(+)-Naloxone inhibits morphine-induced chemotaxis via prevention of heat shock protein 90 cleavage in microglia
(+)-Naloxone inhibits morphine-induced chemotaxis via prevention of heat shock protein 90 cleavage in microglia
复制标题
DOI：
10.1016/j.jfma.2014.12.004
复制
发表时间：
2015-05-01
影响因子：
3.2
通讯作者：
Wong, Chih-Shung
中科院分区：
文献类型：
--
作者：
Tsai, Ru-Yin;Cheng, Yu-Che;Wong, Chih-Shung
Background/Purpose: Microglia have a crucial role in maintaining neuronal homeostasis in the central nervous system. Immune factors released from microglia have important roles in nociceptive signal transduction. Activation of microglia seems to be a shared mechanism in pathological pain and morphine tolerance because pharmacological attenuation of microglia activation provides satisfactory management in both situations.Methods: In the present study, we investigated the effect of 1 nM (+)-naloxone, which is not an opioid receptor antagonist, on morphine-induced activation of microglia EOC13.31 cells.Results: Our results showed that 1 mM morphine enhanced microglia activation and migration, decreased alpha-tubulin acetylation, and induced heat shock protein 90 (HSP90) fragmentation and histone deacetylase 6 (HDAC6) expression. Morphine-induced alpha-tubulin deacetylation and HSP90 fragmentation were HDAC6-dependent. Pretreatment with (+)-naloxone (1 nM) inhibited morphine-evoked microglia activation and chemotaxis and prevented alpha-tubulin deacetylation and HSP90 fragmentation by inhibiting HDAC6 expression.Conclusion: Based on the findings of the present study, we suggest that (+)-naloxone inhibits morphine-induced microglia activation by regulating HDAC6-dependent alpha-tubulin deacetylation and HSP90 fragmentation. Copyright (C) 2015, Elsevier Taiwan LLC & Formosan Medical Association. All rights reserved.
