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Antioxidative roles of sesamin, a functional lignan in sesame seed, and it's effect on lipid-and alcohol-metabolism in the liver: A DNA microarray study

机译:SESAMIN,芝麻籽喹氏菌的抗氧化作用,对肝脏脂质和醇代谢的影响:DNA微阵列研究

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Sesamin was orally administered to rats, and blood, bile and urine were collected periodically. Over 40% of the dose of sesamin was detected in bile as glucuronides of 2-beta, 4-methylenedioxyphenyl)-6-beta, 4-dihydroxyphenyl)-cis-dioxabicyclo[3.3.0]octane and 2-(3, 4-dihydroxyphenyl)-6-beta, 4-dihydroxyphenyl)-cis-dioxabicyclo[3.3.0] octane by 24 hr after administration. Antioxidant activities of these metabolites were compared and catechol metabolites showed strong radical scavenging activities against not only superoxide anion radical but also hydroxyl radical. It was suggested that sesamin was absorbed by the route of portal vein and metabolized to mono- or di-catechol metabolite by drug metabolizing enzymes in the liver cells. Both metabolitesexhibited antioxidant activity in the liver and were finally conjugated with glucuronic acid and to excrete in bile. Sesamin can be classified as a pro-antioxidant.The profiles of gene expression of the liver in rats given sesamin or vehicle were compared. The gene expression levels of the late stage enzymes of beta-oxidation including trifunctional enzyme, acyl-CoA oxidase, bifunctional enzyme and 3-ketoacyl-CoA thiolase were significantly increased by sesamin. On the other hand, the transcription of the genes encoding the enzymes for fatty acid synthesis was decreased. Moreover, in sesamin rats, the gene expression of aldehyde dehydrogenase was increased about 3-fold, whereas alcohol dehydrogenase, liver catalase and CYP2E1 were not changed. These results suggested that sesamin ingestion regulated the transcription levels of hepatic metabolizing enzymes for lipids and alcohol.
机译:SESAMIN口服给予大鼠,周期性地收集血液,胆汁和尿液。在胆汁中以2-β,4-亚甲基二苯基)-6-β,4-二羟基苯基的葡糖醛酸钠检测到超过40%的SESAMIN检测到的血糖醛酸酯 - CIO-DIOxabicyclo [3.3.0]辛烷值和2-(3,4-二羟基苯基)-6-β,4-二羟基苯基)-CIS-DIOxabicyClO [3.3.0]辛烷在给药后24小时。比较这些代谢物的抗氧化活性,并且儿茶酚代谢物呈现出强烈的激进清除活性,不仅对超氧化物阴离子自由基而且羟基。有人建议,芝麻胺被门静脉的途径吸收,并通过肝细胞中的药物代谢酶代谢到单或二 - 儿茶酚代谢物中。在肝脏中代谢物抑制的抗氧化活性,最后与血糖酸和胆汁缀合。 SESAMIN可以被分类为PRO-抗氧化剂。比较了肝脏肝脏在给定芝麻素或载体的大鼠中的基因表达的谱。 SESAMIN显着提高了包括三官能酶,酰基-COA氧化酶,双官能酶和3-酮酰基-COA硫醇酶的β-氧化晚期酶的基因表达水平。另一方面,编码编码脂肪酸合成酶的基因的转录被降低。此外,在芝麻素大鼠中,醛脱氢酶的基因表达增加约3倍,而醇脱氢酶,肝脏过冬酶和CYP2E1没有改变。这些结果表明,SESAMIN摄取调节了脂质和醇的肝脏代谢酶的转录水平。

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