## Abstract Brain‐derived neurotrophic factor (BDNF) promotes a variety of neuromodulatory processes during development as well as in adulthood. This neurotrophin has been associated with synaptic plasticity, suggesting that its regulation may represent one of the mechanisms through which psychotro
Brain-derived neurotrophic factor regulation of N-methyl-D-aspartate receptor-mediated synaptic currents in suprachiasmatic nucleus neurons
✍ Scribed by Y.I. Kim; H.-J. Choi; C.S. Colwell
- Publisher
- John Wiley and Sons
- Year
- 2006
- Tongue
- English
- Weight
- 428 KB
- Volume
- 84
- Category
- Article
- ISSN
- 0360-4012
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✦ Synopsis
Abstract
Light information reaches the suprachiasmatic nucleus (SCN) through a subpopulation of retinal ganglion cells. Previous work raises the possibility that brain‐derived neurotrophic factor (BDNF) and its high‐affinity receptor TrkB may be important as modulators of this excitatory input into the SCN. To test this possibility, we used whole‐cell patch‐clamp methods to measure excitatory currents in rat SCN neurons. These currents were evoked by electrical stimulation of the optic nerve. We found that the amplitude of the N‐methyl‐D‐aspartate (NMDA) component of the evoked excitatory postsynaptic currents (NMDA‐EPSC) was increased by application of BDNF. The neurotrophin also increased the magnitude of NMDA‐evoked currents in SCN neurons. The BDNF enhancement of the NMDA‐EPSC was blocked by treatment with the neurotrophin receptor antagonist K252a as well as treatment with the soluble form of the TrkB receptor engineered as an immunoadhesin (TrkB IgG). Finally, the BDNF enhancement was lost in brain slices treated with the NR2B antagonist ifenprodil. The results demonstrate that BDNF and TrkB receptors are important regulators of retinal glutamatergic synaptic transmission within the SCN. © 2006 Wiley‐Liss, Inc.
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