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  1. Article: Lithocholic acid can carry out in vivo functions of vitamin D.

    Nehring, Jamie A / Zierold, Claudia / DeLuca, Hector F

    Proceedings of the National Academy of Sciences of the United States of America

    2007  Volume 104, Issue 24, Page(s) 10006–10009

    Abstract: The physiological ligand for the vitamin D receptor (VDR) is 1,25-dihydroxyvitamin D(3). Lithocholic acid (LCA), a bile acid implicated in the progression of colon cancer, was recently shown to bind to VDR with low affinity and increase expression of the ...

    Abstract The physiological ligand for the vitamin D receptor (VDR) is 1,25-dihydroxyvitamin D(3). Lithocholic acid (LCA), a bile acid implicated in the progression of colon cancer, was recently shown to bind to VDR with low affinity and increase expression of the xenobiotic enzymes of the CYP3A family. Thus, LCA can induce its own catabolism through the VDR. We have now found that LCA can substitute for vitamin D in the elevation of serum calcium in vitamin D-deficient rats. Further, LCA in the diet will also replace vitamin D in the mobilization of calcium from bone. Further, LCA induces CYP24-hydroxylase mRNA gene expression in the kidney of vitamin D-deficient rats. It is clear, therefore, that LCA can be absorbed into the circulation to bind to the VDR at extra-intestinal sites. These findings lend support for the idea that the VDR may have evolved from an original role in detoxification.
    MeSH term(s) Animals ; Calbindins ; Calcium/blood ; Calcium-Transporting ATPases/metabolism ; Detergents/metabolism ; Detergents/pharmacology ; Dose-Response Relationship, Drug ; Enzyme Induction/drug effects ; Intestines/enzymology ; Intestines/metabolism ; Kidney/enzymology ; Kidney/metabolism ; Lithocholic Acid/metabolism ; Lithocholic Acid/pharmacology ; Male ; RNA, Messenger/metabolism ; Rats ; Rats, Inbred F344 ; Rats, Sprague-Dawley ; Receptors, Calcitriol/genetics ; Receptors, Calcitriol/metabolism ; S100 Calcium Binding Protein G/metabolism ; Species Specificity ; Steroid Hydroxylases/biosynthesis ; Steroid Hydroxylases/genetics ; TRPV Cation Channels/metabolism ; Vitamin D Deficiency/diet therapy ; Vitamin D3 24-Hydroxylase
    Chemical Substances Calbindins ; Detergents ; RNA, Messenger ; Receptors, Calcitriol ; S100 Calcium Binding Protein G ; TRPV Cation Channels ; TRPV6 channel ; Lithocholic Acid (5QU0I8393U) ; Steroid Hydroxylases (EC 1.14.-) ; Vitamin D3 24-Hydroxylase (EC 1.14.15.16) ; Calcium-Transporting ATPases (EC 3.6.3.8) ; Calcium (SY7Q814VUP)
    Language English
    Publishing date 2007-06-12
    Publishing country United States
    Document type Comparative Study ; Journal Article ; Research Support, Non-U.S. Gov't
    ZDB-ID 209104-5
    ISSN 1091-6490 ; 0027-8424
    ISSN (online) 1091-6490
    ISSN 0027-8424
    DOI 10.1073/pnas.0703512104
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  2. Article: Nuclear receptor 4A2 and C/EBPbeta regulate the parathyroid hormone-mediated transcriptional regulation of the 25-hydroxyvitamin D3-1alpha-hydroxylase.

    Zierold, Claudia / Nehring, Jamie A / DeLuca, Hector F

    Archives of biochemistry and biophysics

    2007  Volume 460, Issue 2, Page(s) 233–239

    Abstract: 1Alpha-hydroxylase is the enzyme responsible for the production of the active form of vitamin D, 1,25-dihydroxyvitamin D3. 1Alpha-hydroxylase, found largely in the kidney, is known to be up-regulated by parathyroid hormone (PTH), however the mechanism of ...

