Recombinant BDNF rescues deficits in basal synaptic transmission and hippocampal LTP in BDNF knockout mice.

Abstract:

:Brain-derived neurotrophic factor (BDNF) is expressed at high levels in hippocampal neurons, and its expression is modulated by neural activity. Knockout mice can be used to study the roles of molecules like BDNF in synaptic plasticity with more molecular specificity than is possible using pharmacological approaches. Because in conventional knockouts the disrupted gene product is absent in all tissues throughout the life of the animal, developmental effects may complicate the interpretation of deficits in the adult. Rescue experiments can help to distinguish between developmental and acute requirements for the missing gene product. We here demonstrate that treatment of hippocampal slices from BDNF knockout mice with recombinant BDNF completely reverses deficits in long-term potentiation and significantly improves deficits in basal synaptic transmission at the Schaffer collateral-CA1 synapse. Thus, BDNF has an acute role in hippocampal synaptic function.

journal_name

Neuron

journal_title

Neuron

authors

Patterson SL,Abel T,Deuel TA,Martin KC,Rose JC,Kandel ER

doi

10.1016/s0896-6273(00)80140-3

subject

Has Abstract

pub_date

1996-06-01 00:00:00

pages

1137-45

issue

6

eissn

0896-6273

issn

1097-4199

pii

S0896-6273(00)80140-3

journal_volume

16

pub_type

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