Orfanos C E, Zouboulis C C, Almond-Roesler B, Geilen C C
Department of Dermatology, University Medical Center Benjamin Franklin, Free University of Berlin, Germany.
Drugs. 1997 Mar;53(3):358-88. doi: 10.2165/00003495-199753030-00003.
Since their introduction 15 years ago, retinoids have been increasingly used for topical and systemic treatment of psoriasis and other hyperkeratotic and parakeratotic skin disorders, keratotic genodermatoses, severe acne and acne-related dermatoses, and also for therapy and/or chemoprevention of skin cancer and other neoplasia. Oxidative metabolites of vitamin A (retinol) are natural retinoids present at low levels in the peripheral blood. Synthetic retinoids are classified into 3 generations including nonaromatic, monoaromatic and polyaromatic compounds. They are detectable in plasma 30-60 minutes after systemic administration, and reach maximum concentrations 2 to 4 hours later. Elimination half-life is 10 to 20 hours for isotretinoin, 80 to 175 days for etretinate and 2 to 4 days for, trans-acitretin; the latter, however, partially converts into etretinate. Retinoid concentrations in skin are rather low in contrast to subcutaneous fat tissue. Intracellularly, retinoids interact with cytosolic proteins and specific nuclear receptors. Two classes of nuclear receptors have been suggested to mediate retinoid activity at the molecular level, RARs and RXRs. The expression of retinoid receptors is tissue specific; skin mainly espresses RAR gamma and RXR alpha. Retinoids affect epidermal cell growth and differentiation as well as sebaceous gland activity and exhibit immunomodulatory and anti-inflammatory properties. Current retinoid research targets the development of receptor-selective retinoids for tailoring and/or improving their therapeutic profile. Currently, tretinoin is used systemically for acute promyelocytic leukaemia, etretinate and acitretin for psoriasis and related disorders, as well as other disorders of keratinisation and isotretinoin for seborrhoea, severe acne, rosacea and acneiform dermatoses. Systemic retinoids are also applied for chemoprevention of epithelial skin cancer and cutaneous T cell lymphoma. The major adverse effect of retinoids is teratogenicity; all other adverse effects are dose-dependent and controllable. Contraception is, therefore, essential during retinoid treatment in women of child-bearing age. Clinical monitoring requires physical examination for adverse effects every 3 to 4 weeks and proper laboratory investigations, also including analysis of retinoid bioavailability in selected cases. Topical retinoids are rapidly developing at present and seem promising for the future; their clinical application includes acne, aging, photodamage, precanceroses, skin cancer and disorders of skin pigmentation. The development of receptor-specific retinoids for topical treatment of psoriasis and/or acne may lead to interesting new compounds based on our current concepts of retinoid function.
自15年前被引入以来,维甲酸已越来越多地用于银屑病及其他角化过度和不全角化性皮肤病、角化性遗传性皮肤病、重度痤疮及痤疮相关皮肤病的局部和全身治疗,也用于皮肤癌和其他肿瘤的治疗及/或化学预防。维生素A(视黄醇)的氧化代谢产物是外周血中含量较低的天然维甲酸。合成维甲酸分为三代,包括非芳香族、单芳香族和多芳香族化合物。全身给药后30 - 60分钟可在血浆中检测到它们,2至4小时后达到最大浓度。异维A酸的消除半衰期为10至20小时,阿维A酯为80至175天,阿维A为2至4天;然而,后者会部分转化为阿维A酯。与皮下脂肪组织相比,皮肤中的维甲酸浓度相当低。在细胞内,维甲酸与胞质蛋白和特定核受体相互作用。已提出两类核受体在分子水平介导维甲酸活性,即维甲酸受体(RARs)和维甲酸X受体(RXRs)。维甲酸受体的表达具有组织特异性;皮肤主要表达RARγ和RXRα。维甲酸影响表皮细胞生长和分化以及皮脂腺活性,并具有免疫调节和抗炎特性。当前维甲酸研究的目标是开发受体选择性维甲酸,以调整和/或改善其治疗效果。目前,全反式维甲酸用于急性早幼粒细胞白血病的全身治疗,阿维A酯和阿维A用于银屑病及相关疾病以及其他角化异常疾病的治疗,异维A酸用于脂溢性皮炎、重度痤疮、玫瑰痤疮和痤疮样皮肤病的治疗。全身维甲酸也用于上皮性皮肤癌和皮肤T细胞淋巴瘤的化学预防。维甲酸的主要不良反应是致畸性;所有其他不良反应均与剂量相关且可控。因此,育龄期女性在维甲酸治疗期间必须采取避孕措施。临床监测需要每3至4周进行一次不良反应的体格检查以及适当的实验室检查,在特定病例中还包括维甲酸生物利用度分析。目前局部用维甲酸正在迅速发展,未来似乎很有前景;其临床应用包括痤疮、皮肤老化、光损伤、癌前病变、皮肤癌和皮肤色素沉着异常。基于我们目前对维甲酸功能的认识,开发用于局部治疗银屑病和/或痤疮的受体特异性维甲酸可能会产生有趣的新化合物。