Journal article
Multiple Acyl-Coenzyme A Dehydrogenation Disorder Responsive to Riboflavin: Substrate Oxidation, Flavin Metabolism, and Flavoenzyme Activities in Fibroblasts
Pediatric research, Vol.33(2), pp.129-135
02/1993
DOI: 10.1203/00006450-199302000-00008
PMID: 8433888
Abstract
Multiple acyl-CoA dehydrogenation disorders result from generalized defects in intramitochondrial acyl-CoA dehydrogenation. Fibroblasts from a riboflavin-responsive multiple acyl-CoA dehydrogenation disorder patient catabolizedl4C-butyrate, -octanoate, and -leucine normally after culture in riboflavin-supplemented medium (2 mg/L). After culture in riboflavin-depleted medium (<1.4 µg/L) his cells oxidized the same substrates poorly at 20 to 33% of control (p < 0.05). Patient cells incubated in a wide range of D-[2-l4C]riboflavin concentrations (3, 31.4, and 100 µg/L) synthesized14C-flavin mononucleotide and,4C-flavin adenine dinucleotide (FAD) normally and had normal cytosolicl4C-flavin mononucleotide andl4C-FAD contents, which argues against defects in cellular riboflavin uptake and conversion to flavin mononucleotide and FAD. After culture in 31.4 ng14C-riboflavin/L for 2 wk,l4C-FAD specific radioactivities plateaued and were similar in patient and control cells. However, culturing these uniformly labeled cells in riboflavin-depleted medium for 2 wk lowered the patient’s cellularl4C-FAD content to only 23% of control levels. Similarly, after incubation in lowl4C-riboflavin concentrations (4.4 /µg/L), the patient’s mitochondrial14C-FAD content was only 51% of control after 1 h and 29% of control at 4 h. After a 4-h incubation in a high physiologic concentration of,4C-riboflavin (31.4 µg/L), which raised the patient's cellularl4C-FAD levels 3- to 4-fold, his mitochondrial14C-FAD content rose to normal; control values did not change. We also investigated possible defective FAD binding to flavoenzymes essential for acyl-CoA dehydrogenation. Medium-chain acyl-CoA dehydrogenase activities did not fall significantly in either patient or control mitochondria from cells cultured in riboflavin-depleted medium. However, after culture in riboflavin-depleted medium, the patient's electron transfer flavo-protein activity fell to 59% of control in mitochondrial preparations, which is compatible with decreased matrix FAD content. We postulate that defective maintenance of mitochondrial FAD levels explains this patient’s riboflavin-responsive multiple acyl-CoA dehydrogenation disorder phenotype. © 1993 International Pediatric Research Foundation, Inc.
Details
- Title: Subtitle
- Multiple Acyl-Coenzyme A Dehydrogenation Disorder Responsive to Riboflavin: Substrate Oxidation, Flavin Metabolism, and Flavoenzyme Activities in Fibroblasts
- Creators
- William Rhead - University of IowaVickie RoettgerTeresa MarshaliBrad Amendt - University of Iowa
- Resource Type
- Journal article
- Publication Details
- Pediatric research, Vol.33(2), pp.129-135
- DOI
- 10.1203/00006450-199302000-00008
- PMID
- 8433888
- NLM abbreviation
- Pediatr Res
- ISSN
- 0031-3998
- eISSN
- 1530-0447
- Language
- English
- Date published
- 02/1993
- Academic Unit
- Orthodontics; Anatomy and Cell Biology; Craniofacial Anomalies Research Center; Dental Research
- Record Identifier
- 9984284330202771
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