Department of Pharmacy, College of Medicine, Xi'an Jiaotong University, Xi'an 710061, China.
Inflammation. 2012 Dec;35(6):1872-9. doi: 10.1007/s10753-012-9509-7.
The present work was done to investigate the possible effects of 3,4-oxo-isopropylidene-shikimic acid (ISA) on acetic acid (AA)-induced colitis in rats. Colitis was induced by intracolonic injection of 6 % AA. Several parameters, including macroscopic score and biochemical parameters, were determined to assess the degree of protection. Biochemical parameters such as myeloperoxidase (MPO) activity, malondialdehyde (MDA) and nitric oxide (NO) levels, and superoxide dismutase (SOD) and inducible NO synthase (NOS) activities were measured following standard assay procedures. The study showed that treatment of rats for 6 days with ISA (100 and 200 mg/kg) was able to give complete protection against AA-induced colitis. Moreover, biochemical changes were reversed and brought toward control. These results suggest a beneficial effect of ISA against experimental colitis and the possible mechanism of the protective effects may be partly due to an antioxidant action.
本研究旨在探讨 3,4-氧代异亚丙基莽草酸(ISA)对乙酸(AA)诱导的大鼠结肠炎的可能作用。通过直肠内注射 6%AA 诱导结肠炎。通过测定几种参数,包括宏观评分和生化参数,来评估保护程度。通过标准测定程序测定髓过氧化物酶(MPO)活性、丙二醛(MDA)和一氧化氮(NO)水平、超氧化物歧化酶(SOD)和诱导型一氧化氮合酶(NOS)活性等生化参数。研究表明,ISA(100 和 200mg/kg)治疗大鼠 6 天可完全对抗 AA 诱导的结肠炎。此外,生化变化得到逆转并接近对照。这些结果表明 ISA 对实验性结肠炎具有有益作用,其保护作用的可能机制部分可能归因于抗氧化作用。