1984
DOI: 10.1016/0167-0115(84)90053-3
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Relationship of CCK/gastrin receptor binding to amylase release in dog pancreatic acini

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Cited by 27 publications
(10 citation statements)
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“…In 1984, CCK receptors having pharmacological features different from those of the rodent pancreatic receptor were found on pancreatic acini from the dog [216]. Indeed, gastrin, and the tetrapeptide common to gastrin and CCK, were only 25-fold and 100-fold less potent, respectively, than CCK-8 in inhibiting CCK radioligand binding to these receptors.…”
Section: The Cck-b Receptor In the Normal Pancreas And The Ar4-2j Celmentioning
confidence: 99%
“…In 1984, CCK receptors having pharmacological features different from those of the rodent pancreatic receptor were found on pancreatic acini from the dog [216]. Indeed, gastrin, and the tetrapeptide common to gastrin and CCK, were only 25-fold and 100-fold less potent, respectively, than CCK-8 in inhibiting CCK radioligand binding to these receptors.…”
Section: The Cck-b Receptor In the Normal Pancreas And The Ar4-2j Celmentioning
confidence: 99%
“…Binding Studies were radioiodinatcd by conjugation of the peptide to ,25I-BH reagent and purified by reverse-phase high performance liquid chromatography as previously de scribed [8], Binding assays were carried out on iso lated cells as described [6], ODC Assay ODC activity was measured as previously de scribed [6] with minor modifications. Cytosolic ex tracts were prepared by scraping off cells from dishes, and lysis was performed by freezing and thawing cells in buffer containing 100 mA/ Tris-HCl (pH 7.4), 1 mM EDTA and I mA/ dithiothreitol.…”
Section: Methodsmentioning
confidence: 99%
“…Additionally, no specific gastrin binding was demonstrated in pancreata of foetal rats (day 19 of gestation). In control adult rats, only by using very high amounts of membrane material and high ligand concentrations were specific '251-BH-de~-S03H-ga~trin (2)(3)(4)(5)(6)(7)(8)(9)(10)(11)(12)(13)(14)(15)(16)(17) …”
Section: )mentioning
confidence: 99%
“…[Thr34,Ahx37]-CCK(31-39) (Ahx, aminohexanoic acid), human cles-S03H-[AhxlS]gastrin, des-S03H-gastrin(2 -17) and gastrin-(2-17) were synthesized as described in [13, 141. (2)(3)(4)(5)(6)(7)(8)(9)(10)(11)(12)(13)(14)(15)(16)(17) and gastrin (2 -17) were radiodinated by conjugation with lz5I-BH and purified by reverse-phase HPLC, as described in [16]. The specific activity was 66.6-74.0 GBq/pmol.…”
Section: Chemicalsmentioning
confidence: 99%