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. 1987 Jan;31(1):88–92. doi: 10.1128/aac.31.1.88

Effect of fetal exposure to gentamicin on kidneys of young guinea pigs.

M Lelievre-Pegorier, T Gilbert, R Sakly, A Meulemans, C Merlet-Benichou
PMCID: PMC174658  PMID: 3566243

Abstract

Clearance experiments were performed with young pups born of guinea pigs given a daily injection of 4 mg of gentamicin per kg (body weight) from days 48 to 54 of gestation (term, 68 days). For 3-day-old animals, the glomerular filtration rate was similar to that measured in control guinea pigs of the same age whose mothers were given saline during the same period of gestation. The same applied to fractional excretion of water, urea, total solutes, Na, K, Ca, and Mg but not to fractional phosphate excretion, which increased significantly in the gentamicin group when compared with the controls (mean +/- standard error, 21.7 +/- 4.9 versus 7.3 +/- 1.8%; P less than 0.05; n = 6 for both). The glomerular volume of the juxtamedullary nephrons diminished by about 40%, and their proximal tubule length decreased by about 20%. The glomerular volume of the superficial nephrons also diminished, by about 30%, but their proximal tubule length did not change. The gentamicin concentration was higher in the renal cortex than in the medulla (13.1 +/- 2.6 versus 5.7 +/- 2.2 micrograms/g [dry wt]; P less than 0.01; n = 6 for each). It decreased significantly from days 3 to 20 in both tissues. No functional impairment of the kidney was found in 10-day-old animals, and normal or even supranormal morphometry of the nephrons was observed in the 20-day-old animals. It is concluded that fetal exposure to gentamicin impairs proximal tubular function in the developing animal and might also adversely affect glomerular and tubular growth. However, both the functional and morphometric impairments of nephrons are transitory.

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Selected References

These references are in PubMed. This may not be the complete list of references from this article.

  1. Bankir L., Hollenberg N. K. In vivo staining of the kidney with Alcian blue: an adjunct to morphological and physiological studies. Ren Physiol. 1983;6(3):151–155. doi: 10.1159/000172894. [DOI] [PubMed] [Google Scholar]
  2. Broughton A., Strong J. E. Radioimmunoassay of iodinated gentamicin. Clin Chim Acta. 1976 Jan 2;66(1):125–129. doi: 10.1016/0009-8981(76)90379-x. [DOI] [PubMed] [Google Scholar]
  3. Cowan R. H., Jukkola A. F., Arant B. S., Jr Pathophysiologic evidence of gentamicin nephrotoxicity in neonatal puppies. Pediatr Res. 1980 Nov;14(11):1204–1211. doi: 10.1203/00006450-198011000-00011. [DOI] [PubMed] [Google Scholar]
  4. DAMADIAN R. V., SHWAYRI E., BRICKER N. S. ON THE EXISTENCE OF NON-URINE FORMING NEPHRONS IN THE DISEASED KIDNEY OF THE DOG. J Lab Clin Med. 1965 Jan;65:26–39. [PubMed] [Google Scholar]
  5. Fabre J., Rudhardt M., Blanchard P., Regamey C. Persistence of sisomicin and gentamicin in renal cortex and medulla compared with other organs and serum of rats. Kidney Int. 1976 Dec;10(6):444–449. doi: 10.1038/ki.1976.131. [DOI] [PubMed] [Google Scholar]
  6. Kornguth M. L., Kunin C. M. Distribution of gentamicin and amikacin in rabbit tissues. Antimicrob Agents Chemother. 1977 Jun;11(6):974–977. doi: 10.1128/aac.11.6.974. [DOI] [PMC free article] [PubMed] [Google Scholar]
  7. Lelievre-Pegorier M., Sakly R., Meulemans A., Merlet-Benichou C. Kinetics of gentamicin in plasma of nonpregnant, pregnant, and fetal guinea pigs and its distribution in fetal tissues. Antimicrob Agents Chemother. 1985 Oct;28(4):565–569. doi: 10.1128/aac.28.4.565. [DOI] [PMC free article] [PubMed] [Google Scholar]
  8. Meulemans A., Manuel C., Tran Ba Huy P. Radioimmunoassay of gentamicin in microliter and nanoliter samples of biological fluids. Chemotherapy. 1981;27(1):29–33. doi: 10.1159/000237951. [DOI] [PubMed] [Google Scholar]
  9. STRICKLER J. C., THOMPSON D. D., KLOSE R. M., GIEBISCH G. MICROPUNCTURE STUDY OF INORGANIC PHOSPHATE EXCRETION IN THE RAT. J Clin Invest. 1964 Aug;43:1596–1607. doi: 10.1172/JCI105035. [DOI] [PMC free article] [PubMed] [Google Scholar]
  10. de Rouffignac C., Deiss S., Bonvalet J. P. Détermination du taux individuel de filtration glomérulaire des néphrons accessibles et inaccessibles à la microponction. Pflugers Arch. 1970;315(4):273–290. doi: 10.1007/BF00593456. [DOI] [PubMed] [Google Scholar]

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