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Dietary sodium, glomerular filtration rate autoregulation, and glomerular size distribution profiles in domestic fowl (Gallus gallus)

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Summary

Mammalian glomerular filtration rate (GFR) autoregulation can be impaired by protocols that inhibit tubuloglomrular feedback, such as high sodium intake. Domestic fowl were fed diets containing either high sodium (0.39% Na: High-Na Group) or low sodium (0.03% Na: Low-Na Group). An arterial snare was used to reduce renal arterial perfusion pressure (RAPP) in a stepwise fashion to evaluate GFR autoregulation. Absolute sodium excretion, fractional sodium excretion (FENa), and ambient systemic arterial blood pressure were significantly elevated in the High-Na Group when compared with the Low-Na Group, and pressure natriuresis was abolished by the Low-Na diet. However, GFR autoregulatory profiles were identical in birds fed High-Na and Low-Na diets, suggesting that tubuloglomerular feed-back does not contribute significantly to avian GFR autoregulation. Filtering glomeruli were stained in vivo with alcian blue dye to determine if RAPP-induced reductions in GFR are associated with cessation of filtration (glomerular intermittency) by a portion of the nephron population. RAPP was held below the GFR autoregulatory range (experimental group) or was at ambient systemic arterial pressure (control group) during glomerular staining. Reducing RAPP below the autoregulatory range reduced GFR by 50%, but similar glomerular size distribution profiles were observed for experimental and control groups. These results indicate that sustained glomerular intermittency does not contribute to the decrease in GFR when RAPP is reduced below the autoregulatory range.

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Abbreviations

BW :

body weight

C :

control

E :

excretion

FE :

fractional excretion

FF :

filtration fraction

GFR :

glomerular filtration rate

PAH :

p-amino hippuric acid

RAPP :

renal arterial perfusion pressure

RPF :

renal plasma flow

RT :

reptilian-type

SNGFR :

single nephron glomerular filtration rate

U OSM :

urine osmolarity

UFR :

urine flow rate

References

  • Ames E, Steven K, Skadhauge E (1971) Effects of arginine vasotocin on renal excretion of Na+, K+, Cl, and urea in the hydrated chicken. Am J Physiol 221:1223–1228

    Google Scholar 

  • Aukland K, Oien AH (1987) Renal autoregulation: models combining tubuloglomerular feedback and myogenic response. Am J Physiol 252:F768–F783

    Google Scholar 

  • Boberg U, Seney FD, Persson AEG, Wright FS (1987) Signal for tubuloglomerular feedback control of GFR: responses to both sodium and chloride. Kidney Int 31:420

    Google Scholar 

  • Braun EJ (1976) Intrarenal blood flow distribution in the desert quail following salt loading. Am J Physiol 222:617–629

    Google Scholar 

  • Briggs JP, Schnermann J (1987) The tubuloglomerular feedback mechanism: functional and biochemical aspects. Ann Rev Physiol 49:251–273

    Google Scholar 

  • Brun C (1957) A rapid method for the determination of paraaminohippuric acid in kidney function tests. J Lab Clin Med 37:955–958

    Google Scholar 

  • Carmines PK, Bell PD, Roman RJ, Work J, Navar LG (1985) Prostaglandins in the sodium excretory response to altered renal arterial pressure in dogs. Am J Physiol 248:F8–F14

    Google Scholar 

  • Davis CL, Briggs JP (1987) Effect of reduction in renal artery pressure on atrial natriuretic peptide-induced natriuresis. Am J Physiol 252:F146–F153

    Google Scholar 

  • Dev B, Drescher C, Schnermann J (1974) Resetting of tubuloglomerular feedback sensitivity by dietary salt intake. Pflügers Arch 346:263–277

    Google Scholar 

  • Elger M, Kaune R, Hentschel H (1984) Glomerular intermittency in a freshwater teleost, Carassius gibelis, after transfer to salt water. J Comp Physiol B 154:225–231

    Google Scholar 

  • Fitzgibbons JP, Gennari FJ, Garfinkel HB, Cortell S, Ponte L (1974) Dependence of saline-induced natriuresis upon exposure of the kidney to physical effects of extracellular fluid volume expansion. J Clin Invest 54:1428–1436

    Google Scholar 

  • Gellai M, Valtin H (1979) Chronic vascular constrictions and measurements of renal function in conscious rats. Kid Int 15:419–426

