MK-801, a non-competitive NMDA receptor antagonist, prevents postischemic decrease of inositol 1,4,5-trisphosphate receptor mRNA expression in mongolian gerbil brain

• Published in: Neuroscience letters 1998-10, Vol.255 (2), p.111-114
• Main Authors: Uhm, Chang-Sub, Suh, Young-Suk, Park, Joo-Bae, Sohn, Moon Bang, Rhyu, Im Joo, Kim, Hyun
• Format: Article
• Language: English
• Subjects: Animals; Biological and medical sciences; Brain - metabolism; Calcium Channels - genetics; Dentate Gyrus - metabolism; Dizocilpine Maleate - pharmacology; Gerbillinae; Hippocampus - metabolism; In Situ Hybridization; Inositol 1,4,5-Trisphosphate Receptors; IP 3 receptor; Ischemia; Ischemic Attack, Transient - metabolism; Male; Medical sciences; MK-801; Mongolian gerbil; N-Methyl- d-aspartic acid receptor; Neurology; Receptors, Cytoplasmic and Nuclear - genetics; Receptors, N-Methyl-D-Aspartate - antagonists & inhibitors; Reperfusion Injury - metabolism; RNA, Messenger - metabolism; Time Factors; Tissue Distribution; Vascular diseases and vascular malformations of the nervous system
• ISSN: 0304-3940; 1872-7972
• DOI: 10.1016/S0304-3940(98)00727-7

Changes of inositol 1,4,5-trisphosphate receptor (IP 3R) mRNA expression after transient brain ischemia and the effect of MK-801, a non-competitive N-methyl- d-aspartic acid (NMDA) receptor antagonist, on the IP 3R mRNA expression was studied in mongolian gerbil brain by in situ hybridization. Transient ischemia was induced by ligating left common carotid artery for 10 min, and the animals were allowed recovery from 15 min to 24 h. MK-801 was introduced intraperitoneally 30 min before ischemia. IP 3R mRNA expression was decreased in dentate gyrus and hippocampus from 90 min until 24 h after ischemia. MK-801 pretreatment prevented the change of IP 3R mRNA expression after ischemia. These results suggest that IP 3R mRNA expression in ischemia may be related with NMDA receptor.