Center for Pain and the Brain, Department of Anesthesia, Critical Care and Pain Medicine, Boston Children's Hospital, Boston, MA, USA.
Rhode Island Department of Behavioral Healthcare, Cranston, RI, USA.
Sci Rep. 2020 Mar 27;10(1):5617. doi: 10.1038/s41598-020-62556-0.
Metabolic hormones stabilize brain reward and motivational circuits, whereas excessive opioid consumption counteracts this effect and may impair metabolic function. Here we addressed the role of metabolic processes in the course of the agonist medication-assisted treatment for opioid use disorder (OUD) with buprenorphine or methadone. Plasma lipids, hemoglobin A1C, body composition, the oral glucose tolerance test (oGTT) and the Sweet Taste Test (STT) were measured in buprenorphine- (n = 26) or methadone (n = 32)- treated subjects with OUD. On the whole, the subjects in both groups were overweight or obese and insulin resistant; they displayed similar oGTT and STT performance. As compared to methadone-treated subjects, those on buprenorphine had significantly lower rates of metabolic syndrome (MetS) along with better values of the high-density lipoproteins (HDL). Subjects with- vs. without MetS tended to have greater addiction severity. Correlative analyses revealed that more buprenorphine exposure duration was associated with better HDL and opioid craving values. In contrast, more methadone exposure duration was associated with worse triglycerides-, HDL-, blood pressure-, fasting glucose- and hemoglobin A1C values. Buprenorphine appears to produce beneficial HDL- and craving effects and, contrary to methadone, its role in the metabolic derangements is not obvious. Our data call for further research aimed at understanding the distinctive features of buprenorphine metabolic effects vis-à-vis those of methadone and their potential role in these drugs' unique therapeutic profiles.
代谢激素稳定大脑奖赏和动机回路,而过量的阿片类药物消耗则会抵消这种作用,并可能损害代谢功能。在这里,我们研究了代谢过程在阿片类药物使用障碍(OUD)的激动剂药物辅助治疗中(用丁丙诺啡或美沙酮)的作用。我们测量了接受丁丙诺啡(n=26)或美沙酮(n=32)治疗的 OUD 患者的血浆脂质、糖化血红蛋白 A1C、身体成分、口服葡萄糖耐量试验(oGTT)和甜味测试(STT)。总的来说,两组受试者均超重或肥胖且胰岛素抵抗;他们的 oGTT 和 STT 表现相似。与美沙酮治疗的受试者相比,丁丙诺啡治疗的受试者具有显著更低的代谢综合征(MetS)发生率,以及更好的高密度脂蛋白(HDL)值。与没有 MetS 的受试者相比,有 MetS 的受试者的成瘾严重程度更高。相关分析显示,丁丙诺啡的暴露时间越长,HDL 和阿片类药物渴求值越好。相比之下,美沙酮的暴露时间越长,甘油三酯、HDL、血压、空腹血糖和糖化血红蛋白值越差。丁丙诺啡似乎产生有益的 HDL 和渴求效应,与美沙酮相反,其在代谢紊乱中的作用并不明显。我们的数据呼吁进一步研究,旨在了解丁丙诺啡代谢效应与美沙酮代谢效应的区别及其在这些药物独特治疗特征中的潜在作用。