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首页> 外文期刊>Medicine. >Identify Melatonin as a Novel Therapeutic Reagent in the Treatment of 1-Bromopropane(1-BP) Intoxication
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Identify Melatonin as a Novel Therapeutic Reagent in the Treatment of 1-Bromopropane(1-BP) Intoxication

机译:确定褪黑激素是治疗1-溴丙烷(1-BP)中毒的新型治疗剂

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1-Bromopropane (1-BP) has been used as an alternative for fluoride compounds and 1-BP intoxication may involve lung, liver, and central neural system (CNS). Our previous studies showed that 1-BP impaired memory ability by compromising antioxidant cellular defenses. Melatonin is a powerful endogenous antioxidant, and the objective of this study was to explore the therapeutic role of melatonin in the treatment of 1-BP intoxication. Rats were intragastrically treated with 1-BP with or without melatonin, and then sacrificed on 27th day after 1-BP administration. The Morris water maze (MWM) test was used to evaluate the spatial learning and memory ability of the experimental animals, and NeuN staining was performed to assess neuron loss in hippocampus. We found that rats treated with 1-BP spent more time and swam longer distance before landing on the hidden platform with a comparable swimming speed, which was markedly mitigated by the pretreatment with melatonin in a concentration-dependent manner. In addition, 1-BP-induced notable decrease in neuron population in hippocampus by promoting apoptosis, and melatonin pretreatment attenuated those changes in brain. The GSH/GSSG ratio was proportionately decreased and heme oxygenase 1 was increased in the rats exposed to 1-BP (Figure 6), and administration of melatonin restored them. Meanwhile, MDA, the level of lipid peroxidation product, was significantly increased upon exposed to 1-BP, which was significantly attenuated by melatonin pretreatment, indicating that administration of 1-BP could interfere with redox homeostasis of brain in rat, and such 1-BP-induced biomedical changes were reversed by treatment with melatonin. We conclude that treatment with melatonin attenuates 1-BP-induced CNS toxicity through its ROS scavenging effect.
机译:1-溴丙烷(1-BP)已被用作氟化物的替代品,并且1-BP中毒可能涉及肺,肝和中枢神经系统(CNS)。我们以前的研究表明1-BP通过损害抗氧化剂的细胞防御功能损害了记忆能力。褪黑激素是一种强大的内源性抗氧化剂,本研究的目的是探讨褪黑激素在治疗1-BP中毒中的作用。在有或没有褪黑激素的情况下,用1-BP胃内处理大鼠,然后在1-BP给药后第27天处死大鼠。莫里斯水迷宫(MWM)测试用于评估实验动物的空间学习和记忆能力,NeuN染色用于评估海马神经元的损失。我们发现用1-BP处理的大鼠在以可比的游泳速度降落到隐藏平台上之前花费了更多的时间和更长的游泳距离,而褪黑激素以浓度依赖性的方式显着缓解了这种情况。此外,1-BP诱导的凋亡促进海马神经元数量的显着减少,而褪黑激素预处理则减弱了大脑中的这些变化。在暴露于1-BP的大鼠中,GSH / GSSG比例成比例地降低,血红素加氧酶1升高(图6),褪黑激素的给药使它们恢复。同时,暴露于1-BP时,脂质过氧化产物的MDA水平显着增加,而褪黑素预处理可显着减弱MDA,这表明1-BP的给药可能干扰大鼠脑的氧化还原稳态,而1-BP褪黑激素治疗可逆转BP诱导的生物医学变化。我们得出的结论是,褪黑激素治疗通过其ROS清除作用减弱了1-BP诱导的CNS毒性。

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