TY - JOUR
T1 - Identification of 7α,24-dihydroxy-3-oxocholest-4-en-26-oic and 7α,25-dihydroxy-3-oxocholest-4-en-26-oic acids in human cerebrospinal fluid and plasma
AU - Abdel-Khalik, Jonas
AU - Crick, Peter J.
AU - Yutuc, Eylan
AU - DeBarber, Andrea E.
AU - Duell, P. Barton
AU - Steiner, Robert D.
AU - Laina, Ioanna
AU - Wang, Yuqin
AU - Griffiths, William J.
N1 - Funding Information:
This work was supported by the UK Biotechnology and Biological Sciences Research Council (BBSRC, grant numbers BB/I001735/1 and BB/N015932/1 to WJG, BB/L001942/1 to YW) and the Welsh Government's A4B project. JAK was supported by a PhD studentship from Imperial College Healthcare Charities. Drs L Antoniadou, CS Bartsocas and M Markouri from Athens Medical Center, Rare Diseases Group are thanked for provision of patient samples. Members of the European Network for Oxysterol Research are thanked for informative discussions.
Funding Information:
This work was supported by the UK Biotechnology and Biological Sciences Research Council (BBSRC , grant numbers BB/I001735/1 and BB/N015932/1 to WJG, BB/L001942/1 to YW) and the Welsh Government's A4B project. JAK was supported by a PhD studentship from Imperial College Healthcare Charities. Drs L Antoniadou, CS Bartsocas and M Markouri from Athens Medical Center, Rare Diseases Group are thanked for provision of patient samples. Members of the European Network for Oxysterol Research are thanked for informative discussions.
Publisher Copyright:
© 2018 The Authors
PY - 2018/10
Y1 - 2018/10
N2 - Dihydroxyoxocholestenoic acids are intermediates in bile acid biosynthesis. Here, using liquid chromatography – mass spectrometry, we confirm the identification of 7α,24-dihydroxy-3-oxocholest-4-en-26-oic and 7α,25-dihydroxy-3-oxocholest-4-en-26-oic acids in cerebrospinal fluid (CSF) based on comparisons to authentic standards and of 7α,12α-dihydroxy-3-oxocholest-4-en-26-oic and 7α,x-dihydroxy-3-oxocholest-4-en-26-oic (where hydroxylation is likely on C-22 or C-23) based on exact mass measurement and multistage fragmentation. Surprisingly, patients suffering from the inborn error of metabolism cerebrotendinous xanthomatosis, where the enzyme CYP27A1, which normally introduces the (25 R)26-carboxylic acid group to the sterol side-chain, is defective still synthesise 7α,24-dihydroxy-3-oxocholest-4-en-26-oic acid and also both 25 R- and 25 S-epimers of 7α,12α-dihydroxy-3-oxocholest-4-en-26-oic acid. We speculate that the enzymes CYP46A1 and CYP3A4 may have C-26 carboxylase activity to generate these acids. In patients suffering from hereditary spastic paraplegia type 5 the CSF concentrations of the 7α,24- and 7α,25-dihydroxy acids are reduced, suggesting an involvement of CYP7B1 in their biosynthesis in brain.
AB - Dihydroxyoxocholestenoic acids are intermediates in bile acid biosynthesis. Here, using liquid chromatography – mass spectrometry, we confirm the identification of 7α,24-dihydroxy-3-oxocholest-4-en-26-oic and 7α,25-dihydroxy-3-oxocholest-4-en-26-oic acids in cerebrospinal fluid (CSF) based on comparisons to authentic standards and of 7α,12α-dihydroxy-3-oxocholest-4-en-26-oic and 7α,x-dihydroxy-3-oxocholest-4-en-26-oic (where hydroxylation is likely on C-22 or C-23) based on exact mass measurement and multistage fragmentation. Surprisingly, patients suffering from the inborn error of metabolism cerebrotendinous xanthomatosis, where the enzyme CYP27A1, which normally introduces the (25 R)26-carboxylic acid group to the sterol side-chain, is defective still synthesise 7α,24-dihydroxy-3-oxocholest-4-en-26-oic acid and also both 25 R- and 25 S-epimers of 7α,12α-dihydroxy-3-oxocholest-4-en-26-oic acid. We speculate that the enzymes CYP46A1 and CYP3A4 may have C-26 carboxylase activity to generate these acids. In patients suffering from hereditary spastic paraplegia type 5 the CSF concentrations of the 7α,24- and 7α,25-dihydroxy acids are reduced, suggesting an involvement of CYP7B1 in their biosynthesis in brain.
KW - Bile acid
KW - Brain
KW - Cerebrotendinous xanthomatosis
KW - Cytochrome P450
KW - Hereditary spastic paraplegia type 5
KW - Oxysterol
UR - http://www.scopus.com/inward/record.url?scp=85049486722&partnerID=8YFLogxK
UR - http://www.scopus.com/inward/citedby.url?scp=85049486722&partnerID=8YFLogxK
U2 - 10.1016/j.biochi.2018.06.020
DO - 10.1016/j.biochi.2018.06.020
M3 - Article
C2 - 29960034
AN - SCOPUS:85049486722
SN - 0300-9084
VL - 153
SP - 86
EP - 98
JO - Biochimie
JF - Biochimie
ER -