Ching F P, Otokiti I O, Egert-Omoneukanrin B
Department of Pharmacology, Faculty of Basic Medical Sciences, College of Health Sciences, Niger Delta University, Wilberforce Island, Yenagoa, Nigeria.
Afr J Tradit Complement Altern Med. 2013 May 16;10(4):47-51. doi: 10.4314/ajtcam.v10i4.8. eCollection 2013.
This study was undertaken to evaluate the antidiarrhoeal activity of 3, 7, 4'-trihydroxy-3'-(8″-acetoxy-7″-methyloctyl)-5, 6-dimethoxyflavone, a flavonoid isolated from the stem bark of Stereospermum kunthianum. The antidiarrhoeal activity was evaluated using rodent models with diarrhoea. The normal intestinal transit, castor oil-induced intestinal transit and castor oil-induced diarrhoea tests in mice as well as castor oil-induced intestinal fluid accumulation in rats were employed in the study. The animals were pretreated with distilled water (10 ml/kg for mice, 5 ml/kg for rats), dimethoxyflavone (25 mg/kg or 50 mg/kg), morphine (10 mg/kg), or indomethacin (10 mg/kg) before induction of diarrhoea with castor oil (0.2ml for mice and 2ml for rats). Dimethoxyflavone dose dependently and significantly reduced (P<0.05) castor oil-induced intestinal motility. Its antimotility effect at the dose of 50 mg/kg was higher compared to that of morphine (10 mg/kg). Dimethoxyflavone (25 mg/kg and 50 mg/kg) caused a delay in the onset of diarrhoea reduction in the number and weight of wet stools and total stools in mice with castor oil-induced diarrhoea compared to the distilled water treated mice. Treatment with dimethoxyflavone (25 mg/kg or 50 mg/kg) did not produce any remarkable effect on castor oil-induced intestinal fluid accumulation in rats and normal intestinal transit in mice. The results indicate that dimethoxyflavone possesses antidiarrhoeal activity due to its intestinal antimotility effect and inhibition of other diarrhoeal pathophysiological processes. In conclusion, dimethoxyflavone reduced the frequency and severity of diarrhoea in the diarrhoeal models studied.
本研究旨在评估从昆氏羽叶楸茎皮中分离得到的黄酮类化合物3,7,4'-三羟基-3'-(8″-乙酰氧基-7″-甲基辛基)-5,6-二甲氧基黄酮的止泻活性。使用腹泻啮齿动物模型评估其止泻活性。本研究采用了小鼠的正常肠道转运、蓖麻油诱导的肠道转运和蓖麻油诱导的腹泻试验以及大鼠的蓖麻油诱导的肠液积聚试验。在用蓖麻油(小鼠0.2ml,大鼠2ml)诱导腹泻之前,动物分别用蒸馏水(小鼠10ml/kg,大鼠5ml/kg)、二甲氧基黄酮(25mg/kg或50mg/kg)、吗啡(10mg/kg)或吲哚美辛(10mg/kg)进行预处理。二甲氧基黄酮剂量依赖性地显著降低(P<0.05)蓖麻油诱导的肠道蠕动。其50mg/kg剂量的抗蠕动作用高于吗啡(10mg/kg)。与蒸馏水处理的小鼠相比,二甲氧基黄酮(25mg/kg和50mg/kg)可使蓖麻油诱导腹泻的小鼠腹泻减轻的起始时间延迟,湿粪和总粪便的数量及重量减少。用二甲氧基黄酮(25mg/kg或50mg/kg)处理对大鼠蓖麻油诱导的肠液积聚和小鼠正常肠道转运未产生任何显著影响。结果表明,二甲氧基黄酮因其肠道抗蠕动作用和对其他腹泻病理生理过程的抑制作用而具有止泻活性。总之,在本研究的腹泻模型中,二甲氧基黄酮降低了腹泻的频率和严重程度。