Seif S M, Zenser T V, Ciarochi F F, Davis B B, Robinson A G
J Clin Endocrinol Metab. 1978 Mar;46(3):381-8. doi: 10.1210/jcem-46-3-381.
DDAVP, 1-desamino-8-D-arginine-vasopressin, is a synthetic analog of arginine vasopressin which produces prolonged antidiuresis after intranasal administration to patients with complete central diabetes insipidus. We have studied the mechanism of the prolonged antidiuretic effect by specific radioimmunossay of DDAVP in plasma of patients and by in vitro studies on the adenylate cyclase-cylic AMP system of the rat outer renal medulla. When DDAVP was administredd to patients, all responded, but the duration of response among patients varied from 5-21 h. The peak level of DDAVP in plasma was achieved up to 4 h after administration indicating a slow absorption from the nasal mucosa. The disappearance time of DDAVP from plasma correlated significantly with the duration of antidiuresis, P less than 0.001. On a molar basis DDAVP was 3-fold greater than AVP in its stimulation of outer medullary adenylate cyclase activity and 10-fold greater than AVP in its stimulation of cyclic AMP content. The prolonged antidiuresis of intranasally administered DDAVP is due to slow absorption, presistence in plasma, and enchanced effect on the kidney.
去氨加压素,即1-去氨基-8-D-精氨酸血管加压素,是精氨酸血管加压素的一种合成类似物,给完全性中枢性尿崩症患者鼻内给药后可产生持久的抗利尿作用。我们通过对患者血浆中的去氨加压素进行特异性放射免疫测定以及对大鼠肾外髓质的腺苷酸环化酶 - 环磷酸腺苷系统进行体外研究,来探讨这种持久抗利尿作用的机制。给患者使用去氨加压素后,所有患者均有反应,但患者之间的反应持续时间为5 - 21小时不等。给药后长达4小时血浆中去氨加压素才达到峰值水平,表明其从鼻粘膜吸收缓慢。去氨加压素从血浆中的消失时间与抗利尿持续时间显著相关,P小于0.001。以摩尔为基础,去氨加压素刺激外髓质腺苷酸环化酶活性的能力比血管加压素大3倍,刺激环磷酸腺苷含量的能力比血管加压素大10倍。鼻内给药的去氨加压素产生持久抗利尿作用的原因是吸收缓慢、在血浆中持续存在以及对肾脏的作用增强。