Dreyfus C F, Gershon M D, Haymovits A, Nunez E
Br J Pharmacol. 1976 May;57(1):155-7. doi: 10.1111/j.1476-5381.1976.tb07667.x.
The action of calcitonin was studied on the motility of isolated innervated segments of rabbit and guinea-pig intestines as well as longitudinal muscle with adherent myenteric plexus dissected from the guinea-pig ileum. Calcitonin (0.25 muM) antagonized contractile responses to acetylcholine and the cholinergic response to electrical field stimulation. This hormonal effect was relatively specific since it was not observed at nicotinic receptors or adrenoceptors, nor did calcitonin act as a local anaesthetic or directly on the contractile machinery of smooth muscle. Perivascular adrenergic and intrinsic non-adrenergic inhibitory responses also were unaffected by calcitonin. However, calcitonin did have antihistaminic properties directed against H1-receptors. The concentration of calcitonin required to achieve muscarinic antagonism in our experiments is not reached at the resting level of circulating hormone.
研究了降钙素对兔和豚鼠离体有神经支配肠段以及从豚鼠回肠分离的带有附着肌间神经丛的纵行肌运动的作用。降钙素(0.25μM)拮抗对乙酰胆碱的收缩反应以及对电场刺激的胆碱能反应。这种激素效应相对具有特异性,因为在烟碱受体或肾上腺素受体处未观察到这种效应,降钙素也不充当局部麻醉剂或直接作用于平滑肌的收缩机制。血管周围肾上腺素能和内在非肾上腺素能抑制反应也不受降钙素影响。然而,降钙素确实具有针对H1受体的抗组胺特性。在我们的实验中,达到毒蕈碱拮抗作用所需的降钙素浓度在循环激素的静息水平时未达到。