Gray D A, Erasmus T
Department of Zoology, University of Port Elizabeth, South Africa.
Gen Comp Endocrinol. 1989 Apr;74(1):110-9. doi: 10.1016/0016-6480(89)90119-6.
The physiological roles of plasma osmolality, volume, and angiotensin II (AII) in the control of plasma arginine vasotocin (AVT) have been evaluated in the Kelp gull. Plasma AVT (measured by radioimmunoassay) consistently followed the changes in plasma osmolality induced by dehydration, intravenous (iv) infusion of hypertonic saline, or iv infusion of hypotonic glucose solution. Osmoreceptor control of AVT was further characterized by the stimulatory effect of iv hypertonic mannitol but lack of effect of iv hypertonic urea. A direct volume effect on AVT release was demonstrated during hemorrhage, but blood volume reductions in excess of 10% were required. However, the volume of the extracellular fluid (ECF) compartment does have an important role in modulating the osmotic release of AVT in a way that enables contraction or expansion of ECF to be more expeditiously corrected than would occur if osmoreceptors alone regulated plasma AVT. Any physiological role of plasma AII in the control of plasma AVT is doubtful because after the iv infusion of AII for 60 min at 10, 25, 50, and 100 ng.min-1, only the two highest doses of AII, which produced supraphysiological plasma AII levels, caused elevations of plasma AVT. In addition, the osmotic reactivity of AVT release was not altered by exogenous administration of AII.
在南极鸬鹚中,已对血浆渗透压、容量及血管紧张素II(AII)在控制血浆精氨酸加压催产素(AVT)方面的生理作用进行了评估。血浆AVT(通过放射免疫测定法测量)始终随着脱水、静脉注射高渗盐水或静脉注射低渗葡萄糖溶液所诱导的血浆渗透压变化而变化。静脉注射高渗甘露醇对AVT有刺激作用,而静脉注射高渗尿素则无作用,这进一步说明了AVT受渗透压感受器的控制。在出血期间证实了对AVT释放存在直接的容量效应,但需要超过10%的血容量减少。然而,细胞外液(ECF)区室的容量在调节AVT的渗透释放方面确实具有重要作用,其方式使得ECF的收缩或扩张能够比仅由渗透压感受器调节血浆AVT时更迅速地得到纠正。血浆AII在控制血浆AVT方面的任何生理作用都值得怀疑,因为在以10、25、50和100 ng·min-1的剂量静脉注射AII 60分钟后,只有产生超生理水平血浆AII的两个最高剂量的AII导致了血浆AVT升高。此外,外源性给予AII并未改变AVT释放的渗透反应性。