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Cocaine- and amphetamine-regulated transcript: distribution and function in rat gastrointestinal tract
1Department of Physiological Sciences, BMC F10, Lund University, Lund, Sweden. eva.ekblad@mphy.lu.se
Neurogastroenterology and Motility
|September 26, 2003
Summary
Cocaine- and amphetamine-regulated transcript (CART) peptide is found in enteric neurons throughout the rat gut. CART may modulate nitric oxide transmission and play a role in intestinal adaptation.
Area of Science:
- Neuroscience
- Gastroenterology
Background:
- Cocaine- and amphetamine-regulated transcript (CART) peptide, initially identified in the brain, is also present in the peripheral nervous system.
- The presence and function of CART in the enteric nervous system (ENS) are not fully understood.
Purpose of the Study:
- To investigate the distribution, origin, and projections of CART-expressing enteric neurons in the rat gastrointestinal (GI) tract.
- To explore the potential motor functions of CART in the GI tract.
- To examine the role of CART in intestinal adaptation.
Main Methods:
- Immunocytochemistry and in situ hybridization were used to map CART-expressing neurons in the rat GI tract.
- In vitro studies utilized longitudinal muscle strips from the stomach, ileum, and colon to assess CART's motor effects.
- Contractile and relaxatory responses were measured in response to CART and other known signaling molecules.
Main Results:
- CART peptide was abundant in myenteric neurons across the GI tract, with scarce submucous neurons.
- CART-expressing neurons in the small and large intestines showed short descending projections.
- CART did not directly induce muscle contractions or relaxations but attenuated nitric oxide (NO)-induced relaxations in the colon.
Conclusions:
- CART peptide likely plays a modulatory role in NO transmission within the colon, rather than direct neurotransmission to longitudinal muscles.
- CART may be involved in intestinal adaptation processes.
- An additional hormonal role for CART in the GI tract is also suggested.