Matches in SemOpenAlex for { <https://semopenalex.org/work/W2078467132> ?p ?o ?g. }
- W2078467132 endingPage "128" @default.
- W2078467132 startingPage "118" @default.
- W2078467132 abstract "Whereas acute administration of many types of stimuli induces c-Fos and related proteins in brain, recent work has shown that chronic perturbations cause the region-specific accumulation of novel Fos-like proteins of 35–37 kD. These proteins, termed chronic FRAs (Fos-related antigens), have recently been shown to be isoforms of ΔFosB, which accumulate in brain due to their enhanced stability. In the present study, we sought to extend earlier findings that documented the effects of acute administration of antipsychotic drugs (APDs) on induction of Fos-like proteins by investigating the ability of typical and aytpical APDs, after chronic administration, to induce these ΔFosB isoforms in several brain regions implicated in the clinical actions of these agents. By Western blotting we found that chronic administration of the typical APD, haloperidol, dramatically induces ΔFosB in caudate–putamen (CP), a brain region associated with the extrapyramidal side effects of this drug. A smaller induction was seen in the nucleus accumbens (NAc) and prefrontal cortex (PFC), brain regions associated with the antipsychotic effects of the drug. In contrast, chronic administration of the prototype atypical APD clozapine failed to significantly increase levels of ΔFosB in any of the three brain regions, and even tended to reduce ΔFosB levels in the NAc. Two putative atypical APDs, risperidone and olanzapine, produced small but still significant increases in the levels of ΔFosB in CP, but not NAc or PFC. Studies with selective receptor antagonists suggested that induction of ΔFosB in CP and NAc is most dependent on antagonism of D2–D3 dopamine receptors, with antagonism of D1-like receptors most involved in the PFC. Immunohistochemical analysis confirmed the greater induction of ΔFosB in CP by typical versus atypical APDs, with no significant induction seen in PFC with either class of APD. Together, these findings demonstrate that repeated administration of APDs results in the induction of long-lasting Fos-like transcription factors that could mediate some of the persistent and region-specific changes in brain function associated with chronic drug exposure. Synapse 33:118–128, 1999. © 1999 Wiley-Liss, Inc." @default.
- W2078467132 created "2016-06-24" @default.
- W2078467132 creator A5006828837 @default.
- W2078467132 creator A5021591275 @default.
- W2078467132 creator A5024383091 @default.
- W2078467132 creator A5035129193 @default.
- W2078467132 creator A5049993782 @default.
- W2078467132 creator A5069552705 @default.
- W2078467132 date "1999-08-01" @default.
- W2078467132 modified "2023-10-10" @default.
- W2078467132 title "Region-specific induction of ?FosB by repeated administration of typical versus atypical antipsychotic drugs" @default.
- W2078467132 cites W1527425708 @default.
- W2078467132 cites W153750880 @default.
- W2078467132 cites W1602735100 @default.
- W2078467132 cites W1970782185 @default.
- W2078467132 cites W1973253580 @default.
- W2078467132 cites W1975837516 @default.
- W2078467132 cites W1979017418 @default.
- W2078467132 cites W1985126984 @default.
- W2078467132 cites W1985517071 @default.
- W2078467132 cites W1993624518 @default.
- W2078467132 cites W1993855542 @default.
- W2078467132 cites W1994118834 @default.
- W2078467132 cites W1994773485 @default.
- W2078467132 cites W1997028362 @default.
- W2078467132 cites W1999170649 @default.
- W2078467132 cites W2000890192 @default.
- W2078467132 cites W2006865155 @default.
- W2078467132 cites W2009447429 @default.
- W2078467132 cites W2009449932 @default.
- W2078467132 cites W2010110267 @default.
- W2078467132 cites W2013460039 @default.
- W2078467132 cites W2022769813 @default.
- W2078467132 cites W2036224418 @default.
- W2078467132 cites W2038595150 @default.
- W2078467132 cites W2039964264 @default.
- W2078467132 cites W2042252035 @default.
- W2078467132 cites W2042391155 @default.
- W2078467132 cites W2054228210 @default.
- W2078467132 cites W2054609104 @default.
- W2078467132 cites W2061097819 @default.
- W2078467132 cites W2062610641 @default.
- W2078467132 cites W2070019933 @default.
- W2078467132 cites W2074073259 @default.
- W2078467132 cites W2077707065 @default.
- W2078467132 cites W2078046758 @default.
- W2078467132 cites W2079266000 @default.
- W2078467132 cites W2083252023 @default.
- W2078467132 cites W2084596811 @default.
- W2078467132 cites W2085147949 @default.
- W2078467132 cites W2092416470 @default.
- W2078467132 cites W2095366603 @default.
- W2078467132 cites W2098553579 @default.
- W2078467132 cites W2106918877 @default.
- W2078467132 cites W2111431369 @default.
- W2078467132 cites W2124300506 @default.
- W2078467132 cites W2135090538 @default.
- W2078467132 cites W2153556827 @default.
- W2078467132 cites W2155003995 @default.
- W2078467132 cites W2162811260 @default.
- W2078467132 cites W2169353848 @default.
- W2078467132 cites W2274639366 @default.
- W2078467132 cites W2419358752 @default.
- W2078467132 cites W4292291195 @default.
- W2078467132 doi "https://doi.org/10.1002/(sici)1098-2396(199908)33:2<118::aid-syn2>3.0.co;2-l" @default.
- W2078467132 hasPubMedId "https://pubmed.ncbi.nlm.nih.gov/10400890" @default.
- W2078467132 hasPublicationYear "1999" @default.
- W2078467132 type Work @default.
- W2078467132 sameAs 2078467132 @default.
- W2078467132 citedByCount "90" @default.
- W2078467132 countsByYear W20784671322012 @default.
- W2078467132 countsByYear W20784671322013 @default.
- W2078467132 countsByYear W20784671322014 @default.
- W2078467132 countsByYear W20784671322015 @default.
- W2078467132 countsByYear W20784671322016 @default.
- W2078467132 countsByYear W20784671322017 @default.
- W2078467132 countsByYear W20784671322019 @default.
- W2078467132 countsByYear W20784671322021 @default.
- W2078467132 countsByYear W20784671322023 @default.
- W2078467132 crossrefType "journal-article" @default.
- W2078467132 hasAuthorship W2078467132A5006828837 @default.
- W2078467132 hasAuthorship W2078467132A5021591275 @default.
- W2078467132 hasAuthorship W2078467132A5024383091 @default.
- W2078467132 hasAuthorship W2078467132A5035129193 @default.
- W2078467132 hasAuthorship W2078467132A5049993782 @default.
- W2078467132 hasAuthorship W2078467132A5069552705 @default.
- W2078467132 hasConcept C104317684 @default.
- W2078467132 hasConcept C118552586 @default.
- W2078467132 hasConcept C126322002 @default.
- W2078467132 hasConcept C134018914 @default.
- W2078467132 hasConcept C150194340 @default.
- W2078467132 hasConcept C15744967 @default.
- W2078467132 hasConcept C169760540 @default.
- W2078467132 hasConcept C169900460 @default.
- W2078467132 hasConcept C170493617 @default.
- W2078467132 hasConcept C185592680 @default.
- W2078467132 hasConcept C2776412080 @default.
- W2078467132 hasConcept C2776552330 @default.