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British Journal of Pharmacology
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23 January 1997, Volume 120, Issue 3, Pages 447 – 454 |
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Pharmacological and biochemical evidence for the simultaneous expression of CCKB/gastrin and CCKA receptors in the pig pancreas
C. Philippe1,4, E.F. Lhoste1, M. Dufresne2, L. Moroder3, T. Corring1 & D. Fourmy2 1Laboratoire d’Ecologie et de Physiologie du Système Digestif, INRA, Domaine de Vilvert F-78352 Jouy-en-Josas Cedex, France 2INSERM Unité 151, Institut L. Bugnard, CHU Rangueil, F-31054 Toulouse, France, and 3Max Planck Institut für Biochemie, Martinsried, Germany4Author for correspondence |
| Keywords |
| Pancreas;
CCKA receptor;
CCKB/gastrin receptor;
pig |
| Abstract |
1 In the pig, the secretory response of the pancreas is not inhibited by the antagonist MK329 suggesting that cholecystokininA (CCKA) receptors are not involved. 2 Membranes were isolated from the pancreas of 6 Large White pigs to characterize their CCK receptors. 3 The binding of [125I]-BH-[Thr, Nle]CCK-9 was dependent on pH, maximal after a 90 min incubation period, saturable and reversible. Saturation analysis of the binding demonstrated a single class of high affinity sites (Kd=0.22±0.02 nM) and a binding capacity, Bmax=110.64±12.50 fmol mg-1 protein. 4 Competition binding by agonists and antagonists of CCKA and CCKB/gastrin receptors demonstrated the presence of two distinct binding components, sites presenting a high affinity for [Thr, Nle]CCK-9, gastrin, PD 135158, L-365,260 and a low affinity for MK329, SR 27897, and sites presenting a high affinity for [Thr, Nle]CCK-9, MK329, SR 27897 and a low affinity for gastrin, PD 135158, L-365,260. 5 These pharmacological data demonstrate the presence of both CCKA and CCKB/gastrin receptors in the pig pancreas, the latter being predominant. 6 Two distinct membrane proteins (50 and 85 – 100 kDa, respectively) display pharmacological features of CCKB/gastrin and CCKA receptors. 7 In pigs, as in calves and humans, CCKB/gastrin receptors are predominant in the pancreas. |
Received 22 April, 96; Revised 20 October, 96; Accepted 31 October, 96