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Autonomic, sensory, and motor dysfunction following intrathecal administration of three substance P antagonists.

Autonomic, sensory, and motor dysfunction following intrathecal administration of three substance P antagonists. Research Abstract Details 

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  • Autonomic, sensory, and motor dysfunction following intrathecal administration of three substance P antagonists. Abstract Text:

    b f coxB F Cox,r l schelperR L Schelper,f m faraciF M Faraci,m j brodyM J Brody,

    Antagonists of the putative peptide neurotransmitter substance P have been found to produce pronounced cardiovascular effects when administered into the spinal subarachnoid space. These previous studies have not, however, provided any direct evidence that these effects result from interaction with substance P receptors. The present study was designed to characterize the modification of cardiovascular function resulting from administration of these compounds, and evaluate their effects on the integrity of spinal cord function. Intrathecal administration of two substance P antagonists produced a depressor response accompanied by a reduction of hindquarter vascular resistance. Following administration of a substance P antagonist, the integrated cardiovascular responses to electrical stimulation of the renal afferent nerves and ventrolateral medulla were markedly attenuated. Intrathecal administration to conscious rats of three substance P antagonists led to a variety of sensory and motor dysfunctions, including loss of spontaneous motor function, responsiveness to mechanical and thermal stimuli, and bladder function. No such effects were produced by administration of substance P, luteinizing hormone releasing hormone (LHRH), or LHRH antagonist. These effects from administration of a substance P antagonist were associated with a dose-dependent necrosis of spinal cord tissue. The necrosis may be secondary to ischemia since pretreatment with the vasodilator adenosine significantly delayed or blocked the sensory and motor dysfunctions. This conclusion was supported by the demonstration that cerebrovascular smooth muscle (pial vessels) was constricted by a SP antagonist. Taken together, these data suggest that substance P antagonists appear to non-specifically block transmission in the spinal cord, by mechanisms which may involve reduction of blood flow to the spinal cord.

    Autonomic, sensory, and motor dysfunction following intrathecal administration of three substance P antagonists. Publishing Authors By Initials

    bf coxBF Cox,rl schelperRL Schelper,fm faraciFM Faraci,mj brodyMJ Brody,

    For similar peptides: intercellular signaling peptides and proteins: kinins: tachykinins: substance p research abstracts see: peptides: intercellular signaling peptides and proteins: kinins: tachykinins: substance p research

    PUBMED ID PMID:

    MEDLINE DATE:

    Autonomic, sensory, and motor dysfunction following intrathecal administration of three substance P antagonists. Journal Published:

    PUBLICATION TYPE: Research Support, U.S. Gov't,

    Journal: Experimental brain research. Experimentelle Hirnfo

    VOLUME: 70

    Page Numbers: 61-72

    Journal Abbreviation:

    ISSN: 0014-4819

    DAY: 15

    MONTH: 02

    YEAR: 1988

    Autonomic, sensory, and motor dysfunction following intrathecal administration of three substance P antagonists. Information

    Number of References:

    LANGUAGE: eng

    NlmUniqueID: 43312

    Autonomic, sensory, and motor dysfunction following intrathecal administration of three substance P antagonists. Keywords Mesh Terms:

    KEYWORDS: Substance P

    MESH TERMS: pharmacology

    Chemical & Substance for Abstract: Autonomic, sensory, and motor dysfunction following intrathecal administration of three substance P antagonists. Information

    Substance Name: substance P, Arg(1)-Pro(2)-Trp(7,9)-Leu(

    Registry Number: 83374-71-4

    Grant and Affiliation Information for Autonomic, sensory, and motor dysfunction following intrathecal administration of three substance P antagonists.

    AFFILIATION: Department of Pharmacology, College of Medicine, University of Iowa, Iowa City 52242.

    Country: GERMANY, WEST

    GERMANY, WEST Research PublicationGERMANY, WEST Research Publication

    AGENCY:

    GRANT:

    ACRONYM:

    MEDLINETA: Exp Brain Res

    REFSOURCE:

    DATABASENAME:

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    Number Hits: 0

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