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抗氧化剂的临床药代动力学及其对全身氧化应激的影响。

Clinical pharmacokinetics of antioxidants and their impact on systemic oxidative stress.

作者信息

Schwedhelm Edzard, Maas Renke, Troost Raphael, Böger Rainer H

机构信息

Institute of Experimental and Clinical Pharmacology, Clinical Pharmacology Unit, University Hospital of Hamburg-Eppendorf, Hamburg, Germany.

出版信息

Clin Pharmacokinet. 2003;42(5):437-59. doi: 10.2165/00003088-200342050-00003.

Abstract

Dietary antioxidants play a major role in maintaining the homeostasis of the oxidative balance. They are believed to protect humans from disease and aging. Vitamin C (ascorbic acid), vitamin E (tocopherol), beta-carotene and other micronutrients such as carotenoids, polyphenols and selenium have been evaluated as antioxidant constituents in the human diet. This article addresses data provided from clinical trials, highlighting the clinical pharmacokinetics of vitamin C, vitamin E, beta-carotene, lycopene, lutein, quercetin, rutin, catechins and selenium. The bioavailability of vitamin C is dose-dependent. Saturation of transport occurs with dosages of 200-400 mg/day. Vitamin C is not protein-bound and is eliminated with an elimination half-life (t((1/2))) of 10 hours. In Western populations plasma vitamin C concentrations range from 54-91 micro mol/L. Serum alpha- and gamma-tocopherol range from 21 micro mol/L (North America) to 27 micro mol/L (Europe) and from 3.1 micro mol/L to 1.5 micro mol/L, respectively. alpha-Tocopherol is the most abundant tocopherol in human tissue. The bioavailability of all-rac-alpha-tocopherol is estimated to be 50% of R,R,R-alpha-tocopherol. The hepatic alpha-tocopherol transfer protein (alpha-TTP) together with the tocopherol-associated proteins (TAP) are responsbile for the endogenous accumulation of natural alpha-tocopherol. Elimination of alpha-tocopherol takes several days with a t((1/2)) of 81 and 73 hours for R,R,R-alpha-tocopherol and all-rac-alpha-tocopherol, respectively. The t((1/2)) of tocotrienols is short, ranging from 3.8-4.4 hours for gamma- and alpha-tocotrienol, respectively. gamma-Tocopherol is degraded to 2, 7, 8-trimethyl-2-(beta-carboxyl)-6-hyrdoxychroman by the liver prior to renal elimination. Blood serum carotenoids in Western populations range from 0.28-0.52 micro mol/L for beta-carotene, from 0.2-0.28 for lutein, and from 0.29-0.60 for lycopene. All-trans-carotenoids have a better bioavailability than the 9-cis-forms. Elimination of carotenoids takes several days with a t((1/2)) of 5-7 and 2-3 days for beta-carotene and lycopene, respectively. The bioconversion of beta-carotene to retinal is dose-dependent, and ranges between 27% and 2% for a 6 and 126mg dose, respectively. Several oxidised metabolites of carotenoids are known. Flavonols such as quercetin glycosides and rutin are predominantly absorbed as aglycones, bound to plasma proteins and subsequently conjugated to glucuronide, sulfate, and methyl moieties. The t((1/2)) ranges from 12-19 hours. The bioavailabillity of catechins is low and they are eliminated with a t((1/2)) of 2-4 hours. Catechins are degraded to several gamma-valerolactone derivatives and phase II conjugates have also been identified. Only limited clinical pharmacokinetic data for other polyphenols such as resveratrol have been reported to date.

摘要

膳食抗氧化剂在维持氧化平衡的稳态中起主要作用。它们被认为可以保护人类免受疾病和衰老的影响。维生素C(抗坏血酸)、维生素E(生育酚)、β-胡萝卜素以及其他微量营养素,如类胡萝卜素、多酚和硒,已被评估为人类饮食中的抗氧化成分。本文论述了临床试验提供的数据,重点介绍了维生素C、维生素E、β-胡萝卜素、番茄红素、叶黄素、槲皮素、芦丁、儿茶素和硒的临床药代动力学。维生素C的生物利用度呈剂量依赖性。每日剂量为200 - 400毫克时会出现转运饱和。维生素C不与蛋白质结合,消除半衰期(t(1/2))为10小时。在西方人群中,血浆维生素C浓度范围为54 - 91微摩尔/升。血清α-生育酚和γ-生育酚的浓度范围分别为21微摩尔/升(北美)至27微摩尔/升(欧洲)以及3.1微摩尔/升至1.5微摩尔/升。α-生育酚是人体组织中含量最丰富的生育酚。消旋-α-生育酚的生物利用度估计为RRR-α-生育酚的50%。肝脏中的α-生育酚转运蛋白(α-TTP)与生育酚相关蛋白(TAP)共同负责天然α-生育酚的内源性积累。α-生育酚的消除需要数天时间,RRR-α-生育酚和消旋-α-生育酚的t(1/2)分别为81小时和73小时。生育三烯酚的t(1/2)较短,γ-生育三烯酚和α-生育三烯酚的t(1/2)分别为3.8 - 4.4小时。γ-生育酚在经肾脏排泄之前先在肝脏中降解为2,7,8-三甲基-2-(β-羧基)-6-羟基色满。西方人群血清中的类胡萝卜素浓度,β-胡萝卜素为0.28 - 0.52微摩尔/升,叶黄素为0.2 - 0.28微摩尔/升,番茄红素为0.29 - 0.60微摩尔/升。全反式类胡萝卜素的生物利用度优于9-顺式异构体。类胡萝卜素的消除需要数天时间,β-胡萝卜素和番茄红素的t(1/2)分别为5 - 7天和2 - 3天。β-胡萝卜素向视黄醛的生物转化呈剂量依赖性,6毫克和126毫克剂量时的转化率分别在27%和2%之间。已知类胡萝卜素有几种氧化代谢产物。槲皮素糖苷和芦丁等黄酮醇主要以苷元形式被吸收,与血浆蛋白结合,随后与葡糖醛酸、硫酸盐和甲基部分结合。t(1/2)范围为12 - 19小时。儿茶素的生物利用度较低,消除半衰期为2 - 4小时。儿茶素降解为几种γ-戊内酯衍生物,并且也已鉴定出II相缀合物。迄今为止,仅报道了白藜芦醇等其他多酚类物质有限的临床药代动力学数据。

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