Belozersky Institute of Physico-Chemical Biology, Lomonosov Moscow State University, Moscow, 119234, Russia.
Department of Biochemistry, Sechenov University, Moscow, 119991, Russia.
Biochemistry (Mosc). 2024 Jul;89(7):1161-1182. doi: 10.1134/S0006297924070010.
Charcot-Marie-Tooth (CMT) neuropathy is a polygenic disorder of peripheral nerves with no effective cure. Thiamine (vitamin B1) is a neurotropic compound that improves neuropathies. Our pilot study characterizes therapeutic potential of daily oral administration of thiamine (100 mg) in CMT neuropathy and its molecular mechanisms. The patient hand grip strength was determined before and after thiamine administration along with the blood levels of the thiamine coenzyme form (thiamine diphosphate, ThDP), activities of endogenous holo-transketolase (without ThDP in the assay medium) and total transketolase (with ThDP in the assay medium), and transketolase activation by ThDP [1 - (holo-transketolase/total transketolase),%], corresponding to the fraction of ThDP-free apo-transketolase. Single cases of administration of sulbutiamine (200 mg) or benfotiamine (150 mg) reveal their effects on the assayed parameters within those of thiamine. Administration of thiamine or its pharmacological forms increased the hand grip strength in the CMT patients. Comparison of the thiamin status in patients with different forms of CMT disease to that of control subjects without diagnosed pathologies revealed no significant differences in the average levels of ThDP, holo-transketolase, or relative content of holo and apo forms of transketolase. However, the regulation of transketolase by thiamine/ThDP differed in the control and CMT groups: in the assay, ThDP activated transketolase from the control individuals, but not from CMT patients. Thiamine administration paradoxically decreased endogenous holo-transketolase in CMT patients; this effect was not observed in the control group. Correlation analysis revealed sex-specific differences in the relationship between the parameters of thiamine status in both the control subjects and patients with the CMT disease. Thus, our findings link physiological benefits of thiamine administration in CMT patients to changes in their thiamine status, in particular, the blood levels of ThDP and transketolase regulation.
腓骨肌萎缩症(CMT)神经病是一种多发性周围神经疾病,目前尚无有效治疗方法。硫胺素(维生素 B1)是一种神经营养化合物,可改善神经病变。我们的初步研究描述了每日口服硫胺素(100mg)治疗 CMT 神经病的治疗潜力及其分子机制。在给予硫胺素前后,我们测定了患者的手握力,以及硫胺素辅酶形式(硫胺素二磷酸,ThDP)的血液水平、内源性全转酮醇酶(测定介质中不含 ThDP)和总转酮醇酶(测定介质中含 ThDP)的活性,以及 ThDP 对转酮醇酶的激活作用[1-(全转酮醇酶/总转酮醇酶),%],对应于无 ThDP 的脱辅基转酮醇酶的分数。硫胺素、丁硫胺素(200mg)或苯磷硫胺(150mg)单次给药,其对上述测定参数的影响均在硫胺素范围内。硫胺素或其药理学形式的给药增加了 CMT 患者的手握力。将不同形式 CMT 疾病患者的硫胺素状态与未诊断出病理的对照组进行比较,发现 ThDP、全转酮醇酶或转酮醇酶全酶和脱辅基酶的相对含量的平均水平没有显著差异。然而,硫胺素/ThDP 对转酮醇酶的调节在对照组和 CMT 组之间存在差异:在测定中,ThDP 激活了对照组个体的转酮醇酶,但不激活 CMT 患者的转酮醇酶。硫胺素给药出乎意料地降低了 CMT 患者的内源性全转酮醇酶;而在对照组中则未观察到这种效应。相关性分析显示,对照组和 CMT 患者的硫胺素状态参数之间的关系存在性别特异性差异。因此,我们的研究结果将 CMT 患者给予硫胺素的生理益处与他们的硫胺素状态的变化联系起来,特别是 ThDP 和转酮醇酶调节的血液水平。