PMID- 19168037 OWN - NLM STAT- MEDLINE DCOM- 20090421 LR - 20240319 IS - 1872-6240 (Electronic) IS - 0006-8993 (Print) IS - 0006-8993 (Linking) VI - 1259 DP - 2009 Mar 9 TI - Estradiol increases Pet-1 and serotonin transporter mRNA in the midbrain raphe nuclei of ovariectomized rats. PG - 51-8 LID - 10.1016/j.brainres.2008.12.067 [doi] AB - Previous research has shown that estradiol increases the anorexia associated with serotonin (5-HT) neurotransmission. To examine further the putative relationship between estradiol and 5-HT, we investigated whether estradiol increases the expression of Pet-1 and the 5-HT transporter (5-HTT), two genes implicated in the development and regulation of the 5-HT system. Ovariectomized (OVX) rats (n=5-6/group) were treated with 0, 2, or 10 microg estradiol benzoate (EB) in sesame oil on 2 consecutive days. Food intake and body weight were recorded 2 days later when EB-treated rats typically display signs of behavioral estrus (e.g., reduced feeding). Following the collection of behavioral data, rats were perfused, brains were removed, and coronal sections were cut through the midbrain raphe nuclei. Pet-1 and 5-HTT mRNA levels were quantified throughout the dorsal and median raphe nuclei (DRN and MRN) by conducting in situ hybridization on free-floating tissue sections using (35)S-labeled cDNA probes. As expected, EB treatment decreased food intake and body weight on the day that modeled estrus. At this same time, EB treatment increased Pet-1 and 5-HTT mRNA levels within the DRN and MRN. We conclude that a physiologically relevant regimen of estradiol treatment in OVX rats increases Pet-1 and 5-HTT mRNA levels in the midbrain raphe nuclei at a time when the anorexigenic effect of estradiol is apparent. Further studies are required to determine whether the increased expression of Pet-1 and 5-HTT mRNA plays a causal role in the anorexigenic effect of estradiol. FAU - Rivera, Heidi M AU - Rivera HM AD - Department of Psychology and Program in Neuroscience, Florida State University, Tallahassee, FL 32306-4301, USA. FAU - Oberbeck, Denesa R AU - Oberbeck DR FAU - Kwon, Bumsup AU - Kwon B FAU - Houpt, Thomas A AU - Houpt TA FAU - Eckel, Lisa A AU - Eckel LA LA - eng GR - DK-073936/DK/NIDDK NIH HHS/United States GR - DC-03198/DC/NIDCD NIH HHS/United States GR - R01 DK073936/DK/NIDDK NIH HHS/United States GR - R01 DC003198/DC/NIDCD NIH HHS/United States GR - T32 DC-00044/DC/NIDCD NIH HHS/United States GR - R01 DK073936-03/DK/NIDDK NIH HHS/United States GR - T32 DC000044/DC/NIDCD NIH HHS/United States PT - Journal Article PT - Research Support, N.I.H., Extramural DEP - 20090110 PL - Netherlands TA - Brain Res JT - Brain research JID - 0045503 RN - 0 (Appetite Depressants) RN - 0 (Fev protein, rat) RN - 0 (RNA, Messenger) RN - 0 (Serotonin Plasma Membrane Transport Proteins) RN - 0 (Slc6a4 protein, rat) RN - 0 (Transcription Factors) RN - 1S4CJB5ZGN (estradiol 3-benzoate) RN - 4TI98Z838E (Estradiol) SB - IM MH - Analysis of Variance MH - Animals MH - Appetite Depressants/administration & dosage/pharmacology MH - Body Weight MH - Eating/drug effects MH - Estradiol/administration & dosage/*analogs & derivatives/pharmacology MH - Estrus/drug effects MH - Female MH - Gene Expression/drug effects MH - In Situ Hybridization MH - *Ovariectomy MH - RNA, Messenger/genetics/metabolism MH - Raphe Nuclei/drug effects/*metabolism MH - Rats MH - Rats, Long-Evans MH - Serotonin Plasma Membrane Transport Proteins/genetics/*metabolism MH - Transcription Factors/genetics/*metabolism PMC - PMC2957819 MID - NIHMS88685 EDAT- 2009/01/27 09:00 MHDA- 2009/04/22 09:00 PMCR- 2010/10/20 CRDT- 2009/01/27 09:00 PHST- 2008/09/12 00:00 [received] PHST- 2008/12/29 00:00 [revised] PHST- 2008/12/31 00:00 [accepted] PHST- 2009/01/27 09:00 [entrez] PHST- 2009/01/27 09:00 [pubmed] PHST- 2009/04/22 09:00 [medline] PHST- 2010/10/20 00:00 [pmc-release] AID - S0006-8993(09)00010-9 [pii] AID - 10.1016/j.brainres.2008.12.067 [doi] PST - ppublish SO - Brain Res. 2009 Mar 9;1259:51-8. doi: 10.1016/j.brainres.2008.12.067. Epub 2009 Jan 10.