PAC1 receptor modulation of freezing and flight behavior in periaqueductal gray

dc.contributor.authorYavaş, Ersin
dc.contributor.authorZhuravka, Irina
dc.contributor.authorFanselow, Michael S.
dc.contributor.authorYavaş, Ersin
dc.date.accessioned2025-10-18T10:05:29Z
dc.date.created2023
dc.date.issued2023
dc.departmentFakülteler, İnsan ve Toplum Bilimleri Fakültesi, Psikoloji Bölümü
dc.description.abstractThe midbrain periaqueductal gray (PAG) region is a critical anatomical regulator of fear-related species-specific defensive reactions (SSDRs). Pituitary adenylate-cyclase-activating polypeptide (PACAP), and its main receptor PAC1, play an important role in fear-related behavior and anxiety disorders. However, the function of the PACAP-PAC1 system within the PAG with regards to SSDRs has received little attention. To address this gap, we used transgenic PAC1flox/flox mice to examine both conditional and unconditional defensive reactions. We performed conditional PAC1 gene deletion within the ventrolateral(vl)PAG of PAC1flox/flox mice using an adeno-associated virus (AAV) coding for Cre recombinase. Following viral expression, we used a white noise fear conditioning preparation that produces both an unconditional activity burst to the onset of noise that is followed by conditional freezing. On Day 1, mice received five white noise foot-shock pairings, whereas on Day 2, they were exposed to white noise five times without shock and we scored the activity burst and freezing to the white noise. Following behavioral testing, histology for immunofluorescent analysis was conducted in order to identify PACAP positive cells and stress-induced c-fos activity respectively. We found that PAC1 deletion in vlPAG increased the unconditional activity burst response but disrupted conditional freezing. PAC1 deletion was accompanied by higher c-fos activity following the behavioral experiments. Furthermore, a significant portion of PACAP-EGFP positive cells showed overlapping expression with VGAT, indicating their association with inhibitory neurons. The findings suggested that intact PACAP-PAC1 mechanisms are essential for SSDRs in vlPAG. Therefore, midbrain PACAP contributes to the underlying molecular mechanisms regulating fear responses. PAC1 receptors were conditionally deleted from the ventrolateral PAG where PACAP-positive cells are primarily located, performed fear conditioning experiments were conducted. Lacking PAC1 receptors showed defensive responses inappropriate to the situation such as freezing, activity burst and darting. The findings suggested that intact PACAP-PAC1 mechanisms are essential for intact species-specific defensive reactions in ventrolateral PAG.image
dc.description.sponsorshipWe thank, Daniel Weatherill, Tasmia Amjad and Jeremy Trott for their invaluable contributions to this study.; National Institute of Mental Health [R01MH115678] Funding Source: NIH RePORTER
dc.description.sponsorshipWe thank, Daniel Weatherill, Tasmia Amjad and Jeremy Trott for their invaluable contributions to this study.
dc.identifier.doi10.1111/gbb.12873
dc.identifier.issn1601-1848
dc.identifier.issn1601-183X
dc.identifier.issue6
dc.identifier.orcidYavas, Ersin/0000-0002-5128-3106;
dc.identifier.pmid37983568
dc.identifier.scopus2-s2.0-85177188440
dc.identifier.scopusqualityQ1
dc.identifier.urihttps://doi.org/10.1111/gbb.12873
dc.identifier.urihttps://hdl.handle.net/11772/21279
dc.identifier.volume22
dc.identifier.wosWOS:001104360900001
dc.identifier.wosqualityQ2
dc.indekslendigikaynakWeb of Science
dc.indekslendigikaynakScopus
dc.indekslendigikaynakPubMed
dc.language.isoen
dc.publisherWiley
dc.relation.ispartofGenes Brain and Behavior
dc.relation.publicationcategoryMakale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanı
dc.rightsinfo:eu-repo/semantics/openAccess
dc.snmzWoS_20251016
dc.subjectDarting
dc.subjectEarly Gene Expression
dc.subjectFear Conditioning
dc.subjectFreezing
dc.subjectPac1 Receptor
dc.subjectPeriaqueductal Gray
dc.subjectVgat
dc.titlePAC1 receptor modulation of freezing and flight behavior in periaqueductal gray
dc.typeArticle
dspace.entity.typePublication
relation.isAuthorOfPublicationf74408ac-ac36-45be-a5c3-9cd3072a1868
relation.isAuthorOfPublication.latestForDiscoveryf74408ac-ac36-45be-a5c3-9cd3072a1868

Dosyalar