Kamoi K, Ishibashi M, Yamaji T
Department of Medicine, Nagaoka Red Cross Hospital, Niigata, Japan.
Endocr J. 1997 Apr;44(2):311-7. doi: 10.1507/endocrj.44.311.
Vasopressin (AVP) secretion is principally under osmotic regulation, which is altered by nonosmotic stimuli. It is known that the manner of osmotic regulation of AVP secretion in hypoosmolar state of man consists of four types. The types have (A) random changes in plasma AVP without relation of plasma osmolality; (B) plasma AVP secretion correlated closely to plasma osmolality with a low osmotic threshold for AVP release; (C) nonsuppressible AVP secretion with normal osmotic release of AVP; (D) no abnormalities in AVP secretion. In this study, we found an entirely different type of AVP secretion from the above types in six patients with hyponatremia resulting from various causes during infusion of 5% hypertonic saline. To clarify the mechanism underlying the AVP secretion, we analyzed the interaction between osmotic and nonosmotic stimuli of AVP secretion in these patients. Despite hyponatremia, plasma AVP levels in all patients were not suppressed, which was attributed at least in part to the presence of nonosmotic stimuli for AVP release. These stimuli include nausea, hypotension, blood volume contraction, glucocorticoid deficiency or their combinations. Hypertonic saline infusion increased both serum sodium concentrations and plasma osmolality, although to subnormal levels, and concomitantly, alleviated some of the nonosmotic stimuli for AVP release formerly present in these patients. However, plasma AVP concentrations decreased rapidly during the infusion and reached the nadir in all patients. This phenomenon may be due to alleviation of nonosmotic stimuli for AVP release. Thus, the findings indicate that the potentiating effect of nonosmotic stimuli for AVP secretion may modify the osmotic regulation of AVP secretion in hypoosmolar state, resulting in the type of AVP secretion in this study.
血管加压素(AVP)的分泌主要受渗透压调节,但也会因非渗透压刺激而改变。已知在人体低渗状态下,AVP分泌的渗透压调节方式有四种类型。这些类型包括:(A)血浆AVP随机变化,与血浆渗透压无关;(B)血浆AVP分泌与血浆渗透压密切相关,AVP释放的渗透阈值较低;(C)AVP分泌不可抑制,AVP有正常的渗透释放;(D)AVP分泌无异常。在本研究中,我们发现6例因各种原因导致低钠血症的患者在输注5%高渗盐水期间,其AVP分泌类型与上述类型完全不同。为了阐明AVP分泌的潜在机制,我们分析了这些患者中AVP分泌的渗透压刺激和非渗透压刺激之间的相互作用。尽管存在低钠血症,但所有患者的血浆AVP水平均未被抑制,这至少部分归因于存在AVP释放的非渗透压刺激。这些刺激包括恶心、低血压、血容量减少、糖皮质激素缺乏或它们的组合。输注高渗盐水增加了血清钠浓度和血浆渗透压,尽管仍低于正常水平,同时减轻了这些患者先前存在的一些AVP释放的非渗透压刺激。然而,在输注过程中血浆AVP浓度迅速下降,所有患者均达到最低点。这种现象可能是由于AVP释放的非渗透压刺激减轻所致。因此,这些发现表明,非渗透压刺激对AVP分泌的增强作用可能会改变低渗状态下AVP分泌的渗透压调节,从而导致本研究中的AVP分泌类型。