Effects of hydrogen peroxide on voltage-dependent K+ currents in human cardiac fibroblasts through protein kinase pathways
DC Field | Value | Language |
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dc.contributor.author | Bae, Hyemi | - |
dc.contributor.author | Lee, Donghee | - |
dc.contributor.author | Kim, Young-Won | - |
dc.contributor.author | Choi, Jeongyoon | - |
dc.contributor.author | Lee, Hong Jun | - |
dc.contributor.author | Kim, Sang-Wook | - |
dc.contributor.author | Kim, Taeho | - |
dc.contributor.author | Noh, Yun-Hee | - |
dc.contributor.author | Ko, Jae-Hong | - |
dc.contributor.author | Bang, Hyoweon | - |
dc.contributor.author | Lim, Inja | - |
dc.date.available | 2019-03-08T12:59:05Z | - |
dc.date.issued | 2016-05 | - |
dc.identifier.issn | 1226-4512 | - |
dc.identifier.issn | 2093-3827 | - |
dc.identifier.uri | https://scholarworks.bwise.kr/cau/handle/2019.sw.cau/6961 | - |
dc.description.abstract | Human cardiac fibroblasts (HCFs) have various voltage-dependent K+ channels (VDKCs) that can induce apoptosis. Hydrogen peroxide (H2O2) modulates VDKCs and induces oxidative stress, which is the main contributor to cardiac injury and cardiac remodeling. We investigated whether H2O2 could modulate VDKCs in HCFs and induce cell injury through this process. In whole-cell mode patch-clamp recordings, application of H2O2 stimulated Ca2+-activated (K-ca) currents but not delayed rectifier K+ or transient outward K+ currents, all of which are VDKCs. H2O2 stimulated K-ca currents were blocked by iberiotoxin (IbTX, a large conductance K-ca blocker). The H2O2-stimulating effect on large-conductance K-ca (BKca) currents was also blocked by KT5823 (a protein kinase G inhibitor) and 1 H-[1, 2, 4] oxadiazolo-[4, 3-a] quinoxalin-1-one (ODQ, a soluble guanylate cyclase inhibitor). In addition, 8-bromo-cyclic guanosine 3', 5'-monophosphate (8-Br-cGMP) stimulated BKca currents. In contrast, KT5720 and H-89 (protein kinase A inhibitors) did not block the H2O2-stimulating effect on BKca currents. Using RT-PCR and western blot analysis, three subtypes of K-ca channels were detected in HCFs: BKca channels, small conductance K-ca (SKca) channels, and intermediate-conductance K-ca (IKca) channels. In the annexin V/propidium iodide assay, apoptotic changes in HCFs increased in response to H2O2, but IbTX decreased H2O2-induced apoptosis. These data suggest that among the VDKCs of HCFs, H2O2 only enhances BKca currents through the protein kinase G pathway but not the protein kinase A pathway, and is involved in cell injury through BKca channels. | - |
dc.format.extent | 10 | - |
dc.language | 영어 | - |
dc.language.iso | ENG | - |
dc.publisher | KOREAN JOURNAL OF PHYSIOLOGY & PHARMACOLOGY | - |
dc.title | Effects of hydrogen peroxide on voltage-dependent K+ currents in human cardiac fibroblasts through protein kinase pathways | - |
dc.type | Article | - |
dc.identifier.doi | 10.4196/kjpp.2016.20.3.315 | - |
dc.identifier.bibliographicCitation | KOREAN JOURNAL OF PHYSIOLOGY & PHARMACOLOGY, v.20, no.3, pp 315 - 324 | - |
dc.identifier.kciid | ART002104432 | - |
dc.description.isOpenAccess | Y | - |
dc.identifier.wosid | 000375365400011 | - |
dc.identifier.scopusid | 2-s2.0-84968763990 | - |
dc.citation.endPage | 324 | - |
dc.citation.number | 3 | - |
dc.citation.startPage | 315 | - |
dc.citation.title | KOREAN JOURNAL OF PHYSIOLOGY & PHARMACOLOGY | - |
dc.citation.volume | 20 | - |
dc.type.docType | Article | - |
dc.publisher.location | 대한민국 | - |
dc.subject.keywordAuthor | Ca2+-activated K+ channels | - |
dc.subject.keywordAuthor | Human cardiac fibroblasts | - |
dc.subject.keywordAuthor | Hydrogen peroxide | - |
dc.subject.keywordAuthor | K+ currents | - |
dc.subject.keywordAuthor | Protein kinase | - |
dc.subject.keywordPlus | SMOOTH-MUSCLE-CELLS | - |
dc.subject.keywordPlus | HUMAN DERMAL FIBROBLASTS | - |
dc.subject.keywordPlus | POTASSIUM CURRENT | - |
dc.subject.keywordPlus | ENDOTHELIAL-CELLS | - |
dc.subject.keywordPlus | BKCA-CHANNEL | - |
dc.subject.keywordPlus | CONDUCTANCE | - |
dc.subject.keywordPlus | APOPTOSIS | - |
dc.subject.keywordPlus | PROLIFERATION | - |
dc.subject.keywordPlus | MODULATION | - |
dc.subject.keywordPlus | MYOCYTES | - |
dc.relation.journalResearchArea | Pharmacology & Pharmacy | - |
dc.relation.journalResearchArea | Physiology | - |
dc.relation.journalWebOfScienceCategory | Pharmacology & Pharmacy | - |
dc.relation.journalWebOfScienceCategory | Physiology | - |
dc.description.journalRegisteredClass | scie | - |
dc.description.journalRegisteredClass | scopus | - |
dc.description.journalRegisteredClass | kci | - |
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