Department of Gastroenterology, Huashan Hospital, Fudan University, Shanghai, China.
J Dig Dis. 2009 Nov;10(4):293-9. doi: 10.1111/j.1751-2980.2009.00398.x.
To investigate the effect of Ginkgo biloba extract on gastric precancerous lesions in rats.
80 4-week-old Wistar rats were randomly divided into four groups: a control group, a model group, a low and a high dose Ginkgo biloba extract intervention group; 20 in each group. Gastric precancerous lesions were induced by giving them 100 mg/L N-methyl-N'-nitro-N-nitrosoguanidine (MNNG) solution to drink ad libitum for 20 weeks. In addition to the MNNG, the intervention groups were lavaged with Ginkgo biloba extract (0.5 mg/kg/d in the low dose group, 1.5 mg/kg/d in the high dose group) for 20 weeks. Starting from week 21 all the rats were fed with normal rat chow and tap water. At the end of week 30 the rats were killed. The histopathological changes of their gastric mucosa, ISA, NGI, the serum and gastric mucosal SOD/MDA and the expressions of oncogenes were studied.
The incidence of mild to severe intestinal metaplasia and dysplasia were significantly lower in the intervention groups than those in the model group (P < 0.01). The ISA and NGI in the intervention groups were significantly lower than those in the model group (P < 0.01). In the intervention groups the activity of SOD was increased and the concentration of MDA was decreased (P < 0.01). Expressions of Bcl-2, c-myc and FasL decreased in the intervention groups, whereas the expression of Fas increased. When compared with the model group, the differences were statistically significant (P < 0.01, P < 0.05, respectively).
Ginkgo biloba extract can increase anti-oxidative activity and inhibit the progression of gastric precancerous lesions via the regulation of cell proliferation and apoptosis.
研究银杏叶提取物对大鼠胃癌前病变的影响。
将 80 只 4 周龄 Wistar 大鼠随机分为 4 组:对照组、模型组、低剂量银杏叶提取物干预组和高剂量银杏叶提取物干预组,每组 20 只。除给予 MNNG(100mg/L)溶液自由饮用 20 周诱导胃癌前病变外,干预组还分别给予 0.5mg/kg/d(低剂量组)和 1.5mg/kg/d(高剂量组)银杏叶提取物灌胃 20 周。从第 21 周开始,所有大鼠均给予正常大鼠饲料和自来水。第 30 周末处死大鼠。研究其胃黏膜的组织病理学变化、ISA、NGI、血清和胃黏膜 SOD/MDA 以及癌基因的表达。
干预组轻至重度肠上皮化生和异型增生的发生率明显低于模型组(P<0.01)。干预组的 ISA 和 NGI 明显低于模型组(P<0.01)。干预组 SOD 活性增加,MDA 浓度降低(P<0.01)。干预组 Bcl-2、c-myc 和 FasL 的表达减少,而 Fas 的表达增加。与模型组相比,差异均有统计学意义(P<0.01,P<0.05)。
银杏叶提取物通过调节细胞增殖和凋亡,增加抗氧化活性,抑制胃癌前病变的进展。