伤害
小发夹RNA
基因沉默
NMDA受体
小干扰RNA
RNA干扰
受体
药理学
谷氨酸受体
化学
核糖核酸
细胞生物学
神经科学
医学
生物
基因
生物化学
作者
Raoxiang Zhang,Xuebin Yan,Yonghong Gu,Dong Huang,Li Gan,Rui Han,Lihua Huang
标识
DOI:10.3109/00207454.2013.789873
摘要
Spinal NR2B-containing N-methyl-D-aspartate receptors (NR2B) play a critical role in the formation of central sensitization and persistent pain. Previous studies show that gene silencing of the spinal NR2B subunit by small interfering RNA (siRNA) could alleviate nociception in animals. The siRNA is a 19- to 23-nt RNA duplex, which can be synthesized in vitro or derived from short hairpin RNAs (shRNAs). In the present study, we investigated whether intrathecal injection of shRNAs targeting NR2B (GRIN2B shRNA) could affect nociception on formalin-induced pain in mice. Our results showed that intrathecal injection of GRIN2B shRNA could decrease NR2B mRNA and protein expression levels and hence effectively relieve formalin-induced nociception in mice, suggesting that intrathecal delivery of GRIN2B shRNA can be an efficient way to silence the target gene and provide new insights into the treatment of chronic pain.
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