Literature DB >> 8283205

In vitro electrophysiology of developing genioglossal motoneurons in the rat.

P A Núñez-Abades1, J M Spielmann, G Barrionuevo, W E Cameron.   

Abstract

1. Experiments were performed to determine the change in membrane properties of genioglossal (GG) motoneurons during development. Intracellular recordings were made in 127 GG motoneurons from rats postnatal ages 1-30 days. 2. The input resistance (R(in)) and the membrane time constant (t(aum)) decreased between 5-6 and 13-15 days from 84.8 +/- 25.4 (SD) to 47.0 +/- 18.9 M omega (P < 0.01) and from 10.0 +/- 4.2 to 7.3 +/- 3.3 ms (P < 0.05), respectively. During this period, the rheobase (Irh) increased (P < 0.01) from 0.13 +/- 0.07 to 0.27 +/- 0.14 nA, and the percentage of cells exhibiting inward rectification increased from 5 to 40%. Voltage threshold (Vthr) of the action potential remained unchanged postnatally. 3. There was also a postnatal change in the shape of the action potential. Specifically, between 1-2 and 5-6 days, there was a decrease (P < 0.05) in the spike half-width from 2.23 +/- 0.53 to 1.45 +/- 0.44 ms, resulting, in part, from a steepening (P < 0.05) of the slope of the falling phase of the action potential from 21.6 +/- 10.1 to 32.9 +/- 13.1 mV/ms. The slope of the rising phase also increased significantly (P < 0.01) between 1-2 and 13-15 days from 68.4 +/- 31.0 to 91.4 +/- 44.3 mV/ms. 4. The average duration of the medium afterhyperpolarization (mAHPdur) decreased (P < 0.05) between 1-2 (193 +/- 53 ms) and 5-6 days (159 +/- 43 ms). Whereas the mAHPdur was found to be independent of membrane potential, there was a linear relationship between the membrane potential and the amplitude of the medium AHP (mAHPamp). From this latter relationship, a reversal potential for the mAHPamp was extrapolated to be -87 mV. No evidence for the existence of a slow AHP was found in these developing motoneurons. 5. All cells analyzed (n = 74) displayed adaptation during the first three spikes. The subsequent firing pattern was classified into two groups, adapting and nonadapting. Cells at birth were all adapting, whereas all cells but two from animals 13 days and older were nonadapting. At the intermediate age (5-6 days), the minority (27%) was adapting and the majority (73%) was nonadapting. 6. The mean slope of primary range for the first interspike interval (1st ISI) was approximately 90 Hz/nA. This value was similar for both adapting and nonadapting cells and did not change postnatally.(ABSTRACT TRUNCATED AT 400 WORDS)

Entities:  

Mesh:

Year:  1993        PMID: 8283205     DOI: 10.1152/jn.1993.70.4.1401

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


  13 in total

1.  Neonatal deafferentation does not alter membrane properties of trigeminal nucleus principalis neurons.

Authors:  F S Lo; R S Erzurumlu
Journal:  J Neurophysiol       Date:  2001-03       Impact factor: 2.714

2.  GAD67-GFP+ neurons in the Nucleus of Roller: a possible source of inhibitory input to hypoglossal motoneurons. I. Morphology and firing properties.

Authors:  J F M van Brederode; Y Yanagawa; A J Berger
Journal:  J Neurophysiol       Date:  2010-11-03       Impact factor: 2.714

3.  Reconfiguration of the pontomedullary respiratory network: a computational modeling study with coordinated in vivo experiments.

Authors:  I A Rybak; R O'Connor; A Ross; N A Shevtsova; S C Nuding; L S Segers; R Shannon; T E Dick; W L Dunin-Barkowski; J M Orem; I C Solomon; K F Morris; B G Lindsey
Journal:  J Neurophysiol       Date:  2008-07-23       Impact factor: 2.714

4.  Postnatal development of serotonergic innervation, 5-HT1A receptor expression, and 5-HT responses in rat motoneurons.

Authors:  E M Talley; N N Sadr; D A Bayliss
Journal:  J Neurosci       Date:  1997-06-01       Impact factor: 6.167

5.  Homeostatic dysregulation in membrane properties of masticatory motoneurons compared with oculomotor neurons in a mouse model for amyotrophic lateral sclerosis.

Authors:  Sharmila Venugopal; Chie-Fang Hsiao; Takuma Sonoda; Martina Wiedau-Pazos; Scott H Chandler
Journal:  J Neurosci       Date:  2015-01-14       Impact factor: 6.167

Review 6.  Retracing your footsteps: developmental insights to spinal network plasticity following injury.

Authors:  C Jean-Xavier; S A Sharples; K A Mayr; A P Lognon; P J Whelan
Journal:  J Neurophysiol       Date:  2017-10-25       Impact factor: 2.714

7.  Normal Development and Pathology of Motoneurons: Anatomy, Electrophysiological Properties, Firing Patterns and Circuit Connectivity.

Authors:  Joshua I Chalif; George Z Mentis
Journal:  Adv Neurobiol       Date:  2022

8.  Repetitive firing properties of developing rat brainstem motoneurones.

Authors:  F Viana; D A Bayliss; A J Berger
Journal:  J Physiol       Date:  1995-08-01       Impact factor: 5.182

9.  Diminution of voltage threshold plays a key role in determining recruitment of oculomotor nucleus motoneurons during postnatal development.

Authors:  Livia Carrascal; Jose Luis Nieto-González; Blas Torres; Pedro Nunez-Abades
Journal:  PLoS One       Date:  2011-12-09       Impact factor: 3.240

10.  Maturation of spinal motor neurons derived from human embryonic stem cells.

Authors:  Tomonori Takazawa; Gist F Croft; Mackenzie W Amoroso; Lorenz Studer; Hynek Wichterle; Amy B Macdermott
Journal:  PLoS One       Date:  2012-07-03       Impact factor: 3.240

View more

北京卡尤迪生物科技股份有限公司 © 2022-2023.