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  Long-lasting neurotrophin-induced enhancement of synaptic transmission in the adult hippocampus

Kang, H., & Schuman, E. M. (1995). Long-lasting neurotrophin-induced enhancement of synaptic transmission in the adult hippocampus. Science, 267(5204), 1658-62. doi:10.1126/science.7886457.

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Kang, H., Author
Schuman, Erin M.1, Author           
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1Synaptic Plasticity Department, Max Planck Institute for Brain Research, Max Planck Society, ou_2461710              

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Free keywords: 2-Amino-5-phosphonovalerate/pharmacology Animals Brain-Derived Neurotrophic Factor Carbazoles/pharmacology Dose-Response Relationship, Drug Hippocampus/*drug effects/physiology In Vitro Techniques Indole Alkaloids Long-Term Potentiation/drug effects Male Nerve Growth Factors/*pharmacology Nerve Tissue Proteins/*pharmacology Neuronal Plasticity/drug effects Neurotrophin 3 Protein Kinase C/antagonists & inhibitors Rats Rats, Sprague-Dawley Synapses/drug effects/physiology Synaptic Transmission/*drug effects
 Abstract: The neurotrophins are signaling factors important for the differentiation and survival of distinct neuronal populations during development. To test whether the neurotrophins also function in the mature nervous system, the effects of brain-derived neurotrophic factor (BDNF), nerve growth factor (NGF), and neurotrophic factor 3 (NT-3) on the strength of synaptic transmission in hippocampal slices were determined. Application of BDNF or NT-3 produced a dramatic and sustained (2 to 3 hours) enhancement of synaptic strength at the Schaffer collateral-CA1 synapses; NGF was without significant effect. The enhancement was blocked by K252a, an inhibitor of receptor tyrosine kinases. BDNF and NT-3 decreased paired-pulse facilitation, which is consistent with a possible presynaptic modification. Long-term potentiation could still be elicited in slices previously potentiated by exposure to the neurotrophic factors, which implies that these two forms of plasticity may use at least partially independent cellular mechanisms.

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 Dates: 1995-03-17
 Publication Status: Issued
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 Rev. Type: -
 Identifiers: Other: 7886457
DOI: 10.1126/science.7886457
ISSN: 0036-8075 (Print)0036-8075 (Linking)
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Title: Science
Source Genre: Journal
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Pages: - Volume / Issue: 267 (5204) Sequence Number: - Start / End Page: 1658 - 62 Identifier: -