Tags

Type your tag names separated by a space and hit enter

Effect of tetramethylpyrazine on primary afferent transmission mediated by P2X3 receptor in neuropathic pain states.
Brain Res Bull. 2008 Sep 05; 77(1):27-32.BR

Abstract

Neuropathic pain is the most difficult type of pain to treat. The P2X(3) receptors play a crucial role in facilitating pain transmission at peripheral and spinal sites. The present research investigated the effects of tetramethylpyrazine (TMP) on the primary afferent transmission induced by P2X(3) receptor in neuropathic pain states. Chronic constriction injury (CCI) model was adopted. Sprague-Dawley male rats (n=30) had been randomly divided into normal saline (sham+NS) group (I), TMP group (II), sham group (III), CCI+TMP group (IV), and CCI group (V). Mechanical withdrawal threshold (MWT) and thermal withdrawal latency (TWL) were measured and P2X(3) immunoreactivity in L4/L5 dorsal root ganglion (DRG) and spinal cord was detected by immunohistochemistry. The mechanical withdrawal threshold and thermal withdrawal latency in group V were lower than those in groups I-III or IV (p<0.05), while P2X(3) receptor expression of L4/L5 DRG and spinal cord in group V was higher than those in groups I-III (p<0.01) or group IV (p<0.05). The mechanical withdrawal threshold, thermal withdrawal latency and P2X(3) immunoreactivity of L4/L5 DRG and spinal cord in group IV showed no significant difference compared with those in groups I, II or III (p>0.05). The amplitudes of the currents in group V (CCI) were much larger than those obtained in other groups after application of same concentration adenosine 5'-triphosphate disodium (ATP) (p<0.01). alpha,beta-Methylene-ATP (alpha,beta-meATP)-activated currents in DRG neurons of CCI rats were more obvious than those obtained in other group rats (p<0.01). The results showed that TMP may inhibit the primary afferent transmission of neuropathic pain induced by P2X(3) receptor.

Authors+Show Affiliations

Department of Physiology, Medical College of Nanchang University, Bayi Road 461, Nanchang 330006, PR China.No affiliation info availableNo affiliation info availableNo affiliation info availableNo affiliation info availableNo affiliation info availableNo affiliation info available

Pub Type(s)

Journal Article
Research Support, Non-U.S. Gov't

Language

eng

PubMed ID

18639742

Citation

Gao, Yun, et al. "Effect of Tetramethylpyrazine On Primary Afferent Transmission Mediated By P2X3 Receptor in Neuropathic Pain States." Brain Research Bulletin, vol. 77, no. 1, 2008, pp. 27-32.
Gao Y, Xu C, Liang S, et al. Effect of tetramethylpyrazine on primary afferent transmission mediated by P2X3 receptor in neuropathic pain states. Brain Res Bull. 2008;77(1):27-32.
Gao, Y., Xu, C., Liang, S., Zhang, A., Mu, S., Wang, Y., & Wan, F. (2008). Effect of tetramethylpyrazine on primary afferent transmission mediated by P2X3 receptor in neuropathic pain states. Brain Research Bulletin, 77(1), 27-32. https://doi.org/10.1016/j.brainresbull.2008.02.026
Gao Y, et al. Effect of Tetramethylpyrazine On Primary Afferent Transmission Mediated By P2X3 Receptor in Neuropathic Pain States. Brain Res Bull. 2008 Sep 5;77(1):27-32. PubMed PMID: 18639742.
* Article titles in AMA citation format should be in sentence-case
TY - JOUR T1 - Effect of tetramethylpyrazine on primary afferent transmission mediated by P2X3 receptor in neuropathic pain states. AU - Gao,Yun, AU - Xu,Changshui, AU - Liang,Shangdong, AU - Zhang,Aixia, AU - Mu,Songniu, AU - Wang,Yunxia, AU - Wan,Fang, Y1 - 2008/03/18/ PY - 2008/02/11/received PY - 2008/02/18/accepted PY - 2008/7/22/pubmed PY - 2008/9/13/medline PY - 2008/7/22/entrez SP - 27 EP - 32 JF - Brain research bulletin JO - Brain Res. Bull. VL - 77 IS - 1 N2 - Neuropathic pain is the most difficult type of pain to treat. The P2X(3) receptors play a crucial role in facilitating pain transmission at peripheral and spinal sites. The present research investigated the effects of tetramethylpyrazine (TMP) on the primary afferent transmission induced by P2X(3) receptor in neuropathic pain states. Chronic constriction injury (CCI) model was adopted. Sprague-Dawley male rats (n=30) had been randomly divided into normal saline (sham+NS) group (I), TMP group (II), sham group (III), CCI+TMP group (IV), and CCI group (V). Mechanical withdrawal threshold (MWT) and thermal withdrawal latency (TWL) were measured and P2X(3) immunoreactivity in L4/L5 dorsal root ganglion (DRG) and spinal cord was detected by immunohistochemistry. The mechanical withdrawal threshold and thermal withdrawal latency in group V were lower than those in groups I-III or IV (p<0.05), while P2X(3) receptor expression of L4/L5 DRG and spinal cord in group V was higher than those in groups I-III (p<0.01) or group IV (p<0.05). The mechanical withdrawal threshold, thermal withdrawal latency and P2X(3) immunoreactivity of L4/L5 DRG and spinal cord in group IV showed no significant difference compared with those in groups I, II or III (p>0.05). The amplitudes of the currents in group V (CCI) were much larger than those obtained in other groups after application of same concentration adenosine 5'-triphosphate disodium (ATP) (p<0.01). alpha,beta-Methylene-ATP (alpha,beta-meATP)-activated currents in DRG neurons of CCI rats were more obvious than those obtained in other group rats (p<0.01). The results showed that TMP may inhibit the primary afferent transmission of neuropathic pain induced by P2X(3) receptor. SN - 1873-2747 UR - https://www.unboundmedicine.com/medline/citation/18639742/Effect_of_tetramethylpyrazine_on_primary_afferent_transmission_mediated_by_P2X3_receptor_in_neuropathic_pain_states_ L2 - https://linkinghub.elsevier.com/retrieve/pii/S0361-9230(08)00095-6 DB - PRIME DP - Unbound Medicine ER -