Euterpe oleracea Mart. seed extract protects against renal injury in diabetic and spontaneously hypertensive rats: role of inflammation and oxidative stress

Eur J Nutr. 2018 Mar;57(2):817-832. doi: 10.1007/s00394-016-1371-1. Epub 2017 Jan 20.

Abstract

Purpose: Euterpe oleracea Mart. (açaí) seed extract (ASE), through its anti-hypertensive, antioxidant and anti-inflammatory properties, may be useful to treat or prevent human diseases. Several evidences suggest that oxidative stress and inflammation contribute to the pathogenesis of diabetic nephropathy; therefore, we tested the hypothesis that ASE (200 mg/kg-1day-1) prevents diabetes and hypertension-related oxidative stress and inflammation, attenuating renal injury.

Methods: Male rats with streptozotocin (STZ)-induced diabetes (D), and spontaneously hypertensive rats with STZ-induced diabetes (DH) were treated daily with tap water or ASE (D + ASE and DH + ASE, respectively) for 45 days. The control (C) and hypertensive (H) animals received water.

Results: The elevated serum levels of urea and creatinine in D and DH, and increased albumin excretion in HD were reduced by ASE. Total glomeruli number in D and DH, were increased by ASE that also reduced renal fibrosis in both groups by decreasing collagen IV and TGF-β1 expression. ASE improved biomarkers of renal filtration barrier (podocin and nephrin) in D and DH groups and prevented the increased expression of caspase-3, IL-6, TNF-α and MCP-1 in both groups. ASE reduced oxidative damage markers (TBARS, carbonyl levels and 8-isoprostane) in D and DH associated with a decrease in Nox 4 and p47 subunit expression and increase in antioxidant enzyme activity in both groups (SOD, catalase and GPx).

Conclusion: ASE substantially reduced renal injury and prevented renal dysfunction by reducing inflammation, oxidative stress and improving the renal filtration barrier, providing a nutritional resource for prevention of diabetic and hypertensive-related nephropathy.

Keywords: Diabetes; Euterpe oleracea Mart; Hypertension; Inflammation; Nephropathy; Oxidative stress.

Publication types

  • Comparative Study

MeSH terms

  • Animals
  • Anti-Inflammatory Agents, Non-Steroidal / therapeutic use
  • Antihypertensive Agents / therapeutic use
  • Antioxidants / therapeutic use*
  • Apoptosis
  • Biomarkers / blood
  • Biomarkers / metabolism
  • Biomarkers / urine
  • Diabetes Mellitus, Experimental / complications
  • Diabetes Mellitus, Experimental / diet therapy
  • Diabetes Mellitus, Experimental / immunology
  • Diabetic Nephropathies / complications
  • Diabetic Nephropathies / metabolism
  • Diabetic Nephropathies / pathology
  • Diabetic Nephropathies / prevention & control*
  • Dietary Supplements*
  • Euterpe / chemistry*
  • Fibrosis
  • Glomerular Filtration Barrier / immunology
  • Glomerular Filtration Barrier / metabolism
  • Glomerular Filtration Barrier / pathology
  • Glomerular Filtration Barrier / physiopathology
  • Hypertension / complications
  • Hypertension / diet therapy
  • Hypertension / immunology
  • Hypertension / physiopathology
  • Inflammation Mediators / blood
  • Inflammation Mediators / metabolism
  • Kidney / immunology
  • Kidney / metabolism
  • Kidney / pathology
  • Kidney / physiopathology
  • Oxidative Stress
  • Plant Extracts / therapeutic use*
  • Rats, Inbred SHR
  • Renal Insufficiency / complications
  • Renal Insufficiency / etiology
  • Renal Insufficiency / metabolism
  • Renal Insufficiency / prevention & control*
  • Seeds / chemistry*

Substances

  • Anti-Inflammatory Agents, Non-Steroidal
  • Antihypertensive Agents
  • Antioxidants
  • Biomarkers
  • Inflammation Mediators
  • Plant Extracts