Počet záznamů: 1  

Antihypertensive and metabolic effects of empagliflozin in Ren-2 transgenic rats, an experimental non-diabetic model of hypertension

  1. 1.
    SYSNO ASEP0547427
    Druh ASEPJ - Článek v odborném periodiku
    Zařazení RIVJ - Článek v odborném periodiku
    Poddruh JČlánek ve WOS
    NázevAntihypertensive and metabolic effects of empagliflozin in Ren-2 transgenic rats, an experimental non-diabetic model of hypertension
    Tvůrce(i) Hojná, Silvie (FGU-C) RID, ORCID
    Rauchová, Hana (FGU-C) RID, ORCID
    Malínská, H. (CZ)
    Marková, I. (CZ)
    Hüttl, M. (CZ)
    Papoušek, František (FGU-C)
    Behuliak, Michal (FGU-C) RID, ORCID
    Miklánková, D. (CZ)
    Vaňourková, Z. (CZ)
    Neckář, Jan (FGU-C) RID, ORCID
    Kadlecová, Michaela (FGU-C) RID
    Kujal, P. (CZ)
    Zicha, Josef (FGU-C) RID, ORCID, SAI
    Vaněčková, Ivana (FGU-C) RID, ORCID
    Číslo článku112246
    Zdroj.dok.Biomedicine & Pharmacotherapy. - : Elsevier - ISSN 0753-3322
    Roč. 144, Dec (2021)
    Poč.str.11 s.
    Jazyk dok.eng - angličtina
    Země vyd.FR - Francie
    Klíč. slovaSGLT-2 inhibitor ; cardiac ; renal and metabolic parameters
    Vědní obor RIVED - Fyziologie
    Obor OECDPhysiology (including cytology)
    CEPGA19-06199S GA ČR - Grantová agentura ČR
    Způsob publikováníOpen access
    Institucionální podporaFGU-C - RVO:67985823
    UT WOS000704894600003
    EID SCOPUS85117067903
    DOI10.1016/j.biopha.2021.112246
    AnotaceThe new antidiabetic drugs, gliflozins, inhibit sodium-glucose transporter-2 in renal proximal tubules promoting glucose and sodium excretion. This leads not only to a significant improvement of glucose control but also to the reduction of blood pressure and body weight in both diabetic patients and experimental models. We examined whether these beneficial effects can also be achieved in a non-diabetic hypertensive model, namely in Ren-2 transgenic rats (TGR). Adult 6-month-old hypertensive TGR and their normotensive controls (Hannover Sprague-Dawley rats), were either untreated or treated with empagliflozin (10 mg/kg/day) for two months. Telemetric blood pressure monitoring, renal parameters as well as cardiac function via echocardiography were analyzed during the experiment. At the end of the study, the contribution of major vasoactive systems to blood pressure maintenance was studied. Metabolic parameters and markers of oxidative stress and inflammation were also analyzed. Empagliflozin had no effect on plasma glucose level but partially reduced blood pressure in TGR. Although food consumption was substantially higher in empagliflozin-treated TGR compared to the untreated animals, their body weight and the amount of epididymal and perirenal fat was decreased. Empagliflozin had no effect on proteinuria, but it decreased plasma urea, attenuated renal oxidative stress and temporarily increased urinary urea excretion. Several metabolic (hepatic triglycerides, non-esterified fatty acids, insulin) and inflammatory (TNF-alpha, leptin) parameters were also improved by empagliflozin treatment. By contrast, echocardiography did not reveal any effect of empagliflozin on cardiac function. In conclusion, empagliflozin exerted beneficial antihypertensive, anti-inflammatory and metabolic effects also in a non-diabetic hypertensive model.
    PracovištěFyziologický ústav
    KontaktLucie Trajhanová, lucie.trajhanova@fgu.cas.cz, Tel.: 241 062 400
    Rok sběru2022
    Elektronická adresahttps://doi.org/10.1016/j.biopha.2021.112246
Počet záznamů: 1  

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