Spinal delivery of analgesics in experimental models of pain and analgesia

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Abstract

Systemic administration of analgesics can lead to serious adverse side effects compromising therapeutic benefit in some patients. Information coding pain transmits along an afferent neuronal network, the first synapses of which reside principally in the spinal cord. Delivery of compounds to spinal cord, the intended site of action for some analgesics, is potentially a more efficient and precise method for inhibiting the pain signal. Activation of specific proteins that reside in spinal neuronal membranes can result in hyperpolarization of secondary neurons, which can prevent transmission of the pain signal. This is one of the mechanisms by which opioids induce analgesia. The spinal cord is enriched in such molecular targets, the activation of which inhibit the transmission of the pain signal early in the afferent neuronal network. This review describes the pre-clinical models that enable new target discovery and development of novel analgesics for site-directed pain management.

Original languageEnglish (US)
Pages (from-to)1007-1041
Number of pages35
JournalAdvanced Drug Delivery Reviews
Volume55
Issue number8
DOIs
StatePublished - Aug 15 2003

Bibliographical note

Funding Information:
I would like to extend my great appreciation to Drs Laura S. Stone, Craig W. Stevens, George L. Wilcox, and Richard L. Boortz-Marx, and to Mr Kelley F. Kitto, Ms H. Oanh Nguyen, Mr Brent Grocholski, Ms Cory Goracke, and Mr Scott Thompson for review, comments, and contributions to the various sections of this review. I would like to also thank Dr Tony Yaksh for valuable conversation on the history and use of spinal drug delivery in experimental subjects and humans. Supported by NIDA DA-00509.

Keywords

  • Analgesia
  • Epidural
  • Intrathecal
  • Pain
  • Spinal

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