Brain-derived neurotrophic factor in the ventral midbrain–nucleus accumbens pathway: a role in depression

Abstract

<h2>Abstract</h2><h3>Background</h3> Previous work has shown that brain-derived neurotrophic factor (BDNF) and its receptor, tyrosine kinase receptor B (TrkB), are involved in appetitive behavior. Here we show that BDNF in the ventral tegmental area–nucleus accumbens (VTA–NAc) pathway is also involved in the development of a depression-like phenotype. <h3>Methods</h3> Brain-derived neurotrophic factor signaling in the VTA–NAc pathway was altered in two complementary ways. One group of rats received intra-VTA infusion of vehicle or BDNF for 1 week. A second group of rats received intra-NAc injections of vehicle or adeno-associated viral vectors encoding full-length (TrkB.FL) or truncated (TrkB.T1) TrkB; the latter is kinase deficient and serves as a dominant-negative receptor. Rats were examined in the forced swim test and other behavioral tests. <h3>Results</h3> Intra-VTA infusions of BDNF resulted in 57% shorter latency to immobility relative to control animals, a depression-like effect. Intra-NAc injections of TrkB.T1 resulted in and almost fivefold longer latency to immobility relative to TrkB.FL and control animals, an antidepressant-like effect. No effect on anxiety-like behaviors or locomotion was seen. <h3>Conclusions</h3> These data suggest that BDNF action in the VTA–NAc pathway might be related to development of a depression-like phenotype. This interpretation is intriguing in that it suggests a role for BDNF in the VTA–NAc that is opposite of the proposed role for BDNF in the hippocampus.