Notch1 mediates preconditioning protection induced by GPER in normotensive and hypertensive female rat hearts
| Autor: | Carmine Rocca, Saveria Femminò, Giorgio Aquila, Maria C. Granieri, Ernestina M. De Francesco, Teresa Pasqua, Damiano C. Rigiracciolo, Francesca Fortini, Maria C. Cerra, Marcello Maggiolini, Pasquale Pagliaro, Paola Rizzo, Tommaso Angelone, Claudia Penna |
|---|---|
| Jazyk: | angličtina |
| Rok vydání: | 2018 |
| Předmět: |
0301 basic medicine
Cardiac function curve medicine.medical_specialty Isolated rat hearts Physiology Notch signaling pathway Estrogen receptor Socio-culturale Preconditioning 030204 cardiovascular system & hematology lcsh:Physiology cardioprotection H9c2 NOS PI3K/Akt Reperfusion injury salvage kinases Physiology (medical) 03 medical and health sciences 0302 clinical medicine Internal medicine Medicine Spontaneous hypertensive rat PI3K/AKT/mTOR pathway Original Research Cardioprotection lcsh:QP1-981 biology business.industry Nitric oxide synthase 030104 developmental biology Endocrinology biology.protein business GPER |
| Zdroj: | Frontiers in Physiology Frontiers in Physiology, Vol 9 (2018) |
| Popis: | G protein-coupled estrogen receptor (GPER) is an estrogen receptor expressed in the cardiovascular system. G1, a selective GPER ligand, exerts cardiovascular effects through activation of the PI3K-Akt pathway and Notch signaling in normotensive animals. Here, we investigated whether the G1/GPER interaction is involved in the limitation of infarct size, and improvement of post-ischemic contractile function in female spontaneous hypertensive rat (SHR) hearts. In this model, we also studied Notch signaling and key components of survival pathway, namely PI3K-Akt, nitric oxide synthase (NOS) and mitochondrial K+-ATP (MitoKATP) channels. Rat hearts isolated from female SHR underwent 30 min of global, normothermic ischemia and 120 min of reperfusion. G1 (10 nM) alone or specific inhibitors of GPER, PI3K/NOS and MitoKATP channels co-infused with G1, just before I/R, were studied. The involvement of Notch1 was studied by Western blotting. Infarct size and left ventricular pressure were measured. To confirm endothelial-independent G1-induced protection by Notch signaling, H9c2 cells were studied with specific inhibitor, N-[N-(3,5 difluorophenacetyl)-L-alanyl]-S-phenylglycine t-butyl ester (DAPT, 5 μM), of this signaling. Using DAPT, we confirmed the involvement of G1/Notch signaling in limiting infarct size in heart of normotensive animals. In the hypertensive model, G1-induced reduction in infarct size and improvement of cardiac function were prevented by the inhibition of GPER, PI3K/NOS, and MitoKATP channels. The involvement of Notch was confirmed by western blot in the hypertensive model and by the specific inhibitor in the normotensive model and cardiac cell line. Our results suggest that GPERs play a pivotal role in mediating preconditioning cardioprotection in normotensive and hypertensive conditions. The G1-induced protection involves Notch1 and is able to activate the survival pathway in the presence of comorbidity. Several pathological conditions, including hypertension, reduce the efficacy of ischemic conditioning strategies. However, G1-induced protection can result in significant reduction of I/R injury also female in hypertensive animals. Further studies may ascertain the clinical translation of the present results. |
| Databáze: | OpenAIRE |
| Externí odkaz: |
|