Sudheer Kumar M, Sridhar Reddy B, Kiran Babu S, Bhilegaonkar P M, Shirwaikar A, Unnikrishnan M K
Department of Pharmacology, College of Pharmaceutical Sciences, Manipal 576 119, India.
Indian J Exp Biol. 2004 Feb;42(2):179-85.
Maximum antiinflammatory activity of phytic acid (PA) was seen at an oral dose of 150 mg/kg in the carrageenan induced rat paw edema model. Although PA showed ability to prevent denaturation of proteins, it showed less antiinflammatory activity than ibuprofen. Ability of PA to bring down thermal denaturation of proteins might be a contributing factor in the mechanism of action against inflammation. PA, at all the doses tested, showed significant protection from ulcers induced by ibuprofen, ethanol and cold stress, with a maximum activity at 150 mg/kg. There was a significant increase in gastric tissue malondialdehyde levels in ethanol treated rats but these levels decreased following PA pretreatment. Moreover, pretreatment with PA significantly inhibited various effects of ethanol on gastric mucosa, such as, reduction in the concentration of nonprotein sulfhydryl groups, necrosis, erosions, congestion and hemorrhage. These results suggested that gastro-protective effect of PA could be mediated by its antioxidant activity and cytoprotection of gastric mucosa.
在角叉菜胶诱导的大鼠足爪水肿模型中,植酸(PA)口服剂量为150 mg/kg时显示出最大抗炎活性。尽管PA具有防止蛋白质变性的能力,但其抗炎活性低于布洛芬。PA降低蛋白质热变性的能力可能是其抗炎作用机制的一个促成因素。在所有测试剂量下,PA均显示出对布洛芬、乙醇和冷应激诱导的溃疡有显著保护作用,在150 mg/kg时活性最大。乙醇处理的大鼠胃组织丙二醛水平显著升高,但PA预处理后这些水平降低。此外,PA预处理显著抑制了乙醇对胃黏膜的各种影响,如非蛋白巯基浓度降低、坏死、糜烂、充血和出血。这些结果表明,PA的胃保护作用可能是由其抗氧化活性和胃黏膜细胞保护作用介导的。