Literature DB >> 7124397

Severe functional and structural changes caused by lithium in the developing rat kidney.

S Christensen, P D Ottosen, S Olsen.   

Abstract

Lithium (Li) was administered to rats during maternal pregnancy and/or 8 weeks post-natally, to study the effects on renal function and structure in the developing kidney. Plasma Li was 0.5-1.0 mmol/l 3 and 8 weeks post-natally. Functionally, post-natal Li leads to growth retardation, polyuria with lowering of renal concentration ability, and uremia associated with as much as 80% lowering of the normal glomerular filtration rate (GFR). Pre-natal Li alone did not affect the concentrating ability but caused a 20% increase in GFR when evaluated 8 weeks post-natally. Post-natal Li caused very severe structural changes, consisting of up to 3 mm cortical cysts (= dilated distal convoluted tubules), extensive interstitial fibrosis with cell infiltration, and atrophy of the cortical collecting ducts. Morphometric measurements showed a significant reduction in the volume of the proximal tubular cells. Pre-natal Li caused only slight structural changes, and animals treated both pre- and post-natally were less affected than animals treated post-natally only. The structural changes caused by post-natal Li were unrelated to changes in the concentrating ability but showed a significant correlation with the lowering of the GFR. It is concluded that the post-natally developing rat kidney is particularly sensitive to the nephrotoxic effects of Li, which in low concentrations causes impairment of renal function, leading to uremia. Pre-natal Li exposure by maternal lithium treatment had little effect on renal function and structure when evaluated post-natally.

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Year:  1982        PMID: 7124397     DOI: 10.1111/j.1699-0463.1982.tb00090_90a.x

Source DB:  PubMed          Journal:  Acta Pathol Microbiol Immunol Scand A        ISSN: 0108-0164


  7 in total

1.  Quantitative ultrastructure of human proximal tubules and cortical interstitium in chronic renal disease (hydronephrosis).

Authors:  J C Møller; E Skriver
Journal:  Virchows Arch A Pathol Anat Histopathol       Date:  1985

2.  Ultrastructural quantitation of atubular and hypertrophic glomeruli in rats with lithium-induced chronic nephropathy.

Authors:  N Marcussen; P D Ottosen; S Christensen
Journal:  Virchows Arch A Pathol Anat Histopathol       Date:  1990

3.  Angiotensin II promotes development of the renal microcirculation through AT1 receptors.

Authors:  Kirsten Madsen; Niels Marcussen; Michael Pedersen; Gitte Kjaersgaard; Carie Facemire; Thomas M Coffman; Boye L Jensen
Journal:  J Am Soc Nephrol       Date:  2010-01-07       Impact factor: 10.121

4.  Atubular glomeruli, renal function and hypertrophic response in rats with chronic lithium nephropathy.

Authors:  N Marcussen; S Christensen; J S Petersen; M Shalmi
Journal:  Virchows Arch A Pathol Anat Histopathol       Date:  1991

5.  Lithium-induced uremia in rats - a new model of chronic renal failure.

Authors:  S Christensen; P D Ottosen
Journal:  Pflugers Arch       Date:  1983-11       Impact factor: 3.657

6.  Proximal tubular atrophy: qualitative and quantitative structural changes in chronic obstructive nephropathy in the pig.

Authors:  J C Møller; T M Jørgensen; J Mortensen
Journal:  Cell Tissue Res       Date:  1986       Impact factor: 5.249

Review 7.  Vulnerable periods and processes during central nervous system development.

Authors:  P M Rodier
Journal:  Environ Health Perspect       Date:  1994-06       Impact factor: 9.031

  7 in total

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