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一氧化氮合酶抑制剂α-胍基戊二酸诱发的癫痫发作可被L-精氨酸控制。

Seizures induced by alpha-guanidinoglutaric acid, a nitric oxide synthase inhibitor, are controlled by L-arginine.

作者信息

Habu H, Yokoi I, Kabuto H, Willmore L J, Mori A

机构信息

Department of Neuroscience, Okayama University Medical School, Japan.

出版信息

Biochem Mol Biol Int. 1996 May;39(1):87-95. doi: 10.1080/15216549600201091.

Abstract

We evaluated the effect of manipulation of nitric oxide (NO) synthesis on epileptiform discharges recorded from immobilized rats during intracerebroventricular injection of alpha-guanidinoglutaric acid (GGA), an endogenous convulsant and a NO synthase (NOS) inhibitor, alone or in combined with a NOS substrate, l-arginine (ARG). GGA alone, or combined with 50 mM ARG, resulted in prolonged electrographical seizures while co-injection of either 100 or 200 mM of ARG with GGA caused significantly protection. These data show that ARG inhibited epileptiform discharges in a dose-dependent fashion, suggesting that the discharges initiated by inhibition of NOS with the intrinsic convulsant GGA are abated by increasing the concentration of the NOS substrate ARG.

摘要

我们评估了一氧化氮(NO)合成调控对在脑室内注射内源性惊厥剂及一氧化氮合酶(NOS)抑制剂α-胍基戊二酸(GGA)期间从固定大鼠记录的癫痫样放电的影响,单独注射GGA,或与NOS底物L-精氨酸(ARG)联合注射。单独注射GGA或与50 mM ARG联合注射,都会导致脑电图癫痫发作延长,而将100 mM或200 mM ARG与GGA共同注射则可产生显著的保护作用。这些数据表明,ARG以剂量依赖性方式抑制癫痫样放电,这表明用内源性惊厥剂GGA抑制NOS引发的放电可通过增加NOS底物ARG的浓度而减弱。

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