Bauduin H, Stock C, Launay J F, Vincent D, Potvliege P, Grenier J F
Pflugers Arch. 1977 Nov 25;372(1):69-76. doi: 10.1007/BF00582208.
DbcAMP greater than or equal to 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 neurotransmitter 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.
大于或等于0.1 mM的二丁酰环磷腺苷(dbcAMP)可诱导体外培养的大鼠胰腺碎片排出可分泌的酶。这种效应在性质上类似于通过激素受体起作用的生理促分泌剂的作用:1)它伴随着腺泡细胞顶端出现胞吐图像;2)它依赖能量,但能量供应较低,而氨甲酰胆碱或雨蛙肽反应所需的能量较高,且只能通过氧化磷酸化提供;3)它依赖钙,但未观察到钙的内流或外流有改变;4)它会被已知能破坏微丝微管系统的试剂改变[41]。然而,对dbcAMP的分泌反应在数量上小于激素刺激所获得的反应。基于组织学和生化依据排除了dbcAMP对胰腺腺泡细胞的损伤作用:乳酸脱氢酶(LDH)无明显渗漏;蛋白质合成、2-脱氧-D-葡萄糖和L-亮氨酸摄取未改变。dbcAMP的促分泌作用是可逆的、剂量相关的且具有特异性。它不是由神经递质释放或与它们的受体相互作用介导的。所提供的证据表明dbcAMP与胰腺腺泡细胞直接相互作用,并表明分泌周期的最后一步是该核苷酸衍生物最可能的作用位点。