The present research addresses the hypothesis that lamina I spinothalamic tract (lamI-STT) neurons are an essential substrate for the central representation of nociception and thermoreception as specific sensory modalities, i.e. that they constitute a central pathway that contains the """"""""labeled lines"""""""" of specificity theory for pain and temperature sensation. These experiments focus on the functionally selective organization of this pathway and particularly concentrate on examining attributes which may reflect the distinct functional and anatomical classes of nociceptive and thermoreceptive laml-STT neurons identified physiologically in previous work in the cat. The new lectin (PHA-L) anterograde tracing method will be used to precisely determine the multiple laml-STT a thalamic termination sites, to characterize their morphology and to identify their pathway. The chemical and anatomical selectivity of these terminal projections will be tested with immunohistochemical the detection of endogenous neurochemical, and double-labeling methods for multiple retrograde tracers for the identification of segregated afferent cell groups. In addition, physiological experiments will complement the anatomical localization of the ascending lamI-STI spinal pathway with the individual localization of the axons of identified cells by antidromic activation from a microelectrode at L2. These experiments will directly determine whether lamI-STT axons project separately from the classical STI, as some have proposed, and whether nociceptive and thermoreceptive axons course together. The effects of tonic descending influences on the functional selectivity of these lamI-STT cells and also other non-STT lamina I cells will be examined with reversible spinal cold blocks. Lastly, the sensitivity of these cells to topically applied (intrathecal) morphine will be assessed in order to test their functional differentiation and, by comparing this sensitivity to reported characteristics of intrathecally produced analgesia, to verify the hypothesis that they play an essential role in nociception.

Agency
National Institute of Health (NIH)
Institute
National Institute of Neurological Disorders and Stroke (NINDS)
Type
Research Project (R01)
Project #
5R01NS025616-05
Application #
3410909
Study Section
Neurological Sciences Subcommittee 1 (NLS)
Project Start
1988-02-01
Project End
1995-06-30
Budget Start
1992-07-01
Budget End
1993-06-30
Support Year
5
Fiscal Year
1992
Total Cost
Indirect Cost
Name
St. Joseph's Hosp/Medical Center (Phoenix)
Department
Type
DUNS #
City
Phoenix
State
AZ
Country
United States
Zip Code
85013
Craig, A D Bud (2014) Topographically organized projection to posterior insular cortex from the posterior portion of the ventral medial nucleus in the long-tailed macaque monkey. J Comp Neurol 522:36-63
Craig, A D ' Bud ' (2006) Retrograde analyses of spinothalamic projections in the macaque monkey: input to ventral posterior nuclei. J Comp Neurol 499:965-78
Craig, A D 'Bud'; Zhang, En-Tan (2006) Retrograde analyses of spinothalamic projections in the macaque monkey: input to posterolateral thalamus. J Comp Neurol 499:953-64
Craig, A D (2004) Distribution of trigeminothalamic and spinothalamic lamina I terminations in the macaque monkey. J Comp Neurol 477:119-48
Ito, Shin-Ichi; Craig, A D Bud (2003) Vagal input to lateral area 3a in cat cortex. J Neurophysiol 90:143-54
Andrew, David; Krout, Karl E; Craig, A D Bud (2003) Differentiation of lamina I spinomedullary and spinothalamic neurons in the cat. J Comp Neurol 458:257-71
Craig, A D (2003) Distribution of trigeminothalamic and spinothalamic lamina I terminations in the cat. Somatosens Mot Res 20:209-22
Beggs, J; Jordan, S; Ericson, A-C et al. (2003) Synaptology of trigemino- and spinothalamic lamina I terminations in the posterior ventral medial nucleus of the macaque. J Comp Neurol 459:334-54
Wilson, L B; Andrew, D; Craig, A D (2002) Activation of spinobulbar lamina I neurons by static muscle contraction. J Neurophysiol 87:1641-5
Andrew, D; Craig, A D (2002) Responses of spinothalamic lamina I neurons to maintained noxious mechanical stimulation in the cat. J Neurophysiol 87:1889-901

Showing the most recent 10 out of 45 publications