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[瓜米番荔枝和α-细辛脑的药理学与毒理学]

[Pharmacology and toxicology of Guatteria gaumeri and alpha-asarone].

作者信息

Chamorro G, Salazar M, Salazar S, Mendoza T

机构信息

Departamento de Toxicología, Escuela Nacional de Ciencias Biológicas, I.P.N., México D.F.

出版信息

Rev Invest Clin. 1993 Nov-Dec;45(6):597-604.

PMID:8159883
Abstract

Guatteria gaumeri Greenman (Annonacease) has been used as bark infusion in the traditional mexican medicine for the treatment of hypercholesterolemia and cholelithiasis. The main component is alpha-asarone which has been isolated by different extraction procedures and subsequently synthetized, as well as 16 analogs, derivatives of 4-propenyl-1,2-dimethoxybenzenes 5-substituted. After daily dosing per os of 80 mg/kg of alpha-asarone and the amino and metoxi analogs for seven days to hypercholesterolemic male rats, cholesterol decreased 57.3, 37.5 and 46.9% and triglycerides diminished 42.5, 67.6 and 17.2% respectively. Some of the other analogs showed also important hypolipidemic activity. Similarly alpha-asarone decreased 80.6% the weight of gallstones in hamsters. Studies using adult rat hepatocytes suggest that at least part of the hypolipidemic effect of alpha-asarone could be due to a decrease in the secretion of lipids. Alpha-asarone did not produce any toxic effect after oral administration to rats of 10 or 50 mg/kg for 28 days, or genotoxicity by the dominant lethal test. However long-term exposure of cultivated hepatocytes to micromolar concentrations produced morphologic and ultrastructural alterations, triacylglycerol accumulation and inhibition of protein synthesis and secretion. At the same time both the Ames and sister-chromatid exchange tests showed genotoxic effect. No teratogenicity was observed in pregnant rats during organogenesis but in mice slight fetal toxicity was manifested by hydrocephaly, skeletal defects and fetal weight retardation. There are no data on the possible exposure levels in humans consuming the bark extract, but the toxic effects of alpha-asarone in animals suggest caution in the use of this plant.(ABSTRACT TRUNCATED AT 250 WORDS)

摘要

墨西哥瓜馥木(番荔枝科)在墨西哥传统医学中被用作树皮浸剂,用于治疗高胆固醇血症和胆石症。其主要成分是α-细辛脑,已通过不同提取方法分离出来并随后合成,还有16种类似物,即5-取代的4-丙烯基-1,2-二甲氧基苯衍生物。给高胆固醇血症雄性大鼠每日口服80mg/kg的α-细辛脑以及氨基和甲氧基类似物7天后,胆固醇分别降低了57.3%、37.5%和46.9%,甘油三酯分别减少了42.5%、67.6%和17.2%。其他一些类似物也显示出重要的降血脂活性。同样,α-细辛脑使仓鼠胆结石重量减轻了80.6%。使用成年大鼠肝细胞的研究表明,α-细辛脑的降血脂作用至少部分可能是由于脂质分泌减少。给大鼠口服10或50mg/kg的α-细辛脑28天后未产生任何毒性作用,也未通过显性致死试验产生遗传毒性。然而,将培养的肝细胞长期暴露于微摩尔浓度会导致形态和超微结构改变、三酰甘油积累以及蛋白质合成和分泌受到抑制。同时,艾姆斯试验和姐妹染色单体交换试验均显示出遗传毒性作用。在器官形成期,怀孕大鼠未观察到致畸性,但在小鼠中出现了轻度胎儿毒性,表现为脑积水、骨骼缺陷和胎儿体重发育迟缓。目前尚无关于食用树皮提取物的人类可能接触水平的数据,但α-细辛脑在动物中的毒性作用表明在使用这种植物时应谨慎。(摘要截短至250字)

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