设计师类固醇:过去,现在和未来

J. Fourcroy
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引用次数: 5

摘要

当前的治疗和未来的药物开发取决于对雄激素合成代谢类固醇的发展和调控历史的理解。1962年之后,多项监管变化改变了许多这类化合物的可用性,增加了证明这类药物安全性和有效性的必要性。体育界首先认识到雄激素合成代谢类固醇的合成代谢作用,并使用了大量这些化合物作为“兴奋剂”。随之而来的是一个非法市场,以及旨在逃避检测的新型人造类固醇的开发。最近的发现今天任何新的设计类固醇必须证明安全性和有效性的预期用途。虽然新的雄激素制剂允许更安全和更生理的递送,未来的发展将允许组织选择性治疗,如骨或肌肉。一个有前途的新发展领域包括选择性雄激素受体调节剂。临床医生必须了解雄激素合成代谢类固醇在临床实践中的作用,以提供患者护理。未来非甾体化合物的发展——选择性雄激素受体调节剂——可能会提供更安全、更有效的治疗方法。必须密切注意这些新药的发展。
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Designer steroids: past, present and future
Purpose of reviewCurrent therapy and future drug development depend on an understanding of the developmental and regulatory history of androgenic anabolic steroids. After 1962, multiple regulatory changes altered the availability of many of these compounds and added the need to demonstrate both safety and efficacy for this class of drugs. The athletic community first recognized the anabolic effect of androgenic anabolic steroids and used a multitude of these compounds for ‘doping’. What followed was an illicit market and the development of new designer steroids designed to elude detection. Recent findingsToday any new designer steroid must demonstrate both safety and effectiveness for the intended use. Although new androgen formulations allow safer and more physiologic delivery, future development will allow tissue selective therapies, such as bone or muscle. One promising new area of development includes selective androgen receptor modulators. SummaryClinicians must understand the role of androgenic anabolic steroids in clinical practice to provide patient care. Future development of non-steroidal compounds – selective androgen receptor modulators – will perhaps provide safer and more effective therapy. The development of these new drugs must be watched.
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