Cerebellar globular cells receive strong inhibition mediated by axon collaterals of Purkinje cells

2011 ◽  
Vol 71 ◽  
pp. e322-e323
Author(s):  
Moritoshi Hirono ◽  
Fumihito Saitow ◽  
Moeko Kudo ◽  
Hidenori Suzuki ◽  
Yuchio Yanagawa ◽  
...  
PLoS ONE ◽  
2012 ◽  
Vol 7 (1) ◽  
pp. e29663 ◽  
Author(s):  
Moritoshi Hirono ◽  
Fumihito Saitow ◽  
Moeko Kudo ◽  
Hidenori Suzuki ◽  
Yuchio Yanagawa ◽  
...  

Author(s):  
John C. Eccles ◽  
Masao Ito ◽  
János Szentágothai

Author(s):  
R.V.W. Dimlich ◽  
M.H. Biros

In severe cerebral ischemia, Purkinje cells of the cerebellum are one of the cell types most vulnerable to anoxic damage. In the partial (forebrain) global ischemic (PGI) model of the rat, Paljärvi noted at the light microscopic level that cerebellar damage is inconsistant and when present, milder than in the telencephalon, diencephalon and rostral brain stem. Cerebellar injury was observed in 3 of 4 PGI rats following 5 minutes of reperfusion but in none of the rats after 90 min of reperfusion. To evaluate a time between these two extremes (5 and 90 min), the present investigation used the PGI model to study the effects of ischemia on the ultrastructure of cerebellar Purkinje cells in rats that were sacrificed after 30 min of reperfusion. This time also was chosen because lactic acid that is thought to contribute to ischemic cell changes in PGI is at a maximum after 30 min of reperfusion.


Author(s):  
R.V.W. Dimlich ◽  
M.H. Biros

Although a previous study in this laboratory determined that Purkinje cells of the rat cerebellum did not appear to be damaged following 30 min of forebrain ischemia followed by 30 min of reperfusion, it was suggested that an increase in rough endoplasmic reticulum (RER) and/or polysomes had occurred in these cells. The primary objective of the present study was to morphometrically determine whether or not this increase had occurred. In addition, since there is substantial evidence that glial cells may be affected by ischemia earlier than other cell types, glial cells also were examined. To ascertain possible effects on other cerebellar components, granule cells and neuropil near Purkinje cells as well as neuropil in the molecular layer also were evaluated in this investigation.


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