Ajibo Doris Nnena, Orish Chinna Nneka, Ruggieri Flavia, Bocca Beatrice, Battistini Beatrice, Frazzoli Chiara, Orish Fortune Chimelie, Orisakwe Orish E
Department of Experimental Pharmacology & Toxicology, Faculty of Pharmacy, University of Port Harcourt, PMB, 5323, Port Harcourt, Rivers State, Nigeria.
Department of Anatomy, College of Health Sciences University of Port Harcourt, PMB, 5323, Port Harcourt, Rivers State, Nigeria.
Biol Trace Elem Res. 2024 Aug;202(8):3538-3564. doi: 10.1007/s12011-023-03965-w. Epub 2023 Nov 28.
There is increasing evidence that the imbalance of metals as cobalt (Co) and chromium (Cr) may increase the risk of development and progression of neurodegenerative diseases (NDDs). The human exposure to Co and Cr is derived mostly from industry, orthopedic implants, and polluted environments. Neurological effects of Co and Cr include memory deficit, olfactory dysfunction, spatial disorientation, motor neuron disease, and brain cancer. Mechanisms of Co and Cr neurotoxicity included DNA damage and genomic instability, epigenetic changes, mitochondrial disturbance, lipid peroxidation, oxidative stress, inflammation, and apoptosis. This paper seeks to overview the Co and Cr sources, the mechanisms by which these metals induce NDDs, and their levels in fluids of the general population and patients affected by NDDs. To this end, evidence of Co and Cr unbalance in the human body, mechanistic data, and neurological symptoms were collected using in vivo mammalian studies and human samples.
越来越多的证据表明,钴(Co)和铬(Cr)等金属失衡可能会增加神经退行性疾病(NDDs)发生和发展的风险。人类接触Co和Cr主要源于工业、骨科植入物以及受污染的环境。Co和Cr对神经的影响包括记忆缺陷、嗅觉功能障碍、空间定向障碍、运动神经元疾病和脑癌。Co和Cr神经毒性的机制包括DNA损伤和基因组不稳定、表观遗传变化、线粒体紊乱、脂质过氧化、氧化应激、炎症和细胞凋亡。本文旨在概述Co和Cr的来源、这些金属诱发NDDs的机制,以及它们在普通人群和受NDDs影响患者的体液中的水平。为此,利用体内哺乳动物研究和人体样本收集了人体中Co和Cr失衡的证据、机制数据以及神经症状。