标题:The protective effects of insulin-like growth factor-1 on neurochemical phenotypes of dorsal root ganglion neurons with BDE-209-induced neurotoxicity in vitro
作者:Bai, Xue; Chen, Tianhua; Gao, Yang; Li, Hao; Li, Zhenzhong; Liu, Zhen
作者机构:[Bai, Xue; Chen, Tianhua; Li, Zhenzhong; Liu, Zhen] Shandong Univ, Sch Med, Dept Anat, 44 Wenhua Xi Rd, Jinan 250012, Shandong, Peoples R China.; [G 更多
通讯作者:Liu, Z
通讯作者地址:[Liu, Z]Shandong Univ, Sch Med, Dept Anat, 44 Wenhua Xi Rd, Jinan 250012, Shandong, Peoples R China.
来源:TOXICOLOGY AND INDUSTRIAL HEALTH
出版年:2017
卷:33
期:3
页码:250-264
DOI:10.1177/0748233716638004
关键词:Insulin-like growth factor-1; polybrominated diphenyl ether;; neurotoxicity; neuron; dorsal root ganglion
摘要:Polybrominated diphenyl ethers (PBDEs) exist extensively in the environment as contaminants, in which 2,2',3,3',4,4',5,5',6,6'-decabrominated diphenyl ether (BDE-209) is the most abundant PBDE found in human samples. BDE-209 has been shown to cause neurotoxicity of primary sensory neurons with few effective therapeutic options available. Here, cultured dorsal root ganglion (DRG) neurons were used to determine the therapeutic effects of insulin-like growth factor-1 (IGF-1) on BDE-209-induced neurotoxicity. The results showed that IGF-1 promoted neurite outgrowth and cell viability of DRG neurons with BDE-209-induced neurotoxicity. IGF-1 inhibited oxidative stress and apoptotic cell death caused by BDE-209 exposure. IGF-1 could reverse the decrease in growth-associated protein-43 (GAP-43) and calcitonin gene-related peptide (CGRP), but not neurofilament-200 (NF-200), expression resulting from BDE-209 exposure. The effects of IGF-1 could be blocked by the extracellular signal-regulated protein kinase (ERK1/2) inhibitor PD98059 and the phosphatidylinositol 3-kinase (PI3K) inhibitor LY294002, either alone or in combination. IGF-1 may play an important role in neuroprotective effects on DRG neurons with BDE-209-induced neurotoxicity through inhibiting oxidative stress and apoptosis and regulating GAP-43 and CGRP expression of DRG neurons. Both ERK1/2 and PI3K/Akt signaling pathways were involved in the effects of IGF-1. Thus, IGF-1 might be one of the therapeutic agents on BDE-209-induced neurotoxicity.
收录类别:SCOPUS;SCIE
WOS核心被引频次:1
Scopus被引频次:2
资源类型:期刊论文
原文链接:https://www.scopus.com/inward/record.uri?eid=2-s2.0-85018206961&doi=10.1177%2f0748233716638004&partnerID=40&md5=4756f519054b8d664902faa8f539b518
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