Gupta Saurabh, Khan Arzoo, Vishwas Sukriti, Gulati Monica, Gurjeet Singh Thakur, Dua Kamal, Kumar Singh Sachin, Najda Agnieszka, Sayed Amany A, Almeer Rafa, Abdel-Daim Mohamed M
Chitkara College of Pharmacy, Chitkara University, Punjab 140401, India.
School of Pharmaceutical Sciences, Lovely Professional University, Punjab 144411, India.
Med Hypotheses. 2021 Aug;153:110639. doi: 10.1016/j.mehy.2021.110639. Epub 2021 Jun 29.
Huntington disease (HD) is a type of neurodegenerative disease that is characterized by presence of multiple repeats (more than 36) of cytosine-adenine-guanine (CAG) trinucleotides and mutated huntingtin (mHtt). This can further lead to oxidative stress, enhancement in level of ROS/RNS, mitochondrial dysfunction and neuroinflammations. Many clinical and preclinical trials have been conducted so far for the effective treatment of HD however, none of the drugs has shown complete relief. The regeneration of neurons is a very complicated process and associated with multiple pathological pathways. Hence, finding a unique solution using single drug that could act on multiple pathological pathways is really cumbersome. In the proposed hypothesis the use of demethyleneberberine (DMB) as a potential anti-HD agent has been explained. It is a metabolite of berberine and reported to act on multiple mechanistic pathways that are responsible for HD. Present article highlights new mechanistic insights through which DMB inhibits ROS/RNS, oxidative stress, mitochondrial dysfunctions and neuroinflammation such as NFκB, TNF-α, IL-6 and IL-8, cytokinin. Further its action on cellular apoptosis and neuronal cell death are also reported.
亨廷顿舞蹈症(HD)是一种神经退行性疾病,其特征是存在多个胞嘧啶 - 腺嘌呤 - 鸟嘌呤(CAG)三核苷酸重复序列(超过36个)以及突变的亨廷顿蛋白(mHtt)。这会进一步导致氧化应激、活性氧/氮(ROS/RNS)水平升高、线粒体功能障碍和神经炎症。迄今为止,已经进行了许多临床和临床前试验以有效治疗HD,然而,没有一种药物能完全缓解症状。神经元再生是一个非常复杂的过程,与多种病理途径相关。因此,找到一种能作用于多种病理途径的单一药物的独特解决方案非常困难。在所提出的假说中,已解释了使用去甲基小檗碱(DMB)作为潜在抗HD药物的情况。它是小檗碱的一种代谢产物,据报道可作用于导致HD的多种机制途径。本文重点介绍了DMB抑制ROS/RNS、氧化应激、线粒体功能障碍和神经炎症(如NFκB、TNF-α、IL-6和IL-8、细胞因子)的新机制见解。此外,还报道了其对细胞凋亡和神经元细胞死亡的作用。