Skip to main content
Log in

Effects of changes in intravascular oncotic pressure on renal responses to volume loading in the saltwater-acclimated Pekin duck (Anas platyrhynchos)

  • Published:
Journal of Comparative Physiology B Aims and scope Submit manuscript

Summary

The relative contributions of the intra-and extravascular compartments of the extracellular fluid (ECF) to the control of osmoregulatory renal functions were examined in saltwater-acclimated Pekin ducks. Having established steady-state diuresis and salt gland secretion by continuous infusion of 1 ml·min-1 isotonic Krebs-Ringer-Bicarbonate (KRB) solution, 5% dextran-70 was added to the infusate for 30 min thereby confining volume expansion to the intravascular compartment. General volume expansion by isotonic KRB caused a drop in plasma osmolality by 23 mOsm·kg-1, due to NaCl elimination by the salt glands, and decreases in hematocrit (het) and radioimmunologically measured plasma levels of Arg8-vasotocin (AVT) and Val5-angiotensin II (ANG II), whereas immunoreactivity associated with atrial natriuretic factor (ir-ANF) was increased. Adding 5% dextran-70 to the infusate left plasma osmolality and electrolytes unchanged but was followed by a further decrease in hct and a 36% increase in the plasma colloidosmotic pressure (COP) facilitating fluid shifts from the extra-to the intravascular compartment of the ECF. Plasma levels of AVT and ANG II remained unchanged, but ir-ANF rose three-fold, its increase being three times as great relative to the decrease in hct, as during general volume expansion by isotonic KRB solution. Arterial and central venous pressure measurements did not indicate changes in cardiovascular function. Hyperoncotic infusion initially induced marked antidiuresis with decreased osmolal excretion, despite a slightly elevated urine osmolality. This effects, however, was trasient and not proportional to the rise in COP, but rather seemed to be related to fluid shifts resulting from hyperoncotic loading. With tracer dilution techniques, reductions in both renal plasma flow and glomerular filtration rate were found to contribute to antidiuresis which was associated with reduced fractional water excretion. Salt gland secretion rate did not increase during hyperoncotic intravascular volume expansion but rather tended to decrease. The results of this study are in line with the idea that contributions of the interstitial fluid compartment (IFC) to volume-dependent control of osmoregulatory functions have to be considered. In the present study on saltwater-acclimated ducks, AVT, ANG II, and ir-ANF could be excluded as mediators of the adjustments in renal water and salt handling following fluid shifts due to hyperoncotic intravascular volume expansion.

This is a preview of subscription content, log in via an institution to check access.

Access this article

Price excludes VAT (USA)
Tax calculation will be finalised during checkout.

Instant access to the full article PDF.

Similar content being viewed by others

Abbreviations

ANF :

atrial natriuretic factor

ir-ANF :

ANF-like immunoreactivity

ANG II :

angiotensin II

AVT :

arginine vasotocin

BF :

breathing frequency

b. w. :

body weight

COP :

colloid osmotic pressure

CVP :

central venous pressure

ECF :

extracellular fluid

ERPF :

effective renal plasma flow

FF :

filtration fraction

GFR :

glomerular filtration rate

IFC :

interstitial fluid compartment

i.v. :

intravenous(ly)

hct :

hematocrit

HR :

heart rate

KRB :

Krebs-Ringer Bicarbonate solution

MABP :

mean arterial blood pressure

PAH :

paraaminohippuric acid

SEM :

standard error of mean

References

  • Ackermann U, Pearce JW (1975) On the role of the interstitial volume in the response of the rat to blood volume expansion. Pflügers Arch 359:97–109

    Google Scholar 

  • Aukland K (1989) Is extracellular fluid volume regulated? Acta Physiol Scand 136 Suppl 583:59–67

    Google Scholar 

  • Bie P (1980) Osmoreceptors, vasopressin, and control of renal water excretion. Physiol Rev 60(4):961–1048

