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‘Ischemic tolerance’ phenomenon found in the brain

Kitagawa, Kazuo, Matsumoto, Masayasu, Tagaya, Masafumi, Hata, Ryuji, Ueda, Hirokazu, Niinobe, Michio, Handa, Nobuo, Fukunaga, Ryuzo, Kimura, Kazufumi, Mikoshiba, Katsuhiko, Kamada, Takenobu·1990·Brain Research

Abstract

We investigated the possibility that neuronal cells given a mild ischemic treatment sufficient to perturb the cellular metabolism acquired tolerance to a subsequent, and what would be lethal, ischemic stress in vivo. Cerebral ischemia was produced in the gerbils by occlusion of both common carotids for 5 min, which consistently resulted in delayed neuronal death in the CA1 region of the hippocampus. Minor 2-min ischemia in this model depletes high-energy phosphate compounds and perturbs the protein synthesis, but never causes neuronal necrosis, and therefore was chosen as mild ischemic treatment. Single 2-min ischemia 1 day or 2 days before 5 min ischemia exhibited only partial protective effects against delayed neuronal death. However, two 2-min ischemic treatments at 1 day intervals 2 days before 5 min ischemia exhibited drastically complete protection against neuronal death. The duration and intervals of ischemic treatment, enough to perturb cellular metabolism and cause protein synthesis, were needed respectively, because neither 1-min ischemia nor 2-min ischemia received twice at short intervals exhibited protective effects. This 'ischemic tolerance' phenomenon induced by ischemic stress--which is unquestionably important--and frequent stress in clinical medicine, is intriguing and may open a new approach to investigate the pathophysiology of ischemic neuronal damage.

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Authors
Kitagawa, K., Matsumoto, M., Tagaya, M., Hata, R., Ueda, H., Niinobe, M., Handa, N., Fukunaga, R., Kimura, K., Mikoshiba, K., & Kamada, T.
Venue
Brain Research
Publisher
Elsevier BV
Published
1990-09
Volume
528
Issue
1
Pages
21-24
ISSN
0006-8993 (ISSN-L)
OpenAlex
W2094164804
Cited by
1,091
References
0
FWCI
15.86
Type
journal article
Language
en
Open access
closed

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