PMID- 19190682 OWN - NLM STAT- MEDLINE DCOM- 20090626 LR - 20240326 IS - 1673-7067 (Print) IS - 1995-8218 (Electronic) IS - 1995-8218 (Linking) VI - 25 IP - 1 DP - 2009 Feb TI - Central administration of Orphanin FQ inhibits GnRH secretion by ORL1 receptor in the median eminence of freely moving ovariectomized rats. PG - 1-6 LID - 10.1007/s12264-009-1119-5 [doi] LID - 1 AB - OBJECTIVE: This study aimed to investigate the possible role of Orphanin FQ (OFQ) in the regulation of hypo-thalamic gonadotropin-releasing hormone (GnRH) secretion. METHODS: The method of push-pull perfusion and radioimmuno-assay (RIA) were adopted to examine the secretory profile of GnRH in the median eminence (ME) in freely moving ovari-ectomized (OVX) rats after intracerebroventricular (icv) injection of OFQ and/or [Nphe(1)]NC(1-13)NH(2) (NC13), a competitive antagonists of the opioid receptor-like 1 receptor (ORL1 receptor). RESULTS: GnRH release from ME significantly decreased from 40 min to 80 min after the administration of 20 and 200 nmol OFQ in OVX rats (P < 0.05). This inhibitory effect of 20 nmol OFQ could be abolished by pretreatment with equal dose of NC13. More interestingly, GnRH secretion from ME was increased markedly 60 min after icv injection of 100 and 200 nmol NC13 (P < 0.05). CONCLUSION: Our results suggested central administration of OFQ could inhibit the release of GnRH in the ME of hypothalamus through ORL1 receptor, providing further in vivo evidence supporting the role of OFQ in the control of GnRH secretion. FAU - An, Xiao-Fei AU - An XF AD - Department of Endocrinology, Jiangsu Province Hospital of Traditional Chinese Med, Nanjing 210029, China. anxiaofei2000@163.com FAU - He, Ming AU - He M FAU - Feng, Yi AU - Feng Y FAU - Feng, Hao AU - Feng H FAU - Yu, Jiang-Yi AU - Yu JY LA - eng PT - Journal Article PT - Research Support, Non-U.S. Gov't PL - Singapore TA - Neurosci Bull JT - Neuroscience bulletin JID - 101256850 RN - 0 (Narcotic Antagonists) RN - 0 (Opioid Peptides) RN - 0 (Peptide Fragments) RN - 0 (Receptors, Opioid) RN - 0 (Vasodilator Agents) RN - 0 (nociceptin-(1-13)-NH2, NPhe(1)-) RN - 33515-09-2 (Gonadotropin-Releasing Hormone) RN - 0 (Nociceptin Receptor) RN - 0 (Oprl protein, rat) SB - IM MH - Analysis of Variance MH - Animals MH - Dose-Response Relationship, Drug MH - Female MH - Gonadotropin-Releasing Hormone/*metabolism MH - Median Eminence/*metabolism MH - Narcotic Antagonists MH - Opioid Peptides/*pharmacology MH - Ovariectomy/methods MH - Peptide Fragments/pharmacology MH - Radioimmunoassay MH - Rats MH - Rats, Sprague-Dawley MH - Receptors, Opioid/*metabolism MH - Secretory Pathway/*drug effects MH - Vasodilator Agents/*pharmacology MH - Wakefulness/*physiology MH - Nociceptin Receptor MH - Nociceptin PMC - PMC5552497 EDAT- 2009/02/05 09:00 MHDA- 2009/06/27 09:00 PMCR- 2010/02/01 CRDT- 2009/02/05 09:00 PHST- 2009/02/05 09:00 [entrez] PHST- 2009/02/05 09:00 [pubmed] PHST- 2009/06/27 09:00 [medline] PHST- 2010/02/01 00:00 [pmc-release] AID - 1119 [pii] AID - 10.1007/s12264-009-1119-5 [doi] PST - ppublish SO - Neurosci Bull. 2009 Feb;25(1):1-6. doi: 10.1007/s12264-009-1119-5.