Opioid compounds modulate neurotransmission through a number of different sensory and motor systems. The long-term goals of the present proposal concern the modulation of sensory transmission, especially opioid modulation of nociceptive sensory systems at the spinal level. The immediate intent of this proposal is to concentrate on peripheral mechanisms by examining in detail the localization of delta, mu and kappa opioid receptors to different functional classes of primary afferent neurons. In addition, we will examine relationships between functional properties of afferent neurons and the expression of opioid receptors, vanilloid receptors, and binding sites for the lectin IB4. In making this proposal, immunohistochemical and electrophysiological approaches will be combined to address the following specific aims: Determine what functional classes of primary afferent neurons express opioid receptors. Determine what classes of thermal nociceptors express opioid and vanilloid receptors. Determine in functionally identified sensory neurons, the relationship between the expression of lectin binding sites and opioid and vanilloid receptors. Knowledge obtained from these experiments in the peripheral nervous system will contribute to our understanding of basic opioid mechanisms, and as such will further our understanding of central mechanisms related to the modulation of nociceptive and painful information in both the normal and pathologic states.

Agency
National Institute of Health (NIH)
Institute
National Institute on Drug Abuse (NIDA)
Type
Research Project (R01)
Project #
5R01DA009641-07
Application #
6626824
Study Section
Special Emphasis Panel (ZRG1-IFCN-4 (01))
Program Officer
Thomas, David A
Project Start
1995-09-30
Project End
2004-07-09
Budget Start
2003-01-01
Budget End
2004-07-09
Support Year
7
Fiscal Year
2003
Total Cost
$216,535
Indirect Cost
Name
University of Minnesota Twin Cities
Department
Neurosciences
Type
Schools of Medicine
DUNS #
555917996
City
Minneapolis
State
MN
Country
United States
Zip Code
55455
Brederson, Jill-Desiree; Honda, Christopher N (2015) Primary afferent neurons express functional delta opioid receptors in inflamed skin. Brain Res 1614:105-11
Schramm, Cicely L; Honda, Christopher N (2010) Co-administration of ?- and ?-opioid receptor agonists promotes peripheral opioid receptor function. Pain 151:763-70
Wenk, Heather N; Brederson, Jill-Desiree; Honda, Christopher N (2006) Morphine directly inhibits nociceptors in inflamed skin. J Neurophysiol 95:2083-97
Truong, H; McGinnis, L; Dindo, L et al. (2004) Identification of dorsal root ganglion neurons that innervate the common bile duct of rats. Exp Brain Res 155:477-84
Wenk, H N; Nannenga, M N; Honda, C N (2003) Effect of morphine sulphate eye drops on hyperalgesia in the rat cornea. Pain 105:455-65
Wenk, H N; Honda, C N (2003) Silver nitrate cauterization: characterization of a new model of corneal inflammation and hyperalgesia in rat. Pain 105:393-401
Zhang, X; Honda, C N; Giesler Jr, G J (2000) Position of spinothalamic tract axons in upper cervical spinal cord of monkeys. J Neurophysiol 84:1180-5
Zhang, X; Wenk, H N; Honda, C N et al. (2000) Locations of spinothalamic tract axons in cervical and thoracic spinal cord white matter in monkeys. J Neurophysiol 83:2869-80
Zhang, X; Wenk, H N; Gokin, A P et al. (1999) Physiological studies of spinohypothalamic tract neurons in the lumbar enlargement of monkeys. J Neurophysiol 82:1054-8
Wenk, H N; Honda, C N (1999) Immunohistochemical localization of delta opioid receptors in peripheral tissues. J Comp Neurol 408:567-79

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