Document Detail


Inhibitory control at a synaptic relay.
MedLine Citation:
PMID:  15028756     Owner:  NLM     Status:  MEDLINE    
Abstract/OtherAbstract:
The mammalian medial nucleus of the trapezoid body (MNTB) harbors one of the most powerful terminals in the CNS, the calyx of Held. The mechanisms known to regulate this synaptic relay are relatively ineffective. Here, we report the presence of a remarkably robust and fast-acting glycinergic inhibitory system capable of suppressing calyceal transmission. Evoked glycinergic IPSCs were relatively small in 2-week-old rats, an age by which calyceal maturation has reportedly neared completion. However, by postnatal day 25 (P25), glycinergic transmission had undergone a vigorous transformation, resulting in peak synaptic conductances as high as 280 nS. These are comparable with glutamatergic conductances activated by calyceal inputs. Decay kinetics for IPSCs were severalfold faster than for glycinergic synaptic events reported previously. At physiological temperatures in P25 rats, IPSCs decayed in approximately 1 msec and could be elicited at frequencies up to 500 Hz. Moreover, EPSPs triggered by glutamatergic signals derived from the calyx or simulated by conductance clamp were suppressed when preceded by simulated glycinergic IPSPs. The matching of excitatory transmission in the calyx of Held by a powerful, precision inhibitory system suggests that the relay function of the MNTB may be rapidly modified during sound localization.
Authors:
Gautam B Awatramani; Rostislav Turecek; Laurence O Trussell
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Publication Detail:
Type:  In Vitro; Journal Article; Research Support, U.S. Gov't, P.H.S.    
Journal Detail:
Title:  The Journal of neuroscience : the official journal of the Society for Neuroscience     Volume:  24     ISSN:  1529-2401     ISO Abbreviation:  J. Neurosci.     Publication Date:  2004 Mar 
Date Detail:
Created Date:  2004-03-18     Completed Date:  2004-05-28     Revised Date:  2007-11-14    
Medline Journal Info:
Nlm Unique ID:  8102140     Medline TA:  J Neurosci     Country:  United States    
Other Details:
Languages:  eng     Pagination:  2643-7     Citation Subset:  IM    
Affiliation:
Oregon Hearing Research Center/Vollum Institute, Oregon Health and Science University, Portland, Oregon 97239, USA. awatrama@ohsu.edu
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MeSH Terms
Descriptor/Qualifier:
Animals
Auditory Pathways / physiology*
Brain Stem / cytology,  drug effects,  physiology*
Electric Stimulation / methods
Excitatory Postsynaptic Potentials / drug effects,  physiology
GABA Antagonists / pharmacology
Glutamic Acid / metabolism
Glycine / metabolism
Glycine Agents / pharmacology
Neural Inhibition / drug effects,  physiology*
Neurons / drug effects,  metabolism,  physiology*
Patch-Clamp Techniques
Rats
Sound Localization / physiology
Synapses / physiology*
Synaptic Transmission / drug effects,  physiology
Temperature
Grant Support
ID/Acronym/Agency:
DC04450/DC/NIDCD NIH HHS
Chemical
Reg. No./Substance:
0/GABA Antagonists; 0/Glycine Agents; 56-40-6/Glycine; 56-86-0/Glutamic Acid

From MEDLINE®/PubMed®, a database of the U.S. National Library of Medicine


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