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[黄连总生物碱对实验性胃溃疡的研究]

[Study of total alkaloids from Rhizoma Coptis Chinensis on experimental gastric ulcers].

作者信息

Li Bei, Shang Jing-chuan, Zhou Qi-xin

机构信息

Department of Pharmacology, Chongqing University of Medical Sciences, Chongqing 400016, China.

出版信息

Chin J Integr Med. 2005 Sep;11(3):217-21. doi: 10.1007/BF02836508.

Abstract

OBJECTIVE

To study the effects of total alkaloids (TA) extracted from Rhizoma Coptis Chinensis on experimental gastric ulcer models.

METHODS

Four kinds of experimental ulcer models were established respectively by water-immersion stress, intragastric ethanol, acetic acid erosion, and pylorus ligation. The anti-ulcer effects of TA were evaluated, and compared with that of berberine (Ber) and cimetidine (Cim).

RESULTS

TA showed significant inhibitory effects on ulcerative formation induced by water-immersion stress, intragastric ethanol, and pylorus ligation in dose-dependent manner, and showed therapeutic effect on acetic acid erosion-inducing ulcer, in comparison with the control group. The anti-ulcer activity of Ber was less than TA containing equal content of Ber. TA significantly reduced the free acidity, total acidity and total acid output, but didn't affect the gastric juice volume, gastric pepsin activity, adherent mucus quantity of stomach wall and free mucus dissolving in gastric juice. The suppressive activities of TA on gastric acid secretion didn't occur when it was administered into dodecadactylon at a dose of 360 mg/kg wt. Moreover, when compared with Cim, the inhibitory effect of TA on gastric acid secretion isn't proportional to the inhibitory effects on the formation of the 4 kinds of experimental ulcers.

CONCLUSION

TA is a potent candidate in therapeutic drugs for treating gastric ulcer. Its anti-ulcer effective components and mechanism is not only related to Ber and inhibition of gastric acid, but also to other ingredients of TA and mechanism so far unknown.

摘要

目的

研究从黄连中提取的总生物碱(TA)对实验性胃溃疡模型的影响。

方法

分别通过水浸应激、胃内乙醇、醋酸腐蚀和幽门结扎建立四种实验性溃疡模型。评估TA的抗溃疡作用,并与黄连素(Ber)和西咪替丁(Cim)进行比较。

结果

与对照组相比,TA对水浸应激、胃内乙醇和幽门结扎诱导的溃疡形成具有显著的剂量依赖性抑制作用,对醋酸腐蚀诱导的溃疡具有治疗作用。Ber的抗溃疡活性低于含等量Ber的TA。TA显著降低了游离酸度、总酸度和总酸输出,但不影响胃液体积、胃蛋白酶活性、胃壁黏附黏液量和胃液中游离黏液溶解量。当以360mg/kg体重的剂量将TA给予十二指肠时,未出现对胃酸分泌的抑制作用。此外,与Cim相比,TA对胃酸分泌的抑制作用与对四种实验性溃疡形成的抑制作用不成正比。

结论

TA是治疗胃溃疡的有效候选药物。其抗溃疡有效成分和机制不仅与Ber及胃酸抑制有关,还与TA的其他成分及目前未知的机制有关。

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