Suppr超能文献

人体吸收过程中9-顺式-β-胡萝卜素顺反异构化的证据。

Evidence of cis-trans isomerization of 9-cis-beta-carotene during absorption in humans.

作者信息

You C S, Parker R S, Goodman K J, Swanson J E, Corso T N

机构信息

Division of Nutritional Sciences, Cornell University, Ithaca, NY 14853, USA.

出版信息

Am J Clin Nutr. 1996 Aug;64(2):177-83. doi: 10.1093/ajcn/64.2.177.

Abstract

Absorption and metabolism of [13C]9-cis-beta-carotene ([13C]9c beta C) was studied in three subjects after a single oral dose. Subjects given 1.0 mg [13C]beta-carotene (mean: 99.4% 9-cis-beta-carotene, 0.6% all-trans-beta-carotene; dose A) had substantial concentrations of [13C]all-trans-beta-carotene ([13C]tr beta C) and [13C]all-trans retinol ([13C]retinol) but very low concentrations of [13C]cis-beta-carotene ([13C]cis beta C) in saponified plasma 5 h after dosing, as determined by HPLC and isotope-ratio mass spectrometry. There was no evidence of appreciable absorption of [13C]9-cis retinol. To determine the proportion of [13C]tr beta C and [13C]retinol derived from [13C]9c beta C, a second set of studies in the same subjects was performed with the same isomeric composition except with 13C labeling only in all-trans-beta-carotene (dose B). The results indicated that > 95% of plasma [13C]tr beta C and [13C]retinol observed after dose A was derived from [13C]9c beta C. The concentrations of [13C]tr beta C observed, in excess of that derived from the trace amounts of [13C]tr beta C in the dose, indicated that a significant proportion of the [13C]9c beta C dose was isomerized to [13C]tr beta C before entering the bloodstream. Although precise quantitative estimates of the extent of isomerization of 9-cis-beta-carotene could not be made, it is apparent that cis-trans isomerization of 9-cis-beta-carotene to all-trans-beta-carotene contributed to the near absence of postprandial plasma 9-cis-beta-carotene after its oral administration in humans. The observation of different ratios of beta-carotene to retinol between the two dosing protocols suggests that isomerization did not occur exclusively before uptake by the intestinal mucosa. These results indicate that isomerization of ingested 9-cis-beta-carotene before its secretion into the bloodstream limits the potential supply of 9-cis retinoids to tissues, and increases the vitamin A value of 9-cis-beta-carotene.

摘要

对三名受试者单次口服给药后,研究了[13C]9-顺式-β-胡萝卜素([13C]9c βC)的吸收和代谢情况。给予1.0毫克[13C]β-胡萝卜素的受试者(平均:99.4%为9-顺式-β-胡萝卜素,0.6%为全反式-β-胡萝卜素;剂量A),给药5小时后,通过高效液相色谱法和同位素比质谱法测定,皂化血浆中[13C]全反式-β-胡萝卜素([13C]tr βC)和[13C]全反式视黄醇([13C]视黄醇)浓度较高,但[13C]顺式-β-胡萝卜素([13C]顺式βC)浓度极低。没有证据表明[13C]9-顺式视黄醇有明显吸收。为了确定[13C]tr βC和[13C]视黄醇中源自[13C]9c βC的比例,在同一受试者中进行了另一组研究,其异构体组成相同,但仅在全反式-β-胡萝卜素中进行13C标记(剂量B)。结果表明,剂量A后观察到的血浆[13C]tr βC和[13C]视黄醇中>95%源自[13C]9c βC。观察到的[13C]tr βC浓度超过了剂量中痕量[13C]tr βC衍生的浓度,这表明相当一部分[13C]9c βC剂量在进入血液之前异构化为[13C]tr βC。尽管无法对9-顺式-β-胡萝卜素异构化程度进行精确的定量估计,但很明显,9-顺式-β-胡萝卜素向全反式-β-胡萝卜素的顺反异构化导致其口服给药后人体餐后血浆中几乎不存在9-顺式-β-胡萝卜素。两种给药方案之间β-胡萝卜素与视黄醇比例不同的观察结果表明,异构化并非仅在被肠黏膜摄取之前发生。这些结果表明,摄入的9-顺式-β-胡萝卜素在分泌到血液之前的异构化限制了其向组织提供9-顺式类视黄醇的潜在供应,并增加了9-顺式-β-胡萝卜素的维生素A价值。

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验