CLC number: R741
On-line Access: 2024-08-27
Received: 2023-10-17
Revision Accepted: 2024-05-08
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Cited: 5
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LIU Jian-ren, DING Mei-ping, WEI Er-qing, LUO Jian-hong, SONG Ying, HUANG Jian-zheng, GE Qiu-fu, HU Hua, ZHU Li-jun. GM1 stabilizes expression of NMDA receptor subunit 1 in the ischemic hemisphere of MCAo/reperfusion rat[J]. Journal of Zhejiang University Science B, 2005, 6(4): 254-258.
@article{title="GM1 stabilizes expression of NMDA receptor subunit 1 in the ischemic hemisphere of MCAo/reperfusion rat",
author="LIU Jian-ren, DING Mei-ping, WEI Er-qing, LUO Jian-hong, SONG Ying, HUANG Jian-zheng, GE Qiu-fu, HU Hua, ZHU Li-jun",
journal="Journal of Zhejiang University Science B",
volume="6",
number="4",
pages="254-258",
year="2005",
publisher="Zhejiang University Press & Springer",
doi="10.1631/jzus.2005.B0254"
}
%0 Journal Article
%T GM1 stabilizes expression of NMDA receptor subunit 1 in the ischemic hemisphere of MCAo/reperfusion rat
%A LIU Jian-ren
%A DING Mei-ping
%A WEI Er-qing
%A LUO Jian-hong
%A SONG Ying
%A HUANG Jian-zheng
%A GE Qiu-fu
%A HU Hua
%A ZHU Li-jun
%J Journal of Zhejiang University SCIENCE B
%V 6
%N 4
%P 254-258
%@ 1673-1581
%D 2005
%I Zhejiang University Press & Springer
%DOI 10.1631/jzus.2005.B0254
TY - JOUR
T1 - GM1 stabilizes expression of NMDA receptor subunit 1 in the ischemic hemisphere of MCAo/reperfusion rat
A1 - LIU Jian-ren
A1 - DING Mei-ping
A1 - WEI Er-qing
A1 - LUO Jian-hong
A1 - SONG Ying
A1 - HUANG Jian-zheng
A1 - GE Qiu-fu
A1 - HU Hua
A1 - ZHU Li-jun
J0 - Journal of Zhejiang University Science B
VL - 6
IS - 4
SP - 254
EP - 258
%@ 1673-1581
Y1 - 2005
PB - Zhejiang University Press & Springer
ER -
DOI - 10.1631/jzus.2005.B0254
Abstract: Objective: To determine the protective effect of monosialoganglionside (GM1) and evaluate the influence of GM1 on expression of N-methyl-D-aspartate receptor subunit 1 (NMDAR1) in Sprague-Dawley (SD) rats with focal cerebral ischemia-reperfusion (I/R). Methods: Left middle cerebral artery (MCA) was occluded by an intraluminal suture for 1 h and the brain was reperfused for 72 h in SD rats when infarct volume was measured, GM1 (10 mg/kg) was given ip (intraperitoneally) at 5 min (group A), 1 h (group B) and 2 h (group C) after MCA occlusion (MCAo). Expression of NMDAR1 was detected by Western blot at various time after reperfusion (4 h, 6 h, 24 h, 48 h and 72 h) in ischemic hemispheres of the rats with or without GM1 administered. Results: (1) Adjusted relative infarct volumes of groups A and B were significantly smaller than that of group C and the control group (P<0.01 and P<0.05, respectively). (2) Expression level of NMDAR1 was temporally high at 6 h after reperfusion, and dipped below the normal level at 72 h after reperfusion. GM1 at 5 min after MCAo significantly suppressed the expression of NMDAR1 at 6 h after reperfusion (P<0.05 vs the control). At 72 h after reperfusion, the NMDAR1 expression level of rats treated with GM1 administered (at 5 min or 2 h after MCAo) was significantly higher than that of the control (P<0.05). Conclusion: GM1 can time-dependently reduce infarct volume in rats with focal cerebral I/R partly through stabilizing the expression of NMDAR1.
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