Increased Synaptic Availability of Norepinephrine Following Desipramine is Not Essential for Increases in GR MRNA. Short Communication
Overview
Physiology
Affiliations
Male Sprague-Dawley rats were treated for 7 days with the norepinephrine (NE) uptake inhibitors desipramine (DMI) or (+)-oxaprotiline or the inactive (-)-enantiomer of oxaprotiline. DMI, as previously reported, significantly increased hippocampal glucocorticoid receptor (GR) mRNA while the equipotent NE uptake inhibitor (+)-oxaprotiline like the inactive (-)-oxaprotiline did not alter hippocampal levels of GR mRNA. The results indicate that an increase in the synaptic availability of NE as a consequence of uptake inhibition is not responsible for the action of DMI on GR gene expression.
Patterns of sequence conservation in presynaptic neural genes.
Hadley D, Murphy T, Valladares O, Hannenhalli S, Ungar L, Kim J Genome Biol. 2006; 7(11):R105.
PMID: 17096848 PMC: 1794582. DOI: 10.1186/gb-2006-7-11-r105.
Pariante C, Makoff A, Lovestone S, Feroli S, Heyden A, Miller A Br J Pharmacol. 2001; 134(6):1335-43.
PMID: 11704655 PMC: 1573058. DOI: 10.1038/sj.bjp.0704368.