Literature DB >> 2754484

Primary afferent-evoked synaptic responses and slow potential generation in rat substantia gelatinosa neurons in vitro.

M Yoshimura1, T M Jessell.   

Abstract

1. Primary afferent fiber-evoked synaptic responses and the mechanisms of spike and slow potential generation have been examined in adult rat substantia gelatinosa (SG) neurons in an in vitro transverse spinal cord slice preparation in which an attached dorsal root is retained. Intracellular recordings were made from SG neurons identified by morphological and electrophysiological criteria. Afferent fiber-evoked fast excitatory postsynaptic potentials (fast EPSPs) and slow EPSPs have been analyzed. 2. SG neurons had mean resting membrane potentials of -67.1 +/- 0.5 mV (mean +/- SE), mean input resistance of 257 +/- 17.7 (SE) M omega, and a mean time constant of 21.3 +/- 1.9 ms and exhibited spontaneous EPSPs. 3. Single low-intensity stimuli applied to the dorsal root using a suction electrode produced, in 70% of SG neurons, short-latency, presumed monosynaptic fast EPSPs which had a half decay time of 10-30 ms and an amplitude of 8-28 mV. The conduction velocity of afferent fibers evoking fast EPSPs was 2-7 m/s, corresponding to that of thinly myelinated A-delta-fibers. Dorsal root stimulation at higher intensities evoked, in 10% of SG neurons, long-latency and apparently monosynaptic EPSPs which had a time course and amplitude similar to that evoked by low-intensity stimulation. The conduction velocity of fibers evoking long-latency EPSPs was 0.4-2 m/s, suggesting that they constitute predominantly C-fibers. A-delta- and C-fiber-mediated fast EPSPs were detected in 20% of SG neurons examined. 4. Low-intensity stimuli produced slow EPSPs in 20% of SG neurons. Slow EPSPs were 3-15 mV in amplitude and of up to 2 min in duration. A-delta-fibers appeared to be responsible for the generation of slow EPSPs. Slow EPSPs were associated with an increase in membrane resistance and were decreased in amplitude with membrane hyperpolarization. 5. Action potentials in SG neurons had a mean amplitude of 76.3 +/- 1.1 mV and a mean duration of 1.0 +/- 0.07 ms. Na+ ions represent the main charge carrier during the rising phase of the action potential and Ca2+ ions contribute to the shoulder on the falling phase. 6. In 20% of SG neurons, subthreshold depolarizing pulses were followed by long-lasting slow-inactivating depolarizing potentials which were able to initiate spikes. The slow depolarizing potentials were blocked by TTX and enhanced by application of TEA and Ba2+, suggesting that Na+ and K+ are involved in this slow-inactivating potential.(ABSTRACT TRUNCATED AT 400 WORDS)

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Year:  1989        PMID: 2754484     DOI: 10.1152/jn.1989.62.1.96

Source DB:  PubMed          Journal:  J Neurophysiol        ISSN: 0022-3077            Impact factor:   2.714


  72 in total

1.  Responsiveness of rat substantia gelatinosa neurones to mechanical but not thermal stimuli revealed by in vivo patch-clamp recording.

Authors:  H Furue; K Narikawa; E Kumamoto; M Yoshimura
Journal:  J Physiol       Date:  1999-12-01       Impact factor: 5.182

2.  Actions of opioids on excitatory and inhibitory transmission in substantia gelatinosa of adult rat spinal cord.

Authors:  T Kohno; E Kumamoto; H Higashi; K Shimoji; M Yoshimura
Journal:  J Physiol       Date:  1999-08-01       Impact factor: 5.182

3.  Synaptic reorganization in the substantia gelatinosa after peripheral nerve neuroma formation: aberrant innervation of lamina II neurons by Abeta afferents.

Authors:  I Kohama; K Ishikawa; J D Kocsis
Journal:  J Neurosci       Date:  2000-02-15       Impact factor: 6.167

4.  Correlations between neuronal morphology and electrophysiological features in the rodent superficial dorsal horn.

Authors:  T J Grudt; E R Perl
Journal:  J Physiol       Date:  2002-04-01       Impact factor: 5.182

5.  Mechanisms for ovariectomy-induced hyperalgesia and its relief by calcitonin: participation of 5-HT1A-like receptor on C-afferent terminals in substantia gelatinosa of the rat spinal cord.

Authors:  A Ito; E Kumamoto; M Takeda; K Shibata; H Sagai; M Yoshimura
Journal:  J Neurosci       Date:  2000-08-15       Impact factor: 6.167

6.  Electrophysiological mapping of the nociceptive inputs to the substantia gelatinosa in rat horizontal spinal cord slices.

Authors:  Go Kato; Hidemasa Furue; Toshihiko Katafuchi; Toshiharu Yasaka; Yukihide Iwamoto; Megumu Yoshimura
Journal:  J Physiol       Date:  2004-08-05       Impact factor: 5.182

7.  Inhibitory neurones of the spinal substantia gelatinosa mediate interaction of signals from primary afferents.

Authors:  Jihong Zheng; Yan Lu; Edward R Perl
Journal:  J Physiol       Date:  2010-04-19       Impact factor: 5.182

8.  In vivo responses of mouse superficial dorsal horn neurones to both current injection and peripheral cutaneous stimulation.

Authors:  B A Graham; A M Brichta; R J Callister
Journal:  J Physiol       Date:  2004-10-07       Impact factor: 5.182

9.  Synaptic responses of substantia gelatinosa neurones to dorsal column stimulation in rat spinal cord in vitro.

Authors:  H Baba; M Yoshimura; S Nishi; K Shimoji
Journal:  J Physiol       Date:  1994-07-01       Impact factor: 5.182

10.  Involvement of neurokinin receptors in the induction but not the maintenance of mechanical allodynia in rat flexor motoneurones.

Authors:  Q P Ma; C J Woolf
Journal:  J Physiol       Date:  1995-08-01       Impact factor: 5.182

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