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Brain Res ; 602(1): 165-8, 1993 Jan 29.
Article in English | MEDLINE | ID: mdl-8095425

ABSTRACT

Delayed damage to hippocampal CA1 pyramidal cells was observed in rats subjected to cerebral ischemia caused by 10 min of 4-vessel occlusion. Animals pretreated with alpha-fluoromethylhistidine, a suicide inhibitor of histidine decarboxylase, showed significantly more necrotic cells than did control animals. Mepyramine (H1-antagonist) and (R) alpha-methylhistamine (H3-agonist), but not zolantidine (H2-antagonist), significantly aggravated the delayed neuronal death. These results suggest that histaminergic neurons have a protective role, probably via H1-receptors, in the development of delayed neuronal death caused by cerebral ischemia.


Subject(s)
Brain Ischemia/chemically induced , Hippocampus/blood supply , Neurons/drug effects , Receptors, Histamine/drug effects , Synaptic Transmission/drug effects , Animals , Benzothiazoles , Brain Ischemia/pathology , Cell Death/drug effects , Hippocampus/cytology , Histamine Agonists/toxicity , Histamine H1 Antagonists/toxicity , Histamine H2 Antagonists/toxicity , Male , Methylhistamines/toxicity , Methylhistidines/toxicity , Phenoxypropanolamines , Piperidines/toxicity , Pyrilamine/toxicity , Rats , Rats, Wistar , Thiazoles/toxicity
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