Role of adiponectin as a modulator of testicular function during aging in mice

dc.contributor.authorChoubey, Mayankpor
dc.contributor.authorRanjan, Ashutoshpor
dc.contributor.authorBora, Puran S.por
dc.contributor.authorBaltazar, Fátimapor
dc.contributor.authorMartin, Luc J.por
dc.contributor.authorKrishna, Amitabhpor
dc.date.accessioned2020-10-01T13:30:52Z
dc.date.available2020-10-01T13:30:52Z
dc.date.issued2019
dc.description.abstractThe mechanisms by which testicular functions decline with aging remain largely speculative. Our recent finding showed the importance of adiponectin in the regulation of testicular functions, whereas its concentration declines during male infertility. Thus, the aim of present study was to explore the potential role of adiponectin during aging. The changes in adiponectin, adiponectin-receptors, and insulin receptor proteins expression in the testis were evaluated and compared with the testicular parameters, mass, and testosterone level in the mice from early post-natal to late senescence period. Further, the current study has examined the effect of exogenous adiponectin treatment on testicular functions in aged mice. The results showed a significant decline in adiponectin/adiponectin-receptors expression simultaneously with a significant decline in testicular mass, insulin receptor expression and testosterone synthesis in the testis of aged mice. Exogenous treatment of adiponectin to aged mice resulted in marked improvements in testicular mass, histological features (cells proliferation), insulin receptor expression, testicular glucose uptake, anti-oxidative enzymes activity and testosterone synthesis as compared with the control. Based on these findings, it may be concluded that a marked decline in adiponectin synthesis and action results in decreased insulin sensitivity (development of insulin resistance) and increased oxidative stress which consequently suppresses testicular functions during aging. This study further showed that treatment with adiponectin ameliorates reduced testicular functions by enhanced expression of insulin receptor in the testis of senescent mice. It is thus hypothesized that systemic adiponectin treatment could be a promising therapeutic strategy for improvement of testosterone production and sperm counts during aging.por
dc.description.sponsorshipMayank Choubey greatly acknowledges financial assistance in the form of a Senior Research Fellowship (SRF) from Indian Council of Medical Research (ICMR File No. RBMH/FW/2018/1), New Delhi, India. This work was also supported by University Grant Commission (UGC), New Delhi and Centre of Advanced Study, Department of Zoology, Institute of Science, Banaras Hindu University, Varanasi, India.por
dc.distributioninternationalpor
dc.identifier.doi10.1016/j.bbadis.2018.11.019por
dc.identifier.eissn1879-260X
dc.identifier.issn0925-4439
dc.identifier.pmid30471430por
dc.identifier.urihttps://hdl.handle.net/1822/67193
dc.language.isoengpor
dc.peerreviewedyespor
dc.publisherElsevierpor
dc.relationRBMH/FW/2018/1por
dc.rightsopenAccesspor
dc.subjectAdiponectinpor
dc.subjectAgingpor
dc.subjectAnimalspor
dc.subjectAnimals, Newbornpor
dc.subjectAntioxidantspor
dc.subjectApoptosispor
dc.subjectBiomarkerspor
dc.subjectBlood Glucosepor
dc.subjectBody Weightpor
dc.subjectCaspase 3por
dc.subjectCell Proliferationpor
dc.subjectCell Survivalpor
dc.subjectExtracellular Signal-Regulated MAP Kinasespor
dc.subjectLipid Peroxidationpor
dc.subjectMalepor
dc.subjectMicepor
dc.subjectModels, Biologicalpor
dc.subjectOrgan Sizepor
dc.subjectPhosphorylationpor
dc.subjectProliferating Cell Nuclear Antigenpor
dc.subjectProto-Oncogene Proteins c-bcl-2por
dc.subjectReceptor, Insulinpor
dc.subjectReceptors, Adiponectinpor
dc.subjectSignal Transductionpor
dc.subjectTestispor
dc.subjectTestosteronepor
dc.subjectSenescencepor
dc.subjectMetabolismpor
dc.subjectOxidative-stresspor
dc.subject.wosScience & Technologypor
dc.titleRole of adiponectin as a modulator of testicular function during aging in micepor
dc.typearticlepor
dspace.entity.typePublicationen
oaire.citationEndPage427por
oaire.citationIssue2por
oaire.citationStartPage413por
oaire.citationVolume1865por
sdum.journalBiochimica et Biophysica Acta. Molecular Basis of Diseasepor

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