    Google Scholar 

  • Bouverot P, Hildwein G, Le Goff D (1974) Evaporative water loss, respiratory pattern, gas exchange and acid-base balance during thermal panting in Pekin ducks exposed to moderate heat. Resp Physiol 21:255–269

    Google Scholar 

  • Brummermann M, Simon E (1990) Arterial hypotension in ducks adapted to high salt intake. J Comp Physiol B 160:127–136

    Google Scholar 

  • Chwalbinska-Moneta J (1979) Role of hepatic portal osmoreception in the control of ADH release. Am J Physiol 236:E603-E609

    Google Scholar 

  • Cowley AW Jr, Roman RJ (1989) Neural-hormonal control of blood volume. Proc IUPS (31st Int Congr Physiol Sci, Helsinki, 1989, L4068), Vol. 17, 350

  • Dantzler WH (1988) Comparative physiology of the vertebrate kidney. Zoophysiology vol. 22. Springer, Berlin Heidelberg New York

    Google Scholar 

  • Gauer OH, Henry JP, Behn C (1970) The regulation of extracellular fluid volume. Ann Rev Physiol 32:547–595

    Google Scholar 

  • Genest J, Cantin M (1988) The atrial natriuretic factor: its physiology and biochemistry. Rev Physiol Biochem Pharmacol 110:1–145

    Google Scholar 

  • Gerstberger R, Simon E, Gray DA (1984) Salt gland and kidney responses to intracerebral osmotic stimulation in salt-and water-loaded ducks. Am J Physiol 247:R1022-R1028

    Google Scholar 

  • Goetz KL, Bond GC, Bloxham DD (1975) Atrial receptors and renal function. Physiol Rev 55(2):157–205

    Google Scholar 

  • Goetz KL (1988) Physiology and pathophysiology of atrial peptides. Am J Physiol 254:E1-E15

    Google Scholar 

  • Gray DA, Hammel HT, Simon E (1986) Osmoregulatory effects of angiotensin II in a bird with salt glands (Anas platyrhynchos). J Comp Physiol 156B:315–321

    Google Scholar 

  • Gray DA, Schütz H, Gerstberger R (1991) Plasma ANF responses to blood volume changes in the Pekin duck. Endocrinology (in press)

  • Gray DA, Simon E (1983) Mammalian and avian antidiuretic hormon: studies related to possible species variation in osmoregulatory systems. J Comp Physiol 151 B:241–246

    Google Scholar 

  • Gray DA, Simon E (1985) Control of plasma angiotensis II in a bird with salt glands (Anas platyrhynchos). Gen Comp Endocrin 60:1–13

    Google Scholar 

  • Hall JE, Guyton AC (1976) Changes in renal hemodynamics and renin release caused by increased plasma oncotic pressure. Am J Physiol 231:1550–1556

    Google Scholar 

  • Hammel HT, Simon-Oppermann C, Simon E (1980) Properties of body fluids influencing salt gland secretion in Pekin ducks. Am J Physiol 239:R489-R496

    Google Scholar 

  • Hanwell A, Linzell JL, Peaker M (1972) Nature and location of the receptors for salt gland secretion in the goose. J Physiol (Lond) 226:453–472

    Google Scholar 

  • Holm S (1979) A simple sequentially rejective multiple test procedure. Scand J Statist 6:65–70

    Google Scholar 

  • Keil R, Schütz H, Gray DA, Gerstberger R, Simon E (1990) Hormonal control of renal function in the saltwater-acclimated Pekin duck by AVT and ANF. J Endocrin Invest 13, suppl 2–5:291

    Google Scholar 

  • Knox FG, Haas JA (1982) Factors influencing renal sodium reabsorption in volume expansion. Rev Physiol Biochem Pharmacol 92:75–113

    Google Scholar 

  • Manning RD, Guyton AC (1982) Control of blood volume. Rev Physiol Biochem Pharmacol 93:69–114

    Google Scholar 

  • Marty AT, Zweifach BW (1970) The high oncotic pressure effects of dextrans. Arch Burg 101:421–424

