Eggert Paul
Departmant of Pediatrics, University Children's Hospital, Kiel, Germany.
Acta Paediatr Taiwan. 2002 Jan-Feb;43(1):6-9.
Treatment of primary nocturnal enuresis (PNE) using desmopressin (dDAVP) is based upon the hypothesis that antidiuretic hormone (arginine vasopressin (AVP) secretion is insufficient during the night. Persisting doubts about the theoretical background of this treatment gave reason to different studies: In a first study, AVP regulation in children with PNE was investigated. AVP levels after fluid restriction were compared to those of healthy controls. In order to maintain osmolality, the plasma AVP concentrations of the enuretic children rose to significant higher levels than in the controls. In a second study, the short-time memory of children treated with dDAVP because of PNE was measured. Children under dDAVP showed a significantly better short- time memory.
The results are consistent with the established fact that AVP secretion is a function of plasma osmolality. They contradict the hypothesis that enuretic children have a AVP deficiency which has to be supplemented. Rather, the results point to central action of dDAVP, a defect at the central AVP receptor level or the signal transduction pathway.
使用去氨加压素(dDAVP)治疗原发性夜间遗尿症(PNE)基于这样一种假设,即夜间抗利尿激素(精氨酸加压素(AVP))分泌不足。对这种治疗的理论背景存在的持续疑问促使了不同的研究:在第一项研究中,调查了PNE患儿的AVP调节情况。将限水后患儿的AVP水平与健康对照者的进行比较。为了维持渗透压,遗尿患儿的血浆AVP浓度升至显著高于对照组的水平。在第二项研究中,测量了因PNE接受dDAVP治疗的患儿的短时记忆。接受dDAVP治疗的患儿表现出明显更好的短时记忆。
这些结果与AVP分泌是血浆渗透压的一种功能这一既定事实一致。它们与遗尿患儿存在必须补充的AVP缺乏这一假设相矛盾。相反,结果指向dDAVP的中枢作用、中枢AVP受体水平或信号转导途径存在缺陷。