The projection from auditory cortex to cochlear nucleus in guinea pigs: an in vivo anatomical and in vitro electrophysiological study

被引:29
作者
Jacomme, AV
Nodal, FR
Bajo, VM
Manunta, Y
Edeline, JM
Babalian, A
Rouiller, EM
机构
[1] Univ Fribourg, Dept Med, Div Physiol, CH-1700 Fribourg, Switzerland
[2] Univ Oxford, Physiol Lab, Oxford OX1 3PT, England
[3] Univ Paris 11, CNRS, UMR 6820, NAMC, Orsay, France
关键词
biotinylated dextran amine (BDA); intracellular recording; intracellular staining; corticobulbar axons;
D O I
10.1007/s00221-003-1606-2
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
Previous anatomical experiments have demonstrated the existence of a direct, bilateral projection from the auditory cortex (AC) to the cochlear nucleus (CN). However, the precise relationship between the origin of the projection in the AC and the distribution of axon terminals in the CN is not known. Moreover, the influence of this projection on CN principal cells has not been studied before. The aim of the present study was two-fold. First, to extend the anatomical data by tracing anterogradely the distribution of cortical axons in the CN by means of restricted injections of biotinylated dextran amine (BDA) in physiologically characterized sites in the AC. Second, in an in vitro isolated whole brain preparation (IWB), to assess the effect of electrical stimulation of the AC on CN principal cells from which intracellular recordings were derived. BDA injections in the tonotopically organized primary auditory cortex and dorsocaudal auditory field at high and low best frequency (BF) sites resulted in a consistent axonal labeling in the ipsilateral CN of all injected animals. In addition, fewer labeled terminals were observed in the contralateral CN, but only in the animals subjected to injections in low BF region. The axon terminal fields consisting of boutons en passant or terminaux were found in the superficial granule cell layer and, to a smaller extent, in the three CN subdivisions. No axonal labeling was seen in the CN as result of BDA injection in the secondary auditory area (dorsocaudal belt). In the IWB, the effects of ipsilateral AC stimulation were tested in a population of 52 intracellulary recorded and stained CN principal neurons, distributed in the three CN subdivisions. Stimulation of the AC evoked slow late excitatory postsynaptic potentials (EPSPs) in only two cells located in the dorsal CN. The EPSPs were induced in a giant and a pyramidal cell at latencies of 20 ms and 33 ms, respectively, suggesting involvement of polysynaptic circuits. These findings are consistent with anatomical data showing sparse projections from the AC to the CN and indicate a limited modulatory action of the AC on CN principal cells.
引用
收藏
页码:467 / 476
页数:10
相关论文
共 61 条
[1]   ORIGINS OF AXONS IN CATS ACOUSTIC STRIAE DETERMINED BY INJECTION OF HORSERADISH-PEROXIDASE INTO SEVERED TRACTS [J].
ADAMS, JC ;
WARR, WB .
JOURNAL OF COMPARATIVE NEUROLOGY, 1976, 170 (01) :107-121
[2]   CYTOLOGY OF PERIOLIVARY CELLS AND THE ORGANIZATION OF THEIR PROJECTIONS IN THE CAT [J].
ADAMS, JC .
JOURNAL OF COMPARATIVE NEUROLOGY, 1983, 215 (03) :275-289
[3]   THE EFFERENT PROJECTIONS OF THE CENTRAL NUCLEUS AND THE PERICENTRAL NUCLEUS OF THE INFERIOR COLLICULUS IN THE CAT [J].
ANDERSEN, RA ;
ROTH, GL ;
AITKIN, LM ;
MERZENICH, MM .
JOURNAL OF COMPARATIVE NEUROLOGY, 1980, 194 (03) :649-662
[4]   Central vestibular networks in the guinea-pig: Functional characterization in the isolated whole brain in vitro [J].
Babalian, A ;
Vibert, N ;
Assie, G ;
Serafin, M ;
Muhlethaler, M ;
Vidal, PP .
NEUROSCIENCE, 1997, 81 (02) :405-426
[5]   Inhibitory synaptic interactions between cochlear nuclei:: evidence from an in vitro whole brain study [J].
Babalian, AL ;
Ryugo, DK ;
Vischer, MW ;
Rouiller, EM .
NEUROREPORT, 1999, 10 (09) :1913-1917
[6]   Commissural glycinergic inhibition of bushy and stellate cells in the anteroventral cochlear nucleus [J].
Babalian, AL ;
Jacomme, AV ;
Doucet, JR ;
Ryugo, DK ;
Rouiller, EM .
NEUROREPORT, 2002, 13 (04) :555-558
[7]  
BABALIAN AL, 2001, ARO ABSTR, V24, P197
[8]  
BABALIAN AL, 2002, ARO ABSTR, V25, P8
[9]  
Bajo VM, 1999, J COMP NEUROL, V407, P349, DOI 10.1002/(SICI)1096-9861(19990510)407:3<349::AID-CNE4>3.0.CO
[10]  
2-5