Haisco Pharmaceutical Group Co., Ltd., Chengdu, China.
Saifu Laboratories Co., Ltd., Beijing, China; SAFE Medical Technology Co., Ltd., Hebei, China.
Regul Toxicol Pharmacol. 2024 Dec;154:105731. doi: 10.1016/j.yrtph.2024.105731. Epub 2024 Oct 23.
HSK21542 is a peripherally-restricted kappa opioid receptor (KOR) agonist developed for pain treatment. Because of the CNS pharmacological concern of opioid receptor activation, such as physical dependence and addiction potential, an assessment of abuse potential of HSK21542 was required prior to marketing approval. The preclinical abuse potential assessments for HSK21542 included the following studies: 1) intravenous self-administration study to explore the relative reinforcing efficacy in rats self-administering remifentanil; 2) rat drug discrimination study to examine the pharmacological similarity of the interoceptive or subjective effects of HSK21542 in rats discriminating pentazocine; 3) rat conditioned place preference (CPP) paradigm to test the rewarding effects; 4) rat natural physical dependence-spontaneous withdrawal study in rats chronically treated with HSK21542; 5) naloxone-precipitated withdrawal assay following chronic HSK21542 exposure to evaluate its physical dependence potential. The results showed that HSK21542 was devoid of behavioral evidence of positive reinforcing effect and did not share similar discriminative stimulus effects with pentazocine. HSK21542 also did not produce CPP in rats. In addition, HSK21542 did not produce spontaneous withdrawal or naloxone-precipitated withdrawal in rats with chronic treatments. Collectively, these preclinical findings suggest that HSK21542 has no abuse potential in animals, which demonstrate low abuse potential in humans.
HSK21542 是一种外周受限的 κ 阿片受体 (KOR) 激动剂,开发用于治疗疼痛。由于阿片受体激活的中枢神经系统药理学问题,如身体依赖和成瘾潜力,在获得市场批准之前,需要对 HSK21542 的滥用潜力进行评估。HSK21542 的临床前滥用潜力评估包括以下研究:1)静脉自我给药研究,以探索大鼠自我给予瑞芬太尼的相对强化效力;2)大鼠药物辨别研究,以检查 HSK21542 在大鼠辨别戊唑辛时的内感受或主观效应的药理学相似性;3)大鼠条件性位置偏爱 (CPP) 范式,以测试奖赏效应;4)大鼠自然身体依赖-自发戒断研究,在大鼠慢性给予 HSK21542 时进行;5)纳洛酮诱发的戒断试验,在慢性 HSK21542 暴露后评估其身体依赖潜力。结果表明,HSK21542 没有行为阳性强化作用的证据,也与戊唑辛没有相似的辨别刺激作用。HSK21542 也不会在大鼠中产生 CPP。此外,HSK21542 在慢性治疗的大鼠中不会产生自发戒断或纳洛酮诱发的戒断。总的来说,这些临床前发现表明,HSK21542 在动物中没有滥用潜力,这表明它在人类中具有低滥用潜力。