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用于在小鼠皮肤中递送9-顺式视黄酸的局部应用9-顺式视黄醛。

Topical 9-cis-retinaldehyde for delivery of 9-cis-retinoic acid in mouse skin.

作者信息

Didierjean L, Sass J O, Carraux P, Grand D, Sorg O, Plum C, Nau H, Saurat J H

机构信息

Department of Dermatology, University Hospital, Geneva and DHURDV, Switzerland.

出版信息

Exp Dermatol. 1999 Jun;8(3):199-203. doi: 10.1111/j.1600-0625.1999.tb00371.x.

Abstract

The 9-cis-retinoic acid (9cRA) is an endogenous ligand of retinoid X nuclear receptors (RXRs). Although the epidermis contains five times more RXRs than RARs, little is known on the activity of topical 9cRA. In order to circumvent surface isomerization of topically applied 9cRA into all-trans-retinoic acid (atRA), we used topical 9-cis-retinaldehyde (9cRAL) as a precursor of 9cRA, hypothesizing that keratinocytes would metabolize 9cRAL into 9-cis-retinoic acid (9cRA). Retinoid content was determined by HPLC analysis of mouse tail skin that had been washed after the application of 9cRAL (0.05% for 14 days) to evaluate the metabolites produced within the epidermis. Biologic activities of 9cRAL and atRAL were analysed by assessing hyperplastic and metaplastic responses, by determining epidermal thickness and the levels of mRNAs encoding for specific keratins. atRAL and derived retinoids were found in skin treated with either atRAL or 9cRAL. The metabolite pattern obtained with 9cRAL was similar to that obtained with atRAL except the presence in 9cRAL samples of an unidentified nonpolar metabolite. However, treatment with 9cRAL yielded higher atRAL and lower retinyl ester concentrations. The biologic activities (hyperplastic and metaplastic responses) resulting from topical application of 9cRAL were lower than those induced by atRAL or atRA at similar concentrations. Taken together, these data show that topical 9cRAL does not deliver significant amounts of 9cRA and exerts less biologic activity than atRAL. Contrary to atRAL, 9cRAL does not appear therefore as a pertinent candidate for topical use in humans.

摘要

9-顺式视黄酸(9cRA)是维甲酸X核受体(RXRs)的内源性配体。尽管表皮中RXRs的含量是维甲酸受体(RARs)的五倍,但关于局部应用9cRA的活性却知之甚少。为了避免局部应用的9cRA在表面异构化为全反式视黄酸(atRA),我们使用局部应用的9-顺式视黄醛(9cRAL)作为9cRA的前体,推测角质形成细胞会将9cRAL代谢为9-顺式视黄酸(9cRA)。通过对应用9cRAL(0.05%,持续14天)后洗涤过的小鼠尾部皮肤进行高效液相色谱(HPLC)分析来测定类视黄醇含量,以评估表皮内产生的代谢产物。通过评估增生和化生反应、测定表皮厚度以及编码特定角蛋白的mRNA水平,分析了9cRAL和atRAL的生物学活性。在用atRAL或9cRAL处理的皮肤中均发现了atRAL及其衍生的类视黄醇。9cRAL获得的代谢产物模式与atRAL相似,只是9cRAL样品中存在一种未鉴定的非极性代谢产物。然而,用9cRAL处理产生的atRAL浓度较高,视黄酯浓度较低。在相似浓度下,局部应用9cRAL产生的生物学活性(增生和化生反应)低于atRAL或atRA诱导的活性。综上所述,这些数据表明局部应用9cRAL不会产生大量的9cRA,且其生物学活性低于atRAL。因此,与atRAL不同,9cRAL似乎不是适用于人类局部应用的合适候选物。

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