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成年大鼠肝细胞长期培养中的α-细辛脑毒性

alpha-Asarone toxicity in long-term cultures of adult rat hepatocytes.

作者信息

López M L, Hernández A, Chamorro G, Mendoza-Figueroa T

机构信息

Pharmacology and Toxicology Department, Centro de Investigación y Estudios Avanzados del IPN, México, D.F.

出版信息

Planta Med. 1993 Apr;59(2):115-20. doi: 10.1055/s-2006-959624.

Abstract

In this work we studied the toxic effects of alpha-asarone, a hypolipidemic active principle of Guatteria gaumeri Greenman, on long-term cultures of adult rat hepatocytes cultivated on a feeder layer of 3T3 cells. The exposure for one and two weeks to alpha-asarone (1-50 micrograms/ml) produced intracytoplasmic lipid droplets and at higher concentrations (25-50 micrograms/ml) retraction of the hepatocyte cords and cell detachment. Ultrastructurally, the treated cultures (10 micrograms/ml) showed enlargement and vacuolization of the mitochondria in addition to lipid droplets. The triacylglycerol content increased up to 2.3-fold in the cultures treated for one week with 50 micrograms/ml, whereas the protein content per culture, a rough estimate of cell number and viability, decreased by up to 53% in the cultures treated for two weeks with 50 micrograms/ml. The synthesis and secretion of proteins, measured by the incorporation of [3H]-leucine into cellular and secreted macromolecules, decreased also in the cultures exposed. After one and two week exposure to 50 micrograms/ml of alpha-asarone, the secretion of labeled proteins decreased by 53 and 67%, respectively, whereas the synthesis of cellular and total proteins decreased by 48-67%, respectively. The secretion of proteins was the most sensitive parameter of alpha-asarone toxicity. The mean inhibitory dose (ID50), i.e, that producing 50% inhibition in the incorporation of the labeled precursor, was 22.12 and 5.04 micrograms/ml after one and two weeks exposure, respectively. Our results show that long-term exposure to micromolar concentrations of alpha-asarone produces morphologic and ultrastructural alterations, triacylglycerol accumulation (fatty liver), and inhibition of protein synthesis and secretion.(ABSTRACT TRUNCATED AT 250 WORDS)

摘要

在本研究中,我们研究了瓜馥木属植物高梅瓜馥木(Guatteria gaumeri Greenman)的降血脂活性成分α-细辛醚对在3T3细胞饲养层上培养的成年大鼠肝细胞长期培养物的毒性作用。将α-细辛醚(1-50微克/毫升)暴露1周和2周会产生胞浆内脂滴,在较高浓度(25-50微克/毫升)下会导致肝索收缩和细胞脱离。超微结构上,用10微克/毫升处理的培养物除脂滴外,还显示出线粒体增大和空泡化。用50微克/毫升处理1周的培养物中三酰甘油含量增加高达2.3倍,而每培养物的蛋白质含量(对细胞数量和活力的粗略估计)在用50微克/毫升处理2周的培养物中最多可降低53%。通过将[3H]-亮氨酸掺入细胞和分泌的大分子中来测量的蛋白质合成和分泌,在暴露的培养物中也减少。在暴露于50微克/毫升α-细辛醚1周和2周后,标记蛋白质的分泌分别减少了53%和67%,而细胞和总蛋白质的合成分别减少了48%-67%。蛋白质分泌是α-细辛醚毒性最敏感的参数。平均抑制剂量(ID50),即在标记前体掺入中产生50%抑制的剂量,在暴露1周和2周后分别为22.12和5.04微克/毫升。我们的结果表明,长期暴露于微摩尔浓度的α-细辛醚会产生形态学和超微结构改变、三酰甘油积累(脂肪肝)以及蛋白质合成和分泌的抑制。(摘要截断于250字)

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