This proposal will examine the role of the spinal trigeminal nucleus in the control of the adrenal secretion of catecholamines and the cardiovascular responses evoked by peripheral and central activation of trigeminal neurons. Emphasis is directed at the intranuclear and neurochemical organization as well as the principal projection pathways of the spinal trigeminal nucleus that contribute to the adrenomedullary and autonomic aspects of nociception. Local activation of spinal trigeminal neurons by direct microinjection of glutamate or putative neurotransmitters will assess the relative contribution of rostral and caudal nuclear areas in control of adrenal and autonomic function. Peripheral trigeminal neurons are activated by mechanical radiant heat stimuli. Selective surgical interruption of central pathways or local neuronal inhibition by lidocaine microinjection will delineate the principal projection that underlie adrenal and cardiovascular responses evoked by trigeminal stimulation. Selective sampling of adrenal venous blood by lumboadrenal vein catheterization will permit estimates of adrenal secretion of catecholamines and adrenal blood flow to be determined with high resolution. Plasma catecholamines are assayed by HPLC with electrochemical detection. Carotid arterial blood flow, aortic arterial pressure, heart rate, and expiratory C02 are monitored continuously. Neurophysiological recording techniques will assess the efferent projections of spinal trigeminal neurons that may code for the adrenal and autonomic responses to noxious stimuli. Although the central neural organization that underlies the sensory- discriminative aspects of nociception has received much attention, the central neural organization that underlies the adrenal and autonomic responses to nociception is not well defined. This proposal focuses on the spinal trigeminal system as a model to assess the degree of overlap between the sensory- discriminative and the autonomic aspects of nociception.

Agency
National Institute of Health (NIH)
Institute
National Institute of Neurological Disorders and Stroke (NINDS)
Type
Research Project (R01)
Project #
5R01NS026137-02
Application #
3411801
Study Section
Experimental Cardiovascular Sciences Study Section (ECS)
Project Start
1988-04-01
Project End
1991-03-31
Budget Start
1989-04-01
Budget End
1990-03-31
Support Year
2
Fiscal Year
1989
Total Cost
Indirect Cost
Name
Rhode Island Hospital (Providence, RI)
Department
Type
DUNS #
161202122
City
Providence
State
RI
Country
United States
Zip Code
02903
Tashiro, A; Okamoto, K; Chang, Z et al. (2010) Behavioral and neurophysiological correlates of nociception in an animal model of photokeratitis. Neuroscience 169:455-62
Chang, Z; Okamoto, K; Tashiro, A et al. (2010) Ultraviolet irradiation of the eye and Fos-positive neurons induced in trigeminal brainstem after intravitreal or ocular surface transient receptor potential vanilloid 1 activation. Neuroscience 170:678-85
Okamoto, Keiichiro; Tashiro, Akimasa; Chang, Zheng et al. (2010) Bright light activates a trigeminal nociceptive pathway. Pain 149:235-42
Okamoto, K; Bereiter, D F; Tashiro, A et al. (2009) Ocular surface-evoked Fos-like immunoreactivity is enhanced in trigeminal subnucleus caudalis by prior exposure to endotoxin. Neuroscience 159:787-94
Okamoto, K; Thompson, R; Tashiro, A et al. (2009) Bright light produces Fos-positive neurons in caudal trigeminal brainstem. Neuroscience 160:858-64
Bereiter, David A; Okamoto, Keiichiro; Tashiro, Akimasa et al. (2005) Endotoxin-induced uveitis causes long-term changes in trigeminal subnucleus caudalis neurons. J Neurophysiol 94:3815-25
Hirata, Harumitsu; Okamoto, Keiichiro; Tashiro, Akimasa et al. (2004) A novel class of neurons at the trigeminal subnucleus interpolaris/caudalis transition region monitors ocular surface fluid status and modulates tear production. J Neurosci 24:4224-32
Hirata, Harumitsu; Okamoto, Keiichiro; Bereiter, David A (2003) GABA(A) receptor activation modulates corneal unit activity in rostral and caudal portions of trigeminal subnucleus caudalis. J Neurophysiol 90:2837-49
Bereiter, D A; Bereiter, D F; Hirata, H (2002) Topical cannabinoid agonist, WIN55,212-2, reduces cornea-evoked trigeminal brainstem activity in the rat. Pain 99:547-56
Hirata, H; Takeshita, S; Hu, J W et al. (2000) Cornea-responsive medullary dorsal horn neurons: modulation by local opioids and projections to thalamus and brain stem. J Neurophysiol 84:1050-61

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