Protective effect of Euterpe oleracea Mart (açaí) extract on programmed changes in the adult rat offspring caused by

Graziele Freitas de Bem1, Cristiane Aguiar da Costa, Paola Raquel Braz de Oliveira

  • 1Department of Pharmacology, Institute of Biology, Rio de Janeiro State University, Rio de Janeiro, Brazil.

Insights

Açaí seed extract (ASE) prevents cardiovascular and kidney damage in offspring exposed to maternal low-protein diets. This dietary intervention offers protection against hypertension and oxidative stress, promoting healthier renal function.

Area of Science:

  • Cardiovascular Research
  • Renal Physiology
  • Nutritional Science

Background:

  • Maternal low-protein (LP) diets during pregnancy can lead to cardiovascular and renal issues in offspring.
  • Açaí seed extract (ASE) is investigated for its potential health benefits.

Purpose of the Study:

  • To determine the protective effects of Açaí seed extract (ASE) against cardiovascular and renal alterations in adult offspring of rats fed a low-protein (LP) diet during gestation.

Main Methods:

  • Rats were assigned to four groups: control, ASE, LP diet, and LP diet with ASE supplementation.
  • Offspring were fed a control diet post-weaning and assessed at 4 months for blood pressure, vascular function, and renal parameters.
  • Evaluations included oxidative stress markers, antioxidant activity, and kidney structural analysis.

Main Results:

  • ASE administration prevented hypertension and impaired vasodilation in offspring from LP-fed mothers.
  • ASE normalized elevated urea and creatinine levels and improved renal function markers.
  • ASE treatment reduced oxidative stress by increasing antioxidant enzyme activity and decreasing lipid peroxidation markers in the kidneys.

Conclusions:

  • Supplementation with Açaí seed extract (ASE) during pregnancy protects against hypertension, oxidative stress, and renal damage in offspring.
  • The protective mechanisms likely involve the vasodilator and antioxidant properties of ASE.
  • ASE represents a potential therapeutic strategy for mitigating developmental programming of chronic diseases.
Abstract

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