CYP epoxygenase-derived H2O2 is involved in the endothelium-derived hyperpolarization (EDH) and relaxation of intrarenal arteries

dc.contributor.authorMuñoz Picos, Mercedes
dc.contributor.authorLópez-Oliva Muñoz, María Elvira
dc.contributor.authorPinilla, Estéfano
dc.contributor.authorMartínez Sainz, María Del Pilar
dc.contributor.authorSánchez Pina, Ana Alejandra
dc.contributor.authorRodríguez Prados, Claudia
dc.contributor.authorGarcía Sacristán, Albino
dc.contributor.authorHernández Rodríguez, Medardo Vicente
dc.contributor.authorRivera De Los Arcos, Luis
dc.contributor.authorPrieto Ocejo, Dolores
dc.date.accessioned2025-11-28T16:13:19Z
dc.date.available2025-11-28T16:13:19Z
dc.date.issued2017
dc.description.abstractReactive oxygen species (ROS) like hydrogen peroxide (H2O2) are involved in the in endothelium-derived hyperpolarization (EDH)-type relaxant responses of coronary and mesenteric arterioles. The role of ROS in kidney vascular function has mainly been investigated in the context of harmful ROS generation associated to kidney disease. The present study was sought to investigate whether H2O2 is involved in the endothelium-dependent relaxations of intrarenal arteries as well the possible endothelial sources of ROS generation involved in these responses. Under conditions of cyclooxygenase (COX) and nitric oxide (NO) synthase inhibition, acetylcholine (ACh) induced relaxations and stimulated H2O2 release that were reduced by catalase and by the glutathione peroxidase (GPx) mimetic ebselen in rat renal interlobar arteries, suggesting the involvement of H2O2 in the endothelium-dependent responses. ACh relaxations were also blunted by the CYP2C inhibitor sulfaphenazole and by the NADPH oxidase inhibitor apocynin. Acetylcholine stimulated both superoxide (O2•-) and H2O2 production that were reduced by sulfaphenazole and apocynin. Expression of the antioxidant enzyme CuZnSOD and of the H2O2 reducing enzymes catalase and GPx-1 was found in both intrarenal arteries and renal cortex. On the other hand, exogenous H2O2 relaxed renal arteries by decreasing vascular smooth muscle (VSM) intracellular calcium concentration [Ca2+]i and markedly enhanced endothelial KCa currents in freshly isolated renal endothelial cells. CYP2C11 and CYP2C23 epoxygenases were highly expressed in interlobar renal arteries and renal cortex, respectively, and were co-localized with eNOS in renal endothelial cells. These results demonstrate that H2O2 is involved in the EDH-type relaxant responses of renal arteries and that CYP 2C epoxygenases are physiologically relevant endothelial sources of vasodilator H2O2 in the kidney.
dc.description.departmentDepto. de Fisiología
dc.description.departmentDepto. de Anatomía y Embriología
dc.description.facultyFac. de Farmacia
dc.description.facultyFac. de Veterinaria
dc.description.refereedTRUE
dc.description.sponsorshipMinisterio de Economía y Competitividad (España)
dc.description.statuspub
dc.identifier.citationMuñoz, M., López-Oliva, M. E., Pinilla, E., Martínez, M. P., Sánchez, A., Rodríguez, C., García-Sacristán, A., Hernández, M., Rivera, L., & Prieto, D. (2017). CYP epoxygenase-derived H2O2 is involved in the endothelium-derived hyperpolarization (EDH) and relaxation of intrarenal arteries. Free radical biology & medicine, 106, 168–183. https://doi.org/10.1016/j.freeradbiomed.2017.02.031
dc.identifier.doi10.1016/j.freeradbiomed.2017.02.031
dc.identifier.essn1873-4596
dc.identifier.issn0891-5849
dc.identifier.officialurlhttps://doi.org/10.1016/j.freeradbiomed.2017.02.031
dc.identifier.pmid28212823
dc.identifier.relatedurlhttps://pubmed.ncbi.nlm.nih.gov/28212823/
dc.identifier.urihttps://hdl.handle.net/20.500.14352/127368
dc.journal.titleFree Radical Biology and Medicine
dc.language.isoeng
dc.page.final183
dc.page.initial168
dc.publisherElsevier
dc.relation.projectIDSAF 2012-31631
dc.relation.projectIDSAF2016-77526
dc.rights.accessRightsrestricted access
dc.subject.cdu612
dc.subject.keywordH2O2
dc.subject.keywordEndothelium
dc.subject.keywordRenal arteries
dc.subject.keywordCytochrome P450 (CYP)
dc.subject.keywordEndothelium-derived-hyperpolarization (EDH)
dc.subject.ucmCiencias Biomédicas
dc.subject.ucmFisiología
dc.subject.unesco2411 Fisiología Humana
dc.subject.unesco32 Ciencias Médicas
dc.subject.unesco3205.06 Nefrología
dc.titleCYP epoxygenase-derived H2O2 is involved in the endothelium-derived hyperpolarization (EDH) and relaxation of intrarenal arteries
dc.typejournal article
dc.type.hasVersionVoR
dc.volume.number106
dspace.entity.typePublication
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