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Pharmacokinetics and Pharmacodynamics of Nonsteroidal Androgen Receptor Ligands

机译:非甾体雄激素受体配体的药代动力学和药效动力学

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摘要

Testosterone and structurally related anabolic steroids have been used to treat hypogonadism, muscle wasting, osteoporosis, male contraception, cancer cachexia, anemia, and hormone replacement therapy in aging men or age-related frailty; while antiandrogens may be useful for treatment of conditions like acne, alopecia (male-pattern baldness), hirsutism, benign prostatic hyperplasia (BPH) and prostate cancer. However, the undesirable physicochemical and pharmacokinetic properties of steroidal androgen receptor (AR) ligands limited their clinical use. Nonsteroidal AR ligands with improved pharmacological and pharmacokinetic properties have been developed to overcome these problems. This review focuses on the pharmacokinetics, metabolism, and pharmacology of clinically used and emerging nonsteroidal AR ligands, including antagonists, agonists, and selective androgen receptor modulators.
机译:睾丸激素和与结构相关的合成代谢类固醇已被用于治疗老年男性或与年龄相关的体弱症患者的性腺机能减退,肌肉萎缩,骨质疏松,男性避孕,癌症恶病质,贫血和激素替代疗法。而抗雄激素药可用于治疗痤疮,脱发(男性型秃头),多毛症,前列腺增生(BPH)和前列腺癌。但是,甾体雄激素受体(AR)配体的不良理化和药代动力学特性限制了其临床应用。已经开发出具有改善的药理学和药代动力学性质的非甾族AR配体来克服这些问题。这篇综述的重点是临床使用和新兴的非类固醇AR配体的药代动力学,代谢和药理学,包括拮抗剂,激动剂和选择性雄激素受体调节剂。

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