Matches in SemOpenAlex for { <https://semopenalex.org/work/W2017393472> ?p ?o ?g. }
- W2017393472 endingPage "1788" @default.
- W2017393472 startingPage "1781" @default.
- W2017393472 abstract "This study aimed to delineate the mechanism involved in type 1 diabetes-induced bone loss. The results revealed the alteration of vitamin D metabolic enzyme expression and the downregulation of renal calcium transporter abundance in type 1 diabetic mice. The purpose of this study was to investigate the changes of the expression of vitamin D metabolic enzymes and transcellular calcium-transporting proteins in kidneys from mice with experimentally induced diabetes. Male DBA/2J mice were injected with either vehicle (control) or streptozotocin (STZ) daily for five consecutive days. Bone mineral density was measured by peripheral quantitative computerized tomography, and bone histomorphology was analyzed by Safranin O staining. Real-time PCR and Western blotting were applied to determine the expression of target genes and proteins. Type 1 diabetes produced high urinary calcium excretion and loss of trabecular bone measured at the proximal metaphysis of the tibia and the distal femur. Bone loss was associated with deterioration of trabecular bone microstructure. Quantified PCR results showed that mRNA expression level in the kidney of diabetic mice for 25-hydroxyvitamin D-24-hydroxylase was downregulated at week 10, while those for 25-hydroxyvitamin D-1α-hydroxylase were upregulated at week 20. In addition, mRNA expression levels for renal transient receptor potential V6, plasma membrane Ca-ATPase (PMCA)1b, and vitamin D receptor (VDR) genes were decreased in STZ-treated mice. Western blot analysis showed that protein expression of PMCA1b and VDR was significantly decreased in kidneys from STZ-treated mice compared to that of controls. The limitation in this study is the lack of vitamin D, parathyroid hormone, and phosphorus levels in serum. However, the present study supports the conclusion that the underlying mechanism contributing to type 1 diabetes-associated bone loss may be alterations of vitamin D metabolic enzyme expression and associated decreases in expression of renal calcium transporters." @default.
- W2017393472 created "2016-06-24" @default.
- W2017393472 creator A5024194480 @default.
- W2017393472 creator A5073279162 @default.
- W2017393472 creator A5076081554 @default.
- W2017393472 date "2010-09-29" @default.
- W2017393472 modified "2023-10-18" @default.
- W2017393472 title "Alteration of vitamin D metabolic enzyme expression and calcium transporter abundance in kidney involved in type 1 diabetes-induced bone loss" @default.
- W2017393472 cites W1965960323 @default.
- W2017393472 cites W1970825974 @default.
- W2017393472 cites W1977365677 @default.
- W2017393472 cites W1990365334 @default.
- W2017393472 cites W1997515464 @default.
- W2017393472 cites W2001205177 @default.
- W2017393472 cites W2001846596 @default.
- W2017393472 cites W2015753105 @default.
- W2017393472 cites W2017650323 @default.
- W2017393472 cites W2023320327 @default.
- W2017393472 cites W2023997273 @default.
- W2017393472 cites W2024693050 @default.
- W2017393472 cites W2035683489 @default.
- W2017393472 cites W2037154438 @default.
- W2017393472 cites W2043368155 @default.
- W2017393472 cites W2046583318 @default.
- W2017393472 cites W2050109970 @default.
- W2017393472 cites W2051673925 @default.
- W2017393472 cites W2052751148 @default.
- W2017393472 cites W2053473716 @default.
- W2017393472 cites W2059418097 @default.
- W2017393472 cites W2062621828 @default.
- W2017393472 cites W2078005465 @default.
- W2017393472 cites W2086532628 @default.
- W2017393472 cites W2092785568 @default.
- W2017393472 cites W2096927167 @default.
- W2017393472 cites W2101371788 @default.
- W2017393472 cites W2103435160 @default.
- W2017393472 cites W2104062693 @default.
- W2017393472 cites W2106355527 @default.
- W2017393472 cites W2111672048 @default.
- W2017393472 cites W2119057793 @default.
- W2017393472 cites W2120906476 @default.
- W2017393472 cites W2127176339 @default.
- W2017393472 cites W2128783914 @default.
- W2017393472 cites W2134975242 @default.
- W2017393472 cites W2135062403 @default.
- W2017393472 cites W2151354212 @default.
- W2017393472 cites W2155821999 @default.
- W2017393472 cites W2165433745 @default.
- W2017393472 doi "https://doi.org/10.1007/s00198-010-1404-1" @default.
- W2017393472 hasPubMedCentralId "https://www.ncbi.nlm.nih.gov/pmc/articles/4537183" @default.
- W2017393472 hasPubMedId "https://pubmed.ncbi.nlm.nih.gov/20878391" @default.
- W2017393472 hasPublicationYear "2010" @default.
- W2017393472 type Work @default.
- W2017393472 sameAs 2017393472 @default.
- W2017393472 citedByCount "25" @default.
- W2017393472 countsByYear W20173934722013 @default.
- W2017393472 countsByYear W20173934722014 @default.
- W2017393472 countsByYear W20173934722015 @default.
- W2017393472 countsByYear W20173934722016 @default.
- W2017393472 countsByYear W20173934722017 @default.
- W2017393472 countsByYear W20173934722018 @default.
- W2017393472 countsByYear W20173934722019 @default.
- W2017393472 countsByYear W20173934722020 @default.
- W2017393472 countsByYear W20173934722022 @default.
- W2017393472 crossrefType "journal-article" @default.
- W2017393472 hasAuthorship W2017393472A5024194480 @default.
- W2017393472 hasAuthorship W2017393472A5073279162 @default.
- W2017393472 hasAuthorship W2017393472A5076081554 @default.
- W2017393472 hasBestOaLocation W20173934722 @default.
- W2017393472 hasConcept C104317684 @default.
- W2017393472 hasConcept C124490489 @default.
- W2017393472 hasConcept C126322002 @default.
- W2017393472 hasConcept C134018914 @default.
- W2017393472 hasConcept C170033053 @default.
- W2017393472 hasConcept C179639408 @default.
- W2017393472 hasConcept C2776415932 @default.
- W2017393472 hasConcept C2779280383 @default.
- W2017393472 hasConcept C2780091579 @default.
- W2017393472 hasConcept C519063684 @default.
- W2017393472 hasConcept C55493867 @default.
- W2017393472 hasConcept C555293320 @default.
- W2017393472 hasConcept C71924100 @default.
- W2017393472 hasConcept C86803240 @default.
- W2017393472 hasConceptScore W2017393472C104317684 @default.
- W2017393472 hasConceptScore W2017393472C124490489 @default.
- W2017393472 hasConceptScore W2017393472C126322002 @default.
- W2017393472 hasConceptScore W2017393472C134018914 @default.
- W2017393472 hasConceptScore W2017393472C170033053 @default.
- W2017393472 hasConceptScore W2017393472C179639408 @default.
- W2017393472 hasConceptScore W2017393472C2776415932 @default.
- W2017393472 hasConceptScore W2017393472C2779280383 @default.
- W2017393472 hasConceptScore W2017393472C2780091579 @default.
- W2017393472 hasConceptScore W2017393472C519063684 @default.
- W2017393472 hasConceptScore W2017393472C55493867 @default.
- W2017393472 hasConceptScore W2017393472C555293320 @default.
- W2017393472 hasConceptScore W2017393472C71924100 @default.
- W2017393472 hasConceptScore W2017393472C86803240 @default.
- W2017393472 hasIssue "6" @default.