This application is designed to a) examine the sprouting response of undamaged and damaged trigeminal primary afferent neurons following neonatal peripheral nerve lesions and b) to study some of the mechanisms which may be important in the generation of lesion-induced central terminal arbor abnormalities. To accomplish these goals we propose the following three experiments: 1) The potential of undamaged trigeminal primary afferents to alter their central projections via sprouting, arbor expansion or arbor displacement will be examined by cauterizing all vibrissa follicles of the mystical pad with the exception of those in row C or D. Using intraaxonal and intracellular labeling techniques, we will determine the response of primary afferents with undisturbed peripheral terminations to partial denervation of their central target. 2) We will utilize quantitative electron microscopic techniques to investigate the impact of neonatal infraorbital (IO) nerve transection on the central terminal populations of two subsets of small diameter primary afferent neurons (substance P-like immunoreactive and fluoride resistant acid phosphatase- positive). By examining animals at sequenced intervals after the nerve injury we will determine if the number of terminals per unit area of the substantia gelatinosa and magnocellular region of subnucleus caudalis is maintained, decrease or increased (indicative of sprouting). 3) To determine the importance of patterned primary afferent activity in the development and maintenance of trigeminal primary afferent central terminal arbors, we will expose the IO nerve to tetrodotoxin beginning on the day of birth. This will inhibit primary afferent activity without transecting the nerve, thus causing no apparent disruption in the transport of any trophic substances important to information regarding the response of damaged and undamaged neurons to lesion-induced deafferentation of a portion of the trigeminal system. This knowledge has important clinical benefits in addition to its value as a contribution to our understanding of somatosensory development.

Project Start
Project End
Budget Start
Budget End
Support Year
6
Fiscal Year
1991
Total Cost
Indirect Cost
Name
Saint Louis University
Department
Type
DUNS #
City
Saint Louis
State
MO
Country
United States
Zip Code
63103
Jacquin, Mark F; Arends, Joop J A; Renehan, William E et al. (2015) Whisker-related circuitry in the trigeminal nucleus principalis: Topographic precision. Somatosens Mot Res 32:8-20
Xiang, Chuanxi; Arends, Joop J A; Jacquin, Mark F (2014) Whisker-related circuitry in the trigeminal nucleus principalis: ultrastructure. Somatosens Mot Res 31:141-51
Vadivelu, Sudhakar; Platik, Marina M; Choi, Luke et al. (2005) Multi-germ layer lineage central nervous system repair: nerve and vascular cell generation by embryonic stem cells transplanted in the injured brain. J Neurosurg 103:124-35
Pluto, Charles P; Chiaia, Nicolas L; Rhoades, Robert W et al. (2005) Reducing contralateral SI activity reveals hindlimb receptive fields in the SI forelimb-stump representation of neonatally amputated rats. J Neurophysiol 94:1727-32
Genc, Baris; Ulupinar, Emel; Erzurumlu, Reha S (2005) Differential Trk expression in explant and dissociated trigeminal ganglion cell cultures. J Neurobiol 64:145-56
Gandhi, Rohan; Ryals, Janelle M; Wright, Douglas E (2004) Neurotrophin-3 reverses chronic mechanical hyperalgesia induced by intramuscular acid injection. J Neurosci 24:9405-13
McDonald, John W; Becker, Daniel; Holekamp, Terrence F et al. (2004) Repair of the injured spinal cord and the potential of embryonic stem cell transplantation. J Neurotrauma 21:383-93
Genc, Baris; Ozdinler, P Hande; Mendoza, April E et al. (2004) A chemoattractant role for NT-3 in proprioceptive axon guidance. PLoS Biol 2:e403
Ulupinar, Emel; Unal, Nedim; Erzurumlu, Reha S (2004) Morphometric analysis of embryonic rat trigeminal neurons treated with different neurotrophins. Anat Rec A Discov Mol Cell Evol Biol 277:396-407
Wright, Douglas E; Ryals, Janelle M; McCarson, Kenneth E et al. (2004) Diabetes-induced expression of activating transcription factor 3 in mouse primary sensory neurons. J Peripher Nerv Syst 9:242-54

Showing the most recent 10 out of 178 publications