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Adenine-induced chronic kidney disease induces a similar skeletal phenotype in male and female C57BL/6 mice with more severe deficits in cortical bone properties of male mice.

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  • معلومة اضافية
    • المصدر:
      Publisher: Public Library of Science Country of Publication: United States NLM ID: 101285081 Publication Model: eCollection Cited Medium: Internet ISSN: 1932-6203 (Electronic) Linking ISSN: 19326203 NLM ISO Abbreviation: PLoS One Subsets: MEDLINE
    • بيانات النشر:
      Original Publication: San Francisco, CA : Public Library of Science
    • الموضوع:
    • نبذة مختصرة :
      Competing Interests: The authors have declared that no competing interest exist.
      Chronic kidney disease (CKD) causes bone loss, particularly in cortical bone, through formation of cortical pores which lead to skeletal fragility. Animal models of CKD have shown variability in the skeletal response to CKD between males and females suggesting sex may play a role in this variation. Our aim was to compare the impact of adenine-induced CKD on cortical parameters in skeletally mature male and female C57Bl/6 mice. After 10-weeks of adenine-induced CKD, both male and female adenine mice had high serum parathyroid hormone (PTH), high bone turnover, and cortical porosity compared to non-CKD controls. Both sexes had lower cortical thickness, but only male mice had lower cortical bone area. CKD imparted greater deficits in mechanical properties of male mice compared to female mice. These data demonstrate that both male and female mice develop high PTH/high bone turnover in response to adenine-induced CKD and that cortical bone phenotypes are slightly more severe in males, particularly in mechanical properties deficits.
    • References:
      BMC Nephrol. 2014 May 03;15:69. (PMID: 24885705)
      Bone. 1993 Jul-Aug;14(4):595-608. (PMID: 8274302)
      Kidney Int. 2014 Oct;86(4):810-8. (PMID: 24429401)
      Osteoporos Int. 2013 May;24(5):1721-32. (PMID: 23100118)
      Am J Physiol Renal Physiol. 2014 Dec 1;307(11):F1169-78. (PMID: 25209863)
      Biomed Res Int. 2017;2017:2159739. (PMID: 29181390)
      J Bone Miner Res. 2016 Oct;31(10):1803-1809. (PMID: 27145189)
      JCI Insight. 2019 Feb 21;4(4):. (PMID: 30830862)
      BMC Nephrol. 2013 May 30;14:116. (PMID: 23718816)
      Kidney Int. 2000 Jul;58(1):396-9. (PMID: 10886587)
      Sci Rep. 2019 May 28;9(1):7936. (PMID: 31138895)
      Kidney Int. 2009 Jan;75(2):176-84. (PMID: 18800026)
      Nephrol Dial Transplant. 2013 May;28(5):1140-9. (PMID: 23345625)
      PLoS One. 2015 Apr 13;10(4):e0121705. (PMID: 25874794)
      Bone. 2021 Feb;143:115632. (PMID: 32927105)
      Kidney Int. 2015 Nov;88(5):950-7. (PMID: 26221752)
      Kidney Int. 2014 Jan;85(1):166-73. (PMID: 23903367)
      J Bone Miner Res. 2013 Jan;28(1):2-17. (PMID: 23197339)
      N Engl J Med. 2004 Sep 23;351(13):1296-305. (PMID: 15385656)
      J Bone Miner Res. 2011 Jun;26(6):1368-76. (PMID: 21611975)
      Bone. 2019 Aug;125:16-24. (PMID: 31059864)
      Endocr J. 2006 Jun;53(3):407-13. (PMID: 16723811)
      Calcif Tissue Int. 2020 Apr;106(4):392-400. (PMID: 31832725)
      J Bone Miner Res. 1998 Aug;13(8):1213-20. (PMID: 9718188)
      J Bone Miner Metab. 2017 Sep;35(5):513-521. (PMID: 27830383)
      Curr Opin Nephrol Hypertens. 2019 Jan;28(1):1-9. (PMID: 30320621)
      Osteoporos Int. 2014 Jan;25(1):159-65. (PMID: 23835863)
      J Bone Miner Res. 2013 Aug;28(8):1811-20. (PMID: 23456850)
      J Bone Miner Res. 2014 Apr;29(4):902-10. (PMID: 24038306)
      Sci Rep. 2017 May 22;7(1):2233. (PMID: 28533541)
    • Grant Information:
      F32 DK122731 United States DK NIDDK NIH HHS
    • الرقم المعرف:
      0 (Parathyroid Hormone)
      JAC85A2161 (Adenine)
    • الموضوع:
      Date Created: 20210423 Date Completed: 20210929 Latest Revision: 20210929
    • الموضوع:
      20250114
    • الرقم المعرف:
      PMC8064570
    • الرقم المعرف:
      10.1371/journal.pone.0250438
    • الرقم المعرف:
      33891630