TY - JOUR
T1 - Endothelin receptors in ischemic rat brain and alzheimer brain
AU - Kohzuki, M.
AU - Onodera, H.
AU - Yasujima, M.
AU - Itoyama, Y.
AU - Kanazawa, M.
AU - Sato, T.
AU - Abe, K.
PY - 1995
Y1 - 1995
N2 - Endothelin (ET) binding sites in male Wistar rat brains subjected to a 20-min four-vessel occlusion (transient forebrain ischemia model) which induces hip-pocampal neuron death, and in human brains with Alzheimer disease, were mapped by quantitative in vitro autoradiography employing [125I]ET-1 as a radioligand. Rats were decapitated 4 or 7 days after ischemia. In the rat brain, the [125I]ET-1 binding sites were remarkably increased in the hippocampal CA1 and dentate gyrus, ventral thalamic nucleus, and cortical vessels 4 and 7 days after ischemia, when many reactive astroglia were observed. The [125I]ET-1 binding sites decreased in the cerebral cortex affected by Alzheimer disease. The binding was abolished by 1 μM unlabeled ET-1, ET-3, sarafotoxin S6b, and BQ788 (an ETBantagonist) but not by BQ123 (an ETAantagonist), suggesting that the [125I]ET-1 binding sites are as ETBreceptors. The present findings raise the possibility that a glial ET system could be responsible for the occurrence of ischemic neuron cell death.
AB - Endothelin (ET) binding sites in male Wistar rat brains subjected to a 20-min four-vessel occlusion (transient forebrain ischemia model) which induces hip-pocampal neuron death, and in human brains with Alzheimer disease, were mapped by quantitative in vitro autoradiography employing [125I]ET-1 as a radioligand. Rats were decapitated 4 or 7 days after ischemia. In the rat brain, the [125I]ET-1 binding sites were remarkably increased in the hippocampal CA1 and dentate gyrus, ventral thalamic nucleus, and cortical vessels 4 and 7 days after ischemia, when many reactive astroglia were observed. The [125I]ET-1 binding sites decreased in the cerebral cortex affected by Alzheimer disease. The binding was abolished by 1 μM unlabeled ET-1, ET-3, sarafotoxin S6b, and BQ788 (an ETBantagonist) but not by BQ123 (an ETAantagonist), suggesting that the [125I]ET-1 binding sites are as ETBreceptors. The present findings raise the possibility that a glial ET system could be responsible for the occurrence of ischemic neuron cell death.
KW - Alzheimer
KW - Endothelin receptor
KW - Human
KW - Ischemia
UR - http://www.scopus.com/inward/record.url?scp=0028808182&partnerID=8YFLogxK
UR - http://www.scopus.com/inward/citedby.url?scp=0028808182&partnerID=8YFLogxK
U2 - 10.1097/00005344-199526003-00099
DO - 10.1097/00005344-199526003-00099
M3 - Article
C2 - 8587405
AN - SCOPUS:0028808182
SN - 0160-2446
VL - 26
SP - S329-S331
JO - Journal of cardiovascular pharmacology
JF - Journal of cardiovascular pharmacology
ER -