Does α-lipoic acid therapeutically effective against experimentally induced-acute pulpitis in rats?

MakaleYalnız künye
  • SDG 3 · Sağlık ve Kaliteli Yaşam

Özet

The purpose of the study was to investigate the therapeutic effects of α-lipoic acid (ALA) on an induced-acute pulpitis model in rats. Twenty-four Wistar albino rats were randomly divided into three groups: control, induced-acute pulpitis (PULP) and PULP + ALA groups. In the PULP and PULP + ALA groups, the crowns of the maxillary left incisors were removed horizontally. All exposed pulp tissues were treated with 5 µL LPS solution. In the PULP + ALA group, the rats were treated intraperitoneally with a single dose of ALA (100 mg/kg). The rats were sacrificed 24 h after pulp injury, and the trunk blood and pulp samples were collected and then determined using ELISA assay kits. TNF-α, IL-1β, MMP-1 and MMP-2 levels in the serum and pulp tissues were considerably higher in the PULP group than the control group (p < 0.01–0.001). In the PULP + ALA group, TNF-α, IL-1β, MMP-1 and MMP-2 levels in the serum and pulp tissues decreased significantly compared to the PULP group (p < 0.05–0.001). ALA decreases pro-inflammatory mediators and proteolytic enzymes, which might relieve acute inflammation.

Anahtar Kelimeler

RDL Kalıcı Bağlantı (PID)
https://rdlopen.rawdatalibrary.net/r/adakent/10039Resmi atıflarda kullanılan kalıcı adres
DOI
https://doi.org/10.1111/aej.12618Yayıncı resmi DOI adresi
Tam Kayıt
AlanDeğerDil
dc.contributor.authorKermeoğlu, Fatma
dc.contributor.authorSayıner, Serkan
dc.contributor.authorŞehirli, Ahmet Özer
dc.contributor.authorSavtekin, Gökçe
dc.contributor.authorAksoy, Umut
dc.date.accessioned2026-10-21T19:27:16.341206717Z
dc.date.available2026-10-21T19:27:16.341206717Z
dc.date.issued2023
dc.description.abstractThe purpose of the study was to investigate the therapeutic effects of α-lipoic acid (ALA) on an induced-acute pulpitis model in rats. Twenty-four Wistar albino rats were randomly divided into three groups: control, induced-acute pulpitis (PULP) and PULP + ALA groups. In the PULP and PULP + ALA groups, the crowns of the maxillary left incisors were removed horizontally. All exposed pulp tissues were treated with 5 µL LPS solution. In the PULP + ALA group, the rats were treated intraperitoneally with a single dose of ALA (100 mg/kg). The rats were sacrificed 24 h after pulp injury, and the trunk blood and pulp samples were collected and then determined using ELISA assay kits. TNF-α, IL-1β, MMP-1 and MMP-2 levels in the serum and pulp tissues were considerably higher in the PULP group than the control group (p < 0.01–0.001). In the PULP + ALA group, TNF-α, IL-1β, MMP-1 and MMP-2 levels in the serum and pulp tissues decreased significantly compared to the PULP group (p < 0.05–0.001). ALA decreases pro-inflammatory mediators and proteolytic enzymes, which might relieve acute inflammation.
dc.identifier.doi10.1111/aej.12618
dc.identifier.endpage91
dc.identifier.issn1329-1947
dc.identifier.issue1
dc.identifier.pmid35290687
dc.identifier.scopus2-s2.0-85126217066
dc.identifier.startpage87
dc.identifier.urihttps://rdlopen.rawdatalibrary.net/r/adakent/10039
dc.identifier.volume49
dc.language.isoen
dc.publisherJohn Wiley and Sons Inc
dc.relation.ispartofAustralian Endodontic Journal
dc.rightsinfo:eu-repo/semantics/closedAccess
dc.subjectIL-1β
dc.subjectMMPs
dc.subjectpulpitis
dc.subjectTNF-α
dc.subjectα-lipoic acid
dc.subject.otherAnimals
dc.subject.otherMatrix Metalloproteinase 1
dc.subject.otherMatrix Metalloproteinase 2
dc.subject.otherPulpitis
dc.subject.otherRats
dc.subject.otherRats, Wistar
dc.subject.otherThioctic Acid
dc.subject.otherTumor Necrosis Factor-alpha
dc.subject.othergelatinase A
dc.subject.otherinterstitial collagenase
dc.subject.othertumor necrosis factor
dc.subject.otheranimal
dc.subject.otherrat
dc.subject.otherWistar rat
dc.titleDoes α-lipoic acid therapeutically effective against experimentally induced-acute pulpitis in rats?
dc.typeArticle
dspace.entity.typePublication
rdl.citation.openalex7
rdl.citation.scopus6
rdl.oa.statusclosed
rdl.sdgSDG03
rdl.source.indexSCOPUS
rdl.source.indexPUBMED