Stress-associated ovarian damage, infertility, and delay in achieving pregnancy and treatment options; [Daño ovárico, infertilidad y retraso en la concepción relacionados con el estrés y opciones de tratamiento]

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Many types of stress, including psychological stress, negatively affect reproductive health. This study aimed to investigate the effects of sertraline (a selective serotonin reuptake inhibitor), cerebrolysin (neuroprotective/neurotrophic), and a combination of both against stress-induced ovarian damage, infertility and pregnancy delay in female rats. The rats were divided into five groups (n=14/each group) as healthy (HG), stress control (StC), stress+sertraline (SS), stress+cerebrolysin (SC), and stress+sertraline+cerebrolysin (SSC). To induce stress, animals (except the HG) were kept in a supine position with their forelimbs and hindlimbs (FIM) tied for one hour. Then, sertraline (20mg/kg) was given orally to the SS. Cerebrolysin (2.5ml/kg) was injected into the SC subcutaneously. Sertraline+cerebrolysin was administered to SSC with the same methods and doses. FIM and drug administration continued for 30 days. Six rats from each group were euthanized with high-dose anesthesia, right and left ovarian tissues were removed, and tissues were examined biochemically and histopathologically. The remaining rats were taken for breeding. Exposure to stress in rats caused an increase in malondialdehyde (MDA), tumor necrosis factor-alpha (TNF-α), interleukin-1β (IL-1β), and interleukin-6 (IL-6) levels and a decrease in total glutathione (tGSH). Stress was related to histopathological damage, infertility, and delayed birth. The sertraline and cerebrolysin combination was the most effective in preventing these changes, with sertraline and cerebrolysin alone in second and third places, respectively. Regarding efficacy, selective serotonin reuptake inhibitors (SSRIs) and related drugs may be beneficial in treating stress-related ovarian damage, infertility, and delay in pregnancy. © 2023, Instituto de Investigaciones Clinicas. All rights reserved.

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RDL Kalıcı Bağlantı (PID)
https://rdlopen.rawdatalibrary.net/r/ebyu/12143Resmi atıflarda kullanılan kalıcı adres
DOI
https://doi.org/10.54817/ic.v64n4a8Yayıncı resmi DOI adresi
Tam Kayıt
AlanDeğerDil
dc.contributor.authorAynaoglu Yildiz, Gulsah
dc.contributor.authorYapca, Omer Erkan
dc.contributor.authorDinc, Kemal
dc.contributor.authorGursul, Cebrail
dc.contributor.authorGundogdu, Betul
dc.contributor.authorAktas, Mehmet
dc.contributor.authorSuleyman, Zeynep
dc.contributor.authorBulut, Seval
dc.contributor.authorSuleyman, Halis
dc.date.accessioned2026-10-18T20:27:05.133641525Z
dc.date.available2026-10-18T20:27:05.133641525Z
dc.date.issued2023
dc.description.abstractMany types of stress, including psychological stress, negatively affect reproductive health. This study aimed to investigate the effects of sertraline (a selective serotonin reuptake inhibitor), cerebrolysin (neuroprotective/neurotrophic), and a combination of both against stress-induced ovarian damage, infertility and pregnancy delay in female rats. The rats were divided into five groups (n=14/each group) as healthy (HG), stress control (StC), stress+sertraline (SS), stress+cerebrolysin (SC), and stress+sertraline+cerebrolysin (SSC). To induce stress, animals (except the HG) were kept in a supine position with their forelimbs and hindlimbs (FIM) tied for one hour. Then, sertraline (20mg/kg) was given orally to the SS. Cerebrolysin (2.5ml/kg) was injected into the SC subcutaneously. Sertraline+cerebrolysin was administered to SSC with the same methods and doses. FIM and drug administration continued for 30 days. Six rats from each group were euthanized with high-dose anesthesia, right and left ovarian tissues were removed, and tissues were examined biochemically and histopathologically. The remaining rats were taken for breeding. Exposure to stress in rats caused an increase in malondialdehyde (MDA), tumor necrosis factor-alpha (TNF-α), interleukin-1β (IL-1β), and interleukin-6 (IL-6) levels and a decrease in total glutathione (tGSH). Stress was related to histopathological damage, infertility, and delayed birth. The sertraline and cerebrolysin combination was the most effective in preventing these changes, with sertraline and cerebrolysin alone in second and third places, respectively. Regarding efficacy, selective serotonin reuptake inhibitors (SSRIs) and related drugs may be beneficial in treating stress-related ovarian damage, infertility, and delay in pregnancy. © 2023, Instituto de Investigaciones Clinicas. All rights reserved.
dc.identifier.doi10.54817/ic.v64n4a8
dc.identifier.eissn2477-9393
dc.identifier.endpage523
dc.identifier.issn0535-5133
dc.identifier.issue4
dc.identifier.scopus2-s2.0-85177433104
dc.identifier.startpage513
dc.identifier.urihttps://rdlopen.rawdatalibrary.net/r/ebyu/12143
dc.identifier.volume64
dc.identifier.wosWOS:001141594300009
dc.language.isoen
dc.publisherInstituto de Investigaciones Clinicas
dc.relation.ispartofInvestigacion Clinica (Venezuela)
dc.rightsinfo:eu-repo/semantics/openAccess
dc.subjectcerebrolysin
dc.subjectovarian damage
dc.subjectrats
dc.subjectsertraline
dc.subjectstress
dc.subjectglutathione
dc.subjectinterleukin 1beta
dc.subjectinterleukin 6
dc.subjectmalonaldehyde
dc.subjectthiopental
dc.subjecttumor necrosis factor
dc.subjectanimal experiment
dc.subjectanimal model
dc.subjectanimal tissue
dc.subjectArticle
dc.subjectcontrolled study
dc.subjectemotional stress
dc.subjectenzyme linked immunosorbent assay
dc.subjectfemale
dc.subjectforelimb
dc.subjecthindlimb
dc.subjectinfertility
dc.subjectnonhuman
dc.subjectovary disease
dc.subjectovary tissue
dc.subjectoxidative stress
dc.subjectphysiological stress
dc.subjectpregnancy
dc.subjectrat
dc.subjectreproductive health
dc.titleStress-associated ovarian damage, infertility, and delay in achieving pregnancy and treatment options; [Daño ovárico, infertilidad y retraso en la concepción relacionados con el estrés y opciones de tratamiento]
dc.typeArticle
dspace.entity.typePublication
rdl.citation.scopus2
rdl.citation.wos2
rdl.source.indexSCOPUS
rdl.source.indexWOS
rdl.wos.indexScience Citation Index Expanded (SCI-EXPANDED)