Effect of diazepam on the contents of amino acids and free radical during ischemia /reperfusion injury

Hu Bo , Mei Yuanwu , Wei Guirong , Qiu Xiaoying , Sun Shenggang , Tong E’tang

Current Medical Science ›› 2001, Vol. 21 ›› Issue (2) : 102 -104.

PDF
Current Medical Science ›› 2001, Vol. 21 ›› Issue (2) : 102 -104. DOI: 10.1007/BF02888067
Article

Effect of diazepam on the contents of amino acids and free radical during ischemia /reperfusion injury

Author information +
History +
PDF

Abstract

The protective effect and mechanism of diazepam on ischemia neurons during cerebral ischemia and reperfusion were studied. Sixty-three Wistar rats were divided randomly into nine groups: control group (n=7), ischemia (is) groups including subgroups of is3h, is3-h/repl-h, is3-h/rep2-h, is3-h/rep3-h(n = 7 in each group), diazepam treated groups (10 mg/kg, i. p.), including subgroups of is3-h, is3-h/repl-h, is3-h/rep2-h, is3-h/rep3-h (n=7 in each group) with Zea longa’s animal model of middle cerebral artery occlusion. The comparison between the ischemia group and diazepam-treated group showed that diazepam could obviously decrease the production of glutamate, asparate, MDA and increase the synthesis and release of GABA, SOD and GSH-PX. It was concluded that diazepam exerted its protective effects on neurons through complex mechanisms of regulating the synthesis and release of excitotary/inhibitory amino acids and free radicals.

Keywords

diazepam / excitatory/inhibitory amino acids / free radicals

Cite this article

Download citation ▾
Hu Bo, Mei Yuanwu, Wei Guirong, Qiu Xiaoying, Sun Shenggang, Tong E’tang. Effect of diazepam on the contents of amino acids and free radical during ischemia /reperfusion injury. Current Medical Science, 2001, 21(2): 102-104 DOI:10.1007/BF02888067

登录浏览全文

4963

注册一个新账户 忘记密码

References

[1]

ShuibA, KanthanR. Amplification of inhibitory mechanisms in cerebral ischemia: an alternative approach to neuronal protection. Hisol Histopathol, 1997, 12: 185-185

[2]

FukudaA, MuramatsuK, OkabeA, et al.. Changes in intracellar Ca2+ induced by GABAA receptor activation and reduction in Clgradient in neonatal rat neocortex. J Neurophysiol, 1998, 79(1): 439-439

[3]

Jackson-FriedmanC, LydenP D, NunesS, et al.. High dose baclofen is neuroprotective but also causes intracerebral hemorrhage:a quantal bioassay study using the intraluminal sutsure occlusion method. Exp Neurol, 1997, 147(2): 346-346

[4]

HallE D, FleckT J, OosttveenJ A. Comparative neuroprotective properties of the benzodiazepine receptor full agonist diazepam and the partial agonist PNU-101017 in the gerbil forebrain ischemia model. Brain Res, 1998, 6(1-2): 325-325

[5]

HallE D, AndrusP K, FleckT J, et al.. Neuroprotective properties of the benzodiazepine receptor, partial agonist PNU-101017 in the gerbil forebrain ischemia model. Cereb Blood Flow Metab, 1997, 17(8): 875-875

[6]

SaransaariP, OjaS S. Release of endogenous glutamate, aspartate, GABA and taurine from hippocampal slices from adult and developing mice under cell-damaging conditions. Neurochem Res, 1998, 23(4): 563-563

[7]

Schwartz-BloomR D, McDonough K J, ChaseP J, et al.. Long-term neuroprotection by benzodiazepine: full versus partial agonists after transient cerebral ischemia in gerbil. J Cereb Blood Flow Metab, 1998, 18(5): 548-548

[8]

SakamotoA, OhnishiS T, OhnishiT, et al.. Protective effect of a new anti-oxidant on the rat brain exposed to ischemia-reperfusion injury: inhibition of free radical formation and lipid peroxidation. Free Radic Med Biol, 1991, 11: 385-385

AI Summary AI Mindmap
PDF

82

Accesses

0

Citation

Detail

Sections
Recommended

AI思维导图

/