Literature DB >> 2439159

GABAergic modulation of a substance P-mediated reflex of slow time course in the isolated rat spinal cord.

H Akagi, M Yanagisawa.   

Abstract

The effects of gamma-aminobutyric acid (GABA) and other drugs which interact with GABA receptors were studied on a reflex of slow time course in the spinal cord preparation isolated from the neonatal rat. A single shock to a dorsal root (L3-L5) elicited a stereotyped series of reflexes, consisting of fast and slow components, recorded from the contralateral ventral root of the corresponding segment. The slow component, i.e. the contralateral slow ventral root potential (v.r.p.) had a time-to-peak of 2-5 s and lasted 20-30 s. Bath-application of GABA (5-20 microM) or muscimol (0.05-0.5 microM) caused a decrease in the amplitude of the contralateral slow v.r.p. without producing any change in the d.c. potential recorded from the ventral root. The monosynaptic reflex recorded from the ipsilateral ventral root was not changed by the drugs at these concentrations. Diazepam (0.1-1 microM) potentiated the depolarizing response of the dorsal root to GABA and markedly depressed the contralateral slow v.r.p. Neither the d.c. potential of the ventral root nor the dorsal root was changed by diazepam. The monosynaptic reflex was also unaffected by the drug. Bicuculline (1 microM) suppressed the GABA-induced depolarization recorded from the dorsal root whilst it markedly potentiated the contralateral slow v.r.p. Baclofen at concentrations from 0.01 to 0.1 microM reduced the contralateral slow v.r.p. The inhibitory action of baclofen on the contralateral slow v.r.p. was more marked than on the monosynaptic reflex. 7 The depolarization of the ventral root induced by a brief application of substance P (SP) was depressed by muscimol, diazepam and baclofen, whereas the depolarization was potentiated by bicuculline. 8 The present results suggest that an intraspinal GABAergic inhibitory mechanism plays a role in the modulation of certain slow spinal reflexes. They also support the hypothesis that SP released from certain primary afferent fibres is a neurotransmitter involved in the contralateral slow v.r.p.

Entities:  

Mesh:

Substances:

Year:  1987        PMID: 2439159      PMCID: PMC1853490          DOI: 10.1111/j.1476-5381.1987.tb08998.x

Source DB:  PubMed          Journal:  Br J Pharmacol        ISSN: 0007-1188            Impact factor:   8.739


  21 in total

1.  Antagonism between Lioresal and substance P in rat spinal cord.

Authors:  K Saito; S Konishi; M Otsuka
Journal:  Brain Res       Date:  1975-10-24       Impact factor: 3.252

2.  Quantitative histochemistry of gamma-aminobutyric acid in cat spinal cord with special reference to presynaptic inhibition.

Authors:  Y Miyata; M Otsuka
Journal:  J Neurochem       Date:  1975-09       Impact factor: 5.372

3.  Opiate analgesics and endorphins inhibit rat dorsal root potential in vitro.

Authors:  T Suzue; T Jessell
Journal:  Neurosci Lett       Date:  1980-02       Impact factor: 3.046

4.  A substance P antagonist inhibits a slow reflex response in the spinal cord of the newborn rat.

Authors:  M Yanagisawa; M Otsuka; S Konishi; H Akagi; K Folkers; S Rosell
Journal:  Acta Physiol Scand       Date:  1982-09

5.  An immunohistochemical study of neuronal populations containing neuropeptides or gamma-aminobutyrate within the superficial layers of the rat dorsal horn.

Authors:  S P Hunt; J S Kelly; P C Emson; J R Kimmel; R J Miller; J Y Wu
Journal:  Neuroscience       Date:  1981       Impact factor: 3.590

6.  GABA-ergic influence on the crossed extensor reflex.

Authors:  K Kawasaki; A Matsushita
Journal:  Life Sci       Date:  1982-05-10       Impact factor: 5.037

7.  The role of substance P as a neurotransmitter in the reflexes of slow time courses in the neonatal rat spinal cord.

Authors:  H Akagi; S Konishi; M Otsuka; M Yanagisawa
Journal:  Br J Pharmacol       Date:  1985-03       Impact factor: 8.739

8.  Immunocytochemical localization of glutamate decarboxylase in rat spinal cord.

Authors:  B J McLaughlin; R Barber; K Saito; E Roberts; J Y Wu
Journal:  J Comp Neurol       Date:  1975-12-01       Impact factor: 3.215

9.  The binding of [3H]-diazepam to guinea-pig ileal longitudinal muscle and the in vitro inhibition of contraction by benzodiazepines.

Authors:  J P Hullihan; S Spector; T Taniguchi; J K Wang
Journal:  Br J Pharmacol       Date:  1983-02       Impact factor: 8.739

10.  The development of the dorsal root potential and the responsiveness of primary afferent fibers to gamma-aminobutyric acid in the spinal cord of rat fetuses.

Authors:  N Seno; K Saito
Journal:  Brain Res       Date:  1985-01       Impact factor: 3.252

View more
  6 in total

1.  Inhibitory effects of dopamine on spinal synaptic transmission via dopamine D1-like receptors in neonatal rats.

Authors:  K Kawamoto; K Otsuguro; M Ishizuka; S Ito
Journal:  Br J Pharmacol       Date:  2012-05       Impact factor: 8.739

2.  Evidence for an excitatory action of the benzodiazepine receptor inverse agonist FG 7142 on C-fibre afferents.

Authors:  J Donnerer
Journal:  Naunyn Schmiedebergs Arch Pharmacol       Date:  1989-09       Impact factor: 3.000

3.  Differential contributions of adenosine to hypoxia-evoked depressions of three neuronal pathways in isolated spinal cord of neonatal rats.

Authors:  K Otsuguro; M Wada; S Ito
Journal:  Br J Pharmacol       Date:  2011-09       Impact factor: 8.739

4.  A novel metabotropic glutamate receptor agonist: marked depression of monosynaptic excitation in the newborn rat isolated spinal cord.

Authors:  M Ishida; T Saitoh; K Shimamoto; Y Ohfune; H Shinozaki
Journal:  Br J Pharmacol       Date:  1993-08       Impact factor: 8.739

5.  The effect of centrally acting myorelaxants on NMDA receptor-mediated synaptic transmission in the immature rat spinal cord in vitro.

Authors:  R J Siarey; S K Long; R H Evans
Journal:  Br J Pharmacol       Date:  1992-10       Impact factor: 8.739

6.  The effects of central myorelaxants on synaptically-evoked primary afferent depolarization in the immature rat spinal cord in vitro.

Authors:  R J Siarey; S K Long; M T Tulp; R H Evans
Journal:  Br J Pharmacol       Date:  1994-02       Impact factor: 8.739

  6 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.