Literature DB >> 2460194

Facilitation of the tail-flick reflex by noxious cutaneous stimulation in the rat: antagonism by a substance P analogue.

R A Cridland1, J L Henry.   

Abstract

Effects of noxious cutaneous stimulation on the tail flick reflex were examined in the anaesthetized rat. Noxious stimulation was applied by immersing the distal 4 cm of the tail in water at 55 degrees C for 1.5 min. The tail flick reflex was tested at 3 min intervals by applying a noxious radiant heat stimulus to a region of the tail 10 cm proximal to the tip. Tail immersion reduced reaction time to tail flick by 30% and 20% at 0.5 and 3.5 min after immersion, respectively. Reaction time returned to control at 6.5 min and tended to increase above baseline values at 9.5 and 12.5 min. Naloxone (10 mg/kg, i.p.) potentiated the effects of tail immersion on reaction time and prevented the increase above baseline. When the surface temperature of the skin used to evoke the tail flick reflex was raised by 10 degrees C using innocuous radiant heat, reaction time was not significantly different from the control, suggesting that an increase in skin temperature per se is insufficient to account for the response to immersion. Intrathecal administration of a substance P antagonist (1 nmol) attenuated the response to tail immersion. These results indicate that noxious cutaneous stimulation may release an agent in the spinal cord which facilitates the tail flick reflex, and that this agent is antagonized by a substance P antagonist.

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Year:  1988        PMID: 2460194     DOI: 10.1016/0006-8993(88)90579-3

Source DB:  PubMed          Journal:  Brain Res        ISSN: 0006-8993            Impact factor:   3.252


  5 in total

1.  Spinal neurons exhibiting a specific nociceptive response receive abundant substance P-containing synaptic contacts.

Authors:  Y De Koninck; A Ribeiro-da-Silva; J L Henry; A C Cuello
Journal:  Proc Natl Acad Sci U S A       Date:  1992-06-01       Impact factor: 11.205

2.  A substance P-opioid chimeric peptide as a unique nontolerance-forming analgesic.

Authors:  S E Foran; D B Carr; A W Lipkowski; I Maszczynska; J E Marchand; A Misicka; M Beinborn; A S Kopin; R M Kream
Journal:  Proc Natl Acad Sci U S A       Date:  2000-06-20       Impact factor: 11.205

3.  The effects of neurokinin A, neurokinin B, and eledoisin on substance P analysis.

Authors:  R J Naukam; W C Parris; J R Kambam; J B Kruskal
Journal:  J Clin Monit       Date:  1991-04

4.  Changes in Abeta non-nociceptive primary sensory neurons in a rat model of osteoarthritis pain.

Authors:  Qi Wu; James L Henry
Journal:  Mol Pain       Date:  2010-07-01       Impact factor: 3.395

5.  CP-96,345, a non-peptide antagonist of substance P: II. Actions on substance P-induced hypotension and bronchoconstriction, and on depressor reflexes in mammals.

Authors:  T Griesbacher; J Donnerer; F J Legat; F Lembeck
Journal:  Naunyn Schmiedebergs Arch Pharmacol       Date:  1992-09       Impact factor: 3.000

  5 in total

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