 3.98 +/- 0.36 ms (mean +/- S.D., n = 660). 3. Multiple-electrode recording of spontaneous Purkinje cell CS activity was employed to study the spatial extent of CS synchronicity in the cerebellar cortex. Recordings of CS were obtained from Purkinje cells located on the surface and along the walls of lobule crus 2a. The rostrocaudal band-like distribution of simultaneous (within 1 ms) CS activity in Purkinje cells extended down the sides of the cerebellar folia to the deepest areas recorded (1.6-2.6 mm deep). As shown in previous experiments, the distribution of simultaneous CS activity did not extend significantly (500 microns) in the mediolateral axis of the cerebellar cortex. 4. In two animals a detailed determination of the length of the olivocerebellar fibre bundles was performed by staining the fibres with PHA-L injected into the contralateral inferior olive. This measurement included fibre bundles terminating in twenty-six different areas, ranging from the tops of the various folia to the bottoms of the fissures in both the hemisphere and the vermis. There was a 47.5% difference between the length of the longest measured fibre bundle (15.8 mm, terminating in lobule 6b, zone A) and the length of the shortest measured fibre bundle (8.3 mm, terminating in the cortex at the base of the primary fissure, zone D), after correction for tissue shrinkage. To attain an isochronous conduction time the conduction velocities for these two fibre bundles were calculated to be 4.22 m/s and 2.37 m/s, respectively. 5. By interpolating between measured points a simple formula was derived to estimate the average length of olivocerebellar fibres terminating in any given area of the cerebellar cortex, excluding the paraflocculus, the flocculus and the most lateral regions of the hemisphere. 6. We investigated the most likely mechanisms by which conduction velocity variations with length could result in global isochronicity.(ABSTRACT TRUNCATED AT 400 WORDS)
摘要
  1. 成年大鼠橄榄小脑纤维传导时间的等时性问题,作为小脑浦肯野细胞复杂峰电位活动同步化的基础,已通过潜伏期测量、多电极记录以及菜豆白细胞凝集素(PHA-L)追踪攀缘纤维进行了研究。2. 通过记录小脑不同区域浦肯野细胞的复杂峰电位(CS)反应,来测量橄榄小脑纤维的传导时间。CS由刺激下橄榄附近的橄榄小脑纤维诱发。尽管通过光学显微镜直接测定的长度存在差异,但不同攀缘纤维的传导时间相当一致,为3.98±0.36毫秒(平均值±标准差,n = 660)。3. 采用多电极记录浦肯野细胞CS的自发活动,以研究小脑皮质中CS同步化的空间范围。从位于小叶 Crus 2a表面及沿其壁的浦肯野细胞获取CS记录。浦肯野细胞中同时(1毫秒内)CS活动的前后带状分布沿小脑叶片两侧延伸至记录的最深区域(1.6 - 2.6毫米深)。如先前实验所示,同时CS活动的分布在小脑皮质的内外侧轴上没有显著延伸(500微米)。4. 在两只动物中,通过将PHA-L注入对侧下橄榄对橄榄小脑纤维束进行染色,详细测定了其长度。该测量包括终止于26个不同区域的纤维束,范围从各个叶片顶部到半球和蚓部裂沟底部。校正组织收缩后,最长测量纤维束(15.8毫米,终止于小叶6b,A区)与最短测量纤维束(8.3毫米,终止于初级裂沟底部皮质,D区)的长度相差47.5%。为达到等时传导时间,计算这两个纤维束的传导速度分别为4.22米/秒和2.37米/秒。5. 通过在测量点之间进行插值,得出一个简单公式来估计终止于小脑皮质任何给定区域(不包括旁绒球、绒球和半球最外侧区域)的橄榄小脑纤维的平均长度。6. 我们研究了传导速度随长度变化可能导致整体等时性的最可能机制。(摘要截断于400字)
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2cc2/1143916/fc0ebb2a0ec4/jphysiol00369-0252-a.jpg

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