Ventral Tegmental Area Neurotensin Signaling Links the Lateral Hypothalamus to Locomotor Activity and Striatal Dopamine Efflux in Male Mice
Author(s) -
Christa M. Patterson,
Jenny-Marie T. Wong,
Gina M. Leinninger,
Margaret B. Allison,
Omar S. Mabrouk,
Chelsea Kasper,
Ian E. Gonzalez,
Alexander MacKenzie,
Justin C. Jones,
Robert T. Kennedy,
Martin G. Myers
Publication year - 2015
Publication title -
endocrinology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.674
H-Index - 257
eISSN - 1945-7170
pISSN - 0013-7227
DOI - 10.1210/en.2014-1986
Subject(s) - ventral tegmental area , nucleus accumbens , dopamine , microdialysis , lateral hypothalamus , extracellular , neurotensin , medicine , endocrinology , hypothalamus , mesolimbic pathway , neurotransmitter , dopaminergic , biology , neuroscience , chemistry , neuropeptide , receptor , central nervous system , microbiology and biotechnology
Projections from the lateral hypothalamic area (LHA) innervate components of the mesolimbic dopamine (MLDA) system, including the ventral tegmental area (VTA) and nucleus accumbens (NAc), to modulate motivation appropriately for physiologic state. Neurotensin (NT)-containing LHA neurons respond to multiple homeostatic challenges and project to the VTA, suggesting that these neurons could link such signals to MLDA function. Indeed, we found that pharmacogenetic activation of LHA NT neurons promoted prolonged DA-dependent locomotor activity and NAc DA efflux, suggesting the importance of VTA neurotransmitter release by LHA NT neurons for the control of MLDA function. Using a microdialysis-mass spectrometry technique that we developed to detect endogenous NT in extracellular fluid in the mouse brain, we found that activation of LHA NT cells acutely increased the extracellular concentration of NT (a known activator of VTA DA cells) in the VTA. In contrast to the prolonged elevation of extracellular NAc DA, however, VTA NT concentrations rapidly returned to baseline. Intra-VTA infusion of NT receptor antagonist abrogated the ability of LHA NT cells to increase extracellular DA in the NAc, demonstrating that VTA NT promotes NAc DA release. Thus, transient LHA-derived NT release in the VTA couples LHA signaling to prolonged changes in DA efflux and MLDA function.
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