Effects of umbelliferone isolated from the Ferulago pauciradiata Boiss. & Heldr. Plant on cecal ligation and puncture-induced sepsis model in rats

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Özet

Sepsis is a pathophysiological event involving systemic inflammatory response syndrome, multiple organ failure syndromes, and tissue damage. Overproduction of free radicals as a result of tissue damage during sepsis contributes to cellular toxicity, organ failure, and even mortality. Antioxidants, which scavenge free radicals, play a protective role against various diseases. Previous studies have shown that umbelliferone (UF) has antioxidant and anti-inflammatory effects. Since oxidative stress is naturally associated with sepsis-induced organ dysfunction, the application of antioxidant compounds could potentially illuminate the pathophysiology of sepsis, which does not yet have an effective treatment. The sepsis model induced by cecal ligation and puncture (CLP) was applied to rats. Different doses of UF (10░mg/kg, 20░mg/kg, and 40░mg/kg) on oxidant-antioxidant in septic rats, mRNA of inflammatory mediators such as tumor necrosis factor- α (TNF-α) and interleukin (IL)-1 its effects on expression levels were evaluated in lung, kidney, and liver tissues. When the lung, kidney, and liver tissues of septic rats were compared with those of the control group, it was found that UF administration increased dose-dependent superoxide dismutase activity and glutathione levels and significantly decreased malondialdehyde levels. The effects of UF administration on oxidative parameters were dose-dependent. The 40░mg/kg UF dose showed greater anti-oxidative properties than the 20░mg/kg and 10░mg/kg doses for all the evaluated parameters. Further, the TNF- α mRNA expression of the CLP +40░mg/kg group was reduced to a level comparable to that of the control group. UF has been found to be an effective molecule in reducing oxidative stress by supporting endogenous antioxidants and enhancing the scavenging effects of free radicals. The potent antioxidant property of UF may also be related to the suppression of the cytokine cascade during sepsis. The results suggest that UF administration may represent a new treatment for the prevention of lung, kidney and liver damage caused by septic conditions.

