In vivo BDNF modulation of hippocampal mossy fiber plasticity induced by high frequency stimulation
Article first published online: 16 SEP 2010
Copyright © 2010 Wiley Periodicals, Inc., Inc.
Volume 22, Issue 1, pages 1–8, January 2012
How to Cite
Schjetnan, A. G.-P. and Escobar, M. L. (2012), In vivo BDNF modulation of hippocampal mossy fiber plasticity induced by high frequency stimulation. Hippocampus, 22: 1–8. doi: 10.1002/hipo.20866
- Issue published online: 20 DEC 2011
- Article first published online: 16 SEP 2010
- Manuscript Accepted: 29 JUN 2010
- homeostatic plasticity;
- long-term potentiation;
- structural plasticity;
- learning and memory
Changes in synaptic efficacy and morphology have been proposed as mechanisms underlying learning and memory processes. In our previous studies, high frequency stimulation (HFS) sufficient to induce LTP at the hippocampal mossy fiber (MF) pathway, leads to MF synaptogenesis, in a prominent contralateral form, at the stratum oriens of hippocampal CA3 area. Recently we reported that acute intrahippocampal microinfusion of BDNF induces a lasting potentiation of synaptic efficacy at the MF projection accompanied by a structural reorganization at the CA3 area within the stratum oriens region in a prominent ipsilateral form. It is considered that the capacity of synapses to express plastic changes is itself subject to variation dependent on previous experience. Here we used intrahippocampal microinfusion of BDNF to analyze its effects on functional and structural synaptic plasticity induced by subsequent mossy fiber HFS sufficient to induce LTP in adult rats, in vivo. Our results show that BDNF modifies the ability of the MF pathway to present LTP by HFS. Moreover BDNF modified the structural reorganization pattern produced by HFS, presenting a balanced bilateral appearance. Microinfusion of K252a blocks the functional and morphological effects produced by BDNF, revealing that the BDNF modulation is dependent on its TrkB receptor activation. These findings support the idea that BDNF actions modify subsequent synaptic plasticity; a homeostatic mechanism thought to be essential for synaptic integration among prolonged temporal domains in the adult mammalian brain. © 2010 Wiley Periodicals, Inc., Inc.