Past, present and future of cocaine- and amphetamine-regulated transcript peptide
Gina L C Yosten1, Christopher J Haddock2, Caron M Harada1
1Department of Pharmacology and Physiology, Saint Louis University School of Medicine, St. Louis, MO 63104, USA; Henry and Nasrallah Center for Neuroscience, Saint Louis University School of Medicine, St. Louis, MO 63104, USA.
Physiology & Behavior
|March 11, 2021
Summary
The cocaine- and amphetamine-regulated transcript (CART) peptide
Area of Science:
- Neuroscience
- Molecular Biology
- Pharmacology
Background:
- The cocaine- and amphetamine-regulated transcript (CART) peptide, known since 1981, plays roles in ingestive and reward behaviors.
- Despite its known functions, the CART peptide's therapeutic potential was limited by the lack of an identified receptor.
- Previous research suggested CART acted via a G protein-coupled receptor (GPCR), but its identity remained elusive.
Purpose of the Study:
- To identify the specific G protein-coupled receptor (GPCR) for the CART peptide.
- To elucidate the role of the CART peptide-GPCR interaction in physiological processes.
- To explore the therapeutic potential of targeting the CART peptide-receptor axis.
Main Methods:
- Utilized molecular biology techniques to identify the CART peptide receptor.
- Investigated the interaction between CART peptide and potential GPCR candidates.
- Validated the identified receptor through various experimental approaches.
Main Results:
- Identified GPR160 as the previously orphaned receptor for the CART peptide.
- Confirmed the interaction between CART peptide and GPR160.
- Established GPR160 as a key mediator of CART peptide's actions.
Conclusions:
- The identification of GPR160 as the CART peptide receptor opens new avenues for research.
- This discovery is expected to revitalize interest in CART peptide and its therapeutic applications.
- Targeting the GPR160 receptor presents a promising strategy for developing novel pharmacotherapies.
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