The investigation of possible roles of central 5-HT7 receptors in antipyretic effect mechanism of paracetamol in LPS-induced hyperthermia model of mice

ArticleAçık Erişim

Özet

Aim: This study aimed to investigate the role of the 5-HT7 receptor in fever mechanisms and its possible effect on the antipyretic mechanism of paracetamol. Materials and methods: The study consisted of eight experimental groups and one control group. Group I: healthy, II: LPS, III: LPS + PARA, IV: LPS + AGO, V: LPS + ANTA, VI: LPS + AGO + ANTA, VII: LPS + AGO + PARA, VIII: LPS + ANTA + PARA, and IX: LPS + AGO + ANTA + PARA. Rectal temperatures were measured with a rectal thermometer. At the end of the experiment, tissues were examined molecularly. Real-time PCR mRNA expression analyses were performed for the 5-HT7 receptor, IL-6, and TNF-α in hypothalamus tissue. Results: The mean differences in rectal temperature increased in the LPS, LPS + ANTA, and LPS + AGO + ANTA groups when compared to the healthy group and decreased in the LPS + PARA, LPS + AGO, LPS + AGO + PARA, and LPS + AGO + ANTA + PARA groups when compared to the healthy group. The IL-6 and TNF-α mRNA expression increased in the LPS, LPS + ANTA, and LPS + AGO + ANTA groups when compared to the healthy group in the 2nd and 4th hours. The IL-6 and TNF-α expression decreased in the LPS + PARA, LPS + AGO, LPS + AGO + PARA, and LPS + AGO + ANTA + PARA groups when compared to the LPS group in the 2nd and 4th hours. The 5-HT7 receptor mRNA expression increased in the LPS group when compared to the healthy group in the 2nd hour. The 5-HT7 receptor mRNA expression decreased in the LPS + AGO and LPS + AGO + PARA groups when compared to the LPS group in the 2nd hour. The 5-HT7 receptor mRNA expression increased the in LPS + ANTA and LPS + ANTA + PARA groups when compared to the LPS group in the 2nd hour. Conclusion: The 5-HT7 receptor is a potential defense mechanism in stopping fever and the antipyretic property of paracetamol is not due to the 5-HT7 receptor. © 2019, Springer Nature Switzerland AG.

Anahtar Kelimeler

RDL Kalıcı Bağlantı (PID)
https://rdlopen.rawdatalibrary.net/r/ebyu/13857Resmi atıflarda kullanılan kalıcı adres
DOI
https://doi.org/10.1007/s10787-019-00617-1Yayıncı resmi DOI adresi
Tam Kayıt
AlanDeğerDil
dc.contributor.authorKose, Duygu
dc.contributor.authorCadirci, Elif
dc.contributor.authorHalici, Zekai
dc.contributor.authorSirin, Busra
dc.contributor.authorDincer, Busra
dc.date.accessioned2026-10-18T20:28:39.524081655Z
dc.date.available2026-10-18T20:28:39.524081655Z
dc.date.issued2019
dc.description.abstractAim: This study aimed to investigate the role of the 5-HT7 receptor in fever mechanisms and its possible effect on the antipyretic mechanism of paracetamol. Materials and methods: The study consisted of eight experimental groups and one control group. Group I: healthy, II: LPS, III: LPS + PARA, IV: LPS + AGO, V: LPS + ANTA, VI: LPS + AGO + ANTA, VII: LPS + AGO + PARA, VIII: LPS + ANTA + PARA, and IX: LPS + AGO + ANTA + PARA. Rectal temperatures were measured with a rectal thermometer. At the end of the experiment, tissues were examined molecularly. Real-time PCR mRNA expression analyses were performed for the 5-HT7 receptor, IL-6, and TNF-α in hypothalamus tissue. Results: The mean differences in rectal temperature increased in the LPS, LPS + ANTA, and LPS + AGO + ANTA groups when compared to the healthy group and decreased in the LPS + PARA, LPS + AGO, LPS + AGO + PARA, and LPS + AGO + ANTA + PARA groups when compared to the healthy group. The IL-6 and TNF-α mRNA expression increased in the LPS, LPS + ANTA, and LPS + AGO + ANTA groups when compared to the healthy group in the 2nd and 4th hours. The IL-6 and TNF-α expression decreased in the LPS + PARA, LPS + AGO, LPS + AGO + PARA, and LPS + AGO + ANTA + PARA groups when compared to the LPS group in the 2nd and 4th hours. The 5-HT7 receptor mRNA expression increased in the LPS group when compared to the healthy group in the 2nd hour. The 5-HT7 receptor mRNA expression decreased in the LPS + AGO and LPS + AGO + PARA groups when compared to the LPS group in the 2nd hour. The 5-HT7 receptor mRNA expression increased the in LPS + ANTA and LPS + ANTA + PARA groups when compared to the LPS group in the 2nd hour. Conclusion: The 5-HT7 receptor is a potential defense mechanism in stopping fever and the antipyretic property of paracetamol is not due to the 5-HT7 receptor. © 2019, Springer Nature Switzerland AG.
dc.description.sponsorshipThis study is a part of Duygu KOSE PhD thesis and supported by TUBITAK with project number 112S627. Special thanks for their contribution to Yasin BAYIR; Abdulmecit ALBAYRAK.
dc.identifier.doi10.1007/s10787-019-00617-1
dc.identifier.eissn1568-5608
dc.identifier.endpage1178
dc.identifier.issn0925-4692
dc.identifier.issue6
dc.identifier.pmid31309486
dc.identifier.scopus2-s2.0-85068983455
dc.identifier.startpage1169
dc.identifier.urihttps://rdlopen.rawdatalibrary.net/r/ebyu/13857
dc.identifier.volume27
dc.identifier.wosWOS:000495294000008
dc.language.isoen
dc.publisherBirkhauser Verlag AG
dc.relation.ispartofInflammopharmacology
dc.rightsinfo:eu-repo/semantics/openAccess
dc.subject5-HT7 receptor
dc.subjectFever
dc.subjectHypothalamus
dc.subjectLPS
dc.subjectParacetamol
dc.subjectTNF
dc.subjectAcetaminophen
dc.subjectAnimals
dc.subjectAntipyretics
dc.subjectBody Temperature
dc.subjectDisease Models, Animal
dc.subjectInterleukin-6
dc.subjectLipopolysaccharides
dc.subjectMale
dc.subjectMice
dc.subjectMice, Inbred BALB C
dc.subjectReceptors, Serotonin
dc.subjectRNA, Messenger
dc.subjectTumor Necrosis Factor-alpha
dc.subjectinterleukin 6
dc.subjectmessenger RNA
dc.subjectserotonin 7 receptor
dc.subjecttumor necrosis factor
dc.subjectantipyretic agent
dc.subjectlipopolysaccharide
dc.subjectserotonin receptor
dc.subjectanimal experiment
dc.subjectanimal model
dc.subjectanimal tissue
dc.subjectantipyretic activity
dc.titleThe investigation of possible roles of central 5-HT7 receptors in antipyretic effect mechanism of paracetamol in LPS-induced hyperthermia model of mice
dc.typeArticle
dspace.entity.typePublication
rdl.citation.scopus10
rdl.citation.wos8
rdl.source.indexSCOPUS
rdl.source.indexWOS
rdl.wos.indexScience Citation Index Expanded (SCI-EXPANDED)