Edwards C R, Kitau M J, Chard T, Besser G M
Br Med J. 1973 Aug 18;3(5876):375-8. doi: 10.1136/bmj.3.5876.375.
In seven patients with cranial diabetes insipidus an analogue of vasopressin, DDAVP, produced an antidiuresis lasting up to 20 hours after a single intranasal dose. Lysine vasopressin (LVP) in the same dose produced a less potent antidiuresis which lasted for only three to four hours. The plasma half life of DDAVP was 7.8 and 75.5 min for the fast and slow phases, compared with 2.5 and 14.5 min for LVP. Radioiodine-labelled DDAVP was not destroyed by incubation with late pregnancy plasma, which contains an enzyme that inactivates vasopressin. The slow metabolic clearance of DDAVP, its absorption through the nasal mucosa, and its lack of side effects make this the ideal drug for the treatment of vasopressin-sensitive diabetes insipidus. Patients usually require 10 to 20 mug DDAVP given intranasally twice daily for good clinical control of their diabetes insipidus.
在7例颅咽管性尿崩症患者中,一种血管加压素类似物——去氨加压素(DDAVP),经单次鼻内给药后可产生持续长达20小时的抗利尿作用。相同剂量的赖氨酸加压素(LVP)产生的抗利尿作用较弱,仅持续3至4小时。DDAVP的血浆半衰期在快速和慢速阶段分别为7.8分钟和75.5分钟,而LVP的血浆半衰期分别为2.5分钟和14.5分钟。放射性碘标记的DDAVP与晚期妊娠血浆一起孵育时不会被破坏,晚期妊娠血浆中含有一种可使血管加压素失活的酶。DDAVP代谢清除缓慢、可经鼻黏膜吸收且无副作用,使其成为治疗血管加压素敏感性尿崩症的理想药物。患者通常每日两次鼻内给予10至20微克DDAVP,以实现对尿崩症的良好临床控制。