Activation of extracellular signal-regulated protein kinases 5 in the spinal cord contributes to the neuropathic pain behaviors induced by CCI in rats

Authors: Zhang, Lin1; Xiao, Chun2; Wang, Jun-Ke3; Zhang, Li-Cai2; Zeng, Yin-Ming2

Source: Neurological Research, Volume 31, Number 10, December 2009 , pp. 1037-1043(7)

Publisher: Maney Publishing

Key:
Free Content - Free Content
New Content - New Content
Subscribed Content - Subscribed Content
Free Trial Content - Free Trial Content

Abstract:

Objective: To investigate whether activation and translocation of extracellular signal-regulated kinase 5 (ERK5) is involved in the induction and maintenance of neuropathic pain and observe the effects of activation and translocation of ERK5 on the expression of phosphorylated cAMP response element binding (pCREB) in the chronic neuropathic pain.

Methods: Lumbar intrathecal catheters were chronically implanted in male Sprague-Dawley rats. The left sciatic nerve was loosely ligated proximal to the sciatica's trifurcation at ∼ 1.0 mm intervals with 4-0 silk sutures. The phosphorothioate-modified antisense oligonucleotides (AS-ODNs) were intrathecally administered every 12 hours, 1 day pre-chronic constriction injury (CCI) and 3 day post-CCI. Thermal and mechanical nociceptive thresholds were assessed with the paw withdrawal latency to a radiant heat and von Frey filaments. Expressions of phosphorylated ERK5 (pERK5), pCREB, were assessed by both Western blotting and immunohistochemical analysis.

Results: Intrathecal injection of ERK5 AS-ODN significantly attenuated CCI-induced mechanical allodynia and thermal hyperalgesia. CCI significantly increased the expression of pERK5 neurons in the ipsilateral spinal dorsal horn to injury, not in the contralateral spinal dorsal horn. The time courses of pERK5 expression showed that the levels of both cytosol and nuclear pERK5 were increased at all points after CCI and reached a peak level on post-operative day 5. CCI significantly increased the expression of pERK5 neurons in the laminae I and II of ipsilateral spinal dorsal horn to injury, not in the contralateral spinal dorsal horn. Phospho-CREB-positive neurons were distributed in all laminae of the bilateral spinal cord. Intrathecal injection AS-ODN markedly suppressed the increase of CCI-induced pERK5, pCREB expression in the spinal cord.

Conclusion: The activation of ERK5 pathways contributes to neuropathic pain in CCI rats, and the function of pERK5 may partly be accomplished via the CREB protein-dependent gene expression.

Keywords: EXTRACELLULAR SIGNAL-REGULATED PROTEIN KINASE 5; SPINAL CORD; NEUROPATHIC PAIN; CCI; MITOGEN-ACTIVATED PROTEIN KINASE; CAMP RESPONSE-ELEMENT BINDING PROTEIN

Document Type: Research article

DOI: 10.1179/174313209X405128

Affiliations: 1: Department of Anesthesia, The First Affiliated Hospital, Medical College of Qingdao University, Qingdao, China; Jiangsu Key Laboratory of Anesthesiology, Jiangsu Institute of Anesthesiology, Xuzhou, China; Department of Anesthesia and Critical Ca 2: Jiangsu Key Laboratory of Anesthesiology, Jiangsu Institute of Anesthesiology, Xuzhou, China 3: Department of Anesthesia, The First Affiliated Hospital, China Medical University, Shenyang, China

The full text electronic article is available for purchase. You will be able to download the full text electronic article after payment.

$51.00 plus tax      Refund Policy

 

OR

Back to top

Key:
Free Content - Free Content
New Content - New Content
Subscribed Content - Subscribed Content
Free Trial Content - Free Trial Content
Share this item with others: These icons link to social bookmarking sites where readers can share and discover new web pages.
Page Help Click here for Page Help
Shopping cart
Tools
Sign in






Need to register?
Sign up here
Text size: A | A | A | A