Please use this identifier to cite or link to this item: https://scholarbank.nus.edu.sg/handle/10635/111776
DC FieldValue
dc.titleAcute down-regulation of oxytocin and vasopressin mRNA levels following metrazole-induced seizure in the rat
dc.contributor.authorCarter, D.A.
dc.contributor.authorMurphy, D.
dc.date.accessioned2014-11-28T02:49:34Z
dc.date.available2014-11-28T02:49:34Z
dc.date.issued1993-10-01
dc.identifier.citationCarter, D.A.,Murphy, D. (1993-10-01). Acute down-regulation of oxytocin and vasopressin mRNA levels following metrazole-induced seizure in the rat. Neuroscience Letters 160 (2) : 135-138. ScholarBank@NUS Repository.
dc.identifier.issn03043940
dc.identifier.urihttp://scholarbank.nus.edu.sg/handle/10635/111776
dc.description.abstractFollowing our recent demonstration of metrazole-induced immediate-early gene expression in the hypothalamic supraoptic nucleus (SON), we have now performed a mRNA and transcription analysis to determine the consequences of metrazole treatment for neurohypophyseal peptide gene expression in male rats. Levels of hypothalamic vasopressin (VP) and oxytocin (OT) mRNA were significantly reduced at 2 and 4 h after metrazole (50 mg/kg, i.p.), whereas pro-dynorphin mRNA was significantly elevated at 2 h. No changes in mRNA levels were found at 8, 24 or 48 h after treatment. Another convulsant (kainic acid, 8 mg/kg, i.p.) elicited similar effects on VP and OT mRNAs at 2 h. Specific analysis of the SON, following metrazole, revealed an equivalent effect on VP and OT mRNA levels but a nuclear run-on assay did not detect any change in SON VP gene transcription at 0.5, 1 and 2 h after treatment. The results provide evidence of a novel mechanism which may provide an additional level of control in the regulation of neuropeptide gene expression. © 1993.
dc.sourceScopus
dc.subjectc-fos
dc.subjectc-jun
dc.subjectDynorphin
dc.subjectHypothalamus
dc.subjectMetrazole
dc.subjectOxytocin
dc.subjectSupraoptic nucleus
dc.subjectVasopressin
dc.typeArticle
dc.contributor.departmentINSTITUTE OF MOLECULAR & CELL BIOLOGY
dc.description.sourcetitleNeuroscience Letters
dc.description.volume160
dc.description.issue2
dc.description.page135-138
dc.description.codenNELED
dc.identifier.isiutNOT_IN_WOS
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