    Abstract 1Alpha-hydroxylase is the enzyme responsible for the production of the active form of vitamin D, 1,25-dihydroxyvitamin D3. 1Alpha-hydroxylase, found largely in the kidney, is known to be up-regulated by parathyroid hormone (PTH), however the mechanism of action of PTH and any required transcription factors have not been clearly identified. During gene array analysis we observed that NR4A2, a nuclear orphan receptor, is markedly up-regulated in a porcine kidney cell line (AOK-B50) following PTH stimulation. NR4A2 over-expression increases the endogenous induction of 1alpha-hydroxylase mRNA in the absence of PTH, however optimal stimulation is achieved when both NR4A2 and PTH are present. An unconventional site of action of NR4A2 was localized to a fragment comprising the sequence from -35/+22 of the 1alpha-hydroxylase promoter at a C/EBP consensus site. Study of the involvement of C/EBPbeta in the 1alpha-hydroxylase regulation revealed that the transcriptional enhancement by NR4A2 on the 1alpha-hydroxylase promoter is inhibited by C/EBPbeta. In addition, C/EBPbeta over-expression decreases the endogenous levels of both NR4A2 and 1alpha-hydroxylase mRNA.
    MeSH term(s) 25-Hydroxyvitamin D3 1-alpha-Hydroxylase/biosynthesis ; 25-Hydroxyvitamin D3 1-alpha-Hydroxylase/genetics ; Animals ; CCAAT-Enhancer-Binding Protein-beta/metabolism ; Cell Line ; DNA-Binding Proteins/metabolism ; Gene Expression Profiling ; Gene Expression Regulation, Enzymologic/drug effects ; Gene Expression Regulation, Enzymologic/physiology ; Humans ; Kidney/enzymology ; Nuclear Receptor Subfamily 4, Group A, Member 2 ; Oligonucleotide Array Sequence Analysis ; Parathyroid Hormone/metabolism ; Parathyroid Hormone/pharmacology ; Response Elements/physiology ; Swine ; Transcription Factors/metabolism ; Transcription, Genetic/drug effects ; Transcription, Genetic/physiology ; Up-Regulation/drug effects ; Up-Regulation/physiology
    Chemical Substances CCAAT-Enhancer-Binding Protein-beta ; DNA-Binding Proteins ; NR4A2 protein, human ; Nuclear Receptor Subfamily 4, Group A, Member 2 ; Parathyroid Hormone ; Transcription Factors ; 25-Hydroxyvitamin D3 1-alpha-Hydroxylase (EC 1.14.13.13)
    Language English
    Publishing date 2007-04-15
    Publishing country United States
    Document type Journal Article ; Research Support, Non-U.S. Gov't
    ZDB-ID 523-x
    ISSN 1096-0384 ; 0003-9861
    ISSN (online) 1096-0384
    ISSN 0003-9861
    DOI 10.1016/j.abb.2006.11.028
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  3. Article: Lithocholic acid can carry out in vivo functions of vitamin D

    Nehring, Jamie A / Zierold, Claudia / DeLuca, Hector F

    Proceedings of the National Academy of Sciences of the United States of America. 2007 June 12, v. 104, no. 24

    2007  

    Abstract: The physiological ligand for the vitamin D receptor (VDR) is 1,25-dihydroxyvitamin D₃. Lithocholic acid (LCA), a bile acid implicated in the progression of colon cancer, was recently shown to bind to VDR with low affinity and increase expression of the ... ...

    Abstract The physiological ligand for the vitamin D receptor (VDR) is 1,25-dihydroxyvitamin D₃. Lithocholic acid (LCA), a bile acid implicated in the progression of colon cancer, was recently shown to bind to VDR with low affinity and increase expression of the xenobiotic enzymes of the CYP3A family. Thus, LCA can induce its own catabolism through the VDR. We have now found that LCA can substitute for vitamin D in the elevation of serum calcium in vitamin D-deficient rats. Further, LCA in the diet will also replace vitamin D in the mobilization of calcium from bone. Further, LCA induces CYP24-hydroxylase mRNA gene expression in the kidney of vitamin D-deficient rats. It is clear, therefore, that LCA can be absorbed into the circulation to bind to the VDR at extra-intestinal sites. These findings lend support for the idea that the VDR may have evolved from an original role in detoxification.
    Language English
    Dates of publication 2007-0612
    Size p. 10006-10009.
    Publishing place National Academy of Sciences
    Document type Article
    ZDB-ID 209104-5
    ISSN 1091-6490 ; 0027-8424
    ISSN (online) 1091-6490
    ISSN 0027-8424
    Database NAL-Catalogue (AGRICOLA)

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