Hyperbaric oxygen therapy improves age induced bone dyshomeostasis in non-obese and obese conditions

dc.contributor.authorImerb N.
dc.contributor.authorThonusin C.
dc.contributor.authorPratchayasakul W.
dc.contributor.authorArunsak B.
dc.contributor.authorNawara W.
dc.contributor.authorAeimlapa R.
dc.contributor.authorCharoenphandhu N.
dc.contributor.authorChattipakorn N.
dc.contributor.authorChattipakorn S.C.
dc.contributor.otherMahidol University
dc.date.accessioned2023-06-18T16:47:55Z
dc.date.available2023-06-18T16:47:55Z
dc.date.issued2022-04-15
dc.description.abstractAims: To investigate the effects of hyperbaric oxygen therapy (HBOT) on metabolic disturbance, aging and bone remodeling in D-galactose-induced aging rats with and without obesity by determining the metabolic parameters, aging and oxidative stress markers, bone turnover markers, bone microarchitecture, and bone biomechanical strength. Materials and methods: Male Wistar rats were fed either a normal diet (ND; n = 18) or a HFD (n = 12) for 22 weeks. At week 13, vehicle (0.9% NaCl) was injected into ND-fed rats (NDV; n = 6), while 150 mg/kg/day of D-galactose was injected into 12 ND-fed rats (NDD) and 12 HFD-fed rats (HFDD) for 10 weeks. At week 21, rats were treated with either sham (NDVS, NDDS, or HFDDS; n = 6/ group) or HBOT (NDDH, or HFDDH; n = 6/group) for 14 days. Rats were then euthanized. Blood samples, femora, and tibiae were collected. Key findings: Both NDD and HFDD groups developed aging as indicated by increased AGE level, increased inflammation and oxidative stress as shown by raised serum TNF-α and MDA levels, impaired bone remodeling as indicated by an increase in levels of CTX-1, TRACP-5b, and impaired bone structure/strength, when compared with those of the NDVS group. HFD aggravated these indicators of bone dyshomeostasis in D-galactose-treated rats. HBOT restored bone remodeling and bone structure/strength in the NDD group, however HBOT ameliorated bone dyshomeostasis in the HFDD group. Significance: HBOT is a potential intervention to decrease the risk of osteoporosis and bone fracture in aging with or without obesity.
dc.identifier.citationLife Sciences Vol.295 (2022)
dc.identifier.doi10.1016/j.lfs.2022.120406
dc.identifier.eissn18790631
dc.identifier.issn00243205
dc.identifier.pmid35182555
dc.identifier.scopus2-s2.0-85124751261
dc.identifier.urihttps://repository.li.mahidol.ac.th/handle/20.500.14594/83758
dc.rights.holderSCOPUS
dc.subjectBiochemistry, Genetics and Molecular Biology
dc.titleHyperbaric oxygen therapy improves age induced bone dyshomeostasis in non-obese and obese conditions
dc.typeArticle
mu.datasource.scopushttps://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=85124751261&origin=inward
oaire.citation.titleLife Sciences
oaire.citation.volume295
oairecerif.author.affiliationFaculty of Medicine, Chiang Mai University
oairecerif.author.affiliationMahidol University
oairecerif.author.affiliationInstitute of Molecular Biosciences, Mahidol University
oairecerif.author.affiliationChiang Mai University
oairecerif.author.affiliationAcademy of Science

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