Makino M, Inomata Y, Ito K, Tabata K
Pharmacology & Molecular Biology Research Laboratories, Sankyo Co., Ltd., Tokyo, Japan.
Nihon Yakurigaku Zasshi. 1998 Aug;112(2):97-106. doi: 10.1254/fpj.112.97.
The aim of this study was to assess the effect of plaunotol, an anti-ulcer agent, on trinitrobenzene sulfonic acid (TNB)- and acetic acid-induced colonic lesions in rats. Plaunotol significantly reduced the severity of colonic mucosal lesions induced by TNB at a dose of 600 mg/kg/day. Moreover, plaunotol, at a dose of 600 mg/kg/day, significantly depressed the myeloperoxidase activity of the lesioned area induced by TNB of the rat colon. In the model of colitis induced by acetic acid, plaunotol reduced the area of lesions dose-dependently and significantly at doses of 60, 200 and 600 mg/kg/day as assessed by macroscopic observation. Microscopic observation showed obvious changes by administration of plaunotol such as reduction of epithelial cell necrosis, decreased mucin production and a decreased infiltration of a large number of neutrophils. In conclusion, plaunotol showed a protective effect against colonic lesion formation induced by TNB and acetic acid in rats. This study suggests the possibility that plaunotol may be effective and useful for treatment of inflammatory bowel disease in humans.
本研究旨在评估抗溃疡药物普劳诺托对三硝基苯磺酸(TNB)和乙酸诱导的大鼠结肠损伤的影响。普劳诺托以600毫克/千克/天的剂量显著降低了TNB诱导的结肠黏膜损伤的严重程度。此外,普劳诺托以600毫克/千克/天的剂量显著降低了大鼠结肠TNB诱导损伤区域的髓过氧化物酶活性。在乙酸诱导的结肠炎模型中,通过宏观观察评估,普劳诺托在60、200和600毫克/千克/天的剂量下剂量依赖性地显著减少了损伤面积。微观观察显示,给予普劳诺托后有明显变化,如上皮细胞坏死减少、粘蛋白产生减少以及大量中性粒细胞浸润减少。总之,普劳诺托对大鼠TNB和乙酸诱导的结肠损伤形成具有保护作用。本研究提示普劳诺托可能对人类炎症性肠病的治疗有效且有用。