Author
Listed:
- Karl W. Kafitz
(Institut für Physiologic, Technische Universität München
I. Physiologisches Institut, Universität des Saarlandes)
- Christine R. Rose
(Institut für Physiologic, Technische Universität München
I. Physiologisches Institut, Universität des Saarlandes)
- Hans Thoenen
(Max-Plack-Institut für Neurobiologie)
- Arthur Konnerth
(Institut für Physiologic, Technische Universität München
I. Physiologisches Institut, Universität des Saarlandes)
Abstract
Neurotrophins are a family of structurally related proteins that regulate the survival, differentiation and maintenance of function of different populations of peripheral and central neurons1,2,3. They are also essential for modulating activity-dependent neuronal plasticity4,5,6,7. Here we show that neurotrophins elicit action potentials in central neurons. Even at low concentrations, brain-derived neurotrophic factor (BDNF) excited neurons in the hippocampus, cortex and cerebellum. We found that BDNF and neurotrophin-4/5 depolarized neurons just as rapidly as the neurotransmitter glutamate, even at a more than thousand-fold lower concentration. Neurotrophin-3 produced much smaller responses, and nerve growth factor was ineffective. The neurotrophin-induced depolarization resulted from the activation of a sodium ion conductance which was reversibly blocked by K-252a, a protein kinase blocker which prefers tyrosine kinase Trk receptors8. Our results demonstrate a very rapid excitatory action of neurotrophins, placing them among the most potent endogenous neuro-excitants in the mammalian central nervous system described so far.
Suggested Citation
Karl W. Kafitz & Christine R. Rose & Hans Thoenen & Arthur Konnerth, 1999.
"Neurotrophin-evoked rapid excitation through TrkB receptors,"
Nature, Nature, vol. 401(6756), pages 918-921, October.
Handle:
RePEc:nat:nature:v:401:y:1999:i:6756:d:10.1038_44847
DOI: 10.1038/44847
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