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dc.contributor.authorKutlu, Z.
dc.contributor.authorCelik, M.
dc.contributor.authorBilen, A.
dc.contributor.authorHalıcı, Z.
dc.contributor.authorYıldırım, S.
dc.contributor.authorKarabulut, S.
dc.contributor.authorKarakaya, S.
dc.contributor.authorBostanlık, Delimustafaoğlu F.
dc.contributor.authorAydın, P.
dc.date.accessioned2026-10-29T19:09:03.832659906Z
dc.date.available2026-10-29T19:09:03.832659906Z
dc.date.issued2020
dc.description.abstractSepsis is a pathophysiological event involving systemic inflammatory response syndrome, multiple organ failure syndromes, and tissue damage. Overproduction of free radicals as a result of tissue damage during sepsis contributes to cellular toxicity, organ failure, and even mortality. Antioxidants, which scavenge free radicals, play a protective role against various diseases. Previous studies have shown that umbelliferone (UF) has antioxidant and anti-inflammatory effects. Since oxidative stress is naturally associated with sepsis-induced organ dysfunction, the application of antioxidant compounds could potentially illuminate the pathophysiology of sepsis, which does not yet have an effective treatment. The sepsis model induced by cecal ligation and puncture (CLP) was applied to rats. Different doses of UF (10░mg/kg, 20░mg/kg, and 40░mg/kg) on oxidant-antioxidant in septic rats, mRNA of inflammatory mediators such as tumor necrosis factor- α (TNF-α) and interleukin (IL)-1 its effects on expression levels were evaluated in lung, kidney, and liver tissues. When the lung, kidney, and liver tissues of septic rats were compared with those of the control group, it was found that UF administration increased dose-dependent superoxide dismutase activity and glutathione levels and significantly decreased malondialdehyde levels. The effects of UF administration on oxidative parameters were dose-dependent. The 40░mg/kg UF dose showed greater anti-oxidative properties than the 20░mg/kg and 10░mg/kg doses for all the evaluated parameters. Further, the TNF- α mRNA expression of the CLP +40░mg/kg group was reduced to a level comparable to that of the control group. UF has been found to be an effective molecule in reducing oxidative stress by supporting endogenous antioxidants and enhancing the scavenging effects of free radicals. The potent antioxidant property of UF may also be related to the suppression of the cytokine cascade during sepsis. The results suggest that UF administration may represent a new treatment for the prevention of lung, kidney and liver damage caused by septic conditions.
dc.identifier.articlenumber110206
dc.identifier.doi10.1016/j.biopha.2020.110206
dc.identifier.eissn1950-6007
dc.identifier.issn0753-3322
dc.identifier.pmid32407990
dc.identifier.scopus2-s2.0-85084377191
dc.identifier.urihttps://rdlopen.rawdatalibrary.net/r/bayburt/11997
dc.identifier.volume127
dc.identifier.wosWOS:000543493200087
dc.language.isoen
dc.publisherElsevier Masson SAS
dc.relation.ispartofBiomedicine and Pharmacotherapy
dc.rightsinfo:eu-repo/semantics/openAccess
dc.subjectAntioxidant
dc.subjectCLP
dc.subjectIL-1
dc.subjectTNF-α
dc.subjectUmbelliferone
dc.subject.classificationMedicine, Research & Experimental
dc.subject.classificationPharmacology & Pharmacy
dc.subject.classificationResearch & Experimental Medicine
dc.subject.otherAnimals
dc.subject.otherAntioxidants
dc.subject.otherApiaceae
dc.subject.otherCytokines
dc.subject.otherDisease Models, Animal
dc.subject.otherDose-Response Relationship, Drug
dc.subject.otherFree Radical Scavengers
dc.subject.otherOxidative Stress
dc.subject.otherRats
dc.subject.otherRats, Wistar
dc.subject.otherSepsis
dc.subject.otherUmbelliferones
dc.subject.otherglutathione
dc.subject.otherinterleukin 1
dc.subject.othermalonaldehyde
dc.subject.othermessenger RNA
dc.subject.othersuperoxide dismutase
dc.subject.othertumor necrosis factor
dc.subject.otherumbelliferone
dc.subject.otherantioxidant
dc.subject.othercytokine
dc.subject.otherscavenger
dc.subject.otherumbelliferone derivative
dc.subject.otheranimal experiment
dc.subject.otheranimal model
dc.subject.otheranimal tissue
dc.subject.otherantioxidant activity
dc.subject.othercecal ligation and puncture-induced sepsis
dc.subject.othercontrolled study
dc.subject.otherdose response
dc.subject.otherenzyme activity
dc.subject.otherFerulago pauciradiata
dc.subject.otherhistopathology
dc.subject.otherimmunohistochemistry
dc.subject.otherkidney tissue
dc.subject.otherlipid peroxidation
dc.subject.otherliver tissue
dc.subject.otherlung parenchyma
dc.subject.othermRNA expression level
dc.subject.othernonhuman
dc.subject.otherpriority journal
dc.subject.otherrat
dc.subject.otherReview
dc.subject.otheranimal
dc.subject.otherchemistry
dc.subject.otherdisease model
dc.subject.otherdrug effect
dc.subject.otherisolation and purification
dc.subject.othermetabolism
dc.subject.otherpathophysiology
dc.subject.otherWistar rat
dc.titleEffects of umbelliferone isolated from the Ferulago pauciradiata Boiss. & Heldr. Plant on cecal ligation and puncture-induced sepsis model in rats
dc.typeReview Article
rdl.citation.openalex23
rdl.citation.scopus22
rdl.citation.wos21
rdl.departmentDepartment of Biochemistry, Faculty of Pharmacy, Atatürk University, Erzurum, 25240, Turkey
rdl.departmentDepartment of Biochemistry, Faculty of Medicine, Atatürk University, Erzurum, 25240, Turkey
rdl.departmentDepartment of Internal Medicine, Faculty of Medicine, Atatürk University, Erzurum, 25240, Turkey
rdl.departmentFaculty of Medicine, Department of Pharmacology, Atatürk University, Erzurum, 25240, Turkey
rdl.departmentClinical Research, Development and Design Application and Research Center, Ataturk University, 25240, Erzurum, Turkey
rdl.departmentDepartment of Pathology, Faculty of Veterinary Medicine, Ataturk University, Erzurum, 25240, Turkey
rdl.departmentHealth Services Vocational School, Bayburt University, Bayburt, 69000, Turkey
rdl.departmentDepartment of Pharmacognosy, Faculty of Pharmacy, Ataturk University, Erzurum, 25240, Turkey
rdl.departmentDepartment of Pharmaceutical Botany, Faculty of Pharmacy, Ankara University, Ankara, 06000, Turkey
rdl.departmentDepartment of Anesthesia, Regional Education and Research Hospital, Erzurum, 25240, Turkey
rdl.oa.statusgold
rdl.oa.urlhttps://doi.org/10.1016/j.biopha.2020.110206
rdl.scopus.quartileQ1
rdl.sdgSDG03
rdl.source.indexSCOPUS
rdl.source.indexWOS
rdl.source.indexPUBMED
rdl.wos.indexScience Citation Index Expanded (SCI-EXPANDED)