自纳米乳化给药系统(SNEDDS)吡罗昔康对大鼠胃丙二醛水平及Caspase-3、COX-1、COX-2蛋白表达的保护作用

Iis Wahyuningsih, Kurnia Ambarwati, Erninda Ayu Hapsari, Afifah Fauziyyah, A. Ikhsanudin, D. Pertiwi, W. Widyaningsih
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引用次数: 0

摘要

本研究旨在探讨SNEDDS吡罗西康致溃疡剂对丙二醛(MDA)水平及caspase-3、COX-1、COX-2蛋白表达的保护作用。实验动物为30只1 ~ 2月龄雄性SD大鼠,体重100 ~ 200克,分为5组。口服治疗28天。第29天,采用硫代巴比妥酸反应物质(TBARs)法,用可见分光光度计测定丙二酚(MDA)水平。处死大鼠,取胃脏器免疫组化检测caspase-3、COX-1、COX-2的表达。统计分析显示,吡罗昔康SNEDDS组和吡罗昔康混悬液组caspase-3蛋白表达降低,COX-1表达升高,COX-2表达降低,MDA水平显著降低。含有吡罗昔康的SNEDDS(自纳米乳化药物递送系统)形式对吡罗昔康致溃疡具有保护作用。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Protection Effect of Self-Nanoemulsifying Drug Delivery System (SNEDDS) Piroxicam as Ulcerogenic Agent towards Malondialdehid Level and Protein Expression of Caspase-3, COX-1, COX-2 at Rat Gastric
The aim of this study was to determine the protection effect of SNEDDS piroxicam ulcerogenic agent against malondialdehyde (MDA) level and protein expression of caspase-3, COX-1, COX-2. The research was conducted using the test animals as much as 30 male white Sprague dawley (SD) rats aged 1-2 months with a weight of 100-200 grams divided into 5 groups. Treatment was given for 28 days orally. On the 29th day blood samples were also taken for the determination of MDA (Malondialdehid) levels by Thiobarbituric Acid Reactive Substance (TBARs) method using a visible spectrophotometer. Rats were sacrificed, then gastric organs were taken for immunohistochemical testing of caspase-3 and COX-1 expression, COX-2. The statistical analysis showed that the piroxicam SNEDDS group and the piroxicam suspension group decreased expression of the caspase-3 protein, increased COX-1 expression, decreased COX-2 and significantly decreased MDA levels. The piroxicam-containing SNEDDS (Self-Nanoemulsifying Drug Delivery System) form has protection against ulcogenic piroxicam.
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