Document Detail


Partial transection of the ipsilateral cervical spinal cord evokes a sustained increase in the adrenal section of catecholamines in the cat.
MedLine Citation:
PMID:  2477435     Owner:  NLM     Status:  MEDLINE    
Abstract/OtherAbstract:
The importance of cervical spinal pathways on the adrenal secretion of catecholamines was assessed in chloralose-anesthetized cats. Partial transections of the upper cervical spinal cord were made ipsilateral (n = 21) or contralateral (n = 10) to the adrenal vein sampling catheter. Ipsilateral cuts evoked an immediate increase in the adrenal secretion of epinephrine that remained elevated at 60 min (+89.7 +/- 27.0 ng/min, P less than 0.001) and increased the epinephrine/norepinephrine secretory ratio from 1.99 +/- 0.4 to 5.02 +/- 0.6 by 60 min (P less than 0.01) indicating a preferential augmentation of the secretion of epinephrine. The magnitude of the increase in secretion of epinephrine was well correlated with the cross-sectional area of the ipsilateral cut (rs = 0.681, P less than 0.01). In contrast, partial transections of similar size made contralateral to the adrenal vein sample evoked significantly smaller increases in the adrenal secretion of epinephrine by 60 min (+12.7 +/- 4.8 ng/min) and were not correlated with the cross-sectional area of the cut. The region of transection common to those experiments that caused the greatest increase in the secretion of catecholamines included the deep laminae (laminae V-VII) within the central gray matter as well as a portion of the dorsal columns. Transections restricted to the dorsolateral and lateral funiculi caused small and inconsistent changes in the adrenal secretion of catecholamines. Ipsilateral and contralateral cuts evoked similar effects on peripheral concentrations of catecholamines, on plasma adrenocorticotropin and on plasma angiotensin II, suggesting that the facilitatory effect of ipsilateral cuts on the adrenal secretion of catecholamines was not the result of a humoral mechanism. Arterial pressure and heart rate increased equally by 1 min and returned to prestimulus values by 5 min after transections of the ipsilateral or of the contralateral cervical cord. Electrical stimulation of the ipsilateral cervical spinal cord, caudal to the level of transection, decreased the secretion of epinephrine and arterial pressure by 1 min (-30.5 +/- 9.0%. P less than 0.05) suggesting the presence of an active inhibitory mechanism that persisted after transection. The results indicated that transections of pathways ipsilateral, but not contralateral, to the adrenal medulla that traverse the upper cervical spinal cord evoke a persistent increase in the adrenal secretion of epinephrine, whereas other indices of neuroendocrine or autonomic function do not reflect this tonic influence.(ABSTRACT TRUNCATED AT 400 WORDS)
Authors:
D A Bereiter
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Publication Detail:
Type:  Journal Article; Research Support, U.S. Gov't, P.H.S.    
Journal Detail:
Title:  Journal of the autonomic nervous system     Volume:  27     ISSN:  0165-1838     ISO Abbreviation:  J. Auton. Nerv. Syst.     Publication Date:  1989 Aug 
Date Detail:
Created Date:  1989-11-07     Completed Date:  1989-11-07     Revised Date:  2008-11-21    
Medline Journal Info:
Nlm Unique ID:  8003419     Medline TA:  J Auton Nerv Syst     Country:  NETHERLANDS    
Other Details:
Languages:  eng     Pagination:  181-92     Citation Subset:  IM    
Affiliation:
Section of Neurobiology, Brown University/Rhode Island Hospital, Providence 02903.
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MeSH Terms
Descriptor/Qualifier:
Adrenal Glands / innervation,  metabolism*
Animals
Autonomic Nervous System / physiology
Cardiovascular Physiological Phenomena
Catecholamines / metabolism*
Cats
Electric Stimulation
Female
Functional Laterality / physiology*
Male
Spinal Cord / physiology*
Substance P / pharmacology
Grant Support
ID/Acronym/Agency:
DK26831/DK/NIDDK NIH HHS; NS26137/NS/NINDS NIH HHS
Chemical
Reg. No./Substance:
0/Catecholamines; 33507-63-0/Substance P

From MEDLINE®/PubMed®, a database of the U.S. National Library of Medicine


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