https://scholars.lib.ntu.edu.tw/handle/123456789/519173
DC 欄位 | 值 | 語言 |
---|---|---|
dc.contributor.author | Lee C.-H. | en_US |
dc.contributor.author | HORNG-HUEI LIOU | en_US |
dc.contributor.author | Lu K.-L. | en_US |
dc.contributor.author | Shen Y.-C. | en_US |
dc.contributor.author | Tsai M.-C. | en_US |
dc.date.accessioned | 2020-11-03T09:53:31Z | - |
dc.date.available | 2020-11-03T09:53:31Z | - |
dc.date.issued | 2008 | - |
dc.identifier.uri | https://www.scopus.com/inward/record.uri?eid=2-s2.0-46149126602&doi=10.1016%2fj.neuro.2008.05.002&partnerID=40&md5=dfcb67dc055e134e889820895766cd22 | - |
dc.identifier.uri | https://scholars.lib.ntu.edu.tw/handle/123456789/519173 | - |
dc.description.abstract | Effects of d-amphetamine on the renal outer medullary potassium (ROMK1) channels were tested in the Xenopus oocytes expression system. Xenopus oocytes were injected with mRNA coding for wild-type or mutant ROMK1 channels. Giant inside-out patch-clamp recordings were performed. d-Amphetamine inhibited the activity of ROMK1 channels in a manner that was concentration-dependent but voltage-independent. ROMK1 channels are regulated by intracellular pH (pHi) and protein kinase A (PKA). d-Amphetamine decreased the activity of wild-type and pHi gating residue mutant (K80M) channels over a range of pHi values. However, d-amphetamine failed to reduce channel activity in the presence of PKA inhibitors (H89 and KT 5720) and had no inhibitory effect on the mutants of PKA-phosphorylation sites (S44A, S219A, or S313A), mutants that mimicked the negative charge carried by a phosphate group bound to a serine (S44D, S219D, or S313D), or mutant channels with a positive charge (S219R). These findings suggest that d-amphetamine inhibits ROMK1 channels independently of the pHi. The effects of d-amphetamine on ROMK1 channels may be due to a conformational change induced by PKA-mediated phosphorylation, but not to charge-charge interactions. Crown Copyright ? 2008. | - |
dc.relation.ispartof | NeuroToxicology | - |
dc.subject.classification | [SDGs]SDG3 | - |
dc.subject.other | cyclic AMP dependent protein kinase; cyclic AMP dependent protein kinase inhibitor; dexamphetamine; messenger RNA; potassium channel; protein romk1; animal cell; article; controlled study; drug inhibition; nonhuman; oocyte; priority journal; protein expression; Xenopus; Animals; Carbazoles; Dextroamphetamine; Dopamine Uptake Inhibitors; Dose-Response Relationship, Drug; Dose-Response Relationship, Radiation; Electric Stimulation; Enzyme Inhibitors; Female; Isoquinolines; Membrane Potentials; Microinjections; Mutagenesis, Site-Directed; Oocytes; Patch-Clamp Techniques; Potassium Channels, Inwardly Rectifying; Pyrroles; Serine; Sulfonamides; Xenopus | - |
dc.title | d-Amphetamine inhibits inwardly rectifying potassium channels in Xenopus oocytes expression system | en_US |
dc.type | journal article | en |
dc.identifier.doi | 10.1016/j.neuro.2008.05.002 | - |
dc.identifier.pmid | 18571730 | - |
dc.identifier.scopus | 2-s2.0-46149126602 | - |
dc.relation.pages | 638-646 | - |
dc.relation.journalvolume | 29 | - |
dc.relation.journalissue | 4 | - |
item.cerifentitytype | Publications | - |
item.fulltext | no fulltext | - |
item.openairecristype | http://purl.org/coar/resource_type/c_6501 | - |
item.openairetype | journal article | - |
item.grantfulltext | none | - |
crisitem.author.dept | National Taiwan University Hospital Yun-Lin Branch | - |
crisitem.author.dept | Neurology | - |
crisitem.author.dept | Pharmacology | - |
crisitem.author.dept | Brain and Mind Sciences | - |
crisitem.author.dept | Neurology-NTUH | - |
crisitem.author.orcid | 0000-0001-6537-5346 | - |
crisitem.author.parentorg | National Taiwan University Hospital | - |
crisitem.author.parentorg | College of Medicine | - |
crisitem.author.parentorg | College of Medicine | - |
crisitem.author.parentorg | College of Medicine | - |
crisitem.author.parentorg | National Taiwan University Hospital | - |
顯示於: | 醫學系 |
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