神经病理性疼痛
小胶质细胞
p38丝裂原活化蛋白激酶
小干扰RNA
促炎细胞因子
痛觉超敏
基因沉默
药理学
神经损伤
伤害
医学
化学
炎症
细胞生物学
麻醉
转染
痛觉过敏
内科学
信号转导
生物
受体
MAPK/ERK通路
生物化学
基因
作者
Juhee Shin,Yuhua Yin,Hyewon Park,Seungjo Park,Ursula L. Triantafillu,Yonghyun Kim,Sang Ryong Kim,Sun Yeul Lee,Do Kyung Kim,Jinpyo Hong,Dong Woon Kim
出处
期刊:Nanomedicine
[Future Medicine]
日期:2018-07-01
卷期号:13 (13): 1607-1621
被引量:51
标识
DOI:10.2217/nnm-2018-0054
摘要
Aim: To investigate whether p38 small-interfering RNA-loaded nanoparticles (p38 siRNA NPs) attenuate spinal nerve ligation (SNL)-induced neuropathic pain in rats by suppressing spinal microglia activation via p38 targeting. Materials & methods: After synthesizing p38 siRNA NPs with sonication, physical characteristics were measured for size and zeta potential. p38 siRNA NPs were then administrated intrathecally into SNL rats if they could reduce pain behavior excellently. Results: p38 siRNA NPs significantly reduced mechanical allodynia as well as microgliosis in the spinal dorsal horns of SNL rats, consistent with a downregulation of p38-related proinflammatory mediators. Conclusion: As p38 in the spinal microglia plays a critical role in neuropathic pain, we expect that p38 siRNA NPs could be a promising tool for the treatment of neuropathic pain.
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