首页> 外文期刊>Boletin Latinoamericano y del Caribe de Plantas Medicinales y Aromaticas >Herbal extracts differentially inhibit oxidative effects caused by the biotransformation of nifurtimox, nitrofurantoin and acetaminophen on rat liver microsomes
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Herbal extracts differentially inhibit oxidative effects caused by the biotransformation of nifurtimox, nitrofurantoin and acetaminophen on rat liver microsomes

机译:草药提取物不同程度地抑制硝呋替莫,硝基呋喃妥因和对乙酰氨基酚对大鼠肝微粒体的生物转化所引起的氧化作用。

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Inflammation is a cellular defensive mechanism associated to oxidative stress. The administration of nitrofurantoin, nifurtimox and acetaminophen generates oxidative stress by their biotransformation through CYP450 system. The main adverse effect described for the first two drugs is gastrointestinal inflammation and that of the last, hepatitis. Therefore, standardised dry extracts from Rosmarinus officinalis, Buddleja globosa Hope, Cynara scolymus L., Echinacea purpurea and Hedera helix were tested to evaluate their capacity to decrease drug-induced oxidative stress. For that, rat liver microsomes were incubated with drugs in the presence of NADPH (specific CYP450 system cofactor) to test oxidative damage on microsomal lipids, thiols, and GST activity. All drugs tested induced oxidation of microsomal lipids and thiols, and inhibition of GST activity. Herbal extracts prevented these phenomena in different extension. These results show that antioxidant phytodrugs previously evaluated could alleviate drugs adverse effects associated to oxidative stress.
机译:炎症是与氧化应激相关的细胞防御机制。硝基呋喃妥因,尼呋替莫和对乙酰氨基酚的给药通过经由CYP450系统的生物转化而产生氧化应激。前两种药物的主要不良反应是胃肠道炎症,最后一种是肝炎。因此,对来自迷迭香,Buddleja globosa Hope,Cynara scolymus L.,紫锥菊和Hedera螺旋的标准化干提取物进行了测试,以评估其降低药物诱导的氧化应激的能力。为此,将大鼠肝微粒体与在NADPH(特异性CYP450系统辅因子)存在下的药物一起孵育,以测试对微粒体脂质,硫醇和GST活性的氧化损伤。所有测试的药物均可诱导微粒体脂质和硫醇氧化,并抑制GST活性。草药提取物以不同的方式阻止了这些现象。这些结果表明,先前评估过的抗氧化剂植物药可以减轻药物与氧化应激相关的不良影响。

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