Matches in SemOpenAlex for { <https://semopenalex.org/work/W2000470286> ?p ?o ?g. }
- W2000470286 endingPage "14" @default.
- W2000470286 startingPage "1" @default.
- W2000470286 abstract "This work compares the effects on brain stimulation reward (BSR) when combining D2 dopamine receptor and AMPA glutamate receptor manipulations in the sublenticular central extended amygdala (SLEAc) and the nucleus accumbens shell (NAc shell). Thirty-seven male Long Evans rats received medial forebrain bundle (MFB) stimulation electrodes and bilateral injection guide cannulae aimed at either the SLEAc or the NAc shell. The rate-frequency paradigm was used to assess drug-induced changes in stimulation reward effectiveness and in response rate following 0.5 μl infusions of 0.50 μg of 1,2,3,4-tetrahydro-6-nitro-2,3-dioxo-benzo[f]quinoxaline-7-sulfonamide (NBQX) (AMPA receptor antagonist), 10.0 μg of quinpirole (D2 receptor agonist), 0.25 μg of AMPA (AMPA receptor agonist), 3.0 μg of eticlopride (D2 receptor antagonist), 0.50 μg of NBQX with 10.0 μg of quinpirole, and 0.25 μg of AMPA with 3.0 μg of eticlopride. The drugs were injected both ipsi- and contralateral to the stimulation site. AMPA blockade and D2 stimulation synergized to reduce BSR's reward efficacy when directed at the SLEAc contralateral to the stimulation site whereas changes in reward efficacy were primarily D2-dependent following injections into the ipsilateral SLEAc. When injected into the NAc shell the drugs had only one significant effect on the frequency required to maintain half-maximal responding: injections of NBQX with quinpirole ipsilateral to the stimulation site increased required frequency significantly more than did injections of saline. Contrary to expectations, stimulating AMPA receptors with and without co-blockade of D2 receptors also decreased the stimulation's reward efficacy, although these effects may reflect general behavioral disruption more than effects on reward per se. These results indicate a role for the SLEAc in BSR and also suggest that SLEAc neurons ipsi- and contralateral to the stimulated MFB play their roles in BSR through different mechanisms." @default.
- W2000470286 created "2016-06-24" @default.
- W2000470286 creator A5003438720 @default.
- W2000470286 creator A5011478099 @default.
- W2000470286 creator A5050136259 @default.
- W2000470286 date "2012-11-01" @default.
- W2000470286 modified "2023-09-25" @default.
- W2000470286 title "Brain stimulation reward is altered by affecting dopamine–glutamate interactions in the central extended amygdala" @default.
- W2000470286 cites W1935412124 @default.
- W2000470286 cites W1945424073 @default.
- W2000470286 cites W1966001294 @default.
- W2000470286 cites W1966891940 @default.
- W2000470286 cites W1969817492 @default.
- W2000470286 cites W1970761553 @default.
- W2000470286 cites W1972252766 @default.
- W2000470286 cites W1976064429 @default.
- W2000470286 cites W1979532884 @default.
- W2000470286 cites W1983445937 @default.
- W2000470286 cites W1987243354 @default.
- W2000470286 cites W1989783934 @default.
- W2000470286 cites W1989809574 @default.
- W2000470286 cites W1993631201 @default.
- W2000470286 cites W2005041180 @default.
- W2000470286 cites W2012012876 @default.
- W2000470286 cites W2013752543 @default.
- W2000470286 cites W2019772841 @default.
- W2000470286 cites W2021072779 @default.
- W2000470286 cites W2025936719 @default.
- W2000470286 cites W2027441566 @default.
- W2000470286 cites W2032372936 @default.
- W2000470286 cites W2032738876 @default.
- W2000470286 cites W2035197880 @default.
- W2000470286 cites W2042335457 @default.
- W2000470286 cites W2043212816 @default.
- W2000470286 cites W2043843299 @default.
- W2000470286 cites W2044860425 @default.
- W2000470286 cites W2054154676 @default.
- W2000470286 cites W2069422686 @default.
- W2000470286 cites W2071969308 @default.
- W2000470286 cites W2075627875 @default.
- W2000470286 cites W2079336138 @default.
- W2000470286 cites W2084702088 @default.
- W2000470286 cites W2087874796 @default.
- W2000470286 cites W2091447309 @default.
- W2000470286 cites W2095489665 @default.
- W2000470286 cites W2095951518 @default.
- W2000470286 cites W2104513822 @default.
- W2000470286 cites W2106828113 @default.
- W2000470286 cites W2110293865 @default.
- W2000470286 cites W2115601524 @default.
- W2000470286 cites W2129557089 @default.
- W2000470286 cites W2138008736 @default.
- W2000470286 cites W2141657914 @default.
- W2000470286 cites W2142522676 @default.
- W2000470286 cites W2151763167 @default.
- W2000470286 cites W2168125354 @default.
- W2000470286 cites W2172010489 @default.
- W2000470286 cites W2483005372 @default.
- W2000470286 cites W2502741214 @default.
- W2000470286 cites W4238505877 @default.
- W2000470286 cites W4295332810 @default.
- W2000470286 doi "https://doi.org/10.1016/j.neuroscience.2012.08.019" @default.
- W2000470286 hasPubMedId "https://pubmed.ncbi.nlm.nih.gov/22906479" @default.
- W2000470286 hasPublicationYear "2012" @default.
- W2000470286 type Work @default.
- W2000470286 sameAs 2000470286 @default.
- W2000470286 citedByCount "5" @default.
- W2000470286 countsByYear W20004702862013 @default.
- W2000470286 countsByYear W20004702862014 @default.
- W2000470286 countsByYear W20004702862015 @default.
- W2000470286 countsByYear W20004702862016 @default.
- W2000470286 countsByYear W20004702862017 @default.
- W2000470286 crossrefType "journal-article" @default.
- W2000470286 hasAuthorship W2000470286A5003438720 @default.
- W2000470286 hasAuthorship W2000470286A5011478099 @default.
- W2000470286 hasAuthorship W2000470286A5050136259 @default.
- W2000470286 hasConcept C126322002 @default.
- W2000470286 hasConcept C134018914 @default.
- W2000470286 hasConcept C15744967 @default.
- W2000470286 hasConcept C160268369 @default.
- W2000470286 hasConcept C169760540 @default.
- W2000470286 hasConcept C170493617 @default.
- W2000470286 hasConcept C185592680 @default.
- W2000470286 hasConcept C24998067 @default.
- W2000470286 hasConcept C2776552330 @default.
- W2000470286 hasConcept C2776669363 @default.
- W2000470286 hasConcept C2778125517 @default.
- W2000470286 hasConcept C2778296116 @default.
- W2000470286 hasConcept C2778938600 @default.
- W2000470286 hasConcept C2779917531 @default.
- W2000470286 hasConcept C2780062018 @default.
- W2000470286 hasConcept C2780076171 @default.
- W2000470286 hasConcept C513476851 @default.
- W2000470286 hasConcept C61174792 @default.
- W2000470286 hasConcept C64948172 @default.
- W2000470286 hasConcept C71924100 @default.
- W2000470286 hasConcept C98274493 @default.
- W2000470286 hasConceptScore W2000470286C126322002 @default.