Division of Medicinal and Process Chemistry, Central Drug Research Institute, Lucknow 226001, U.P, India.
Phytomedicine. 2010 Jul;17(8-9):569-74. doi: 10.1016/j.phymed.2009.10.016. Epub 2009 Dec 3.
In the present study, the gastroprotective mechanism of Xylocarpus granatum fruit and its active constituents gedunin and photogedunin was investigated. Chloroform fraction (Fr-CHCl(3)) of X. granatum fruit was evaluated against cold restraint (CRU), aspirin (AS), alcohol (AL) and pyloric ligation (PL) induced gastric ulcer models in rats and histamine (HA) induced duodenal ulcer model in guinea pigs. Potential anti-ulcer activity of Fr-CHCl(3) was observed against CRU (58.28%), AS (67.81%), AL (84.38%), PL (65.66%) and HA (61.93%) induced ulcer models. The standard drug omeprazole (10mg/kg, p.o.) showed 68.25% protection against CRU, 57.08% against AS and 69.42% against PL model and 70.79% against HA induced duodenal ulcer. Sucralfate, another standard drug (500 mg/kg, p.o.) showed 62.72% protection in AL induced ulcer model. Fr-CHCl(3) significantly reduced free acidity (51.42%), total acidity (30.76%) and upregulated mucin secretion by 58.37% respectively. Phytochemical investigations of Fr-CHCl(3) yielded gedunin (36%), photogedunin (2%). Further, Fr-CHCl(3) and its compounds gedunin and photogedunin significantly inhibited H(+) K(+)-ATPase activity in vitro with IC(50) of 89.37, 56.86 and 66.54 microg/ml respectively as compared to the IC(50) value of omeprazole (30.24 microg/ml) confirming their anti-secretory activity. Conclusively, Fr-CHCl(3) of Xylocarpus granatum was found to possess anti-ulcerogenic activity which might be due to its anti-secretory activity and subsequent strengthening of the defensive mechanism. This study is the first of its kind to show significant anti-secretory effect of gedunin and photogedunin. Therefore it could act as a potent therapeutic agent against peptic ulcer disease.
在本研究中,研究了石榴果及其活性成分吉杜宁和光吉杜宁的胃保护机制。评估了石榴果的氯仿部分(Fr-CHCl(3))对大鼠冷束缚(CRU)、阿司匹林(AS)、酒精(AL)和幽门结扎(PL)诱导的胃溃疡模型以及组胺(HA)诱导的豚鼠十二指肠溃疡模型的作用。Fr-CHCl(3)对 CRU(58.28%)、AS(67.81%)、AL(84.38%)、PL(65.66%)和 HA(61.93%)诱导的溃疡模型显示出潜在的抗溃疡活性。标准药物奥美拉唑(10mg/kg,po)对 CRU 的保护率为 68.25%,对 AS 为 57.08%,对 PL 为 69.42%,对 HA 诱导的十二指肠溃疡为 70.79%。另一种标准药物硫糖铝(500mg/kg,po)对 AL 诱导的溃疡模型的保护率为 62.72%。Fr-CHCl(3)可分别显著降低游离酸度(51.42%)、总酸度(30.76%)和增加粘蛋白分泌 58.37%。Fr-CHCl(3)的植物化学研究得到了吉杜宁(36%)和光吉杜宁(2%)。此外,Fr-CHCl(3)及其化合物吉杜宁和光吉杜宁在体外显著抑制 H(+)K(+)-ATP 酶活性,IC(50)分别为 89.37、56.86 和 66.54μg/ml,与奥美拉唑(30.24μg/ml)的 IC(50)值相比,证实了其抗分泌活性。总之,发现 Xylocarpus granatum 的 Fr-CHCl(3)具有抗溃疡活性,这可能是由于其抗分泌活性和随后增强的防御机制。这项研究是首例显示吉杜宁和光吉杜宁具有显著抗分泌作用的研究。因此,它可以作为治疗消化性溃疡疾病的有效药物。