    Google Scholar 

  • Gerstberger R, Kaul R, Gray DA, Simon E (1985) Arginine vasotocin and glomerular filtration rate in saltwater-acclimated ducks. Am J Physiol 248:F663–F667

    Google Scholar 

  • Gregg CM, Wideman RF (1990) Morphological and functional comparisons of normal and hypertrophied kidneys of adult domestic fowl Gallus gallus. Am J Physiol. 258:F403–F413

    Google Scholar 

  • Kare MR, Biely J (1948) The toxicity of sodium chloride and its relation to water intake in baby chicks. Poultry Sci 27:751–758

    Google Scholar 

  • Martindale L (1957) The effect of high dietary sodium chloride on renal function in chicks. Br Poult Sci 16:577–581

    Google Scholar 

  • Moore LC, Schnermann J, Yarimizu S (1979) Feedback mediation of SNGFR autoregulation in hydropenic and DOCA- and saltloaded rats. Am J Physiol 237:F63–F74

    Google Scholar 

  • Navar LG (1978) Renal autoregulation: perspectives from whole kidney and single nephron studies. Am J Physiol 234:F357–F370

    Google Scholar 

  • Niznik RA, Wideman RF, Cowen BS, Kissell RE (1985) Induction of urolithiasis in single comb white leghorn pullets: effect on glomerular number. Poultry Sci 64:1430–1437

    Google Scholar 

  • Nutrient requirements of poultry, Eighth Revised Edition (1984) National Academy Press, Washington D.C.

  • Riddle O (1930) Complete atrophy of kidney in pigeons following section of the ureter. Proc Soc Exp Biol Med 27:1022–1023

    Google Scholar 

  • Schnermann J, Schubert G, Briggs J (1986) Tubuloglomerular feedback responses with native and artificial tubular fluid. Am J Physiol 250:F16–F21

    Google Scholar 

  • Scott ML, Nesheim MC, Young RJ (1982) Essential inorganic elements. In: Nutrition of the chicken, Third edition. M.L. Scott and Associates, Ithaca, NY

    Google Scholar 

  • Sjoquist M, Goransson A (1985) Tinme-dependent heterogeneity of filtration rate in the autoregulating rat kidney. Acta Physiol Scand 123:151–158

    Google Scholar 

  • Unflat JG, Kissell RE, Wideman RF, Muir FV (1985) A comparison of two techniques for determining glomerular size distributions in domestic fowl. Poultry Sci 64:1210–1215

    Google Scholar 

  • Waugh WW (1977) Photometry of inulin and polyfructosan by use of a cysteine/tryptophan reaction. Clin Chem 23:639–645

    Google Scholar 

  • Wideman RF, Avian kidney anatomy and physiology. In: Dietert RM (Ed) CRC Critical Reviews in Poultry Biology Vol 1, CRC Press, Boca Raton, FL, pp 133–176

  • Wideman RF (1989) Maturation of glomerular size distribution profiles in domestic fowl Gallus gallus. J Morphol 201:205–213

    Google Scholar 

  • Wideman RF, Braun EJ (1982) Ureteral urine collection from anesthetized domestic fowl. Lab Animal Sci 32:298–301

    Google Scholar 

  • Wideman RF, Laverty G (1986) Kidney function in domestic fowl with chronic occlusion of the ureter and caudal renal vein. Poultry Sci 65:2148–2155

    Google Scholar 

  • Wideman RF, Gregg CM (1988) Model for evaluating avian renal hemodynamics and glomerular filtration rate autoregulation. Am J Physiol 254:R925–R932

    Google Scholar 

  • Wideman RF, Braun EJ, Anderson GL (1981) Microanatomy of the renal cortex in the domestic fowl. J Morphol 168:249–267

    Google Scholar 

  • Wideman RF, Satnick JL, Mitsos WJ, Bennett KR, Smith SR (1987) Effect of saline adaptation and renal portal sodium infusion on glomerular size distributions and kidney function in domestic fowl. Poultry Sci 66:348–356

    Google Scholar 

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Vena, V.E., Lac, T.H. & Wideman, R.F. Dietary sodium, glomerular filtration rate autoregulation, and glomerular size distribution profiles in domestic fowl (Gallus gallus). J Comp Physiol B 160, 7–16 (1990). https://doi.org/10.1007/BF00258757

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