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来自卡朱卡拉巴豆的反式脱氢巴豆素的抗溃疡活性。

Antiulcerogenic activity of trans-dehydrocrotonin from Croton cajucara.

作者信息

Brito A R, Rodríguez J A, Hiruma-Lima C A, Haun M, Nunes D S

机构信息

Dep. de Fisiologia e Biofísica, Universidade Estadual de Campinas, São Paulo, Brasil.

出版信息

Planta Med. 1998 Mar;64(2):126-9. doi: 10.1055/s-2006-957388.

Abstract

trans-Dehydrocrotonin (DHC), the major diterpene isolated from Croton cajucara Benth, was assayed for antiulcerogenic activity in four induced gastric ulcer models in the rat. At an oral dose of 100 mg/kg DHC showed a significant antiulcerogenic effect on ulcers induced by hypothermic restraint stress, ethanol, and pylorus ligature. No significant changes in indomethacin-induced gastric lesions or modifications in gastric parameters such as wall mucus, secretion rate, pH, and total acid content were found after DHC treatment. The acute toxicological effects of DHC were assessed in mice. The LD50 values were 876 mg/kg and 47.2 mg/kg for oral and intraperitoneal administrations, respectively. The cytotoxicity of DHC was also studied. A dose-dependent inhibition of cell viability was observed in V-79 fibroblast cell cultures with an IC50 of 240 microM. The high yields of DHC obtained from dried C. cajucara barks as well as its good antiulcerogenic activity and low toxicity support the pharmacological study of this compound as a potential new antiulcerogenic drug.

摘要

反式脱氢巴豆素(DHC)是从克罗顿卡尤卡拉本特中分离出的主要二萜类化合物,在大鼠的四种诱导性胃溃疡模型中检测了其抗溃疡活性。口服剂量为100mg/kg时,DHC对低温束缚应激、乙醇和幽门结扎诱导的溃疡显示出显著的抗溃疡作用。DHC治疗后,吲哚美辛诱导的胃损伤或胃参数如壁黏液、分泌率、pH值和总酸含量均未发现明显变化。在小鼠中评估了DHC的急性毒理学效应。口服和腹腔注射的LD50值分别为876mg/kg和47.2mg/kg。还研究了DHC的细胞毒性。在V-79成纤维细胞培养物中观察到细胞活力的剂量依赖性抑制,IC50为240μM。从干燥的卡尤卡拉树皮中获得的高产率DHC及其良好的抗溃疡活性和低毒性支持了对该化合物作为潜在新型抗溃疡药物的药理学研究。

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