Modulation of the voltage-gated sodium- and calcium-dependent potassium channels in rat vestibular and facial nuclei after unilateral labyrinthectomy and facial nerve transsection:: An in situ hybridization study

被引:21
作者
Patkó, T [1 ]
Vassias, I [1 ]
Vidal, PP [1 ]
De Waele, C [1 ]
机构
[1] Ctr Univ St Peres, CNRS Paris 5, LNRS, F-75270 Paris 06, France
关键词
Na alpha channels; SK channels; deafferentiation; medial vestibular nucleus; facial motoneurons; axotomy;
D O I
10.1016/S0306-4522(02)00829-1
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
We investigated whether the expression in the vestibular and facial nuclei of the voltage-dependent Na alphaI and Na alphaIII channels and of the Ca2+-activated K+-channel subunits, small-conductance (SK) 1, SK2 and SK3, is affected by unilateral inner-ear lesion including both labyrinthectomy and transsection of the facial nerve. Specific sodium (Na alphaI, Na alphaIII) and potassium (SK1, SK2, SK3) radioactive oligonucleotides were used to probe sections of rat vestibular and facial nuclei by in situ hybridization methods. The signal was detected with films or by emulsion photography. Animals were killed at various times following the lesion: 1 day, 3 days, 8 days or 30 days. In normal adult animals, mRNAs for Na alphaI, and SKI, SK2, and SK3 channels were found in several brainstem regions including the lateral, medial, superior and inferior vestibular nuclei and the facial nuclei. In contrast, there was little Na alphaIII subunit mRNA anywhere in the brainstem. Following unilateral inner ear lesion in rats, the medial vestibular nuclei were probed with Na alphaI, Na alphaIII, SK1, SK2 and SK3 oligonucleotide probes: autoradiography indicated no difference between the two sides, at any of the times studied. Na alphaI and SK2 mRNAs were less abundant and Na alphaIII, SKI and SK3 mRNAs were more abundant in the axotomized facial nuclei motoneurons than in controls. Removal of vestibular input did not affect the abundance of the mRNAs for the sodium- or calcium-dependent potassium channels in the deafferented vestibular nuclei. There is thus no evidence that modulation of these conductances contributes to the recovery of a normal resting discharge of the deafferented vestibular neurons and consequently to the functional recovery of the postural and oculomotor deficits observed at the acute stage. However, facial axotomy induced a long-term modulation of both Na and SK conductances mRNAs in the facial motoneurons ipsilateral to the lesion. Presumably, retrograde injury factors resulting from axotomy were able to alter durably the membrane properties and thus the excitability of the facial motoneurons. (C) 2003 IBRO. Published by Elsevier Science Ltd. All rights reserved.
引用
收藏
页码:265 / 280
页数:16
相关论文
共 60 条
[1]   INTRACELLULAR STUDIES IN THE FACIAL NUCLEUS ILLUSTRATING A SIMPLE NEW METHOD FOR OBTAINING VIABLE MOTONEURONS IN ADULT-RAT BRAIN-SLICES [J].
AGHAJANIAN, GK ;
RASMUSSEN, K .
SYNAPSE, 1989, 3 (04) :331-338
[2]   SODIUM-CHANNEL MESSENGER-RNA-I, MESSENGER-RNA-II AND MESSENGER-RNA-III IN THE CNS - CELL-SPECIFIC EXPRESSION [J].
BLACK, JA ;
YOKOYAMA, S ;
HIGASHIDA, H ;
RANSOM, BR ;
WAXMAN, SG .
MOLECULAR BRAIN RESEARCH, 1994, 22 (1-4) :275-289
[3]  
BRYSCH W, 1991, EXP BRAIN RES, V86, P562
[4]   THE MOLECULAR-BASIS OF NEURONAL EXCITABILITY [J].
CATTERALL, WA .
SCIENCE, 1984, 223 (4637) :653-661
[5]  
Curthoys I S, 1995, J Vestib Res, V5, P67, DOI 10.1016/0957-4271(94)00026-X
[6]   Lack of growth-associated protein-43 reemergence or of growth-associated protein-43 mRNA modulation in deafferented vestibular nuclei during the first 6 weeks after unilateral inner ear lesion [J].
de Waele, C ;
Loquet, G ;
Torres, AC ;
Vidal, PP .
EXPERIMENTAL BRAIN RESEARCH, 2000, 132 (04) :464-475
[7]  
DEWAELE C, 1994, EUR J NEUROSCI, V6, P565
[8]   MEDIAL VESTIBULAR NUCLEUS IN THE GUINEA-PIG - APAMIN-INDUCED RHYTHMIC BURST FIRING - AN IN-VITRO AND IN-VIVO STUDY [J].
DEWAELE, C ;
SERAFIN, M ;
KHATEB, A ;
YABE, T ;
VIDAL, PP ;
MUHLETHALER, M .
EXPERIMENTAL BRAIN RESEARCH, 1993, 95 (02) :213-222
[9]   NEUROCHEMISTRY OF THE CENTRAL VESTIBULAR PATHWAYS [J].
DEWAELE, C ;
MUHLETHALER, M ;
VIDAL, PP .
BRAIN RESEARCH REVIEWS, 1995, 20 (01) :24-46
[10]  
DEWAELE C, 1988, SOC NEUR ABSTR, V14, P331