吴少华, 罗晓东, 马云保, 郝小江, 吴大刚. 一支箭中抗胃溃疡的倍半萜内酯苷J. 药学学报, 2002, 37(1): 33-36.
引用本文: 吴少华, 罗晓东, 马云保, 郝小江, 吴大刚. 一支箭中抗胃溃疡的倍半萜内酯苷J. 药学学报, 2002, 37(1): 33-36.
WU Shao-hua, LUO Xiao-dong, MA Yun-bao, HAO Xiao-jiang, WU Da-gang. ANTI-GASTRIC ULCER SESQUITERPENE LACTONE GLYCOSIDES FROM CREPIS NAPIFERAJ. Acta Pharmaceutica Sinica, 2002, 37(1): 33-36.
Citation: WU Shao-hua, LUO Xiao-dong, MA Yun-bao, HAO Xiao-jiang, WU Da-gang. ANTI-GASTRIC ULCER SESQUITERPENE LACTONE GLYCOSIDES FROM CREPIS NAPIFERAJ. Acta Pharmaceutica Sinica, 2002, 37(1): 33-36.

一支箭中抗胃溃疡的倍半萜内酯苷

ANTI-GASTRIC ULCER SESQUITERPENE LACTONE GLYCOSIDES FROM CREPIS NAPIFERA

  • 摘要: 目的研究一支箭(Crepis napifera (Franch.) Babc.)根中抗胃溃疡的活性成分。方法采用柱色谱方法进行分离纯化,得到2个化合物,用NMR,MS,UV,IR光谱技术和化学方法进行鉴定;测定化合物1对大鼠体内由阿司匹林导致胃损伤的影响和对胃酸分泌的作用。结果分离得到2个倍半萜内酯苷类化合物,taraxinic acid-1′-O-β-D-glucopyranoside (1)和11,13-dihydro-taraxinic acid-1′-O-β-D-glucopyranoside (2)。化合物1以80 mg·kg-1的剂量ig给药,可以有效地抑制鼠体内由于阿司匹林导致的胃损伤,并以70 mg·kg-1的剂量iv不会影响鼠体胃内由组胺刺激产生的胃酸分泌物。结论化合物1为保护胃粘膜,抗胃溃疡的活性成分。

     

    Abstract: AIMThe anti-gastric ulcer constituents from the roots of Crepis napifera (Franch) Babc (Compositae) were studied. METHODSSolvent partition, Si gel and Rp-18 column chromatography, crystallization and spectral methods were used to extract, isolate and identify two compounds. The activity of compound 1 was tested on the mouse stomach by determining the effect on aspirin-induced gastric lesions and on histamine-stimulated gastric acid secretion. RESULTSTwo sesquiterpene lactone glycosides, taraxinic acid-1′-O-β-D-glucopyranoside (1) and 11,13-dihydro-taraxinic acid-1′-O-β-D-glucopyranoside (2) were obtained. Compound 1 at the dose of 80 mg·kg-1 po inhibited significantly the development of aspirin-induced gastric lesions in the rat and at an iv dose of 70 mg·kg-1 did not affect histamine-stimulated gastric acid secretion in the lumen-perfused rat stomach. CONCLUSIONCompound 1 is the active component of the plant which protects gastric mucosa and exhibits anti-gastric ulcer action.

     

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