Cholecystokinin receptor
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cholecystokinin A receptor | |
---|---|
Identifiers | |
Symbol | CCKAR |
Entrez | 886 |
HUGO | 1570 |
OMIM | 118444 |
RefSeq | NM_000730 |
UniProt | P32238 |
Other data | |
Locus | Chr. 4 p15.2-p15.1 |
cholecystokinin B receptor | |
---|---|
Identifiers | |
Symbol | CCKBR |
Entrez | 887 |
HUGO | 1571 |
OMIM | 118445 |
RefSeq | NM_176875 |
UniProt | P32239 |
Other data | |
Locus | Chr. 11 p15.4 |
Cholecystokinin receptors or CCK receptors are a group of G-protein coupled receptors which bind the peptide hormones cholecystokinin (CCK) or gastrin.[1] There are two different subtypes CCKA and CCKB which are ~50% homologous:[2] Various cholecystokinin antagonists have been developed and are used in research, although the only drug of this class that has been widely marketed to date is the anti-ulcer drug proglumide.
protein | gene | tissue distribution | preferred ligand | function |
---|---|---|---|---|
CCKA (CCK1) | CCKAR | primarily gastrointestinal tract, lesser amounts in the CNS | sulfated CCK >> nonsulfated CCK ≈ nonsulfated CCK | stimulation of bicarb secretion, gall bladder emptying and inhibiting gut motility |
CCKB (CCK2) | CCKBR | primarily CNS, lesser amounts in the gastrointestinal tract | gastrin ≈ CCK (receptor does not descriminate between sulfated and nonsulfated peptides) | regulation of nociception, anxiety, memory and hunger |
References
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External links
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- ↑ Noble F, Wank SA, Crawley JN, Bradwejn J, Seroogy KB, Hamon M, Roques BP (1999). "International Union of Pharmacology. XXI. Structure, distribution, and functions of cholecystokinin receptors" ([dead link]). Pharmacol. Rev. 51 (4): 745–81. PMID 10581329.
- ↑ Dufresne M, Seva C, Fourmy D (2006). "Cholecystokinin and gastrin receptors". Physiol. Rev. 86 (3): 805–47. doi:10.1152/physrev.00014.2005. PMID 16816139.
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