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局部用脂质体 5α-还原酶抑制剂诱导仓鼠颊部皮脂腺器官选择性凋亡:痤疮的治疗策略。

Selective induction of apoptosis in the hamster flank sebaceous gland organ by a topical liposome 5-alpha-reductase inhibitor: a treatment strategy for acne.

机构信息

AntiCancer, Inc, University of California San Diego, San Diego, California 92111, USA.

出版信息

J Dermatol. 2010 Feb;37(2):156-62. doi: 10.1111/j.1346-8138.2009.00778.x.

Abstract

Acne is a very widespread cosmesis problem. Isotretinoin, a synthetic oral retinoid is used to treat acne, which is androgen dependent. Numerous side-effects occur from this treatment. 5-alpha-Reductase plays a critical role in normal and pathological androgen-dependent processes. We have taken the approach to develop a selective, effective, topically-applied 5-alpha-reductase inhibitor to modify unwanted or pathological processes in the pilosebaceous unit such as acne. Toward this goal, we have previously developed a selective liposome hair follicle targeting system. We demonstrate in this report that the 5-alpha-reductase inhibitor N,N-diethyl-4-methyl-3-oxo-4-aza-5alpha-androstane-17beta-carboxamide (4-MA) incorporated into liposomes induces apoptosis and inhibits growth of the dihydrotestosterone (DHT)-dependent hamster flank organ sebaceous gland. We have compared topical application of liposome 4-MA and solvent-formulated 4-MA and observed selective efficacy of topical application of liposome 4-MA by the reduction of size and induction of apoptosis only in the treated hamster flank organ. Apoptosis induced by liposome 4-MA in the treated flank organ sebaceous gland cells was observed both by assays for DNA fragments (transferase deoxytidyl uridine end labeling) and by observation of condensed and fragmented nuclei. When 4-MA was topically applied formulated in ethanol and glycerol without liposomes, the selective efficacy was lost. Liposome 4-MA did not significantly affect prostate weight, testosterone/DHT ratios or bodyweight gain compared to controls indicating safety as well as efficacy of topical application of liposome 4-MA for pathological processes such as acne.

摘要

痤疮是一种非常普遍的美容问题。异维 A 酸是一种合成的口服维 A 酸类药物,用于治疗雄激素依赖性痤疮。这种治疗会产生许多副作用。5α-还原酶在正常和病理雄激素依赖性过程中起着关键作用。我们已经采取了开发一种选择性、有效、局部应用的 5α-还原酶抑制剂的方法,以改变毛发皮脂腺单位中不需要的或病理过程,如痤疮。为此,我们之前开发了一种选择性的脂质体毛囊靶向系统。我们在本报告中证明,将 5α-还原酶抑制剂 N,N-二乙基-4-甲基-3-氧代-4-氮杂-5α-雄甾烷-17β-羧酰胺(4-MA)掺入脂质体中可诱导凋亡并抑制二氢睾酮(DHT)依赖性仓鼠侧腹器官皮脂腺的生长。我们比较了脂质体 4-MA 和溶剂配方 4-MA 的局部应用,观察到脂质体 4-MA 的局部应用具有选择性疗效,仅在治疗的仓鼠侧腹器官中减少大小并诱导凋亡。通过脱氧尿苷末端标记转移酶测定和观察浓缩和碎片化的核,观察到脂质体 4-MA 在治疗的侧腹器官皮脂腺细胞中诱导的凋亡。当 4-MA 以不含脂质体的乙醇和甘油配方局部应用时,选择性疗效丧失。与对照组相比,脂质体 4-MA 对前列腺重量、睾酮/DHT 比值或体重增加没有显著影响,表明脂质体 4-MA 局部应用治疗痤疮等病理过程的安全性和疗效。

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