P2X(3) Receptor in Primary Afferent Neurons Mediates the Relief of Visceral Hypersensitivity by Electroacupuncture in an Irritable Bowel Syndrome Rat Model.
P2X(3) Receptor in Primary Afferent Neurons Mediates the Relief of Visceral Hypersensitivity by Electroacupuncture in an Irritable Bowel Syndrome Rat Model.
复制标题
初级传入神经元中的 P2X3 受体通过电针介导肠易激综合征大鼠模型内脏过敏的缓解
DOI:
10.1155/2020/8186106
复制
发表时间:
2020
影响因子:
2
通讯作者:
Wu H
中科院分区:
文献类型:
--
作者:
Zhang F;Ma Z;Weng Z;Zhao M;Zheng H;Wu L;Lu Y;Bao C;Liu Y;Liu H;Wu H
Background Electroacupuncture (EA) has been confirmed effectiveness in the treatment of irritable bowel syndrome (IBS), and P2X3 receptors in the peripheral and central neurons participate in the acupuncture-mediated relief of the visceral pain in IBS. Objective To reveal the neurobiological mechanism that P2X3 receptor of colonic primary sensory neurons in the dorsal root ganglia of the lumbosacral segment is involved in the alleviation of visceral hypersensitivity by EA in an IBS rat model. Methods The IBS chronic visceral pain rat model was established according to the method of Al-Chaer et al. EA at the bilateral He-Mu points, including ST25 and ST37, was conducted for intervention. The behavioral studies, histopathology of colon, electrophysiology, immunofluorescence histochemistry, and real-time polymerase chain reaction assays were used to observe the role of P2X3 receptor in the colon and related DRG in relieving visceral hypersensitivity by EA. Results EA significantly reduced the behavior scores of the IBS rats under different levels (20, 40, 60, 80 mmHg) of colorectal distention stimulation and downregulated the expression levels of P2X3 receptor protein and mRNA in colon and related DRG of the IBS rats. EA also regulated the electrical properties of the membranes, including the resting membrane potential, rheobase, and action potential of colon-associated DRG neurons in the IBS rats. Conclusion EA can regulate the P2X3 receptor protein and mRNA expression levels in the colon and related DRG of IBS rats with visceral pain and then regulate the excitatory properties of DRG neurons.
登录
查看更多内容
影响因子:
24.5
作者:
Tillisch, K
通讯作者:
Tillisch, K
DOI:
10.1073/pnas.252537299
发表时间:
2002-12-24
影响因子:
11.1
作者:
Jarvis, MF;Burgard, EC;Faltynek, C
通讯作者:
Faltynek, C
DOI:
10.5114/pg.2018.78343
发表时间:
2018-01-01
影响因子:
1.3
作者:
Pietrzak, Anna;Skrzydlo-Radomanska, Barbara;Rydzewska, Grazyna
通讯作者:
Rydzewska, Grazyna
影响因子:
3.3
作者:
Wang HJ;Xu X;Xie RH;Rui YY;Zhang PA;Zhu XJ;Xu GY
通讯作者:
Xu GY
DOI:
10.1152/ajpgi.00257.2012
发表时间:
2012-10-01
影响因子:
4.5
作者:
Feng, Bin;La, Jun-Ho;Gebhart, G. F.
通讯作者:
Gebhart, G. F.