Literature DB >> 34396787

Renal mass reduction increases the response to exogenous insulin independent of acid-base status or plasma insulin levels in rats.

Elinor C Mannon1, Christina L Sartain1, Trevin C Wilkes2, Jingping Sun1, Aaron J Polichnowski3, Paul M O'Connor1.   

Abstract

Impairments in insulin sensitivity can occur in patients with chronic kidney disease (CKD). Correction of metabolic acidosis has been associated with improved insulin sensitivity in CKD, suggesting that metabolic acidosis may directly promote insulin resistance. Despite this, the effect of acid or alkali loading on insulin sensitivity in a rodent model of CKD (remnant kidney) has not been directly investigated. Such studies could better define the relationship between blood pH and insulin sensitivity. We hypothesized that in remnant kidney rats, acid or alkali loading would promote loss of pH homeostasis and consequently decrease insulin sensitivity. To test this hypothesis, we determined the impact of alkali (2 wk) or acid (5-7 days) loading on plasma electrolytes, acid-base balance, and insulin sensitivity in either sham control rats, 2/3 nephrectomized rats, or 5/6 nephrectomized rats. Rats with 5/6 nephrectomy had the greatest response to insulin followed by rats with 2/3 nephrectomy and sham control rats. We found that treatment with 0.1 M sodium bicarbonate solution in drinking water had no effect on insulin sensitivity. Acid loading with 0.1 M ammonium chloride resulted in significant reductions in pH and plasma bicarbonate. However, acidosis did not significantly impair insulin sensitivity. Similar effects were observed in Zucker obese rats with 5/6 nephrectomy. The effect of renal mass reduction on insulin sensitivity could not be explained by reduced insulin clearance or increased plasma insulin levels. We found that renal mass reduction alone increases sensitivity to exogenous insulin in rats and that this is not acutely reversed by the development of acidosis.NEW & NOTEWORTHY Impairments in insulin sensitivity can occur in patients with chronic kidney disease, and previous work has suggested that metabolic acidosis may be the underlying cause. Our study investigated the effect of acid or alkali loading on insulin sensitivity in a rodent model of chronic kidney disease. We found that renal mass reduction increases the blood glucose response to insulin and that this is not acutely reversed by the development of acidosis.

Entities:  

Keywords:  Zucker obese rat; blood glucose; chronic kidney disease; insulin resistance; metabolic acidosis

Mesh:

Substances:

Year:  2021        PMID: 34396787      PMCID: PMC8560408          DOI: 10.1152/ajprenal.00679.2020

Source DB:  PubMed          Journal:  Am J Physiol Renal Physiol        ISSN: 1522-1466


  28 in total

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Journal:  Clin Sci (Lond)       Date:  2018-06-20       Impact factor: 6.124

Review 2.  Mechanisms of muscle wasting in chronic kidney disease.

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Journal:  Nephron       Date:  1975       Impact factor: 2.847

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Authors:  Jeffrey A Kraut; Ira Kurtz
Journal:  Am J Kidney Dis       Date:  2005-06       Impact factor: 8.860

6.  Cardiovascular dysfunction in Zucker obese and Zucker diabetic fatty rats: role of hydronephrosis.

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9.  Severe renal mass reduction impairs recovery and promotes fibrosis after AKI.

Authors:  Aaron J Polichnowski; Rongpei Lan; Hui Geng; Karen A Griffin; Manjeri A Venkatachalam; Anil K Bidani
Journal:  J Am Soc Nephrol       Date:  2014-02-07       Impact factor: 10.121

10.  Insulin resistance as an independent predictor of cardiovascular mortality in patients with end-stage renal disease.

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Journal:  J Am Soc Nephrol       Date:  2002-07       Impact factor: 10.121

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  1 in total

Review 1.  Comparison of the surgical resection and infarct 5/6 nephrectomy rat models of chronic kidney disease.

Authors:  Ryan J Adam; Adaysha C Williams; Alison J Kriegel
Journal:  Am J Physiol Renal Physiol       Date:  2022-04-04
  1 in total

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