Mood-related disorders such as anxiety and depression are linked to dysfunction in many brain structures, including the hippocampus. Many effective and promising new drugs for the treatment of mood-related disorders target, directly or indirectly, G protein-coupled receptors (GPCRs) that modulate the activity of multiple effectors. The relative significance of specific GPCR-effector interactions to normal and pathological mood-related behaviors, and pertinent anatomic loci, are unclear. The premise of this proposal is that a better understanding of GPCR-effector interactions, obtained with an interdisciplinary approach spanning molecular, ultrastructural, electrophysiological, and behavioral levels of analysis, will ultimately improve how we understand and treat mental disorders with strong affective components. The focus of this study is the G protein-gated inwardly-rectifying K+ (Girk/KIR3) channel, which mediates the postsynaptic inhibitory effect of many neurotransmitters - including several linked mood-related behavior such as GABA, serotonin, and adenosine - that influence neuronal excitability via activation of GPCRs. Recent studies have identified new modes of Girk regulation and a striking GPCR-dependent compartmentalization of Girk signaling in the hippocampus. The goal of the proposed research is to build on this foundation by pursuing factors influencing the strength and sensitivity of GPCR-Girk signaling, mechanisms underlying the GPCR-dependent compartmentalization of Girk signaling in the hippocampus, and the contributions made by hippocampal GPCR-Girk signaling to mood-related behavior and cognition. Effort will be centered on three inter-related Specific Aims: (1) To understand the Girk1-dependent potentiation of GPCR-Girk signaling. Structural insights into the positive contribution made by the Girk1 subunit to GPCR-Girk signaling will be pursued, and the hypothesis that Girk1 strengthens the physical interaction between receptor and channel will be tested. (2) To identify factors underlying the GPCR-dependent compartmentalization of Girk signaling. The hypothesis that the molecular composition and subcellular distribution of hippocampal Girk signaling differs in a GPCR- dependent manner will be tested. (3) To measure the impact of hippocampal GPCR-Girk signaling on mood and cognition. Mood-related behavior and cognition will be measured in constitutive knockout mice exhibiting diminished or enhanced GPCR signaling, and in mice following pharmacologic and/or genetic manipulation of Girk signaling in the hippocampus. The molecular, subcellular, and behavioral insights gleaned from these studies will enhance our understanding of neuronal GPCR-Girk signaling, while offering new insights into the molecular and anatomic basis of mood-related behavior and cognition. Accordingly, the proposed research aligns with several high-priority research areas at the National Institute of Mental Health and constitutes a necessary step toward a more comprehensive understanding of, and more effective treatments for, mood- related disorders.

Public Health Relevance

Anxiety disorders and depression are linked to dysfunction in brain regions involved with emotion. Many effective and promising new treatments for such disorders target proteins on the surface of neurons (receptors), which control the activity of many proteins inside the neurons (effectors), in these brain regions. The proposed research will shed new light on receptor-effector interactions in pertinent brain regions that shape anxiety-related behavior, paving the way toward a more comprehensive understanding of, and improved treatments for, mood-related disorders.

Agency
National Institute of Health (NIH)
Institute
National Institute of Mental Health (NIMH)
Type
Research Project (R01)
Project #
5R01MH061933-12
Application #
8420341
Study Section
Neurotransporters, Receptors, and Calcium Signaling Study Section (NTRC)
Program Officer
Asanuma, Chiiko
Project Start
2000-07-01
Project End
2017-01-31
Budget Start
2013-02-01
Budget End
2014-01-31
Support Year
12
Fiscal Year
2013
Total Cost
$352,515
Indirect Cost
$112,515
Name
University of Minnesota Twin Cities
Department
Pharmacology
Type
Schools of Medicine
DUNS #
555917996
City
Minneapolis
State
MN
Country
United States
Zip Code
55455
Victoria, Nicole C; Marron Fernandez de Velasco, Ezequiel; Ostrovskaya, Olga et al. (2016) G Protein-Gated K(+) Channel Ablation in Forebrain Pyramidal Neurons Selectively Impairs Fear Learning. Biol Psychiatry 80:796-806
Montandon, Gaspard; Ren, Jun; Victoria, Nicole C et al. (2016) G-protein-gated Inwardly Rectifying Potassium Channels Modulate Respiratory Depression by Opioids. Anesthesiology 124:641-50
Herman, Melissa A; Sidhu, Harpreet; Stouffer, David G et al. (2015) GIRK3 gates activation of the mesolimbic dopaminergic pathway by ethanol. Proc Natl Acad Sci U S A 112:7091-6
Marron Fernandez de Velasco, Ezequiel; Hearing, Matthew; Xia, Zhilian et al. (2015) Sex differences in GABA(B)R-GIRK signaling in layer 5/6 pyramidal neurons of the mouse prelimbic cortex. Neuropharmacology 95:353-60
Kotecki, Lydia; Hearing, Matthew; McCall, Nora M et al. (2015) GIRK Channels Modulate Opioid-Induced Motor Activity in a Cell Type- and Subunit-Dependent Manner. J Neurosci 35:7131-42
Slesinger, Paul A; Wickman, Kevin (2015) Preface. Int Rev Neurobiol 123:xi-xii
Marron Fernandez de Velasco, Ezequiel; McCall, Nora; Wickman, Kevin (2015) GIRK Channel Plasticity and Implications for Drug Addiction. Int Rev Neurobiol 123:201-38
Wydeven, Nicole; Marron Fernandez de Velasco, Ezequiel; Du, Yu et al. (2014) Mechanisms underlying the activation of G-protein-gated inwardly rectifying K+ (GIRK) channels by the novel anxiolytic drug, ML297. Proc Natl Acad Sci U S A 111:10755-60
Lujan, Rafael; Marron Fernandez de Velasco, Ezequiel; Aguado, Carolina et al. (2014) New insights into the therapeutic potential of Girk channels. Trends Neurosci 37:20-9
Wydeven, Nicole; Posokhova, Ekaterina; Xia, Zhilian et al. (2014) RGS6, but not RGS4, is the dominant regulator of G protein signaling (RGS) modulator of the parasympathetic regulation of mouse heart rate. J Biol Chem 289:2440-9

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