Login / Signup

<i>Limosilactobacillus fermentum</i> prevents gut-kidney oxidative damage and the rise in blood pressure in male rat offspring exposed to a maternal high-fat diet.

Luciana Caroline Paulino do NascimentoEvandro Leite de SouzaMicaelle Oliveira de Luna FreireValdir de Andrade BragaThatyane Mariano Rodrigues de AlbuqeurqueCláudia Jacques LagranhaJosé Luiz de Brito Alves
Published in: Journal of developmental origins of health and disease (2022)
Oxidative stress along the gut-kidney axis is a risk factor for developing arterial hypertension in offspring from dams fed a high-fat diet. Considering the antioxidant capacity of probiotic strains, this study evaluated the effects of a daily multistrain formulation with <i>Limosilactobacillus fermentum</i> 139, 263, and 296 on blood pressure (BP), renal function, and oxidative stress and along the gut-kidney axis in male offspring from dams fed a high-fat high-cholesterol (HFHC) diet during pregnancy and lactation. Dams were fed a diet control or HFHC diet during pregnancy and lactation. At 100 days of age, part of the male offspring from dams fed a HFHC diet received <i>Limosilactobacillus fermentum</i> formulation for 4 weeks (HFHC + Lf) daily. After the 4-week intervention, BP (tail-cuff plethysmography) and urinary and biochemical variables were measured. In addition, malondialdehyde levels, enzymatic activities of superoxide dismutase, catalase, glutathione-S-transferase, and nonenzymatic antioxidant defense (thiols content) were measured in the colon and renal cortex. Male offspring from dams fed a HFHC had increased blood pressure, impaired renal function, and oxidative stress along the gut-kidney axis. Administration of <i>Limosilactobacillus fermentum</i> reduced systolic, diastolic, and mean blood pressure levels and alleviated renal function impairment and oxidative stress along the gut-kidney axis in male offspring from dams fed a HFHC diet. Administration of <i>Limosilactobacillus fermentum</i> formulation attenuated programmed hypertension in the HFHC group through oxidative stress modulation along the gut-kidney axis.
Keyphrases