Recombinant Rat Cholecystokinin receptor type A (Cckar)

1. This study demonistrated that Cckar and Melanin-concentrating hormone colization in neuron in the lateral hypothalamus (LH) and zona incerta (ZI), but MCHR1 mRNA is widely expressed throughout the brain. PMID:24978951
2. Data suggest that Apo AIV (apolipoprotein AIV) in NTS (nucleus of the solitary tract) or/and peripheral Cck (cholecystokinin) require vagal Cck1r/Cckar signaling to elicit satiation; high-fat diet reduces satiating capacity of these signals. PMID:24564397
3. factors secondary to obesity and/or diabetes rather than impaired CCK-1 receptor signaling may contribute to altered CART expression PMID:23545074
4. CCK-A receptors are located on the cell bodies of cholinergic interneurons in the corpus striatum. PMID:22981453
5. Activation of duodenal PKC-delta leads to the stimulation of CCK release and activation of the CCK-A receptor signaling axis to lower glucose production in normal rats. PMID:21984583
6. Data indicate that the Homo-Phe derivative 2 (VL-0797) enhanced 12-fold the affinity for the rat CCK(1)-R affinity and 15-fold for the human CCK(1)-R relative to the reference compound 12 (VL-0395). PMID:21728335
7. Data suggest L-364,718 potentiates electroacupuncture analgesia through the CCK-A receptor of pain-excited and pain-inhibited neurons in the nucleus parafascicularis. PMID:20953702
8. CCK1 and CCK2 receptors are expressed on pancreatic stellate cells and induce collagen production PMID:20843811
9. our results demonstrate for the first time, that CCK-1 receptor plays a crucial role in both meal-induced and fasting insulin sensitization PMID:20624386
10. Present study examined the contribution of genetics, sex and early maternal environment to anxiety-like behaviors and locomotion in CCK1 knockout rats, suggesting that the mutation may predispose (rather than induce) the animals to an anxious phenotype. PMID:20347877
11. The results of this study showed that increased oil intake in cck-1 receptor deficient rats is driven by both peripheral deficits to satiation and altered orosensory sensitivity. PMID:19887078
12. Gastric leptin may exert acute sympathoinhibitory and cardiovascular effects via vagal transmission and CCK(1) receptor activation and may play a separate role to adipose leptin in short-term cardiovascular regulation. PMID:19940076
13. Activation of high-affinity CCK(A) receptors elicits Ca(2+) oscillations, whereas stimulation of low-affinity CCK(A) receptors evokes a sustained Ca(2+) plateau; these modes are mediated through L-type Ca(2+) channel and involve G(q) protein. PMID:12016125
14. These results indicate that CCKB, but not CCKA receptors are involved in anxiety, as tested by microinjection of cholecystokinin agonists. PMID:12373548
15. endogenous CCK appears to act in part by a paracrine or neurocrine mechanism at CCKARs peripheral to the blood-brain barrier to inhibit gastric emptying PMID:12388446
16. Endogenous CCK appears to act in part at CCKARs peripheral to the blood-brain barrier to inhibit food intake PMID:12414437
17. None of the three known phases of the febrile response of rats to lipopolysaccharides requires the CCK-A receptor. PMID:12562931
18. results demonstrate that cholecystokinin stimulates tyrosine phosphorylation of three sites in focal adhesion kinase and proline-rich kinase 2 but differs in participation of cholecystokinin receptor A and by protein kinase C and [Ca2+] PMID:12651850
19. CCK-AR and CCK-BR gene were present in pulmonary vascular endothelial cells, macrophages, bronchial epithelial cells and alveolar epithelial cells, which play an important role in mediating the regulatory actions of CCK-8 on these cells. PMID:12800239
20. peripheral and central responses to enterostatin are mediated through or dependent on peripheral and central CCK-A receptors PMID:12855414
21. CCK-A receptors play an important role in the regulation of central dopamine transmission, as revealed by studies of the CCK-A receptor-deficient Otsuka Long Evans Tokushima Fatty (OTLEF) rat strain. PMID:12932815
22. spatial memory was impaired in the OLETF rats with genetic abnormality in cck-a receptor PMID:14607104
23. the data identified CCK-A and CCK-B receptor mRNAs in the rat retina and demonstrated that they are functional, stimulating tyrosine phosphorylation pathways. PMID:14698681
24. involvement of type A CCK receptors in the mediation of the inhibitory effect of large doses of ethanol on the gastric emptying PMID:14700745
25. acute pancreatitis induced by bile-pancreatic duct ligation associates with a temporal increase in pancreatic cholecystokinin-A receptor protein expression, p38 mitogen activated protein kinase activation, and nuclear factor-kappaB activation PMID:14988658
26. apo A-IV released from the intestinal mucosa during lipid absorption stimulates the release of endogenous CCK that activates CCK(1) receptors on vagal afferent nerve terminals initiating feedback inhibition of gastric motility. PMID:15117731
27. Differential roles for cholecystokinin a receptors in energy balance in rats and mice. PMID:15123537
28. The OLETF rats showed a large hysteresis. PMID:15178543
29. Taste preference in Otsuka Long-Evans Tokushima fatty (OLETF) rats with deficiency of this receptor. PMID:15358606
30. These findings demonstrate that compared with controls, OLETF rats differ in their gustatory functions with an overall augmented sensitivity for sweet that progresses during prediabetes. PMID:16081877
31. Lack of CCK-1 receptors, or other OLETF-related abnormalities, resulted in a satiation deficit, leading to increased meal size, hyperphagia, and increased weight gain as early as 2-4 postnatal days. PMID:16099824
32. Cholecystokinin-8 activates the brainstem and myenteric neurons through the CCK1 receptor. PMID:16112401
33. CCK1 receptors have a role in stress and pain responses in rats PMID:16289472
34. under 'basal' conditions, a portion of the glandular protein synthesis, as well as the whole increase in synthesis in response to administration of pentagastrin, engaged both types of CCK receptors. PMID:16556659
35. OLETF rats do not express deficits in controlling gastric emptying rates; however, they exhibit decreased behavioral and vagal responsiveness to gastric distension that may contribute to the increased meal size in these animals. PMID:16728725
36. REVIEW: hyperphagia and obesity in OLETF rats without CCK-1 receptors PMID:16815799
37. Report effects of cholecystokinin-58 on type 1 cholecystokinin receptor function and regulation. PMID:18776046
38. cholecystokinin CCK1 and serotonin 5-HT3 receptors are mediators of the excitatory effects of cholecystokinin and 5-HT, respectively, on pancreatic vagal afferent discharge PMID:19026634
39. Fischer 344 rats lacking the cholecystokinin-1 receptor gene show normal feeding and body weight. PMID:19111529
40. The findings suggest that in addition to previously described deficits in peripheral satiety signals and augmented orexigenic regulation, the anorectic effect of CART peptide may also be diminished in CCK-1 deficient rats. PMID:19533109
41. endogenous CCK-1 receptor signaling in infants is a potential pathway through which maternal-pup interactions regulate the development and functional organization of emotional circuits that control anxiety-like behavior in the offspring. PMID:20001102

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UNIGENE: Rn.10184

KEGG: rno:24889

STRING: 10116.ENSRNOP00000063137