Literature DB >> 17923323

Phosphorylation of c-Jun N-terminal kinase isoforms and their different roles in spinal cord dorsal horn and primary somatosensory cortex.

Ming-Gang Liu1, Fu-Kang Zhang, She-Wei Guo, Lan-Feng Zhao, Yang-Yuan An, Xiu-Yu Cui, Jun Chen.   

Abstract

The present study was undertaken to investigate whether isoforms of c-Jun N-terminal kinase (JNK 46 kDa and 54 kDa), one component of the mitogen-activated protein kinase (MAPK) family, might show region-related differential activation patterns in both naïve and pain-experiencing rats. In naïve rats, no significant difference was observed in total expression level of the two JNK isoforms between spinal cord and primary somatosensory cortex (S1 area). However, phosphorylated JNK 46 kDa was normally expressed in the S1 area, but not in the spinal cord, while neither of the two structures contained phosphorylated JNK 54 kDa. Subcutaneous bee venom (BV)-induced persistent pain stimulation resulted in a significant increase in the phosphorylation of both JNK isoforms in each area for a long period (lasting at least 48 h). Nevertheless, JNK 46 kDa exhibited a much higher activation than JNK 54 kDa in the spinal cord, whereas the same noxious stimulation elicited evident activation of JNK 54 kDa in the S1 area, leaving JNK 46 kDa less affected. Intraplantar injection of sterile saline solution, causing acute and transient pain, produced almost the same changes in activation profile of the two JNK isoforms as found in the BV-treated rats. These results implicate that individual members of the JNK family may be associated with specific regions of nociceptive processing. Also, the two JNK isoforms are supposed to function differently according to their locations within the rat central nervous system.

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Year:  2007        PMID: 17923323     DOI: 10.1016/j.neulet.2007.09.001

Source DB:  PubMed          Journal:  Neurosci Lett        ISSN: 0304-3940            Impact factor:   3.046


  6 in total

1.  Spinal sample showing p-JNK and P38 associated with the pain signaling transduction of glial cell in neuropathic pain.

Authors:  J Cao; J-s Wang; X-h Ren; W-d Zang
Journal:  Spinal Cord       Date:  2014-11-11       Impact factor: 2.772

Review 2.  The nociceptive and anti-nociceptive effects of bee venom injection and therapy: a double-edged sword.

Authors:  Jun Chen; William R Lariviere
Journal:  Prog Neurobiol       Date:  2010-06-15       Impact factor: 11.685

Review 3.  Roles of the hippocampal formation in pain information processing.

Authors:  Ming-Gang Liu; Jun Chen
Journal:  Neurosci Bull       Date:  2009-10       Impact factor: 5.203

4.  Role of JNK isoforms in the development of neuropathic pain following sciatic nerve transection in the mouse.

Authors:  Giusi Manassero; Ivan E Repetto; Stefano Cobianchi; Valeria Valsecchi; Christophe Bonny; Ferdinando Rossi; Alessandro Vercelli
Journal:  Mol Pain       Date:  2012-05-22       Impact factor: 3.395

5.  Synaptic Homeostasis and Allostasis in the Dentate Gyrus Caused by Inflammatory and Neuropathic Pain Conditions.

Authors:  Rui-Rui Wang; Yan Wang; Su-Min Guan; Zhen Li; Saurabh Kokane; Fa-Le Cao; Wei Sun; Chun-Li Li; Ting He; Yan Yang; Qing Lin; Jun Chen
Journal:  Front Synaptic Neurosci       Date:  2018-01-31

6.  Nociception-induced spatial and temporal plasticity of synaptic connection and function in the hippocampal formation of rats: a multi-electrode array recording.

Authors:  Xiao-Yan Zhao; Ming-Gang Liu; Dong-Liang Yuan; Yan Wang; Ying He; Dan-Dan Wang; Xue-Feng Chen; Fu-Kang Zhang; Hua Li; Xiao-Sheng He; Jun Chen
Journal:  Mol Pain       Date:  2009-09-22       Impact factor: 3.395

  6 in total

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