Renal and myocardial histopathology and morphometry in rats with adenine - Induced chronic renal failure: Influence of gum acacia

Badreldin H. Ali, Ibrahim Inuwa, Mohamed Al Za'Abi, Shadia Al Bahlani, Halima Al Issaei, Aishwarya Ramkumar, Thulasi Madanagopal, Abedrrahim Nemmar, Denise M. Malheiros, Roberto Zatz

Research output: Contribution to journalArticle

14 Citations (Scopus)

Abstract

Background/Aim: Chronic kidney disease (CKD) is associated with increased occurrence of cardiovascular system dysfunction. Previous studies have revealed a number of alterations in the kidneys and heart during CKD. However, unbiased quantitative studies on these structures in this disease have so far not been addressed. Materials and Methods: We induced CKD in rats by feeding adenine (0.75% w/w, four weeks) and using unbiased stereological methods, investigated the effect of the ensuing CKD on the kidneys and left ventricular structure. Since gum acacia (GA) has previously been shown to ameliorate the severity of CKD in humans and rodents, we investigated the effect of giving GA (15% w/v in the drinking water concomitantly with adenine) on the kidneys and left ventricular structure using the above model. Results: The CKD was confirmed by standard biochemical indices in plasma and urine and by accumulation of the uremic toxin indoxyl sulfate. Additionally, it increased blood pressure. In rats with CKD absolute volume of left ventricle was significantly increased, and the volume density and absolute volume of myocardial capillaries were decreased, whilst the same parameters of myocardium and interstitial tissue were increased. Renal morphometry demonstrated significant increase in kidney volume and interstitial tissue in adenine- treated rats. Similarly, glomerular Bowman's capsule was significantly thickened. The myocardial and renal changes were significantly mitigated by GA treatment. Conclusions: These results add to our existing knowledge of the pathophysiology of adenine - CKD and provides plausible histopathological and morphometric evidence for the usefulness of GA in CKD.

Original languageEnglish
Pages (from-to)818-828
Number of pages11
JournalCellular Physiology and Biochemistry
Volume34
Issue number3
DOIs
Publication statusPublished - Apr 12 2014

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Gum Arabic
Adenine
Chronic Renal Insufficiency
Chronic Kidney Failure
Kidney
Indican
Bowman Capsule
Cardiovascular System
Drinking Water
Heart Ventricles
Rodentia
Myocardium
Urine
Blood Pressure

Keywords

  • Adenine
  • Gum acacia
  • Heart remodeling
  • Left ventricle
  • Rat
  • Renal failure

ASJC Scopus subject areas

  • Physiology
  • Medicine(all)

Cite this

Renal and myocardial histopathology and morphometry in rats with adenine - Induced chronic renal failure : Influence of gum acacia. / Ali, Badreldin H.; Inuwa, Ibrahim; Al Za'Abi, Mohamed; Al Bahlani, Shadia; Al Issaei, Halima; Ramkumar, Aishwarya; Madanagopal, Thulasi; Nemmar, Abedrrahim; Malheiros, Denise M.; Zatz, Roberto.

In: Cellular Physiology and Biochemistry, Vol. 34, No. 3, 12.04.2014, p. 818-828.

Research output: Contribution to journalArticle

Ali, Badreldin H. ; Inuwa, Ibrahim ; Al Za'Abi, Mohamed ; Al Bahlani, Shadia ; Al Issaei, Halima ; Ramkumar, Aishwarya ; Madanagopal, Thulasi ; Nemmar, Abedrrahim ; Malheiros, Denise M. ; Zatz, Roberto. / Renal and myocardial histopathology and morphometry in rats with adenine - Induced chronic renal failure : Influence of gum acacia. In: Cellular Physiology and Biochemistry. 2014 ; Vol. 34, No. 3. pp. 818-828.
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AU - Inuwa, Ibrahim

AU - Al Za'Abi, Mohamed

AU - Al Bahlani, Shadia

AU - Al Issaei, Halima

AU - Ramkumar, Aishwarya

AU - Madanagopal, Thulasi

AU - Nemmar, Abedrrahim

AU - Malheiros, Denise M.

AU - Zatz, Roberto

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N2 - Background/Aim: Chronic kidney disease (CKD) is associated with increased occurrence of cardiovascular system dysfunction. Previous studies have revealed a number of alterations in the kidneys and heart during CKD. However, unbiased quantitative studies on these structures in this disease have so far not been addressed. Materials and Methods: We induced CKD in rats by feeding adenine (0.75% w/w, four weeks) and using unbiased stereological methods, investigated the effect of the ensuing CKD on the kidneys and left ventricular structure. Since gum acacia (GA) has previously been shown to ameliorate the severity of CKD in humans and rodents, we investigated the effect of giving GA (15% w/v in the drinking water concomitantly with adenine) on the kidneys and left ventricular structure using the above model. Results: The CKD was confirmed by standard biochemical indices in plasma and urine and by accumulation of the uremic toxin indoxyl sulfate. Additionally, it increased blood pressure. In rats with CKD absolute volume of left ventricle was significantly increased, and the volume density and absolute volume of myocardial capillaries were decreased, whilst the same parameters of myocardium and interstitial tissue were increased. Renal morphometry demonstrated significant increase in kidney volume and interstitial tissue in adenine- treated rats. Similarly, glomerular Bowman's capsule was significantly thickened. The myocardial and renal changes were significantly mitigated by GA treatment. Conclusions: These results add to our existing knowledge of the pathophysiology of adenine - CKD and provides plausible histopathological and morphometric evidence for the usefulness of GA in CKD.

AB - Background/Aim: Chronic kidney disease (CKD) is associated with increased occurrence of cardiovascular system dysfunction. Previous studies have revealed a number of alterations in the kidneys and heart during CKD. However, unbiased quantitative studies on these structures in this disease have so far not been addressed. Materials and Methods: We induced CKD in rats by feeding adenine (0.75% w/w, four weeks) and using unbiased stereological methods, investigated the effect of the ensuing CKD on the kidneys and left ventricular structure. Since gum acacia (GA) has previously been shown to ameliorate the severity of CKD in humans and rodents, we investigated the effect of giving GA (15% w/v in the drinking water concomitantly with adenine) on the kidneys and left ventricular structure using the above model. Results: The CKD was confirmed by standard biochemical indices in plasma and urine and by accumulation of the uremic toxin indoxyl sulfate. Additionally, it increased blood pressure. In rats with CKD absolute volume of left ventricle was significantly increased, and the volume density and absolute volume of myocardial capillaries were decreased, whilst the same parameters of myocardium and interstitial tissue were increased. Renal morphometry demonstrated significant increase in kidney volume and interstitial tissue in adenine- treated rats. Similarly, glomerular Bowman's capsule was significantly thickened. The myocardial and renal changes were significantly mitigated by GA treatment. Conclusions: These results add to our existing knowledge of the pathophysiology of adenine - CKD and provides plausible histopathological and morphometric evidence for the usefulness of GA in CKD.

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