Effects of drugs on the production of stress ulcer in the rat.

L Nagy, G Mózsik, M Fiegler, E Gerber, T Past, C Ruzsa, Z Vezekényi, T Jávor
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Abstract

The authors studied the effect of drugs with different mechanisms of action on the prevention of stress ulcer production in the rat. Stress ulcer was induced by a method developed by the authors: intact, starved rats were swum in water at 23 degrees C for 5 hours. Atropine (0.1-0.5 and 1.0 mg/kg i.m.), cimetidine (1.0-5.0 and 25 mg/kg i.p.), prostacyclin (PGI2) (5.0-25.0 and 100 micrograms/kg i.p.) and phentolamine (0.35-1.75-3.5 and 7.0 mg/kg i.m.) were shown to decrease the production of stress ulcers significantly, in a dose-dependent fashion. Propranolol (0.35-1.75-3.5 and 7.0 mg/kg i.m.) did not influence the production of stress ulcers. The finding that drugs with different actions could considerably reduce or prevent the production of stress ulcer appears to indicate the complexity of the neural, hormonal and biochemical processes involved in the pathogenesis. On the basis of the present results the authors suggest the use of a preventive therapeutic regimen in clinical practice with an appropriate combination of drugs.

药物对应激性溃疡大鼠产生的影响。
作者研究了不同作用机制的药物对大鼠应激性溃疡产生的预防作用。应激性溃疡的诱导方法是由作者发明的:将完整的、饥饿的大鼠在23℃的水中游泳5小时。阿托品(0.1-0.5和1.0 mg/kg i.p.)、西咪替丁(1.0-5.0和25 mg/kg i.p.)、前列腺素(PGI2)(5.0-25.0和100微克/kg i.p.)和酚妥拉明(0.35-1.75-3.5和7.0 mg/kg i.p.)显示出以剂量依赖的方式显著减少应激性溃疡的产生。心得安(0.35 ~ 1.75 ~ 3.5和7.0 mg/kg i.m)不影响应激性溃疡的产生。不同作用的药物可以显著减少或预防应激性溃疡的产生,这一发现似乎表明了其发病机制中涉及的神经、激素和生化过程的复杂性。根据目前的结果,作者建议在临床实践中使用预防治疗方案,并适当联合用药。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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