Matches in SemOpenAlex for { <https://semopenalex.org/work/W2018703690> ?p ?o ?g. }
- W2018703690 endingPage "450" @default.
- W2018703690 startingPage "441" @default.
- W2018703690 abstract "N-Methyl-d-aspartate, kainate, and quisqualate released endogenous adenosine from superfused slices of rat parietal cortex.N-Methyl-d-aspartate-evoked adenosine release was blocked byd,1-2-amino-5-phosphono-valeric acid and ( + )-5-methyl-10,11-dihydro-5H-dibenzo[a,d]cyclohepten-5,10-imine hydrogen maleate (MK-801), indicating that it was receptor-mediated, although it did not show the expected potentiation in the absence of Mg2+. In contrast,N-methyl-d-aspartate-evoked release of [3H]noradrenaline from the same slices was markedly potentiated in Mg2+-free medium. Therefore, the lack of Mg2+ modulation ofN-methyl-d-aspartate-evoked adenosine release was not due to depolarization-induced alleviation of the Mg2+ block in the slices. Kainate-evoked adenosine release was diminished by the non-specific excitatory amino acid antagonist, γ-d-glutamyl-glycine, and kainate- and quisqualate-evoked adenosine release was diminished by 6,7-dinitroquinoxaline-2,3-dione, indicating that these agonists release adenosine by acting atnon-N-methyl-d-aspartate receptors. Tetrodotoxin decreasedN-methyl-d-aspartate- and kainate-evoked adenosine release by 40% and 19% respectively, indicating that release was mediated in part by propagated action potentials in the slices. Total release of adenosine byN-methyl-d-aspartate, kainate or quisqualate was not diminished in the absence of Ca2+. A second exposure to kainate following restoration of Ca2+ to slices previously depolarized in the absence of Ca2+resulted in an amount of adenosine release equal to an initial release by slices in the presence of Ca2+, a result suggesting the presence of separate Ca2+-dependent and Ca2+-independent pools of adenosine. The present experiments demonstrate that activation of all three major subtypes of excitatory amino acid receptors in the cortex releases adenosine, possibly from separate Ca2+-dependent and -independent pools. Adenosine released from the cortex following excitatory amino acid stimulation may, by acting at inhibitory P1 purinoceptors, diminish excitatory neurotransmission and protect against excitotoxicity." @default.
- W2018703690 created "2016-06-24" @default.
- W2018703690 creator A5052221889 @default.
- W2018703690 creator A5067356159 @default.
- W2018703690 date "1990-01-01" @default.
- W2018703690 modified "2023-09-27" @default.
- W2018703690 title "N-methyl-d-aspartate, kainate and quisqualate release endogenous adenosine from rat cortical slices" @default.
- W2018703690 cites W1031173056 @default.
- W2018703690 cites W1502934874 @default.
- W2018703690 cites W1559801920 @default.
- W2018703690 cites W1775883263 @default.
- W2018703690 cites W1968162207 @default.
- W2018703690 cites W1968693309 @default.
- W2018703690 cites W1969010113 @default.
- W2018703690 cites W1978507389 @default.
- W2018703690 cites W1979028943 @default.
- W2018703690 cites W1987085388 @default.
- W2018703690 cites W1995473185 @default.
- W2018703690 cites W1996590069 @default.
- W2018703690 cites W1997568797 @default.
- W2018703690 cites W2003341655 @default.
- W2018703690 cites W2004110685 @default.
- W2018703690 cites W2007884285 @default.
- W2018703690 cites W2012191069 @default.
- W2018703690 cites W2012398018 @default.
- W2018703690 cites W2015202249 @default.
- W2018703690 cites W2016719792 @default.
- W2018703690 cites W2016759315 @default.
- W2018703690 cites W2017597964 @default.
- W2018703690 cites W2018654901 @default.
- W2018703690 cites W2020749289 @default.
- W2018703690 cites W2023657406 @default.
- W2018703690 cites W2026213310 @default.
- W2018703690 cites W2030816469 @default.
- W2018703690 cites W2033838661 @default.
- W2018703690 cites W2035750459 @default.
- W2018703690 cites W2035997751 @default.
- W2018703690 cites W2037335023 @default.
- W2018703690 cites W2037772094 @default.
- W2018703690 cites W2042935005 @default.
- W2018703690 cites W2047579513 @default.
- W2018703690 cites W2048814561 @default.
- W2018703690 cites W2050453552 @default.
- W2018703690 cites W2050482922 @default.
- W2018703690 cites W2050886880 @default.
- W2018703690 cites W2054402374 @default.
- W2018703690 cites W2055991501 @default.
- W2018703690 cites W2057537207 @default.
- W2018703690 cites W2057998065 @default.
- W2018703690 cites W2064379457 @default.
- W2018703690 cites W2071679166 @default.
- W2018703690 cites W2075056521 @default.
- W2018703690 cites W2075970322 @default.
- W2018703690 cites W2076908838 @default.
- W2018703690 cites W2077027022 @default.
- W2018703690 cites W2080876088 @default.
- W2018703690 cites W2083306923 @default.
- W2018703690 cites W2089960690 @default.
- W2018703690 cites W2092544119 @default.
- W2018703690 cites W2100040827 @default.
- W2018703690 cites W2160136423 @default.
- W2018703690 doi "https://doi.org/10.1016/0306-4522(90)90280-h" @default.
- W2018703690 hasPubMedId "https://pubmed.ncbi.nlm.nih.gov/1982346" @default.
- W2018703690 hasPublicationYear "1990" @default.
- W2018703690 type Work @default.
- W2018703690 sameAs 2018703690 @default.
- W2018703690 citedByCount "73" @default.
- W2018703690 countsByYear W20187036902013 @default.
- W2018703690 countsByYear W20187036902016 @default.
- W2018703690 countsByYear W20187036902018 @default.
- W2018703690 countsByYear W20187036902023 @default.
- W2018703690 crossrefType "journal-article" @default.
- W2018703690 hasAuthorship W2018703690A5052221889 @default.
- W2018703690 hasAuthorship W2018703690A5067356159 @default.
- W2018703690 hasConcept C12554922 @default.
- W2018703690 hasConcept C126322002 @default.
- W2018703690 hasConcept C134018914 @default.
- W2018703690 hasConcept C160268369 @default.
- W2018703690 hasConcept C170493617 @default.
- W2018703690 hasConcept C182683403 @default.
- W2018703690 hasConcept C185592680 @default.
- W2018703690 hasConcept C189184402 @default.
- W2018703690 hasConcept C2776991684 @default.
- W2018703690 hasConcept C2778938600 @default.
- W2018703690 hasConcept C55493867 @default.
- W2018703690 hasConcept C61174792 @default.
- W2018703690 hasConcept C67018056 @default.
- W2018703690 hasConcept C67907053 @default.
- W2018703690 hasConcept C71924100 @default.
- W2018703690 hasConcept C86803240 @default.
- W2018703690 hasConceptScore W2018703690C12554922 @default.
- W2018703690 hasConceptScore W2018703690C126322002 @default.
- W2018703690 hasConceptScore W2018703690C134018914 @default.
- W2018703690 hasConceptScore W2018703690C160268369 @default.
- W2018703690 hasConceptScore W2018703690C170493617 @default.
- W2018703690 hasConceptScore W2018703690C182683403 @default.
- W2018703690 hasConceptScore W2018703690C185592680 @default.
- W2018703690 hasConceptScore W2018703690C189184402 @default.