Ahlem Clarence N, Kennedy Michael R, Page Theodore M, Reading Christopher L, White Steven K, McKenzie John J, Cole Phaedra I, Stickney Dwight R, Frincke James M
Int J Clin Exp Med. 2011;4(2):119-35. Epub 2011 Apr 23.
17α-Ethynyl-androst-5ene-3β, 7β, 17β-triol (HE3286) is an orally bioavailable analogue of androst-5-ene-3β,7β,17β-triol, a non-glucocorticoid anti-inflammatory metabolite of the adrenal steroid, dehydroepiandrosterone. The pharmacology of HE3286 was characterized in preparation for clinical trials in type 2 diabetes mellitus and other diseases of inflammation. Interactions with nuclear hormone receptors and P450 enzymes were measured in vitro. Drug metabolism was studied preclinically in mice, rats, dogs, and monkeys. Neurological and cardiopulmonary safety and dose-ranging and chronic toxicity studies were conducted in rats and dogs in accordance with FDA guidelines. Pharmacokinetics and metabolites were measured in Phase I clinical trials. HE3286 was differentially metabolized between species. HE3286 and metabolites did not bind or transactivate steroid binding nuclear hormone receptors or inhibit P450 enzymes. There were no adverse effects in safety pharmacology and canine toxicology studies. Although HE3286 did not elicit systemic toxicity in rats, mild estrogenic effects were observed, but without apparent association to hormonal changes. Safety margins were greater than 20-fold in rats and dogs with respect to the most commonly used clinical dose of 10 mg/day. The terminal half-life in humans was 8 hours in males and 5.5 hours in females. HE3286 is the first derivative of the DHEA metabolome to undergo a comprehensive pharmacological and safety evaluation. The results of these investigations have shown that HE3286 has a low potential for toxicity and possesses pharmacological properties generally suitable for use in human medicine. The favorable profile of HE3286 warrants further exploration of this new class of anti-inflammatory agents.
17α-乙炔基-雄甾-5-烯-3β,7β,17β-三醇(HE3286)是雄甾-5-烯-3β,7β,17β-三醇的口服生物可利用类似物,后者是肾上腺类固醇脱氢表雄酮的一种非糖皮质激素抗炎代谢产物。对HE3286的药理学特性进行了研究,为开展2型糖尿病及其他炎症性疾病的临床试验做准备。在体外测定了其与核激素受体和细胞色素P450酶的相互作用。在小鼠、大鼠、犬和猴身上进行了临床前药物代谢研究。按照美国食品药品监督管理局(FDA)的指导原则,在大鼠和犬身上开展了神经和心肺安全性、剂量范围及慢性毒性研究。在Ⅰ期临床试验中测定了药代动力学和代谢产物。HE3286在不同物种间的代谢存在差异。HE3286及其代谢产物不与类固醇结合核激素受体结合或使其反式激活,也不抑制细胞色素P450酶。在安全性药理学和犬类毒理学研究中未发现不良反应。尽管HE3286在大鼠中未引发全身毒性,但观察到了轻微的雌激素样作用,但与激素变化无明显关联。相对于最常用的临床剂量10毫克/天,大鼠和犬的安全系数大于20倍。在人类中,男性的终末半衰期为8小时,女性为5.5小时。HE3286是脱氢表雄酮代谢组中首个接受全面药理学和安全性评估的衍生物。这些研究结果表明,HE3286的毒性潜力较低,具有一般适用于人类医学的药理学特性。HE3286的良好特性值得进一步探索这类新型抗炎药物。