Bioactive Peptides from Ruditapes philippinarum Attenuate Hypertension and Cardiorenal Damage in Deoxycorticosterone Acetate-Salt Hypertensive Rats

Molecules. 2023 Nov 15;28(22):7610. doi: 10.3390/molecules28227610.

Abstract

Hypertension is a common disease that affects human health and can lead to damage to the heart, kidneys, and other important organs. In this study, we investigated the regulatory effects of bioactive peptides derived from Ruditapes philippinarum (RPP) on hypertension and organ protection in deoxycorticosterone acetate (DOCA)-salt hypertensive rats. We found that RPPs exhibited significant blood pressure-lowering properties. Furthermore, the results showed that RPPs positively influenced vascular remodeling and effectively maintained a balanced water-sodium equilibrium. Meanwhile, RPPs demonstrated anti-inflammatory potential by reducing the serum levels of inflammatory cytokines (TNF-α, IL-2, and IL-6). Moreover, we observed the strong antioxidant activity of RPPs, which played a critical role in reducing oxidative stress and alleviating hypertension-induced damage to the aorta, heart, and kidneys. Additionally, our study explored the regulatory effects of RPPs on the gut microbiota, suggesting a possible correlation between their antihypertensive effects and the modulation of gut microbiota. Our previous studies have demonstrated that RPPs can significantly reduce blood pressure in SHR rats. This suggests that RPPs can significantly improve both essential hypertension and DOAC-salt-induced secondary hypertension and can ameliorate cardiorenal damage caused by hypertension. These findings further support the possibility of RPPs as an active ingredient in functional anti-hypertensive foods.

Keywords: DOCA–salt hypertensive rats; Ruditapes philippinarum peptides; antihypertension; cardiorenal protection; gut microbiota; oxidative stress.

MeSH terms

  • Acetates / pharmacology
  • Animals
  • Antihypertensive Agents / therapeutic use
  • Blood Pressure
  • Desoxycorticosterone* / adverse effects
  • Humans
  • Hypertension* / chemically induced
  • Hypertension* / drug therapy
  • Peptides / pharmacology
  • Rats
  • Rats, Inbred SHR

Substances

  • Desoxycorticosterone
  • Antihypertensive Agents
  • Peptides
  • Acetates