This subproject is one of many research subprojects utilizing theresources provided by a Center grant funded by NIH/NCRR. The subproject andinvestigator (PI) may have received primary funding from another NIH source,and thus could be represented in other CRISP entries. The institution listed isfor the Center, which is not necessarily the institution for the investigator.As human and rodent trace amine receptors diverge in structure, subtype number and brain distribution, we postulate that non-human primates will provide a more suitable model for uncovering the physiological and pharmacological relevance of trace amine subtypes. In this regard, there is a 96% sequence identity for Trace Amine Associated Receptor 1 (TAAR1) in non-human primate and human. To establish fundamental information needed to explore TAAR subtype function, we are investigating non-human primate TAAR subtype structure, pharmacology, signal transduction and brain distribution. We utilize luciferase assays sensitive to different signal transduction pathways to uncover agonists as well as antagonists that block agonist-induced receptor activation. We are mapping TAAR subtype mRNA and protein distribution in primate brain using real-time RT-PCR and immunohistochemistry, to discern which receptor subtypes are expressed in brain. Our studies form the basis for investigating the physiological and pharmacological relevance of trace amine receptors in a primate model, and provide novel leads for developing therapeutic agents to treat addiction and neuropsychiatric disorders.
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