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dc.contributor.authorGéa, Luíza Paulpt_BR
dc.contributor.authorAguiar, Bianca Wollenhaupt dept_BR
dc.contributor.authorWatts, Devon Patrickpt_BR
dc.contributor.authorMaich, William Thomaspt_BR
dc.contributor.authorKapczinski, Flávio Pereirapt_BR
dc.contributor.authorSharma, Roohiept_BR
dc.contributor.authorMishra, Ram K.pt_BR
dc.contributor.authorRosa, Adriane Ribeiropt_BR
dc.contributor.authorFrey, Benício Noronhapt_BR
dc.date.accessioned2024-11-27T06:51:41Zpt_BR
dc.date.issued2022pt_BR
dc.identifier.issn2666-9153pt_BR
dc.identifier.urihttp://hdl.handle.net/10183/281551pt_BR
dc.description.abstractBackground High levels of inflammation and oxidative stress are observed in bipolar disorder (BD) being further associated with mood symptoms and cognitive dysfunction. Due to the crosstalk between the periphery and central nervous system, the blood-brain barrier (BBB) disruption has been considered a key mechanism of the BD pathophysiology. This study aimed to evaluate claudin-5 expression in the brain of a model of mania induced by D-amphetamine (AMPH). Methods Wistar rats were injected with AMPH (2 mg/kg i.p.) and treated with lithium (47.5 mg/kg i.p.). Locomotor behavior was assessed, followed by euthanasia, blood collection, and brain removal. Tumor necrosis factor (TNF) α and thiobarbituric acid reactive substances (TBARS) were quantified in the serum and brain tissue, and claudin-5 was quantified in the brain. Results AMPH-injected animals exhibited increased locomotor activity. In the serum, TBARS levels were augmented in lithium-treated groups, while TNFα was not detected. In the brain, TBARS and TNFα did not differ between groups but were positively andstrongly correlated in the striatum of AMPH-injected rats. Contrary to our hypothesis, AMPH and lithium injections did not affect claudin-5 levels in the brain. Limitations The main limitations include the lack of a dynamic marker of BBB integrity and limited number of biomarkers analyzed. Conclusions This is one of the first attempts to investigate the effects of AMPH on BBB integrity, and no disruption was observed. Still, we provide rationale for future research to elucidate the importance of BBB disruption in BD, recently proposed as a marker of illness progression.en
dc.format.mimetypeapplication/pdfpt_BR
dc.language.isoengpt_BR
dc.relation.ispartofJournal of affective disorders reports. [Amsterdam]. Vol. 9 (July 2022), 100368, 7 p.pt_BR
dc.rightsOpen Accessen
dc.subjectBipolar disorderen
dc.subjectTranstorno bipolarpt_BR
dc.subjectEstresse oxidativopt_BR
dc.subjectAmphetamineen
dc.subjectLithiumen
dc.subjectBarreira hematoencefálicapt_BR
dc.subjectBlood-brain barrieren
dc.subjectAnfetaminapt_BR
dc.subjectLítiopt_BR
dc.subjectTumor necrosis factor αen
dc.subjectFatores de necrose tumoralpt_BR
dc.subjectThiobarbituric acid reactive substancesen
dc.subjectSubstâncias reativas com ácido tiobarbitúricopt_BR
dc.titleInvestigation of blood-brain barrier disruption in an animal model of mania induced by D-amphetaminept_BR
dc.typeArtigo de periódicopt_BR
dc.identifier.nrb001211145pt_BR
dc.type.originEstrangeiropt_BR


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