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Japanese

EFFECTS OF SO-CALLED CEREBRAL CIRCULATION OR METABOLISM FACILITATING AGENTS ON CEREBRAL FUNCTION UNDERGOING TEMPORARY ANOXIA : AN EXPERIMENTAL STUDY IN THE ISOLATED, PERFUSED RAT'S BRAIN MODEL Yasuhiko Sumi 1 , Hiromu Yamada 1 , Noboru Sakai 1 , Yusuke Tanabe 1 , Toshifumi Hirata 1 12nd Dept. of Surgery, Gifu Univ. School of Medicine pp.1109-1116
Published Date 1980/11/1
DOI https://doi.org/10.11477/mf.1406204668
  • Abstract
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Experimental studies were performed on effects on cerebral circulation and metabolism of 3 drugs, using an isolated, perfused rat's brain preparation. Perfusion was done with fluorocarbon emulsion. Perfusion pressure was kept constant and perfusion was interrupted temporarily for 3 minutes. Changes in EEG, perfusion rate and histological findings, induced by drug administration, were observed. The results obtained were as follows.

1) Hydrogenated ergot alkaloids: Tendency of spontaneous gradual reduction in EEG activities, as observed in control experiments, was alleviated and tendency of induction of fast activities wasnoted. Perfusion rate increased significantly. These findings suggested that this drug was effec-tive in maintaining normal metabolism of brain cells and in preventing insufficiency of cerebral circulation, under adverse conditions.

2) Hydrocortisone: No significant changes were observed in EEG activities. However a significant increase in perfusion rate was seen at the later stage of perfusion. It was inferred that this drug might alleviate swelling of capillary endothelial cells and astrocytic process and, consequently, dilate cerebral capillaries, resulting in increased circulation of an injured brain.

3) Thyrotropin releasing hormone-tartrate: EEG showed an earlier post-interruption recovery to control EEG after resuming perfusion, and EEG improvement continued for a fairly long period. There was a significant increase in perfusion rate. It was supposed that this drug had, besides its action of a hypothalamic releasing hormone, a central nervous stimulatory action, and the observed increase in perfusion rate might be due to metabolic regulation.


Copyright © 1980, Igaku-Shoin Ltd. All rights reserved.

基本情報

電子版ISSN 2185-405X 印刷版ISSN 0006-8969 医学書院

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