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首页> 外文期刊>Drug and Chemical Toxicology >Oxidative stress after sulfur mustard intoxication and its reduction by melatonin: efficacy of antioxidant therapy during serious intoxication
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Oxidative stress after sulfur mustard intoxication and its reduction by melatonin: efficacy of antioxidant therapy during serious intoxication

机译:硫芥菜中毒后的氧化应激及其褪黑激素的降低:严重中毒期间抗氧化剂治疗的功效

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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, subcutane-ously) 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 carbonyla-tion was slowed due to melatonin intake. In conclusion, melatonin seems to be a prospective compound in reducing SM toxicity impact in the rat.
机译:芥菜(SM)是一种重要的化学战剂,但SM毒性的机理尚未得到充分认识。然而,氧化应激和随后的大分子在人体内的破坏被认为是SM毒性的关键步骤之一。用纯净(即蒸馏)SM中毒的大鼠作为模型生物,皮内施用0(对照),5,20和80 mg / kg体重的剂量。将具有强抗氧化能力的褪黑激素(分别皮下注射25和50 mg / kg)应用于另一组暴露于相同剂量SM的大鼠中。血浆蛋白总量,三氧化二铁还原能力(FRAP),在血浆中测定了硫代巴比妥酸反应性物质(TBARS)和血浆蛋白羰基。发现用于对照的总血浆蛋白显着减少,并且用褪黑激素处理了最低剂量的SM。褪黑激素还能够增强低分子量抗氧化剂的产生,因为与SM相比,SM致毒的大鼠在被SM致毒后的FRAP水平显着(P≤0.01)增加了20和80 mg / kg。对照用褪黑激素治疗。褪黑激素也降低了TBARS水平,代表脂质过氧化(LPO)降低。但是,LPO对于SM毒性影响似乎不太重要。更可靠的参数是血浆总蛋白羰基水平。由于SM,羰基水平显着增加,而由于褪黑激素的摄入,羰基化反应减慢。总之,褪黑激素似乎是减少大鼠SM毒性影响的前瞻性化合物。

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