Rosen J, Negro-Vilar A
Ligand Pharmaceuticals, San Diego, CA 92121, USA.
J Musculoskelet Neuronal Interact. 2002 Mar;2(3):222-4.
A novel approach to the treatment of osteoporosis in men, and possibly women, is the development of selective androgen receptor modulators (SARMs) that can stimulate formation of new bone with substantially diminished proliferative activity in the prostate, as well as reduced virilizing activity in women. Over the last several years, we have developed a program to discover and develop novel, non-steroidal, orally-active selective androgen receptor modulators (SARMs) that provide improved therapeutic benefits and reduce risk and side effects. In recent studies, we have used a skeletally mature orchiectomized (ORX) male rat as an animal model of male hypogonadism for assessing the efficacy of LGD2226, a nonsteroidal, non-aromatizable, and non-5alpha-reducible SARM. We assessed the activity of LGD2226 on bone turnover, bone mass and bone strength, and also evaluated the effects exerted on classic androgen-dependent targets, such as prostate, seminal vesicles and muscle. A substantial loss of bone density was observed in ORX animals, and this loss was prevented by SARMs, as well as standard androgens. Biochemical markers of bone turnover revealed an early increase of bone resorption in androgen-deficient rats that was repressed in ORX animals treated with the oral SARM, LGD2226, during a 4-month treatment period. Differences in architectural properties and bone strength were detected by histomorphometric and mechanical analyses, demonstrating beneficial effects of LGD2226 on bone quality in androgen-deficient rats. Histomorphometric analysis of cortical bone revealed distinct anabolic activity of LGD2226 in periosteal bone. LGD2226 was able to prevent bone loss and maintain bone quality in ORX rats by stimulating bone formation, while also inhibiting bone turnover. LGD2226 also exerted anabolic activity on the levator ani muscle. Taken together, these results suggest that orally-active, non-steroidal SARMs may be useful therapeutics for both muscle and bone in elderly hypogonadal men through their anabolic activities. Since SARMs both prevent bone loss, and also stimulate formation of new bone, they may have significant advantages relative to currently used anti-resorptive therapies. Coupled with their activity in muscle and their ability to maintain or restore libido, they offer new therapeutic approaches for male and female hormone replacement.
一种治疗男性(可能也适用于女性)骨质疏松症的新方法是开发选择性雄激素受体调节剂(SARM),这类药物能够刺激新骨形成,同时大幅降低前列腺的增殖活性,并减少女性的男性化活性。在过去几年里,我们开展了一个项目,旨在发现和开发新型的、非甾体的、口服活性的选择性雄激素受体调节剂(SARM),以提供更好的治疗效果并降低风险和副作用。在最近的研究中,我们使用骨骼成熟的去势(ORX)雄性大鼠作为男性性腺功能减退的动物模型,来评估LGD2226的疗效,LGD2226是一种非甾体、不可芳香化且不可5α还原的SARM。我们评估了LGD2226对骨转换、骨量和骨强度的活性,还评估了其对经典雄激素依赖性靶器官(如前列腺、精囊和肌肉)的影响。在ORX动物中观察到骨密度大幅下降,而SARM以及标准雄激素可预防这种下降。骨转换的生化标志物显示,雄激素缺乏的大鼠骨吸收早期增加,但在用口服SARM LGD2226治疗4个月的ORX动物中,这种增加受到抑制。通过组织形态计量学和力学分析检测到结构特性和骨强度的差异,证明LGD2226对雄激素缺乏大鼠的骨质量有有益影响。皮质骨的组织形态计量学分析显示LGD2226在骨膜骨中有明显的合成代谢活性。LGD2226能够通过刺激骨形成同时抑制骨转换,来预防ORX大鼠的骨质流失并维持骨质量。LGD2226还对提肛肌发挥合成代谢活性。综上所述,这些结果表明,口服活性非甾体SARM通过其合成代谢活性,可能对老年性腺功能减退男性的肌肉和骨骼都是有用的治疗药物。由于SARM既能预防骨质流失,又能刺激新骨形成,它们相对于目前使用的抗吸收疗法可能具有显著优势。再加上它们在肌肉中的活性以及维持或恢复性欲的能力,它们为男性和女性激素替代提供了新的治疗方法。