Changes in the synaptic efficacy of excitatory and inhibitory transmission can perturb the delicate balance of excitation and inhibition within the brain and thus profoundly modulate cognitive processes. The overall goal of this research proposal is to understand the mechanisms by which TRPV1, a non-selective cation channel, may be involved in the modulation of synaptic efficacy at both excitatory and inhibitory synapses in the hippocampus and dentate gyrus, two key brain areas involved in learning and memory formation and where TRPV1 is highly expressed. TRPV1 is generally thought to be expressed presynaptically, and might retrogradely be activated by different lipid ligands including endocannabinoids (eCBs). The experiments proposed here are designed to test the possibility that TRPV1 may act postsynaptically to reduce the number or responsiveness of glutamate and GABA receptors. In addition, I will test the possibility that eCBs, which typically signal in a retrograde manner by activating presynaptic cannabinoid receptors, could also act in an autocrine manner to regulate postsynaptic receptor function via TRPV1. First, I will analyze the cellular and molecular mechanism underlying TRPV1 activation as well as the mechanism downstream by which TRPV1-mediated physiological effect at CNS synapses. Second, I will expand our analyses to understand the contribution of several G-protein coupled receptors in regulating TRPV1- mediated changes of synaptic efficacy. This information is essential to gain a better understanding on the role of brain TRPV1 in regulating synaptic and neural circuit function.

Public Health Relevance

TRPV1 channels have recently become an attractive molecular target for the development of new drugs to control pain in the peripheral nervous system. Undesirable side-effects may arise from unknown and previously unexplored TRPV1 functions in the central nervous system. Unmasking the role of TRPV1 in the central nervous system is not only relevant to the development of novel analgesic strategies but it may also provide new insights into the cellular basis underlying brain function under normal and pathophysiological conditions.

Agency
National Institute of Health (NIH)
Institute
National Institute of Neurological Disorders and Stroke (NINDS)
Type
Postdoctoral Individual National Research Service Award (F32)
Project #
5F32NS071821-02
Application #
8098896
Study Section
Special Emphasis Panel (ZRG1-F03B-H (20))
Program Officer
Talley, Edmund M
Project Start
2010-07-01
Project End
2012-06-30
Budget Start
2011-07-01
Budget End
2012-06-30
Support Year
2
Fiscal Year
2011
Total Cost
$53,042
Indirect Cost
Name
Albert Einstein College of Medicine
Department
Neurosciences
Type
Schools of Medicine
DUNS #
110521739
City
Bronx
State
NY
Country
United States
Zip Code
10461
Hashimotodani, Yuki; Nasrallah, Kaoutsar; Jensen, Kyle R et al. (2017) LTP at Hilar Mossy Cell-Dentate Granule Cell Synapses Modulates Dentate Gyrus Output by Increasing Excitation/Inhibition Balance. Neuron 95:928-943.e3
Chávez, Andrés E; Hernández, Vivian M; Rodenas-Ruano, Alma et al. (2014) Compartment-specific modulation of GABAergic synaptic transmission by TRPV1 channels in the dentate gyrus. J Neurosci 34:16621-9
Castillo, Pablo E; Younts, Thomas J; Chavez, Andres E et al. (2012) Endocannabinoid signaling and synaptic function. Neuron 76:70-81
Rodenas-Ruano, Alma; Chávez, Andrés E; Cossio, Maria J et al. (2012) REST-dependent epigenetic remodeling promotes the developmental switch in synaptic NMDA receptors. Nat Neurosci 15:1382-90
Chavez, Andres E; Chiu, Chiayu Q; Castillo, Pablo E (2010) TRPV1 activation by endogenous anandamide triggers postsynaptic long-term depression in dentate gyrus. Nat Neurosci 13:1511-8