Why the study?
Perivascular adipose tissue regulates vascular tonus with an anticontractile effect that may become dysfunctional in hypertension, prompting evaluation of whether dietary supplementation with egg white hydrolysate interferes with this function in DOCA-salt hypertensive animals.
Does Egg White Hydrolysate (EWH) improve perivascular adipose tissue (PVAT) dysfunction in DOCA-salt hypertensive rats?
Does Egg White Hydrolysate (EWH) improve perivascular adipose tissue (PVAT) dysfunction in DOCA-salt hypertensive rats?
Dietary supplementation with Egg White Hydrolysate improves perivascular adipose tissue dysfunction in severe hypertension by modulating the renin-angiotensin system, redox balance, and inflammation.
• DOCA-salt hypertension promotes loss of the anticontractile effect of m PVAT in resistance arteries. • EWH prevents the m PVAT damage caused by DOCA-salt hypertension. • EWH modulates RAS axis and reduces redox balance and inflammatory state in DOCA-salt hypertensive rats. Perivascular adipose tissue (PVAT) regulates vascular tonus with an anticontractile effect, which may be dysfunctional in hypertension. An Egg White Hydrolysate (EWH), a bioactive food, restores endothelium dysfunction and reduces blood pressure levels in malignant hypertension. We aimed to evaluate whether dietary supplementation with EWH interferes with the PVAT function in the mesenteric resistance arteries (MRA) of DOCA-salt hypertensive animals and the mechanisms involved. Male rats were divided into 4 groups and treated for 8 weeks. For 4 weeks, DOCA-salt or vehicle-treated rats (SHAM) were induced, and after that, some rats were co-treated with DOCA-salt or vehicle plus EWH (1 g/kg/day) for 4 weeks more. MRA and/or their PVAT ( m PVAT) were used for functional, molecular, and biochemical analysis. The anticontractile effect of m PVAT in response to norepinephrine (NE) was observed only in MRA rings with PVAT of the SHAM group, while this effect was abolished in DOCA-salt rings. The EWH treatment did not change the anticontractile effect of m PVAT in SHAM but partially restored it in DOCA-salt rats. Acute aliskiren incubation reduced NE-induced contraction only in MRA with PVAT of DOCA-salt rats. EWH prevented the overactivation of the renin levels and ACE activity in m PVAT of DOCA-salt rats; while did not change AT1R expression, but increased AT2R expression. In m PVAT, EWH blocked the increase of MDA, ROS and pro-inflammatory cytokines observed in DOCA-salt rats. EWH improved PVAT dysfunction in MRA of severe hypertension. This beneficial effect could be mediated by an ameliorated redox balance, inflammatory state, and RAS axis.
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Abreu et al. (2024) studied this question.
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