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Updated: Nov 4, 2025

A Protocol for Measuring Cue Reactivity in a Rat Model of Cocaine Use Disorder
Published on: June 18, 2018
Overcoming Stress, Hunger, and Pain: Cocaine- and Amphetamine-Regulated Transcript Peptide's Promise
Willis K Samson1, Daniela Salvemini1, Gina L C Yosten1
1Department of Pharmacology and Physiology and Henry and Amelia Nasrallah Center for Neuroscience Saint Louis University School of Medicine, St Louis, MO 63104, USA.
The cocaine- and amphetamine-regulated transcript peptide (CARTp) and its receptor GPR160 are crucial for regulating appetite, thirst, and pain. Their newly understood roles highlight therapeutic potential.
Area of Science:
- Neuroendocrinology
- Molecular Pharmacology
- Physiology
Background:
- The cocaine- and amphetamine-regulated transcript (CART) peptide (CARTp) has demonstrated broad pharmacologic actions.
- The physiological relevance of CARTp's actions remained largely unestablished until recent discoveries.
Purpose of the Study:
- To review the diverse actions of CARTp.
- To highlight the physiological importance and therapeutic potential of the CARTp-GPR160 system.
Main Methods:
- Literature review of CARTp's pharmacologic actions.
- Discussion of recent findings on CARTp receptor identification and function.
- Exploration of molecular and genetic approaches to investigate CARTp's roles.
Main Results:
- The identification of GPR160 as a CARTp receptor.
- The CARTp-GPR160 interaction is essential for circadian regulation of appetite and thirst.
- This interaction is also implicated in the transmission of nerve injury-induced pain.
Conclusions:
- The CARTp-GPR160 system plays a vital role in fundamental physiological processes.
- Further research using molecular approaches may uncover additional functions.
- This ligand/receptor pair holds significant therapeutic potential for various conditions.
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