Nephrectomy Does not Exacerbate Cancellous Bone loss in Thalassemic Mice.


Journal

Scientific reports
ISSN: 2045-2322
Titre abrégé: Sci Rep
Pays: England
ID NLM: 101563288

Informations de publication

Date de publication:
08 05 2020
Historique:
received: 19 09 2019
accepted: 20 04 2020
entrez: 10 5 2020
pubmed: 10 5 2020
medline: 2 12 2020
Statut: epublish

Résumé

Patients with β-thalassemia have an increased risk of developing chronic kidney disease which is associated with osteoporosis and periodontitis. The purpose of this study was to evaluate mandibular and femoral bone change in heterozygous β-globin knockout (BKO) mice following 5/6 nephrectomy (Nx). Female and male BKO mouse blood smears demonstrated microcytic hypochromic anemia. Serum urea nitrogen, creatinine, calcium, and phosphorus levels were not changed in BKO mice. Nx increased the serum levels of urea nitrogen in both wild type (WT) and BKO mice and the level was much higher in BKO males. Serum level of creatinine was increased in Nx WT but not BKO mice. However, serum calcium and phosphorus levels were not altered. Nx induced comparable renal fibrosis in BKO mice and WT controls. Bone loss was observed in mandibular cancellous bone but not cortical bone of both male and female BKO mice. Nx decreased cancellous bone volume and cortical thickness in WT. Interestingly, BKO mice were resistant to Nx-induced cancellous bone loss. However, cortical thickness and cortical bone mineral density were reduced in Nx male BKO mice. Nx increased mRNA levels of type I collagen, Osx and Trap in WT but not BKO mice. Similarly, Nx reduced cancellous bone volume in femurs and increased osteoblast number and osteoclast number in WT not BKO mice. Serum FGF23 and erythropoietin levels were markedly increased in BKO mice. Nx decreased serum erythropoietin but not FGF23 levels. Since WT treated with erythropoietin exhibited a significant reduction in cancellous bone volume, it was possible that lower level of erythropoietin in Nx BKO mice prevented the Nx-induced cancellous bone loss.

Identifiants

pubmed: 32385316
doi: 10.1038/s41598-020-64681-2
pii: 10.1038/s41598-020-64681-2
pmc: PMC7210954
doi:

Substances chimiques

Biomarkers 0
Fgf23 protein, mouse 0
Fibroblast Growth Factor-23 7Q7P4S7RRE
Nitrogen N762921K75

Types de publication

Journal Article Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

7786

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Auteurs

Sutada Lotinun (S)

Department of Physiology, Faculty of Dentistry, Chulalongkorn University, Bangkok, Thailand. sutada.l@chula.ac.th.
Skeletal Disorders Research Unit, Faculty of Dentistry, Chulalongkorn University, Bangkok, Thailand. sutada.l@chula.ac.th.

Korakot Atjanasuppat (K)

Skeletal Disorders Research Unit, Faculty of Dentistry, Chulalongkorn University, Bangkok, Thailand.

Jutatip Limsuvech (J)

Skeletal Disorders Research Unit, Faculty of Dentistry, Chulalongkorn University, Bangkok, Thailand.

Asada Leelahavanichkul (A)

Department of Microbiology, Faculty of Medicine, Chulalongkorn University, Bangkok, Thailand.

Saovaros Svasti (S)

Thalassemia Research Center, Institute of Molecular Biosciences, and Department of Biochemistry, Faculty of Science, Mahidol University, Bangkok, Thailand.

Nateetip Krishnamra (N)

Department of Physiology, Faculty of Science, Mahidol University, Bangkok, Thailand.

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