Involvement of coerulospinal noradrenergic pathway in fentanyl-induced muscular rigidity in rats

Neurosci Lett. 1990 Jan 1;108(1-2):183-8. doi: 10.1016/0304-3940(90)90728-r.

Abstract

Unilateral, site-specific microinjection of fentanyl (2.5 micrograms/50 nl) into the locus coeruleus (LC) in Sprague-Dawley rats anesthetized with ketamine evoked a significant increase in the electromyographic activity recorded from both caudal lateral extensor and gastrocnemius muscles. This correlate of opiate-induced muscular rigidity was appreciably antagonized by a pretreatment with the specific alpha 1-adrenoceptor blocker, prazosin (250 micrograms/kg, i.v.). On the other hand, an equimolar dose (0.65 mumol/kg) of the specific alpha 2-adrenoceptor blocker, yohimbine (0.23 mg/kg, i.v.) failed to prevent the occurrence of fentanyl-induced EMG activation. We suggest that the coerulospinal noradrenergic pathway may be directly involved in the elicitation of muscular rigidity by fentanyl, possibly via alpha 1-adrenoceptors in the spinal cord.

MeSH terms

  • Adrenergic Fibers / drug effects
  • Adrenergic Fibers / physiology*
  • Animals
  • Dose-Response Relationship, Drug
  • Fentanyl*
  • Locus Coeruleus / drug effects
  • Locus Coeruleus / physiopathology*
  • Male
  • Microinjections
  • Muscle Rigidity / chemically induced*
  • Muscle Rigidity / physiopathology
  • Prazosin / pharmacology
  • Rats
  • Rats, Inbred Strains
  • Spinal Cord / drug effects
  • Spinal Cord / physiopathology*
  • Yohimbine / pharmacology

Substances

  • Yohimbine
  • Fentanyl
  • Prazosin