Sterols and oxysterols in plasma from Smith-Lemli-Opitz syndrome patients

Autor: Jonas Abdel-Khalik, Michael Ogundare, Peter J. Crick, Brian W. Bigger, William J. Griffiths, Libin Xu, Ingemar Björkhem, Andrew A. M. Morris, Yuqin Wang, Mei Kwun Kwok, Ned A. Porter, Akira Honda, Cedric H.L. Shackleton, Peter E. Clayton, Karin Tuschl
Jazyk: angličtina
Předmět:
0301 basic medicine
medicine.medical_specialty
7-Dehydrocholesterol reductase
Oxidoreductases Acting on CH-CH Group Donors
congenital
hereditary
and neonatal diseases and abnormalities

Oxysterol
Free Radicals
Endocrinology
Diabetes and Metabolism

Clinical Biochemistry
Reductase
Biochemistry
Article
03 medical and health sciences
7-Dehydrocholesterol
chemistry.chemical_compound
Plasma
Dehydrocholesterols
Endocrinology
Internal medicine
Blood plasma
medicine
polycyclic compounds
Humans
Molecular Biology
Liquid chromatography–
Sterol
mass spectrometry
Cholesterol
Cholestadienols
nutritional and metabolic diseases
Oxysterols
Cell Biology
medicine.disease
3. Good health
Smith-Lemli-Opitz Syndrome
Sterols
030104 developmental biology
chemistry
Smith–Lemli–Opitz syndrome
Mutation
8-Dehydrocholesterol
Molecular Medicine
lipids (amino acids
peptides
and proteins)
Zdroj: The Journal of Steroid Biochemistry and Molecular Biology.
ISSN: 0960-0760
DOI: 10.1016/j.jsbmb.2016.03.018
Popis: Smith-Lemli-Opitz syndrome (SLOS) is a severe autosomal recessive disorder resulting from defects in the cholesterol synthesising enzyme 7-dehydrocholesterol reductase (Δ7-sterol reductase, DHCR7, EC 1.3.1.21) leading to a build-up of the cholesterol precursor 7-dehydrocholesterol (7-DHC) in tissues and blood plasma. Although the underling enzyme deficiency associated with SLOS is clear there are likely to be multiple mechanisms responsible for SLOS pathology. In an effort to learn more of the aetiology of SLOS we have analysed plasma from SLOS patients to search for metabolites derived from 7-DHC which may be responsible for some of the pathology. We have identified a novel hydroxy-8-dehydrocholesterol, which is either 24- or 25-hydroxy-8-dehydrocholesterol and also the known metabolites 26-hydroxy-8-dehydrocholesterol, 4-hydroxy-7-dehydrocholesterol, 3β,5α-dihydroxycholest-7-en-6-one and 7α,8α-epoxycholesterol. None of these metabolites are detected in control plasma at quantifiable levels (0.5ng/mL).
Databáze: OpenAIRE