par Bauduin, Henri 
;Stock, Christiane;Launay, Jean François;Vincent, D.;Potvliege, P.;Grenier, Jacques J.F.
Référence Pflügers Archiv, 372, 1, page (69-76)
Publication Publié, 1977-01
;Stock, Christiane;Launay, Jean François;Vincent, D.;Potvliege, P.;Grenier, Jacques J.F.Référence Pflügers Archiv, 372, 1, page (69-76)
Publication Publié, 1977-01
Article révisé par les pairs
| Résumé : | DbcAMP≥0.1 mM induces the discharge of exportable enzymes from rat pancreas fragments incubated in vitro. This effect is qualitatively similar to the action of physiological secretagogues acting via hormone receptors: 1) it is accompanied by the appearance of exocytotic images at the acinar cell apex; 2) it is energy dependent but energy supply is low while that required for the carbamylcholine or caerulein response is high and can only be afforded by oxidative phosphorylation; 3) it is calcium dependent, but no alteration of inward or outward calcium movement can be observed; 4) it is altered by agents known to disrupt the microfilamentous microtubular system [41]. However, the secretory response to DbcAMP is quantitatively less than that obtained with hormonal stimuli. A damaging effect of DbcAMP on pancreatic acinar cells is ruled out on histological and biochemical grounds: there is no significant leakage of LDH; protein synthesis, 2-deoxy-d-glucose and l-leucine uptake are unaltered. The secretagogue effect of DbcAMP is reversible, dose-related and specific. It is not mediated by neuro-transmitter release or by interaction with their receptors. The evidence presented points to a direct interaction of DbcAMP on the pancreatic acinar cell and suggests the last step of the secretory cycle as the most probable site of action of the nucleotide derivative. © 1977 Springer-Verlag. |
