Myxobacterial natural products: An under-valued source of products for drug discovery for neurological disorders

被引:22
作者
Dehhaghi, Mona [1 ,2 ,3 ]
Mohammadipanah, Fatemeh [1 ,2 ]
Guillemin, Gilles J. [3 ]
机构
[1] Univ Tehran, Sch Biol, Dept Microbial Biotechnol, Tehran, Iran
[2] Univ Tehran, Coll Sci, Ctr Excellence Phylogeny Living Organisms, Tehran, Iran
[3] Macquarie Univ, Fac Med & Hlth Sci, Neuropharmacol Grp, Sydney, NSW, Australia
基金
澳大利亚研究理事会;
关键词
Drug discovery; Neurodegenerative diseases; Natural products; Myxobacteria; SORANGIUM-CELLULOSUM MYXOBACTERIA; MICROTUBULE-STABILIZING AGENTS; POLYUNSATURATED FATTY-ACIDS; GLIDING BACTERIA; STRUCTURE ELUCIDATION; AXONAL-TRANSPORT; MYXOCOCCUS-XANTHUS; CHONDROMYCES-CROCATUS; TERRESTRIAL MYXOBACTERIUM; CYSTOBACTER-FERRUGINEUS;
D O I
10.1016/j.neuro.2018.02.017
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
Age-related disorders impose noticeable financial and emotional burdens on society. This impact is becoming more prevalent with the increasing incidence of neurodegenerative diseases and is causing critical concerns for treatment of patients worldwide. Parkinson's disease, Alzheimer's disease, multiple sclerosis and motor neuron disease are the most prevalent and the most expensive to treat neurodegenerative diseases globally. Therefore, exploring effective therapies to overcome these disorders is a necessity. Natural products and their derivatives have increasingly attracted attention in drug discovery programs that have identified microorganisms which produce a large range of metabolites with bioactive properties. Myxobacteria, a group of Gram-negative bacteria with large genome size, produce a wide range of secondary metabolites with significant chemical structures and a variety of biological effects. They are potent natural product producers. In this review paper, we attempt to overview some secondary metabolites synthesized by myxobacteria with neuroprotective activity through known mechanisms including production of polyunsaturated fatty acids, reduction of apoptosis, immunomodulation, stress reduction of endoplasmic reticulum, stabilization of microtubules, enzyme inhibition and serotonin receptor modulation. (C) 2018 Elsevier B.V. All rights reserved.
引用
收藏
页码:195 / 203
页数:9
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