Department of Internal Medicine (Pharmacogenomics), Washington University School of Medicine (J.W., L.Z., A.F., E.C., G.W.D.) and Mitochondria in Motion, Inc. (J.W., L.Z.), St. Louis Missouri.
Department of Internal Medicine (Pharmacogenomics), Washington University School of Medicine (J.W., L.Z., A.F., E.C., G.W.D.) and Mitochondria in Motion, Inc. (J.W., L.Z.), St. Louis Missouri
J Pharmacol Exp Ther. 2024 Oct 18;391(2):361-374. doi: 10.1124/jpet.124.002258.
Mitochondrial dysfunction is a hallmark of many genetic neurodegenerative diseases, but therapeutic options to reverse mitochondrial dysfunction are limited. While recent studies support the possibility of improving mitochondrial fusion/fission dynamics and motility to correct mitochondrial dysfunction and resulting neurodegeneration in Charcot-Marie-Tooth disease (CMT) and other neuropathies, the clinical utility of reported compounds and relevance of preclinical models are uncertain. Here, we describe motor and sensory neuron dysfunction characteristic of clinical CMT type 2 A in a CRISPR/Casp-engineered Mfn2 Thr105Met (T105M) mutant knock-in mouse. We further demonstrate that daily oral treatment with a novel mitofusin activator derived from the natural product piperine can reverse these neurologic phenotypes. Piperine derivative 8015 promoted mitochondrial fusion and motility in Mfn2-deficient cells in a mitofusin-dependent manner and reversed mitochondrial dysfunction in cultured fibroblasts and reprogrammed motor neurons from a human CMT2A patient carrying the MFN2 T105M mutation. Like previous mitofusin activators, 8015 exhibited stereospecific functionality, but the more active stereoisomer, 8015-P2, is unique in that it has subnanomolar potency and undergoes entero-hepatic recirculation which extends its in vivo half-life. Daily administration of 8015-P2 to Mfn2 T105M knock-in mice for 6 weeks normalized neuromuscular and sensory dysfunction and corrected histological/ultrastructural neurodegeneration and neurogenic myoatrophy. These studies describe a more clinically relevant mouse model of CMT2A and an improved mitofusin activator derived from piperine. We posit that 8015-P2 and other piperine derivatives may benefit CMT2A or other neurodegenerative conditions wherein mitochondrial dysdynamism plays a contributory role. SIGNIFICANCE STATEMENT: Mitochondrial dysfunction is widespread and broadly contributory in neurodegeneration, but difficult to target therapeutically. Here, we describe 8015-P2, a new small molecule mitofusin activator with ∼10-fold greater potency and improved in vivo pharmacokinetics versus comparators, and demonstrate its rapid reversal of sensory and motor neuron dysfunction in an Mfn2 T105M knock-in mouse model of Charcot-Marie-Tooth disease type 2 A. These findings further support the therapeutic approach of targeting mitochondrial dysdynamism in neurodegeneration.
线粒体功能障碍是许多遗传性神经退行性疾病的标志,但逆转线粒体功能障碍的治疗选择有限。尽管最近的研究支持改善线粒体融合/裂变动力学和运动性以纠正 Charcot-Marie-Tooth 病(CMT)和其他神经病变中的线粒体功能障碍和由此导致的神经退行性变的可能性,但报告的化合物的临床实用性和临床前模型的相关性尚不确定。在这里,我们描述了 CRISPR/Cas 工程 Mfn2 Thr105Met(T105M)突变敲入小鼠中临床 CMT 2A 型的运动和感觉神经元功能障碍。我们进一步证明,新型 mitofusin 激活剂 8015 的每日口服治疗可逆转这些神经表型。哌啶衍生物 8015 以依赖于 mitofusin 的方式促进 Mfn2 缺陷细胞中的线粒体融合和运动性,并逆转培养的成纤维细胞和携带 MFN2 T105M 突变的人类 CMT2A 患者的重编程运动神经元中的线粒体功能障碍。与以前的 mitofusin 激活剂一样,8015 表现出立体特异性功能,但更活跃的立体异构体 8015-P2 的独特之处在于它具有亚纳摩尔的效力,并经历肠肝再循环,从而延长了其体内半衰期。8015-P2 每日给药 6 周可使 Mfn2 T105M 敲入小鼠的神经肌肉和感觉功能正常化,并纠正组织学/超微结构神经退行性变和神经源性肌萎缩。这些研究描述了一种更具临床相关性的 CMT2A 小鼠模型和一种源自胡椒碱的改良 mitofusin 激活剂。我们假设 8015-P2 和其他胡椒碱衍生物可能有益于 CMT2A 或其他其中线粒体功能障碍起作用的神经退行性疾病。