Please use this identifier to cite or link to this item: http://hdl.handle.net/11452/30041
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dc.contributor.authorSerter Kocaoğlu, Sema-
dc.date.accessioned2022-12-22T08:05:41Z-
dc.date.available2022-12-22T08:05:41Z-
dc.date.issued2020-09-07-
dc.identifier.citationYurtseven, D. G. vd. (2020). "Immunohistochemical evidence for glutamatergic regulation of nesfatin-1 neurons in the rat hypothalamus". Brain Sciences, 10(9).en_US
dc.identifier.issn2076-3425-
dc.identifier.urihttps://doi.org/10.3390/brainsci10090630-
dc.identifier.urihttps://www.mdpi.com/2076-3425/10/9/630-
dc.identifier.urihttp://hdl.handle.net/11452/30041-
dc.description.abstractNesfatin-1, identified as an anorexigenic peptide, regulates the energy metabolism by suppressing food intake. The majority of nesfatin-1-synthesizing neurons are concentrated in various hypothalamic nuclei, especially in the supraoptic (SON), arcuate (ARC) and paraventricular nuclei (PVN). We tested the hypothesis that the glutamatergic system regulates nesfatin-1 neurons through glutamate receptors. Therefore, the first aim of the proposed studies was to examine effects of different glutamate agonists in the activation of nesfatin-1 neurons using c-Fos double immunohistochemical labeling. Experimental groups were formed containing male and female rats which received intraperitoneal injections of glutamate agonists kainic acid, alpha-amino-3-hydroxy-5-methyl-4-isoxazolepropionic acid (AMPA) and N-methyl-D-aspartate (NMDA) while the control rats received vehicle. The significant increase in the number of c-Fos-expressing nesfatin-1 neurons after agonist injections were observed both in female and male subjects and some of these effects were found to be sexually dimorphic. In addition, treatment with specific glutamate antagonists 6-cyano-7-nitroquinoxaline-2,3-dione (CNQX) or dizocilpine (MK-801) before each of the three agonist injections caused a statistically significant reduction in the number of activated nesfatin-1 neurons in the hypothalamic nuclei including supraoptic, paraventricular and arcuate nuclei. The second aim of the study was to determine the expression of glutamate receptor subunit proteins in the nesfatin-1 neurons by using a double immunofluorescence technique. The results showed that the glutamate receptor subunits, which may form homomeric or heteromeric functional receptor channels, were expressed in the nesfatin-1 neurons. In conclusion, the results of this study suggest that nesfatin-1 neurons respond to glutamatergic signals in the form of neuronal activation and that the glutamate receptors that are synthesized by nesfatin-1 neurons may participate in the glutamatergic regulation of these neurons.en_US
dc.language.isoenen_US
dc.publisherMDPIen_US
dc.rightsinfo:eu-repo/semantics/openAccessen_US
dc.rightsAtıf Gayri Ticari Türetilemez 4.0 Uluslararasıtr_TR
dc.rights.urihttp://creativecommons.org/licenses/by-nc-nd/4.0/*
dc.subjectGlutamateen_US
dc.subjectNesfatin-1en_US
dc.subjectC-Fosen_US
dc.subjectHypothalamusen_US
dc.subjectRaten_US
dc.subjectBlood-brain-barrieren_US
dc.subjectSubunit messenger-RNAsen_US
dc.subjectC-fosen_US
dc.subjectReceptor subunitsen_US
dc.subjectUltrastructural-localizationen_US
dc.subjectSatiety moleculeen_US
dc.subjectKainic aciden_US
dc.subjectExpressionen_US
dc.subjectKainateen_US
dc.subjectActivationen_US
dc.subjectNeurosciences & neurologyen_US
dc.titleImmunohistochemical evidence for glutamatergic regulation of nesfatin-1 neurons in the rat hypothalamusen_US
dc.typeArticleen_US
dc.identifier.wos000580138200001tr_TR
dc.identifier.scopus2-s2.0-85090779765tr_TR
dc.relation.tubitakTÜBİTAKtr_TR
dc.relation.publicationcategoryMakale - Uluslararası Hakemli Dergitr_TR
dc.contributor.departmentBursa Uludağ Üniversitesi/Tıp Fakültesi/Histoloji ve Embriyoloji Anabilim Dalı.tr_TR
dc.contributor.orcid0000-0001-5757-8450tr_TR
dc.contributor.orcid0000-0003-3463-7483tr_TR
dc.identifier.volume10tr_TR
dc.identifier.issue9tr_TR
dc.relation.journalBrain Sciencesen_US
dc.contributor.buuauthorGök, Duygu Yurtseven-
dc.contributor.buuauthorMinbay, Zehra-
dc.contributor.buuauthorEzigör, Özhan-
dc.contributor.researcheridABE-5128-2020tr_TR
dc.contributor.researcheridABC-1475-2020tr_TR
dc.contributor.researcheridAAW-4867-2021tr_TR
dc.relation.collaborationYurt içitr_TR
dc.identifier.pubmed32932902tr_TR
dc.subject.wosNeurosciencesen_US
dc.indexed.wosSCIEen_US
dc.indexed.scopusScopusen_US
dc.indexed.pubmedPubMeden_US
dc.wos.quartileQ3en_US
dc.contributor.scopusid57193760779tr_TR
dc.contributor.scopusid8220935200tr_TR
dc.contributor.scopusid6603109907tr_TR
dc.subject.scopusNucleobindin; Pyroglutamyl-Histidyl-Glycine; DNA-Binding Proteinsen_US
dc.subject.emtree6 cyano 7 nitro 2,3 quinoxalinedioneen_US
dc.subject.emtreeAMPA receptor agonisten_US
dc.subject.emtreeKainic aciden_US
dc.subject.emtreeN methyl dextro aspartic acid receptoren_US
dc.subject.emtreeN methyl dextro aspartic acid receptor stimulating agenten_US
dc.subject.emtreeNesfatin 1en_US
dc.subject.emtreeNeurotransmitteren_US
dc.subject.emtreeUnclassified drugen_US
dc.subject.emtreeAdulten_US
dc.subject.emtreeAnimal experimenten_US
dc.subject.emtreeAnimal modelen_US
dc.subject.emtreeAnimal tissueen_US
dc.subject.emtreeArticleen_US
dc.subject.emtreeCell countingen_US
dc.subject.emtreeControlled studyen_US
dc.subject.emtreeEnergy metabolismen_US
dc.subject.emtreeFemaleen_US
dc.subject.emtreeFood intakeen_US
dc.subject.emtreeGABAergic transmissionen_US
dc.subject.emtreeGlutamatergic synapseen_US
dc.subject.emtreeHippocampusen_US
dc.subject.emtreeHypothalamusen_US
dc.subject.emtreeImmunofluorescenceen_US
dc.subject.emtreeImmunofluorescence testen_US
dc.subject.emtreeImmunohistochemistryen_US
dc.subject.emtreeImmunoreactivityen_US
dc.subject.emtreeMaleen_US
dc.subject.emtreeNonhumanen_US
dc.subject.emtreeProtein expressionen_US
dc.subject.emtreeProtein phosphorylationen_US
dc.subject.emtreeRaten_US
dc.subject.emtreeSynaptic transmissionen_US
dc.subject.emtreeVaccinationen_US
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