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Anti-secretory and cyto-protective effects of peganine hydrochloride isolated from the seeds of Peganum harmala on gastric ulcers

机译:从骆驼蓬种子分离的盐酸豌豆碱对胃溃疡的抗分泌和细胞保护作用。

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摘要

Gastroprotective mechanism of peganine hydrochloride isolated from Peganum harmala seeds was investigated. Peganine hydrochloride was evaluated against cold restraint (CRU), aspirin (AS), alcohol (AL) and pyloric ligation (PL) induced gastric ulcer models in rats. Potential anti-ulcer activity of peganine was observed against CRU (50.0%), AS (58.5%), AL (89.41%) and PL (62.50%) induced ulcer models. The reference drug omeprazole (10 mg/kg, p.o.) showed 77.45% protection against CRU, 49.97% against AS and 69.42% against PL model. Sucralfate, another reference drug (500 mg/kg, p.o.) showed 62.50% protection in AL induced ulcer model. Peganine significantly reduced free acidity (33.38%), total acidity (38.09%) and upregulated mucin secretion by 67.91%, respectively. Further, peagnine significantly inhibited H+ K+-ATPase activity in vitro with IC50 of 73.47 μg/ml as compared to the IC50 value of omeprazole (30.24 μg/ml) confirming its anti-secretory activity.
机译:研究了从Peganum harmala种子中分离的盐酸豌豆碱的胃肠道保护作用。评估了盐酸胍对大鼠的冷约束(CRU),阿司匹林(AS),酒精(AL)和幽门结扎(PL)诱发的胃溃疡模型的抵抗力。观察到了针对CRU(50.0%),AS(58.5%),AL(89.41%)和PL(62.50%)诱导的溃疡模型产生的豌豆潜在的抗溃疡活性。参比药物奥美拉唑(10 mg / kg,p.o.)对CRU有77.45%的保护,对AS有49.97%的保护,对PL模型有69.42%。硫糖铝,另一种参考药物(500 mg / kg,口服)在AL诱导的溃疡模型中显示出62.50%的保护作用。豌豆素分别显着降低了游离酸(33.38%),总酸度(38.09%)和上调了粘蛋白分泌67.91%。此外,与奥美拉唑的IC50值(30.24μg/ ml)相比,在体外,尿素能显着抑制H + K + -ATPase活性,IC50为73.47μg/ ml,从而证实了其抗分泌活性。

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