    Google Scholar 

  • Morimoto T, Miki K, Nose H, Tanaka Y, Yamada S (1981) Transvascular fluid shift after blood volume modification in relation to compliances of the total vascular bed and interstitial fluid space. Jap J Physiol 31:869–878

    Google Scholar 

  • Nishimura H, Miwa T, Bailey JR (1984) Renal handling of sodium chloride and its control in birds. J Exp Zool 232:697–705

    Google Scholar 

  • Phillips MI, Kimura B, Wang H, Hoffman WE (1989) Effects of vagotomy on brain and plasma atrial natriuretic peptide during hemorrhage. Am J Physiol 257:R1393–1399

    Google Scholar 

  • Ploucha JM, Fink GD (1986) Hemodynamics of hemorrhage in the conscious rat and chicken. Am J Physiol 251:R846-R850

    Google Scholar 

  • Sawchenko PE, Friedman MI (1979) Sensory functions of the liver —a review. Am J Physiol 236(1):R5-R20

    Google Scholar 

  • Schindler SL, Gildersleeve RP (1987) Comparison of recovery from hemorrhage in birds and mammals. Comp Biochem Physiol 87A:533–542

    Google Scholar 

  • Schütz H, Gerstberger R (1990) Atrial natriuretic factor (ANF) controls salt gland secretion through interaction with high-affinity receptors. Endocrinology 127:1718–1726

    Google Scholar 

  • Sharples JA, Green R (1989) Renal function during intravenous albumin infusion in the anaesthetized rat. Proc of the 31st Int Congr Physiol Sci, Helsinki, Finland P1223:41

  • Shideman JR, Evans RL, Bierer DW, Quebbemann AJ (1981) Renal venous portal contribution to PAH and uric acid clearance in the chicken. Am J Physiol 240:F46-F53

    Google Scholar 

  • Shiraishi Y, Fujimura S, Handa M, Kimura T, Ota K, Nakada T (1990) Vasopressin and atrial natriuretic peptide release in cardiopulmonary denervated dogs. Am J Physiol 258:R704-R710

    Google Scholar 

  • Simon E (1982) The osmoregulatory system of birds with salt glands. Comp Biochem Physiol 71A:547–556

    Google Scholar 

  • Simon-Oppermann C, Gerstberger R (1989) Role of kidneys in osmoregulation of birds with salt glands: integration of central neurohormonal control. In: Chadwick A, Hughes M (eds) Progress in osmoregulation and prolactin secretion, Leeds Philos Soc, England, pp 183–205

    Google Scholar 

  • Von Amelen H, Laniado M, Röcker L, Kirsch KA (1985) Effects of dehydration on the vasopressin response to immersion. J Appl Physiol 58:114–120

    Google Scholar 

  • Wong NLM, Wong EFC, Au GH, Hu DCK (1988) Effect of α-and β-adrenergic stimulation on atrial natriuretic peptide release in vitro. Am J Physiol 255:E260-E264

    Google Scholar 

  • Yokota SD, Benyajati S, Dantzler WH (1985) Comparative aspects of glomerular filtration in vertebrates. Renal Physiol, Basel 8:193–221

    Google Scholar 

  • Zucker IH, Gilmore C, Dietz J, Gilmore JP (1977) Effect of volume expansion and veratrine on salt gland secretion in the goose. Am J Physiol 232:R185-R189

    Google Scholar 

Download references

Author information

Authors and Affiliations

Authors

Rights and permissions

Reprints and permissions

About this article

Cite this article

Keil, R., Gerstberger, R. & Simon, E. Effects of changes in intravascular oncotic pressure on renal responses to volume loading in the saltwater-acclimated Pekin duck (Anas platyrhynchos). J Comp Physiol B 161, 179–187 (1991). https://doi.org/10.1007/BF00262882

Download citation

  • Accepted:

  • Issue Date:

  • DOI: https://doi.org/10.1007/BF00262882

Key words

Navigation