Can amniotic fluid protect developing fetal lungs against the harmful effects of oxidative stress?

ArticleAçık Erişim

Özet

Background/aim: Preterm births cause fetuses to be born without completing the development of their organs. Due to this undesirable situation, it is the pulmonary tissue which has to be most exposed to harmful effects of extrauterine environment. Early disappearance of the prophylactic and constructive effects of amniotic fluid (AF) on developing tissues, such as pulmonary tissue, facilitates the formation of pulmonary morbidities resulting from oxygen. Setting out from this knowledge, we wanted, in addition to assessing the beneficent effects of AF on pulmonary tissue, to study the importance of AF in morbidities of this tissue thought to originate from oxygen. Materials and methods: In this experimental study, while the study group was made up of the fetuses of pregnant rats exposed to hyperbaric oxygen, (hyperoxic pregnant rat fetuses-HPRF), the control group was formed of the fetuses of the rats pregnant in the usual room setting (normoxic pregnant rat fetuses-NPRF). The pulmonary and hepatic tissues taken from the fetuses of these pregnant rats on the 21st day of their pregnancy were compared biochemically and histologically. For biochemical assessment, total glutathione (tGSH), catalase (CAT), malondialdehyde (MDA), tumor necrosis factor-alpha (TNF-α) values and for histopathological assessment, apoptosis, alveolar wall count (AWC), vena centralis count (VCC) were included. Results: Statistical significance was found in the pulmonary tissue values of tGSH on behalf of NPRF, and MDA on behalf of HPRF (p < 0.05). In liver tissue, statistical significance was detected in tGSH and CAT values in favor of NPRF and in MDA, and TNF-α values in favor of HPRF (p < 0.05). Conclusion: Our study has demonstrated that AF protects the pulmonary tissue from the harmful effects of oxygen in the intrauterine period. In addition, our data have suggested that the pulmonary tissue’s being deprived of the useful effects of AF owing to premature birth may be an important trigger in the occurrence of the pulmonary morbidities thought to result from oxygen. © TÜBİTAK.

Anahtar Kelimeler

RDL Kalıcı Bağlantı (PID)
https://rdlopen.rawdatalibrary.net/r/ebyu/12160Resmi atıflarda kullanılan kalıcı adres
DOI
https://doi.org/10.55730/1300-0144.5564Yayıncı resmi DOI adresi
Tam Kayıt
AlanDeğerDil
dc.contributor.authorKorkmaz, Levent
dc.contributor.authorAlan, Cumali
dc.contributor.authorTopal, İsmail
dc.contributor.authorTayfur, Mahir
dc.contributor.authorBozkurt, Ali Seydi
dc.contributor.authorGürsul, Cebrail
dc.contributor.authorBaştuğ, Osman
dc.date.accessioned2026-10-18T20:27:05.865189986Z
dc.date.available2026-10-18T20:27:05.865189986Z
dc.date.issued2023
dc.description.abstractBackground/aim: Preterm births cause fetuses to be born without completing the development of their organs. Due to this undesirable situation, it is the pulmonary tissue which has to be most exposed to harmful effects of extrauterine environment. Early disappearance of the prophylactic and constructive effects of amniotic fluid (AF) on developing tissues, such as pulmonary tissue, facilitates the formation of pulmonary morbidities resulting from oxygen. Setting out from this knowledge, we wanted, in addition to assessing the beneficent effects of AF on pulmonary tissue, to study the importance of AF in morbidities of this tissue thought to originate from oxygen. Materials and methods: In this experimental study, while the study group was made up of the fetuses of pregnant rats exposed to hyperbaric oxygen, (hyperoxic pregnant rat fetuses-HPRF), the control group was formed of the fetuses of the rats pregnant in the usual room setting (normoxic pregnant rat fetuses-NPRF). The pulmonary and hepatic tissues taken from the fetuses of these pregnant rats on the 21st day of their pregnancy were compared biochemically and histologically. For biochemical assessment, total glutathione (tGSH), catalase (CAT), malondialdehyde (MDA), tumor necrosis factor-alpha (TNF-α) values and for histopathological assessment, apoptosis, alveolar wall count (AWC), vena centralis count (VCC) were included. Results: Statistical significance was found in the pulmonary tissue values of tGSH on behalf of NPRF, and MDA on behalf of HPRF (p < 0.05). In liver tissue, statistical significance was detected in tGSH and CAT values in favor of NPRF and in MDA, and TNF-α values in favor of HPRF (p < 0.05). Conclusion: Our study has demonstrated that AF protects the pulmonary tissue from the harmful effects of oxygen in the intrauterine period. In addition, our data have suggested that the pulmonary tissue’s being deprived of the useful effects of AF owing to premature birth may be an important trigger in the occurrence of the pulmonary morbidities thought to result from oxygen. © TÜBİTAK.
dc.identifier.doi10.55730/1300-0144.5564
dc.identifier.eissn1303-6165
dc.identifier.endpage120
dc.identifier.issn1300-0144
dc.identifier.issue1
dc.identifier.pmcidPMC10387876
dc.identifier.pmid36945927
dc.identifier.scopus2-s2.0-85149124585
dc.identifier.startpage109
dc.identifier.urihttps://rdlopen.rawdatalibrary.net/r/ebyu/12160
dc.identifier.volume53
dc.identifier.wosWOS:000941667500014
dc.language.isoen
dc.publisherTurkiye Klinikleri
dc.relation.ispartofTurkish Journal of Medical Sciences
dc.rightsinfo:eu-repo/semantics/openAccess
dc.subjectAmniotic fluid
dc.subjectbronchopulmonary dysplasia
dc.subjecthyperbaric oxygen
dc.subjectoxidative stress
dc.subjectAnimals
dc.subjectFemale
dc.subjectHumans
dc.subjectLung
dc.subjectOxygen
dc.subjectPregnancy
dc.subjectPremature Birth
dc.subjectRats
dc.subjectTumor Necrosis Factor-alpha
dc.subjectcaspase 3
dc.subjectcysteine aspartyl protease
dc.subjectglutathione
dc.subjectglutathione peroxidase
dc.subjectheparin
dc.subjectmalonaldehyde
dc.subjecttumor necrosis factor
dc.subjectunclassified drug
dc.subjectxylazine
dc.subjectamnion fluid
dc.subjectanimal experiment
dc.subjectanimal model
dc.subjectanimal tissue
dc.subjectapoptosis
dc.subjectArticle
dc.subjectbiochemical analysis
dc.subjectcentrifugation
dc.titleCan amniotic fluid protect developing fetal lungs against the harmful effects of oxidative stress?
dc.typeArticle
dspace.entity.typePublication
rdl.citation.scopus0
rdl.citation.trdizin0
rdl.citation.wos0
rdl.departmentERZİNCAN BİNALİ YILDIRIM ÜNİVERSİTESİ
rdl.departmentT.C. SAĞLIK BAKANLIĞI
rdl.oa.statusgold
rdl.source.indexSCOPUS
rdl.source.indexWOS
rdl.source.indexTRDIZIN
rdl.source.indexPUBMED
rdl.wos.indexScience Citation Index Expanded (SCI-EXPANDED)