Literature DB >> 2120802

Cerebral blood flow and neuronal damage during progressive cerebral ischemia in gerbils.

M Matsumoto1, T Hatakeyama, K Morimoto, T Yanagihara.   

Abstract

A combined autoradiographic and immunohistochemical method was used to correlate the extent of focal cerebral ischemia and morphologic ischemic damage following unilateral carotid occlusion in 16 gerbils for 5-30 minutes. Immunohistochemical lesions detectable by the reaction for microtubule-associated proteins 1 and 2 were visible in the subiculum-CA1 and CA2 regions of the hippocampus and layer III/IV of the cerebral cortex after 5 minutes of ischemia (n = 4). Local blood flow was promptly reduced but still heterogeneous after 10 minutes of ischemia (n = 4); local blood flow in immunohistochemical lesions was less than 5 ml/100 g/min except in highly vulnerable regions, where flow values of 5-15 ml/100 g/min were observed. After 15 minutes of ischemia (n = 4) local blood flow in less vulnerable regions including the thalamus and caudoputamen also declined to less than 5 ml/100 g/min, and immunohistochemical lesions became visible in those regions after 30 minutes of ischemia (n = 4). On the other hand, many brain regions tolerated local blood flow of less than 5 ml/100 g/min without ischemic damage. The present study demonstrates that selective tissue vulnerability during progressive cerebral ischemia depends on the degree of hypoperfusion and on factors inherent to neurons in various brain regions.

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Year:  1990        PMID: 2120802     DOI: 10.1161/01.str.21.10.1470

Source DB:  PubMed          Journal:  Stroke        ISSN: 0039-2499            Impact factor:   7.914


  6 in total

1.  The characteristics of blood-brain barrier in three different conditions--infarction, selective neuronal death and selective loss of presynaptic terminals--following cerebral ischemia.

Authors:  K Kitagawa; M Matsumoto; T Ohtsuki; M Tagaya; T Okabe; R Hata; H Ueda; N Handa; K Sobue; T Kamada
Journal:  Acta Neuropathol       Date:  1992       Impact factor: 17.088

2.  Blockade of Acid-Sensing Ion Channels Attenuates Recurrent Hypoglycemia-Induced Potentiation of Ischemic Brain Damage in Treated Diabetic Rats.

Authors:  Ashish K Rehni; Vibha Shukla; Miguel A Perez-Pinzon; Kunjan R Dave
Journal:  Neuromolecular Med       Date:  2019-05-27       Impact factor: 3.843

3.  Early MEK1/2 inhibition after global cerebral ischemia in rats reduces brain damage and improves outcome by preventing delayed vasoconstrictor receptor upregulation.

Authors:  Sara Ellinor Johansson; Stine Schmidt Larsen; Gro Klitgaard Povlsen; Lars Edvinsson
Journal:  PLoS One       Date:  2014-03-18       Impact factor: 3.240

4.  Total Flavonoids in Caragana (TFC) Promotes Angiogenesis and Enhances Cerebral Perfusion in a Rat Model of Ischemic Stroke.

Authors:  Qiansong He; Shirong Li; Lailai Li; Feiran Hu; Ning Weng; Xiaodi Fan; Shixiang Kuang
Journal:  Front Neurosci       Date:  2018-09-12       Impact factor: 4.677

5.  Ischemia-Triggered Glutamate Excitotoxicity From the Perspective of Glial Cells.

Authors:  Denisa Belov Kirdajova; Jan Kriska; Jana Tureckova; Miroslava Anderova
Journal:  Front Cell Neurosci       Date:  2020-03-19       Impact factor: 5.505

6.  Cerebrovascular Senescence Is Associated With Tau Pathology in Alzheimer's Disease.

Authors:  Annie G Bryant; Miwei Hu; Becky C Carlyle; Steven E Arnold; Matthew P Frosch; Sudeshna Das; Bradley T Hyman; Rachel E Bennett
Journal:  Front Neurol       Date:  2020-09-16       Impact factor: 4.003

  6 in total

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