Pregabalin Alters Nociceptive Behavior and Expression Level of P2X3 Receptor in the Spinal Dorsal Horn in a Rat Model Induced by Chronic Compression of the Dorsal Root Ganglion. Issue 12 (17th October 2013)
- Record Type:
- Journal Article
- Title:
- Pregabalin Alters Nociceptive Behavior and Expression Level of P2X3 Receptor in the Spinal Dorsal Horn in a Rat Model Induced by Chronic Compression of the Dorsal Root Ganglion. Issue 12 (17th October 2013)
- Main Title:
- Pregabalin Alters Nociceptive Behavior and Expression Level of P2X3 Receptor in the Spinal Dorsal Horn in a Rat Model Induced by Chronic Compression of the Dorsal Root Ganglion
- Authors:
- Yu, Jianfeng
Fu, Peng
Zhang, Yan
Liu, Shuzhen
Cui, Donghong - Abstract:
- <abstract abstract-type="main"> <title>ABSTRACT</title> <p>P2X3 receptors are present in the spinal dorsal horn (SDH) and play an essential role in the regulation of nociception and pain. Pregabalin (PGB) has been used as a new antiepileptic drug in the treatment of neuropathic pain. However, it is unclear whether PGB‐induced analgesia was associated with the P2X3 receptor in SDH. Here, rats were randomly divided into four groups (<italic>n</italic> = 12 per group), including 2 sham operation groups, which was treated by normal saline (Sham + NS group) or PGB (Sham + PGB group), other 2 groups with chronic compression of the dorsal root ganglion, a normal saline‐treated CCD group (CCD+NS group), and a PGB‐treated CCD group (CCD + PGB group). A rat model of neuropathic pain was used by compressing the right L4 and L5 dorsal root ganglia. Each group was evaluated using the mechanical withdrawal threshold (MWT). The mRNA and protein levels of the P2X3 receptor in the ipsilateral SDH were measured by RT‐PCR, western blot, and immunofluorescence on 14 day after CCD operation. CCD rats showed the highest mechanical hyperalgesia and the lowest pain threshold in the four groups. Simultaneously, CCD rats showed higher P2X3 mRNA and protein expression in ipsilateral side of the SDH than the sham operation rats. However, the MWT was increased and expression of P2X3 mRNA and protein in the ipsilateral SDH in CCD rats was decreased 3 days after PGB treatment. Thus, PGB may partially<abstract abstract-type="main"> <title>ABSTRACT</title> <p>P2X3 receptors are present in the spinal dorsal horn (SDH) and play an essential role in the regulation of nociception and pain. Pregabalin (PGB) has been used as a new antiepileptic drug in the treatment of neuropathic pain. However, it is unclear whether PGB‐induced analgesia was associated with the P2X3 receptor in SDH. Here, rats were randomly divided into four groups (<italic>n</italic> = 12 per group), including 2 sham operation groups, which was treated by normal saline (Sham + NS group) or PGB (Sham + PGB group), other 2 groups with chronic compression of the dorsal root ganglion, a normal saline‐treated CCD group (CCD+NS group), and a PGB‐treated CCD group (CCD + PGB group). A rat model of neuropathic pain was used by compressing the right L4 and L5 dorsal root ganglia. Each group was evaluated using the mechanical withdrawal threshold (MWT). The mRNA and protein levels of the P2X3 receptor in the ipsilateral SDH were measured by RT‐PCR, western blot, and immunofluorescence on 14 day after CCD operation. CCD rats showed the highest mechanical hyperalgesia and the lowest pain threshold in the four groups. Simultaneously, CCD rats showed higher P2X3 mRNA and protein expression in ipsilateral side of the SDH than the sham operation rats. However, the MWT was increased and expression of P2X3 mRNA and protein in the ipsilateral SDH in CCD rats was decreased 3 days after PGB treatment. Thus, PGB may partially reverse mechanical hyperalgesia in CCD rats by inhibiting P2X3 receptor expression in the ipsilateral SDH. Anat Rec, 296:1907–1912, 2013. © 2013 Wiley Periodicals, Inc.</p> </abstract> … (more)
- Is Part Of:
- Anatomical record. Volume 296:Issue 12(2013:Dec.)
- Journal:
- Anatomical record
- Issue:
- Volume 296:Issue 12(2013:Dec.)
- Issue Display:
- Volume 296, Issue 12 (2013)
- Year:
- 2013
- Volume:
- 296
- Issue:
- 12
- Issue Sort Value:
- 2013-0296-0012-0000
- Page Start:
- 1907
- Page End:
- 1912
- Publication Date:
- 2013-10-17
- Subjects:
- Anatomy -- Periodicals
Evolution (Biology) -- Periodicals
Morphology -- Periodicals
571.3 - Journal URLs:
- http://www3.interscience.wiley.com/cgi-bin/jhome/113463905 ↗
http://onlinelibrary.wiley.com/journal/10.1002/(ISSN)1932-8494 ↗
http://onlinelibrary.wiley.com/ ↗ - DOI:
- 10.1002/ar.22816 ↗
- Languages:
- English
- ISSNs:
- 1932-8486
- Deposit Type:
- Legaldeposit
- View Content:
- Available online (eLD content is only available in our Reading Rooms) ↗
- Physical Locations:
- British Library DSC - 0898.005000
British Library DSC - BLDSS-3PM
British Library HMNTS - ELD Digital store - Ingest File:
- 3104.xml