It has been amply demonstrated that there are two physiologic stimuli which control the release of antidiuretic hormone (ADH) from the posterior pituitary. The first, delineated by the experiments of E. B. Verney (1947)(1948),1 involves alterations in intracellular volume in "osmoreceptor" cells which are probably in the supraoptic and paraventricular hypothalamic nuclei. The second and more recently defined stimulus appears to involve isotonic changes in some parameter (s) of the extracellular volume.2-10 While the location of the "volume receptors" is unknown, there is evidence to suggest their locus in the left atrium and adjacent pulmonary venous bed and their communication cephalad via the vagus nerves.8,11-13 Carter et al14 have reported a 40-year-old patient with inappropriate secretion of ADH and hyponatremia secondary to head trauma in whom there appeared to be a "dissociation" of osmolar and volume control stimuli.In this patient ADH secretion during the early stages of illness was autonomous of both receptor systems. As recovery pro¬ gressed over one to two months there was evidence for volume inhibition of ADH secretion ; water diuresis occurred in re¬ sponse to water or salt loading. During this same period ADH secretion remained in¬ dependent of osmoreceptor control. Eventu¬ ally complete recovery occurred. Schwartz et al noted a suggestive transient inhibition of inappropriate ADH secretion in a patient with bronchogenic carcinoma during infusion of slightly hypertonic saline.15 However urine osmolality in this patient decreased to only 150 mOsm, and sodium excretion increased tenfold during the study period.It is the purpose of this report to describe an instance of dissociation of volume and osmolar control of ADH release in a sixmonth-old infant who had manifestations of transient brain damage and diabetes insipidus.
Report of CaseA Negro male infant was the fifth child of a 22-year-old mother. Birth weight was 2.3 kg (5 lb). Gestation was essentially uncomplicated, but the infant was born prematurely at eight months. He appeared normal at birth and remained in the nursery only three days. The feeding history was not reliable. He was bottle-fed, but no conclusion regarding the amounts given is possible. An episode of diarrhea occurred at three months but cleared spontaneously. Rice and bean soup were reportedly introduced at five months. No vitamins or other solid food had been given. At six months the child entered the University Hospital with a history of poor weight gain and slow development. During the previous month stools had been numerous and loose and had become mucosanguineous two or three days before ad¬ mission. There was a history of weight loss during this month. The child had not laughed or smiled Downloaded From: http://archpedi.jamanetwork.com/ by a Oakland University User on 06/03/2015