Masukawa T, Sai M, Tochino Y
Department of Biology and Clinical Physiology, Faculty of Pharmaceutical Sciences, Setsunan University, Osaka, Japan.
Jpn J Pharmacol. 1989 Sep;51(1):125-7. doi: 10.1254/jjp.51.125.
The anti-hypoxic effect (assessed by a standard hypoxia survival test) 3 hr after 2-cyclohexene-1-one (CHX) was completely abolished by injections of L-cysteine after CHX. Under these conditions, brain GSH was depleted to about 50% of the control level in CHX-treated mice and recovered to about 80% of control level following L-cysteine post-treatment. However, D-cysteine could not cause such effects. Intracerebroventricular injection of CHX, which caused a selective depletion of brain GSH, produced an anti-hypoxic effect. Thus, the anti-hypoxic effect may be related to the decrease of brain GSH levels.
在2-环己烯-1-酮(CHX)处理3小时后的抗缺氧作用(通过标准缺氧存活试验评估),在CHX处理后注射L-半胱氨酸可使其完全消除。在这些条件下,CHX处理的小鼠脑内谷胱甘肽(GSH)水平降至对照水平的约50%,L-半胱氨酸处理后恢复至对照水平的约80%。然而,D-半胱氨酸不会产生这种作用。脑室内注射CHX导致脑内GSH选择性耗竭,产生了抗缺氧作用。因此,抗缺氧作用可能与脑内GSH水平降低有关。