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J Neurophysiol 95: 3893-3897, 2006. First published May 10, 2006; doi:10.1152/jn.00123.2006
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Functional GABAA-Receptor–Mediated Inhibition in the Neonatal Dorsal Horn

L. Bremner, M. Fitzgerald and M. Baccei

Department of Anatomy and Developmental Biology, University College London, London, United Kingdom

Submitted 6 March 2006; accepted in final form 17 March 2006

Neonatal nociceptive circuits and dorsal horn cells are characterized by an apparent lack of inhibitory control: receptive fields are large and thresholds low in the first weeks of life. It has been suggested that this may reflect immature GABAA-receptor (GABAAR) signaling whereby an early developmental shift in transmembrane anion gradient is followed by a longer period of low Cl extrusion capacity. To investigate whether functional GABAAR-mediated inhibition does indeed undergo postnatal regulation at the level of dorsal horn circuits, we applied the selective GABAAR antagonist gabazine to the spinal cord in anesthetized rat pups [postnatal day (P) 3 or 21] while recording spike activity in single lumbar dorsal horn cells in vivo. At both ages, blockade of GABAAR activity resulted in enlarged hind paw receptive field areas and increased activity evoked by low- and high-intensity cutaneous stimulation, revealing comparable inhibition of dorsal horn cell firing by spinal GABAARs at P3 and P21. This inhibition did not require descending pathways to the spinal cord because perforated patch-clamp recordings of deep dorsal horn neurons in P3 spinal cord slices also showed an increase in evoked spike activity after application of gabazine. We conclude that spinal GABAergic inhibitory transmission onto single dorsal horn cells "in vivo" is functional at P3 and that low Cl extrusion capacity does not restrict GABAergic function over the normal range of evoked sensory activity. The excitability of neonatal spinal sensory circuits could reflect immaturity in other intrinsic or descending inhibitory networks rather than weak spinal GABAergic inhibition.


Address for reprint requests and other correspondence: L. Bremner, Department of Anatomy and Developmental Biology, University College London, Medawar Building, Gower Street, London WC1E 6BT, UK (E-mail: l.bremner{at}ucl.ac.uk)




This article has been cited by other articles:


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J. Neurophysiol.Home page
R. A. Ingram, M. Fitzgerald, and M. L. Baccei
Developmental Changes in the Fidelity and Short-Term Plasticity of GABAergic Synapses in the Neonatal Rat Dorsal Horn
J Neurophysiol, June 1, 2008; 99(6): 3144 - 3150.
[Abstract] [Full Text] [PDF]


Home page
J. Physiol.Home page
L. R. Bremner and M. Fitzgerald
Postnatal tuning of cutaneous inhibitory receptive fields in the rat
J. Physiol., March 15, 2008; 586(6): 1529 - 1537.
[Abstract] [Full Text] [PDF]




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