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芥子气中毒后的氧化应激及其通过褪黑素的减少:严重中毒期间抗氧化治疗的疗效。

Oxidative stress after sulfur mustard intoxication and its reduction by melatonin: efficacy of antioxidant therapy during serious intoxication.

机构信息

Center of Advanced Studies, University of Defence/Trebesska 1575, Hradec Kralove, Czech Republic.

出版信息

Drug Chem Toxicol. 2011 Jan;34(1):85-91. doi: 10.3109/01480545.2010.505238. Epub 2010 Oct 19.

DOI:10.3109/01480545.2010.505238
PMID:20958112
Abstract

Sulfur mustard (SM) is an important chemical warfare agent. The mechanism of SM toxicity still has not been fully recognized. However, oxidative stress and following the damaging of macromolecules in the human body is considered one of the crucial steps in SM toxicity. Rats intoxicated with pure (i.e., distilled) SM were used as a model organism. The doses, 0 (control), 5, 20, and 80 mg/kg of body weight, were applied intradermally. A hormone with strong antioxidant potency, melatonin, was applied (25 and 50 mg/kg, subcutaneously) into the other group of rats exposed with the same doses of SM. Total plasma protein, ferric-reducing antioxidant power (FRAP), thiobarbituric-acid-reactive substances (TBARS), and plasma protein carbonyls were assayed in blood plasma. A significant decrease of total plasma proteins was found for control, and the lowest dose of SM was treated with melatonin. Melatonin was also able to enhance the production of low-molecular-weight antioxidants, as the SM-intoxicated rats had significantly (P ≤ 0.01) increasing FRAP levels after intoxication with SM in doses of 20 and 80 mg/kg, when compared to the control treated with melatonin. Melatonin also decreased TBARS level, representing reduced lipid peroxidation (LPO). However, LPO seems to be of less importance for SM toxic impact. The more reliable parameter was the level of total plasma protein carbonyls. The carbonyl levels were significantly increased due to SM, and the carbonylation was slowed due to melatonin intake. In conclusion, melatonin seems to be a prospective compound in reducing SM toxicity impact in the rat.

摘要

硫芥(SM)是一种重要的化学战剂。SM 毒性的机制尚未完全被认识。然而,氧化应激以及随后人体大分子的损伤被认为是 SM 毒性的关键步骤之一。使用纯(即蒸馏)SM 中毒的大鼠作为模型生物。应用 0(对照)、5、20 和 80mg/kg 体重的剂量进行皮内注射。将具有强抗氧化能力的激素褪黑素(25 和 50mg/kg,皮下注射)应用于暴露于相同剂量 SM 的另一组大鼠中。测定血浆中的总血浆蛋白、铁还原抗氧化能力(FRAP)、硫代巴比妥酸反应物质(TBARS)和血浆蛋白羰基。发现对照组的总血浆蛋白显著下降,而用褪黑素处理的 SM 最低剂量最低。褪黑素还能够增强低分子量抗氧化剂的产生,因为与用褪黑素处理的对照组相比,SM 中毒的大鼠在 20 和 80mg/kg 的剂量下,SM 中毒后 FRAP 水平显著(P≤0.01)升高。褪黑素还降低了 TBARS 水平,代表脂质过氧化(LPO)减少。然而,LPO 对 SM 毒性的影响似乎不太重要。更可靠的参数是总血浆蛋白羰基水平。由于 SM,羰基水平显著增加,由于褪黑素的摄入,羰基化作用减慢。总之,褪黑素似乎是一种有前途的化合物,可降低大鼠 SM 毒性的影响。

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