Literature DB >> 12930812

Developmental learning in a pain-related system: evidence for a cross-modality mechanism.

Alexandra Waldenström1, Jonas Thelin, Erik Thimansson, Anders Levinsson, Jens Schouenborg.   

Abstract

The nociceptive spinal reflex system performs highly precise sensorimotor transformations that require functionally specified synaptic strengths. The specification is gradually attained during early development and appears to be learning dependent. Here we determine the time course of this specification for heat-nociceptive tail withdrawal reflexes and analyze which types of primary afferents are important for the learning by applying various forms of noninvasive sensory deprivations. The percentage of erroneous heat-nociceptive tail withdrawal reflexes (i.e., movements directed toward the stimulation) decreased gradually from 64.1 +/- 2.5% (mean +/- SEM) to <10% during postnatal days 10-21. This improvement was completely blocked by anesthetizing the tail during the adaptation period, confirming that an experience-dependent mechanism is involved in the specification of synaptic strengths. However, the results show that the adaptation occurs to a significant extent despite local analgesia and protection of the tail from noxious input, provided that tactile sensitivity is preserved. Therefore, it appears that a nociceptive input is not necessary for the adaptation, and that input from tactile receptors can be used to guide the nociceptive synaptic organization during development. Sensory deprivation in the adult rat failed to affect the heat-nociceptive withdrawal reflex system, indicating that the adaptation has a "critical period" during early development. These findings provide a key to the puzzle of how pain-related systems can be functionally adapted through experience despite the rare occurrence of noxious input during early life.

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Mesh:

Year:  2003        PMID: 12930812      PMCID: PMC6740755     

Source DB:  PubMed          Journal:  J Neurosci        ISSN: 0270-6474            Impact factor:   6.167


  27 in total

1.  C-fiber activity-dependent maturation of glycinergic inhibition in the spinal dorsal horn of the postnatal rat.

Authors:  Stephanie C Koch; Keri K Tochiki; Stefan Hirschberg; Maria Fitzgerald
Journal:  Proc Natl Acad Sci U S A       Date:  2012-07-09       Impact factor: 11.205

2.  Neonatal Injury Alters Sensory Input and Synaptic Plasticity in GABAergic Interneurons of the Adult Mouse Dorsal Horn.

Authors:  Jie Li; Mark L Baccei
Journal:  J Neurosci       Date:  2019-08-16       Impact factor: 6.167

3.  Action-based body maps in the spinal cord emerge from a transitory floating organization.

Authors:  Marcus Granmo; Per Petersson; Jens Schouenborg
Journal:  J Neurosci       Date:  2008-05-21       Impact factor: 6.167

4.  Activity-dependent modulation of glutamatergic signaling in the developing rat dorsal horn by early tissue injury.

Authors:  Jie Li; Suellen M Walker; Maria Fitzgerald; Mark L Baccei
Journal:  J Neurophysiol       Date:  2009-08-12       Impact factor: 2.714

5.  Pacemaker neurons within newborn spinal pain circuits.

Authors:  Jie Li; Mark L Baccei
Journal:  J Neurosci       Date:  2011-06-15       Impact factor: 6.167

6.  Tolerance, opioid-induced allodynia and withdrawal associated allodynia in infant and young rats.

Authors:  M H Zissen; G Zhang; A McKelvy; J T Propst; J J Kendig; S M Sweitzer
Journal:  Neuroscience       Date:  2006-10-19       Impact factor: 3.590

7.  Connectivity of pacemaker neurons in the neonatal rat superficial dorsal horn.

Authors:  Jie Li; Elizabeth Kritzer; Neil C Ford; Shahriar Arbabi; Mark L Baccei
Journal:  J Comp Neurol       Date:  2015-02-17       Impact factor: 3.215

Review 8.  The development of pain circuits and unique effects of neonatal injury.

Authors:  Chelsie L Brewer; Mark L Baccei
Journal:  J Neural Transm (Vienna)       Date:  2019-08-09       Impact factor: 3.575

9.  Transcriptional expression of voltage-gated Na⁺ and voltage-independent K⁺ channels in the developing rat superficial dorsal horn.

Authors:  M L Blankenship; D E Coyle; M L Baccei
Journal:  Neuroscience       Date:  2012-12-07       Impact factor: 3.590

10.  Postnatal tuning of cutaneous inhibitory receptive fields in the rat.

Authors:  Lindsay R Bremner; Maria Fitzgerald
Journal:  J Physiol       Date:  2007-12-13       Impact factor: 5.182

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