Lang Ryan M, Chawla Riddhi, Patel Sugandha, Abrams Charles K, Dobrowsky Rick T
Department of Pharmacology and Toxicology, University of Kansas, Lawrence, Kansas 66045, United States.
Department of Neurology and Rehabilitation, College of Medicine, University of Illinois Chicago, Chicago Illinois 60612, United States.
ACS Pharmacol Transl Sci. 2024 Dec 13;8(1):124-135. doi: 10.1021/acsptsci.4c00464. eCollection 2025 Jan 10.
Mutations in connexin 32 (Cx32) are a common cause of Charcot-Marie-Tooth 1X (CMT1X) disease, an inherited peripheral neuropathy characterized by progressive neuromuscular weakness and demyelination. There are no approved pharmacologic therapies for CMT1X, and identifying new treatments that slow the onset and severity of neuromuscular decline may aid disease management. Cemdomespib is an orally bioavailable small molecule that improved demyelination and neuromuscular junction (NMJ) morphology in mice lacking Cx32 expression. However, whether a similar efficacy may manifest in models of CMT1X arising from Cx32 mutations that cause the organellar accumulation of the protein was unclear. Additionally, it was unclear whether cemdomespib therapy slowed the rate of demyelination/NMJ degeneration or stabilized nerve and NMJ morphology to levels present at the initiation of drug therapy. To address these issues, 4-month-old R75W-Cx32 mice, which accumulate the mutant Cx32 in golgi, were treated for 0, 10, or 20 weeks with 0 or 3 mg/kg cemdomespib. Grip strength, motor nerve conduction velocity (MNCV), femoral nerve myelination, and NMJ morphology were quantified. Daily drug therapy significantly slowed the decline in grip strength over the course of treatment, while 20 weeks of drug treatment significantly improved MNCV and decreased the g-ratio and the number of thinly myelinated femoral nerve axons. Similarly, 20 weeks of cemdomespib therapy improved the NMJ morphology and the overlap between presynaptic (synaptophysin) and postsynaptic (α-bungarotoxin) markers. These data show that cemdomespib therapy slows the rate of neuromuscular decline and demyelination and may present a disease-modifying approach for patients with gain-of-function Cx32 mutations.
连接蛋白32(Cx32)突变是夏科-马里-图斯病1X型(CMT1X)的常见病因,这是一种遗传性周围神经病变,其特征为进行性神经肌肉无力和脱髓鞘。目前尚无批准用于CMT1X的药物治疗方法,确定能延缓神经肌肉衰退发作和严重程度的新治疗方法可能有助于疾病管理。塞姆多司匹布是一种口服生物可利用的小分子,可改善缺乏Cx32表达的小鼠的脱髓鞘和神经肌肉接头(NMJ)形态。然而,在由导致该蛋白细胞器积累的Cx32突变引起的CMT1X模型中是否会表现出类似疗效尚不清楚。此外,尚不清楚塞姆多司匹布治疗是否会减缓脱髓鞘/NMJ变性的速度,或将神经和NMJ形态稳定至药物治疗开始时的水平。为解决这些问题,对4月龄在高尔基体中积累突变型Cx32的R75W-Cx32小鼠,分别用0或3mg/kg塞姆多司匹布治疗0、10或20周。对握力、运动神经传导速度(MNCV)、股神经髓鞘形成和NMJ形态进行了量化。每日药物治疗在治疗过程中显著减缓了握力下降,而20周的药物治疗显著改善了MNCV,并降低了g比值和薄髓鞘股神经轴突数量。同样,20周的塞姆多司匹布治疗改善了NMJ形态以及突触前(突触素)和突触后(α-银环蛇毒素)标记物之间的重叠。这些数据表明,塞姆多司匹布治疗可减缓神经肌肉衰退和脱髓鞘速度,可能为功能获得性Cx32突变患者提供一种疾病修饰方法。