Masukawa T, Sai M, Tochino Y
Faculty of Pharmaceutical Sciences, Setsunan University, Osaka, Japan.
Life Sci. 1989;44(5):311-8. doi: 10.1016/0024-3205(89)90224-5.
The effect of various reduced glutathione (GSH) depletors on the survival time under normobaric and hypobaric hypoxia was examined in mice. The survival time was markedly prolonged in mice treated with glutathione S-transferase substrate, 2-cyclohexene-1-one (50-100 mg/kg, ip) and phorone (100-250 mg/kg, ip). The anti-hypoxic effect lasted for at least 3 hr and the maximum effect was found 0.5 hr after injection. Further, both compounds significantly elevated blood glucose levels 0.5-1 hr after treatment. The extent of the elevated blood glucose was nearly comparable to that of the mice treated with glucose (1-2 g/kg, ip), which was found to possess an anti-hypoxic effect. However, a GSH synthesis inhibitor, buthionine sulfoximine, could cause neither a prolongation of survival time of hypoxic mice nor an elevation of blood glucose. Moreover, unlike the depletion of hepatic GSH, brain GSH was markedly decreased by 2-cyclohexene-1-one and phorone, but not by buthionine sulfoximine. These findings suggest that the elevated blood glucose may involve in one of the mechanisms of the anti-hypoxic effect of 2-cyclohexene-1-one and phorone. A relationship between the anti-hypoxic effect and the depletion of brain GSH was also discussed.
研究了多种还原型谷胱甘肽(GSH)耗竭剂对小鼠在常压和低压缺氧条件下存活时间的影响。用谷胱甘肽S-转移酶底物2-环己烯-1-酮(50 - 100毫克/千克,腹腔注射)和佛尔酮(100 - 250毫克/千克,腹腔注射)处理的小鼠,其存活时间显著延长。抗缺氧作用持续至少3小时,注射后0.5小时出现最大效果。此外,两种化合物在处理后0.5 - 1小时均显著提高血糖水平。血糖升高的程度与用葡萄糖(1 - 2克/千克,腹腔注射)处理的小鼠几乎相当,而葡萄糖被发现具有抗缺氧作用。然而,GSH合成抑制剂丁硫氨酸亚砜胺既不能延长缺氧小鼠的存活时间,也不能提高血糖水平。此外,与肝脏GSH的耗竭不同,2-环己烯-1-酮和佛尔酮可使脑GSH显著降低,而丁硫氨酸亚砜胺则无此作用。这些发现表明,血糖升高可能参与了2-环己烯-1-酮和佛尔酮抗缺氧作用的机制之一。还讨论了抗缺氧作用与脑GSH耗竭之间的关系。