Schlondorff D, Weber H, Trizna W, Fine L G
Am J Physiol. 1978 Jan;234(1):F16-21. doi: 10.1152/ajprenal.1978.234.1.F16.
Newborns show an inability to concentrate maximally their urine. The vasopressin responsiveness of adenylate cyclase was, therefore, examined in membranes obtained from kidneys of neonatal and adult rats and from renal medulla and isolated collecting tubules of newborn and adult rabbits. In spite of higher basal and NaF-stimulated activity, vasopressin failed to stimulate adenylate cyclase from neonatal rat kidneys. In neonatal and adult rabbits, basal and NaF-stimulated adenylate cyclase activities of renal medullary membranes were comparable but vasopressin stimulation was significantly lower in the newborns. No change in hormonal activation constant was observed. This hyporesponsiveness of neonatal adenylate cyclase to vasopressin was confirmed with single isolated rabbit collecting tubules for adenylate cyclase determination, a highly sensitive preparation. It is intriguing to speculate that the low vasopressin stimulation of the medullary adenylate cyclase in the developing kidney may contribute to the known limitations of the urinary concentrating mechanism in the newborn period.
新生儿表现出无法最大限度地浓缩尿液的能力。因此,研究人员检测了新生大鼠和成年大鼠肾脏、新生兔和成年兔肾髓质及分离的集合小管的细胞膜中腺苷酸环化酶对血管加压素的反应性。尽管基础活性和氟化钠刺激的活性较高,但血管加压素未能刺激新生大鼠肾脏的腺苷酸环化酶。在新生兔和成年兔中,肾髓质细胞膜的基础腺苷酸环化酶活性和氟化钠刺激的活性相当,但血管加压素刺激在新生兔中显著较低。未观察到激素激活常数的变化。通过高度敏感的单一分离兔集合小管进行腺苷酸环化酶测定,证实了新生腺苷酸环化酶对血管加压素的低反应性。有趣的是,可以推测发育中的肾脏髓质腺苷酸环化酶对血管加压素的低刺激可能导致新生儿期已知的尿液浓缩机制的局限性。