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罗勒黄酮的体内辐射防护作用:小鼠的存活率

In vivo radioprotection by ocimum flavonoids: survival of mice.

作者信息

Uma Devi P, Ganasoundari A, Rao B S, Srinivasan K K

机构信息

Department of Radiobiology, Kasturba Medical College, Manipal, India.

出版信息

Radiat Res. 1999 Jan;151(1):74-8.

PMID:9973087
Abstract

Two flavonoids, orientin and vicenin, isolated from the leaves of the Indian plant Ocimum sanctum were tested for their radioprotective effect in mice. Both compounds provided protection against death from gastrointestinal syndrome as well as bone marrow syndrome when injected intraperitoneally (i.p.) before whole-body exposure to 11 Gy gamma radiation. The optimum drug dose for protection was 50 microg/kg body weight: An increase in the drug dose did not increase protection. No acute toxicity was observed at doses as high as 100 mg/kg body weight of either compound. Maximum protection was obtained when either compound was injected i.p. 30 min before irradiation. Changing the route of administration or the interval between drug injection (i.p.) and irradiation reduced protection. Drug treatment after irradiation was not very effective. Vicenin was slightly better than orientin in increasing survival at 30 days; protection by vicenin also lasted longer. Dose modification factors (DMFs) for the LD50 were 1.37 for vicenin and 1.30 for orientin. Radical scavenging activity has been demonstrated for both orientin and vicenin, and this appears to be one of the mechanisms of protection by these flavonoids.

摘要

从印度植物圣罗勒的叶子中分离出的两种黄酮类化合物,即荭草苷和异荭草苷,在小鼠体内进行了辐射防护作用测试。在全身暴露于11 Gyγ射线之前腹腔注射(i.p.)这两种化合物,均可提供针对胃肠道综合征和骨髓综合征所致死亡的保护作用。保护的最佳药物剂量为50μg/kg体重:药物剂量增加并未增强保护作用。两种化合物在高达100mg/kg体重的剂量下均未观察到急性毒性。在照射前30分钟腹腔注射任一化合物,均可获得最大保护作用。改变给药途径或药物注射(i.p.)与照射之间的间隔会降低保护作用。照射后进行药物治疗效果不佳。在提高30天生存率方面,异荭草苷略优于荭草苷;异荭草苷的保护作用持续时间也更长。荭草苷和异荭草苷的半数致死量(LD50)的剂量修正因子(DMF)分别为1.37和1.30。已证实荭草苷和异荭草苷均具有自由基清除活性,这似乎是这些黄酮类化合物发挥保护作用的机制之一。

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