Literature DB >> 12466442

Developmental changes in short-term synaptic depression in the neonatal mouse spinal cord.

Yan Li1, R E Burke.   

Abstract

We examined age-dependent changes in short-term synaptic depression of monosynaptic excitatory postsynaptic potentials (EPSPs) recorded in lumbar motoneurons in hemisected spinal cords of neonatal Swiss-Webster mice between postnatal day 2 (P2) and 12 (P12). We used four paradigms that sample the input-output dependence on stimulation history in different but complementary ways: 1) paired-pulse depression; 2) steady-state depression during constant frequency trains; 3) modulation during irregular stimulation sequences; and 4) recovery after high-frequency conditioning trains. Paired-pulse synaptic depression declined more than steady-state depression during 10-pulse trains at frequencies from 0.125 to 8 Hz in this age range. Depression during sequences of irregular stimulations that more closely mimic physiological activation also declined with postnatal age. On the other hand, the overall rate of synaptic recovery after a 4-Hz conditioning train exhibited surprisingly little change between P2 and P12. Control experiments indicated that these observations depend primarily, if not exclusively, on changes in presynaptic transmitter release. The data were examined using quantitative models that incorporate factors that have been suggested to exist at more specialized central synapses. The model that best predicted the observations included two presynaptic compartments that are depleted during activation, plus two superimposed processes that enhance transmitter release by different mechanisms. One of the latter produced rapidly-decaying enhancement of transmitter release fraction. The other mechanism indirectly enhanced the rate of renewal of one of the depleted presynaptic compartments. This model successfully predicted the constant frequency and irregular sequence data from all age groups, as well as the recovery curves following short, high-frequency tetani. The results suggest that a reduction in release fraction accounts for much of the decline in synaptic depression during early postnatal development, although changes in both enhancement processes also contribute. The time constants of resource renewal showed surprisingly little change through the first 12 days of postnatal life.

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Year:  2002        PMID: 12466442     DOI: 10.1152/jn.00406.2002

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


  7 in total

1.  Primary afferent synapses on developing and adult Renshaw cells.

Authors:  George Z Mentis; Valerie C Siembab; Ricardo Zerda; Michael J O'Donovan; Francisco J Alvarez
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2.  Activity Regulates the Incidence of Heteronymous Sensory-Motor Connections.

Authors:  Alana I Mendelsohn; Christian M Simon; L F Abbott; George Z Mentis; Thomas M Jessell
Journal:  Neuron       Date:  2015-06-18       Impact factor: 17.173

3.  Functional maturation of the macaque's lateral geniculate nucleus.

Authors:  J Anthony Movshon; Lynne Kiorpes; Michael J Hawken; James R Cavanaugh
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4.  Functionally reduced sensorimotor connections form with normal specificity despite abnormal muscle spindle development: the role of spindle-derived neurotrophin 3.

Authors:  Neil A Shneider; George Z Mentis; Joshua Schustak; Michael J O'Donovan
Journal:  J Neurosci       Date:  2009-04-15       Impact factor: 6.167

5.  Preservation of VGLUT1 synapses on ventral calbindin-immunoreactive interneurons and normal locomotor function in a mouse model of spinal muscular atrophy.

Authors:  Vatsala Thirumalai; Rachel M Behrend; Swetha Birineni; Wenfang Liu; Dvir Blivis; Michael J O'Donovan
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Review 6.  Enabling techniques for in vitro studies on mammalian spinal locomotor mechanisms.

Authors:  Shawn Hochman; Elizabeth A Gozal; Heather B Hayes; JoAnna T Anderson; Stephen P DeWeerth; Young-Hui Chang
Journal:  Front Biosci (Landmark Ed)       Date:  2012-06-01

7.  The Classical Complement Pathway Mediates Microglia-Dependent Remodeling of Spinal Motor Circuits during Development and in SMA.

Authors:  Aleksandra Vukojicic; Nicolas Delestrée; Emily V Fletcher; John G Pagiazitis; Sethu Sankaranarayanan; Ted A Yednock; Ben A Barres; George Z Mentis
Journal:  Cell Rep       Date:  2019-12-03       Impact factor: 9.423

  7 in total

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