Effects of Taxifolin in Spontaneously Hypertensive Rats with a Focus on Erythrocyte Quality.
Tomas JasenovecDominika RadosinskaMarta KollarovaPeter BalisStefan ZoradNorbert VrbjarIveta BernatovaSona CacanyiovaLubomira TothovaJana RadošinskáPublished in: Life (Basel, Switzerland) (2022)
Oxidative stress and multiple erythrocyte abnormalities have been observed in hypertension. We focused on the effects of angiotensin-converting enzyme 2 (ACE2) inhibition by MLN-4760 inhibitor on angiotensin peptides, oxidative stress parameters, and selected erythrocyte quality markers in spontaneously hypertensive rats (SHR). We also investigated the potential effects of polyphenolic antioxidant taxifolin when applied in vivo and in vitro following its incubation with erythrocytes. SHRs were divided into four groups: control, taxifolin-treated, MLN-4760-treated, and MLN-4760 with taxifolin. MLN-4760 administration increased the blood pressure rise independent of taxifolin treatment, whereas taxifolin decreased it in control SHRs. Body weight gain was also higher in ACE2-inhibited animals and normalized after taxifolin treatment. However, taxifolin did not induce any change in angiotensin peptide concentrations nor a clear antioxidant effect. We documented an increase in Na,K-ATPase enzyme activity in erythrocyte membranes of ACE2-inhibited SHRs after taxifolin treatment. In conclusion, ACE2 inhibition deteriorated some selected RBC properties in SHRs. Although taxifolin treatment did not improve oxidative stress markers, our data confirmed the blood pressure-lowering potential, anti-obesogenic effect, and some "erythroprotective" effects of this compound in both control and ACE2-inhibited SHRs. In vitro investigations documenting different effects of taxifolin on erythrocyte properties from control and ACE2-inhibited SHRs accentuated the irreplaceability of in vivo studies.
Keyphrases
- angiotensin converting enzyme
- angiotensin ii
- oxidative stress
- blood pressure
- weight gain
- body mass index
- dna damage
- type diabetes
- ischemia reperfusion injury
- metabolic syndrome
- machine learning
- newly diagnosed
- induced apoptosis
- signaling pathway
- diabetic rats
- artificial intelligence
- weight loss
- replacement therapy
- birth weight
- big data
- heat stress