Retrotope, Inc., Los Altos, CA, USA.
Trends Pharmacol Sci. 2020 Apr;41(4):236-248. doi: 10.1016/j.tips.2020.01.010. Epub 2020 Feb 26.
Oxidative stress is a common feature of genetic and idiopathic neurological diseases that thus far have been intractable to drug therapy. Polyunsaturated fatty acids (PUFAs) form cellular, mitochondrial, retinal, and other membranes highly important in neuronal function. However, PUFAs are susceptible to the noxious lipid peroxidation (LPO) chain reaction, which is a common feature of various neurological and age-related pathologies, making this pathway an attractive target for therapeutic intervention. Regioselective deuteration that reinforces oxidation-prone, bis-allylic sites of PUFAs is a novel, nonantioxidant treatment modality that dramatically reduces LPO, potentially mitigating numerous diseases through preservation of membrane properties and amelioration of oxidative stress. Animal disease models and several ongoing human clinical trials highlight the potential of the deuterated-PUFA (D-PUFA) drug candidates currently in development.
氧化应激是遗传和特发性神经疾病的共同特征,迄今为止,这些疾病对药物治疗仍然难以治疗。多不饱和脂肪酸 (PUFA) 形成细胞、线粒体、视网膜和其他对神经元功能非常重要的膜。然而,PUFA 容易受到有害的脂质过氧化 (LPO) 连锁反应的影响,LPO 是各种神经和与年龄相关的病理学的共同特征,这使得该途径成为治疗干预的有吸引力的目标。加强 PUFAs 中易氧化的双烯丙基位点的区域选择性氘化是一种新颖的非抗氧化治疗方式,可通过维持膜特性和减轻氧化应激来显著降低 LPO,从而潜在地改善多种疾病。动物疾病模型和几项正在进行的人类临床试验突出了目前正在开发的氘化 -PUFA (D-PUFA) 药物候选物的潜力。