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The Sciatic Nerve Cuffing Model of Neuropathic Pain in Mice
Published on: July 16, 2014
Targeting druggable kinases in neuropathic pain
Harrison Benson1, Komalpreet Kaur1, Mahmoud Salama Ahmed2,3
1Department of Pharmaceutical Sciences, Jerry H. Hodge School of Pharmacy, Texas Tech University Health Science Center, Amarillo, TX, USA.
Abstract:
Despite the prevalence of neuropathic pain and the opioid crisis, there has been little progress in the development of non-opioid alternative therapies. Protein kinases orchestrate multiple key pathophysiological events in the progression of pain signaling pathways. This review highlights druggable kinases and the associated scaffolds as well as molecular modalities to reverse mechanical allodynia and thermal hyperalgesia in neuropathy models whether preclinically or clinically.
Insights
Developing non-opioid pain therapies remains challenging. This review explores protein kinases as potential targets to reverse neuropathic pain, offering hope beyond the opioid crisis.
Area of Science:
- Neuroscience
- Pharmacology
- Pain Management
Background:
- Neuropathic pain is prevalent, yet effective non-opioid treatments are scarce.
- The opioid crisis necessitates alternative pain management strategies.
Purpose of the Study:
- To review druggable protein kinases involved in pain signaling.
- To identify molecular strategies for reversing neuropathic pain symptoms.
Main Methods:
- Literature review of preclinical and clinical studies.
- Focus on protein kinases and their associated molecular modalities.
Main Results:
- Protein kinases play crucial roles in pain pathway progression.
- Specific kinases and scaffolds show potential for therapeutic intervention.
Conclusions:
- Targeting protein kinases offers a promising avenue for non-opioid neuropathic pain therapies.
- Further research into kinase inhibitors could yield novel analgesics.
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