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首页> 外文期刊>Journal of gastroenterology and hepatology >S-allyl cysteine alleviates nonsteroidal anti-inflammatory drug-induced gastric mucosal damages by increasing cyclooxygenase-2 inhibition, heme oxygenase-1 induction, and histone deacetylation inhibition
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S-allyl cysteine alleviates nonsteroidal anti-inflammatory drug-induced gastric mucosal damages by increasing cyclooxygenase-2 inhibition, heme oxygenase-1 induction, and histone deacetylation inhibition

机译:S-烯丙基半胱氨酸通过增加对环氧合酶2的抑制,血红素加氧酶1的诱导和组蛋白去乙酰化的抑制来减轻非甾体类抗炎药诱导的胃粘膜损伤

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摘要

Background and AimNonsteroidal anti-inflammatory drugs (NSAIDs), the most highly prescribed drugs in the world for the treatment of pain, inflammation, and fever, are associated with gastric mucosal damages including ulcer directly or indirectly. This study was aimed to document the preventive effects of an organosulfur constituent of garlic, S-allyl cysteine (SAC), against NSAIDs-induced gastric damages, as well the elucidation of its pharmacological actions, such as anti-inflammatory, anti-oxidative, and cytoprotective actions.
机译:背景和Aim非甾体抗炎药(NSAID)是世界上用于治疗疼痛,炎症和发烧的处方最高的药物,与胃粘膜损害(包括溃疡)直接或间接相关。这项研究旨在证明大蒜中的有机硫成分S-烯丙基半胱氨酸(SAC)对NSAIDs引起的胃部损害的预防作用,以及其药理作用的阐明,例如抗炎,抗氧化,和细胞保护作用。

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