Literature DB >> 6642092

Renal enlargement: comparative autoradiographic studies of 3H-thymidine uptake in diabetic and uninephrectomized rats.

R Rasch, J O Nörgaard.   

Abstract

Incorporation of 3H-thymidine into renal cortical tissue has been studied by light microscopic autoradiography in streptozotocin-diabetic rats, uninephrectomized rats, uninephrectomized diabetic rats, insulin-treated diabetic rats and control rats. The percentage of labelled cortical nuclei (the labelling index) was determined separately in glomeruli, proximal tubules and distal tubules after 2, 4 and 6 days on autoradiographs from 1 micron thick plastic embedded sections. The incorporation of thymidine in glomerular nuclei was consistently low (less than 1%) and no differences were found between the control and experimental groups. In both proximal and distal tubules an increase in thymidine incorporation was seen on day 2 followed by a decline on days 4 and 6. The maximal labelling on day 2 in proximal tubules was 9.1% in the uninephrectomized diabetic group, 3.7% in the diabetic group and 1.4% in the uninephrectomized group. In distal tubules the corresponding values were 5.2, 3.5 and 1.1%. The increase in kidney weight after 6 days was 83, 62 and 37%, respectively. Estimates of the net increase in the number of cortical tubular cells in the different experimental groups showed that the kidney enlargement followed different patterns with respect to the extent of cellular hyperplasia and hypertrophy. The kidney growth in uninephrectomized diabetic rats was dominated by tubular cellular hyperplasia, in the diabetic group hyperplasia and hypertrophy participated to approximately the same extent, whereas cellular hypertrophy was most pronounced in the uninephrectomized animals. Nuclear labelling in the insulin-treated diabetic rats was not different from that of control rats and consequently a hyperplastic effect of streptozotocin can be ruled out.(ABSTRACT TRUNCATED AT 250 WORDS)

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Year:  1983        PMID: 6642092     DOI: 10.1007/BF00279944

Source DB:  PubMed          Journal:  Diabetologia        ISSN: 0012-186X            Impact factor:   10.122


  22 in total

1.  Some aspects of compensatory hyperplasia of the kidney.

Authors:  G E WILLIAMS
Journal:  Br J Exp Pathol       Date:  1961-08

2.  Glomerular size and structure in diabetes mellitus. I. Early abnormalities.

Authors:  R Osterby; H J Gundersen
Journal:  Diabetologia       Date:  1975-06       Impact factor: 10.122

3.  Accretion and turnover of RNA in the renoprival kidney.

Authors:  R A Malt; D A Lemaitre
Journal:  Am J Physiol       Date:  1968-05

4.  Effect of streptozotocin-induced diabetes on kidney weight and compensatory hypertrophy in the rat.

Authors:  J Ross; J K Goldman
Journal:  Endocrinology       Date:  1971-04       Impact factor: 4.736

5.  A quantitative cytochemical investigation of the relationship between cell mass and initiation of DNA synthesis in mouse fibroblasts in vitro.

Authors:  D Killander; A Zetterberg
Journal:  Exp Cell Res       Date:  1965-10       Impact factor: 3.905

6.  Chemical aspects of compensatory renal hypertrophy.

Authors:  I W Halliburton; R Y Thomson
Journal:  Cancer Res       Date:  1965-12       Impact factor: 12.701

7.  Morphometry of the renal corpuscle during postnatal growth and compensatory hypertrophy.

Authors:  G Olivetti; P Anversa; M Melissari; A V Loud
Journal:  Kidney Int       Date:  1980-04       Impact factor: 10.612

8.  Alterations in glomerular RNA in diabetic rats: roles of glucagon and insulin.

Authors:  P Cortes; F Dumler; K K Venkatachalam; J Goldman; K S Sastry; H Venkatachalam; J Bernstein; N W Levin
Journal:  Kidney Int       Date:  1981-10       Impact factor: 10.612

9.  Renal hypertrophy in experimental diabetes: a comparison to compensatory hypertrophy.

Authors:  K Seyer-Hansen
Journal:  Diabetologia       Date:  1978-05       Impact factor: 10.122

10.  Uridine triphosphate and RNA synthesis during diabetes-induced renal growth.

Authors:  P Cortes; N W Levin; F Dumler; A H Rubenstein; C P Verghese; K K Venkatachalam
Journal:  Am J Physiol       Date:  1980-04
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  35 in total

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Journal:  Biochem J       Date:  2003-10-15       Impact factor: 3.857

Review 2.  The pathobiology of diabetic vascular complications--cardiovascular and kidney disease.

Authors:  Stephen P Gray; Karin Jandeleit-Dahm
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Authors:  C A Pollock; M S Nobes; A Z Gyory; P T Heng; M J Field
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Journal:  Am J Pathol       Date:  2002-11       Impact factor: 4.307

6.  Ornithine decarboxylase inhibitor eliminates hyperresponsiveness of the early diabetic proximal tubule to dietary salt.

Authors:  Cynthia M Miracle; Timo Rieg; Hadi Mansoury; Volker Vallon; Scott C Thomson
Journal:  Am J Physiol Renal Physiol       Date:  2008-06-18

7.  Tubular lesions in streptozotocin-diabetic rats.

Authors:  R Rasch
Journal:  Diabetologia       Date:  1984-07       Impact factor: 10.122

8.  The impact of renal growth, regression and regrowth in experimental diabetes mellitus on number and size of proximal and distal tubular cells in the rat kidney.

Authors:  J R Nyengaard; A Flyvbjerg; R Rasch
Journal:  Diabetologia       Date:  1993-11       Impact factor: 10.122

9.  Loss of mitotic activity and the expression of vimentin in glomerular epithelial cells of developing human kidneys.

Authors:  M Nagata; Y Yamaguchi; K Ito
Journal:  Anat Embryol (Berl)       Date:  1993-03

10.  The impact of experimental diabetes mellitus in rats on glomerular capillary number and sizes.

Authors:  J R Nyengaard; R Rasch
Journal:  Diabetologia       Date:  1993-03       Impact factor: 10.122

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