Laurberg P, Rehfeld J F
Second University Clinic of Internal Medicine, Kommunehospitalet, Aarhus, Denmark.
J Endocrinol. 1987 Oct;115(1):77-82. doi: 10.1677/joe.0.1150077.
Cholecystokinin (CCK) is a heterogeneous gut hormone which is also synthetized in extra-intestinal endocrine cells and neurons. In order to examine the possibility that CCK peptides are local modulators of calcitonin secretion, we have studied the structure-activity relationship on calcitonin secretion from perfused canine thyroid lobes as well as the presence and molecular nature of CCK in the thyroid. Peptides containing the intact COOH-terminal tetrapeptide amide of CCK (CCK-4, CCK-5, pentagastrin, CCK-8 and gastrin-17) all induced dose-dependent (0.1, 3 and 100 nmol/l) increases in calcitonin release (P less than 0.05, n = 4) with biphasic secretion during 6-min infusion periods. The deamidated tetrapeptide and the COOH-terminal tripeptide were without effect. Gel chromatography of neutral water and acid-ethanol extracts of thyroid tissue, monitored by sequence-specific CCK and gastrin radioimmunoassays, disclosed a variety of CCK and gastrin peptides of which a predominant form resembled small molecular forms like CCK-4 and CCK-5. The presence in the thyroid of small CCK-like peptides and the pronounced effect of such peptides on calcitonin secretion suggest that calcitonin secretion is modulated by local release of small CCK peptides. They could originate from intrathyroidal nerves or from sub-populations of C-cells.
胆囊收缩素(CCK)是一种异质性肠激素,也在肠外内分泌细胞和神经元中合成。为了研究CCK肽是否是降钙素分泌的局部调节因子,我们研究了灌注犬甲状腺叶降钙素分泌的构效关系以及甲状腺中CCK的存在和分子性质。含有完整CCK羧基末端四肽酰胺的肽(CCK-4、CCK-5、五肽胃泌素、CCK-8和胃泌素-17)在6分钟输注期间均诱导降钙素释放呈剂量依赖性(0.1、3和100 nmol/l)增加(P<0.05,n = 4),且分泌呈双相性。脱酰胺四肽和羧基末端三肽无作用。通过序列特异性CCK和胃泌素放射免疫测定监测甲状腺组织中性水提取物和酸乙醇提取物的凝胶色谱,发现了多种CCK和胃泌素肽,其中一种主要形式类似于CCK-4和CCK-5等小分子形式。甲状腺中存在小的CCK样肽以及此类肽对降钙素分泌的显著作用表明,降钙素分泌受小CCK肽局部释放的调节。它们可能源自甲状腺内神经或C细胞亚群。