Megala Jayaraman, Geetha Arumugam
Indian J Exp Biol. 2015 Oct;53(10):657-64.
The edible fruits of Pithecellobium dulce (Roxb.) Benth. are traditionally used for various gastric complications in India. Here, we investigated the antiulcer activity of hydroalcoholic fruit extract of P. dulce (HAEPD) by applying cysteamine induced duodenal ulcer model in rats. Duodenal ulcer was induced in male albino Wistar rats by oral administration of cysteamine @ 420 mg/kg body wt. as a single dose. The rats were pre-administered orally with HAEPD @ 200 mg/kg body wt. for 30 days prior to ulcer induction. Rats pre-administered with ranitidine @ 30 mg/kg body wt. served as reference drug control. Ulcer score, thiobarbituric acid reactive substances (TBARS), glycoproteins, superoxide dismutase, catalase and glutathione peroxidase and reduced glutathione levels were measured in the duodenum. Rats pre-administered with the HAEPD showed significantly reduced ulcer score comparable to that of ranitidine pretreated rats. The co-administration of HAEPD lowered the TBARS level and also restored the levels of glycoproteins, enzymatic and non-enzymatic antioxidants. Histopathological observations confirmed the presence of inflammation, necrosis and hemorrhagic spots in the duodenum of ulcer control rats which were significantly reduced due to HAEPD treatment. No abnormal alterations were observed in normal rats treated with HAEPD at the dosage studied. The results demonstrated antioxidant and cytoprotective nature of P. dulce, and thereby its significant anti ulcer property.
猴耳环(Pithecellobium dulce (Roxb.) Benth.)的可食用果实传统上用于治疗印度的各种胃部并发症。在此,我们通过在大鼠中应用半胱胺诱导的十二指肠溃疡模型,研究了猴耳环水醇提取物(HAEPD)的抗溃疡活性。通过口服给予420 mg/kg体重的半胱胺单剂量,在雄性白化Wistar大鼠中诱导十二指肠溃疡。在溃疡诱导前30天,给大鼠口服预先给予200 mg/kg体重的HAEPD。预先给予30 mg/kg体重雷尼替丁的大鼠作为参考药物对照。在十二指肠中测量溃疡评分、硫代巴比妥酸反应性物质(TBARS)、糖蛋白、超氧化物歧化酶、过氧化氢酶和谷胱甘肽过氧化物酶以及还原型谷胱甘肽水平。预先给予HAEPD的大鼠显示溃疡评分显著降低,与雷尼替丁预处理的大鼠相当。HAEPD的共同给药降低了TBARS水平,还恢复了糖蛋白、酶促和非酶促抗氧化剂的水平。组织病理学观察证实溃疡对照大鼠的十二指肠中存在炎症、坏死和出血点,而HAEPD治疗使其显著减少。在所研究的剂量下,用HAEPD治疗的正常大鼠未观察到异常改变。结果证明了猴耳环的抗氧化和细胞保护性质,从而其具有显著的抗溃疡特性。