Caniggia A, Nuti R, Vattimo A, Galli M, Turchetti V, Franci B, Martorelli T, Righi G
Minerva Med. 1983 Apr 28;74(18):993-1010.
(Asu) E-CT is a deaminodicarba-analog of the synthetic eel-calcitonin (E-CT) that shows specific activity and the potency reasonably high in comparison with that of the most potent natural hormone. The structure of its molecule indicates that the disulphide bond in calcitonins is not essential for the biological activity but only for the maintenance of the specific conformation by forming an intramolecular bridge. The instability of calcitonins should mainly be attributed to the presence of the disulfide bond and (Asu)E-CT proved to be more stable "in vitro" than native calcitonins. The more prolonged hypocalcemic effect of E-CT and its aminosuberic analog (Asu)E-CT has been accounted for to a greater stability of and persistence at the receptor site. (Asu) E-CT has been largely studied in Japan on experimental animals and successfully used in the treatment of hypercalcemia in man. On the contrary investigations on human administration of this analog are very scarce. The present paper reports studies carried out in normal subjects and Paget's disease patients to investigate the effects of (Asu)E-CT in man in comparison with the effects of synthetic human calcitonin (H-CT) and synthetic salmon calcitonin (S-CT). Two different experimental procedures have been used: 1) rapid intravenous injection of (Asu)E-CT (80 MRC. U.) or respectively of H-CT and S-CT (100 MRC. U.) in 15 subjects (7 normals and 8 with Paget's disease); 2) slow 7 days continuous subcutaneous infusion of similar daily amounts of (Asu)E-CT, H-CT and S-CT administered by a microjet pump device in 21 subjects (7 normals and 14 with Paget's disease). The intravenous administration of (Asu)E-CT induced a rapid and persistent decrease in total plasma calcium, ionized calcium and plasma phosphate that was more evident in Paget's disease patients than in normal subjects. No clearly cut differences have been observed with the hypocalcemic and hypophosphatemic effect of H-CT and S-CT administered intravenously; nevertheless the hypocalcemic effect proved to be more persistent in Paget's disease patients treated with (Asu)E-CT. After intravenous infusion of (Asu)E-CT the plasma level of cAMP rose more evidently in pagetic than in normal subjects but the rise was lower than in H-CT and S-CT treated subjects.(ABSTRACT TRUNCATED AT 400 WORDS)
(天冬氨酸)鳗鱼降钙素(E-CT)是合成鳗鱼降钙素的脱氨二碳类似物,与最有效的天然激素相比,它具有特定活性且效价相当高。其分子结构表明,降钙素中的二硫键对生物活性并非必不可少,而仅通过形成分子内桥来维持特定构象。降钙素的不稳定性主要应归因于二硫键的存在,并且(天冬氨酸)E-CT在“体外”被证明比天然降钙素更稳定。E-CT及其氨基辛二酸类似物(天冬氨酸)E-CT的降钙作用持续时间更长,这被认为是由于其在受体部位具有更高的稳定性和持久性。(天冬氨酸)E-CT在日本已在实验动物上进行了大量研究,并成功用于治疗人类高钙血症。相反,关于这种类似物在人体给药方面的研究非常稀少。本文报告了在正常受试者和佩吉特病患者中进行的研究,以比较(天冬氨酸)E-CT与合成人降钙素(H-CT)和合成鲑鱼降钙素(S-CT)在人体中的作用。使用了两种不同的实验程序:1)对15名受试者(7名正常人和8名佩吉特病患者)快速静脉注射(天冬氨酸)E-CT(80 MRC单位)或分别注射H-CT和S-CT(100 MRC单位);2)对21名受试者(7名正常人和14名佩吉特病患者)使用微喷射泵装置缓慢皮下连续输注7天相似日剂量的(天冬氨酸)E-CT、H-CT和S-CT。静脉注射(天冬氨酸)E-CT导致总血浆钙、离子钙和血浆磷酸盐迅速且持续下降,在佩吉特病患者中比在正常受试者中更明显。静脉注射H-CT和S-CT的降钙和降磷作用未观察到明显差异;然而,在接受(天冬氨酸)E-CT治疗的佩吉特病患者中,降钙作用被证明更持久。静脉输注(天冬氨酸)E-CT后,佩吉特病患者血浆中环磷酸腺苷(cAMP)水平的升高比正常受试者更明显,但低于接受H-CT和S-CT治疗的受试者。(摘要截短至400字)