Endothelial dysfunction (ED) is a hallmark of heart failure (HF). Clinically, most cases of HF is due to CAD. On the other hand, ED is seen in patient with severe HF of non-ischemic origin. Mechanisms leading to the development of secondary type of ED are still not clear. Aim of the present study was to describe the development of secondary type of coronary ED in Tgαq*44 mice as well as to elucidate the involvement of aldosterone in this phenomenon. Both coronary endothelium-dependent and endothelium-independent responses were assessed in isolated Tgαq*44 hearts and age-matched FVB mice. In addition, level of 6-keto-PGF1α in cardiac effluent and production of 02- in cardiac tissue were assessed. Despite increased generation of O2- in cardiac tissue, endothelial function was not altered in Tgαq*44 mice at the age of 4 months. However, coronary ED developed, as evidenced by impaired NO-induced but not PGI2-induced vasodilatation in Tgαq*44 mice at the age of 14 months. Interestingly, there was a compensatory increase in basal PGI2 production in Tgαq*44 hearts. Treatment of Tgαq*44 mice with canrenone, aldosteron receptor antagonist improved both survival and NO-mediated vasodilatation in Tgαq*44 mice but had no effects on heart hypertrophy, pulmonary congestion and basal PGI2 production. In conclusion, development of coronary ED is secondary to cardiomyocytes pathology in T ; gαq*44 mice and is characterized by decreased NO bioavailability and compensatory increase in PGI2 production in coronary circulation. Development of secondary type of coronary ED in Tgαq*44 mice is at last partly related to aldosterone in Tgαq*44 mice.
3 lut 2023
27 cze 2022
8
0
http://dl.cm-uj.krakow.pl:8080/publication/4763
Nazwa wydania | Data |
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ZB-104209 | 3 lut 2023 |
Drelicharz, Łukasz
Przyborowski, Kamil
Bartuś, Magdalena
Wnuk, Mateusz
Kosiniak-Kamysz, Władysław
Włoch, Alicja
Stompór, Małgorzata