New insights in dihydropyrimidine dehydrogenase deficiency: a pivotal role for beta-aminoisobutyric acid?

Biochem J. 2004 Apr 1;379(Pt 1):119-24. doi: 10.1042/BJ20031463.

Abstract

DPD (dihydropyrimidine dehydrogenase) constitutes the first step of the pyrimidine degradation pathway, in which the pyrimidine bases uracil and thymine are catabolized to beta-alanine and the R-enantiomer of beta-AIB (beta-aminoisobutyric acid) respectively. The S-enantiomer of beta-AIB is predominantly derived from the catabolism of valine. It has been suggested that an altered homoeostasis of beta-alanine underlies some of the clinical abnormalities encountered in patients with a DPD deficiency. In the present study, we demonstrated that only a slightly decreased concentration of beta-alanine was present in the urine and plasma, whereas normal levels of beta-alanine were present in the cerebrospinal fluid of patients with a DPD deficiency. Therefore the metabolism of beta-alanine-containing peptides, such as carnosine, may be an important factor involved in the homoeostasis of beta-alanine in patients with DPD deficiency. The mean concentration of beta-AIB was approx. 2-3-fold lower in cerebrospinal fluid and urine of patients with a DPD deficiency, when compared with controls. In contrast, strongly decreased levels (10-fold) of beta-AIB were present in the plasma of DPD patients. Our results demonstrate that, under pathological conditions, the catabolism of valine can result in the production of significant amounts of beta-AIB. Furthermore, the observation that the R-enantiomer of beta-AIB is abundantly present in the urine of DPD patients suggests that significant cross-over exists between the thymine and valine catabolic pathways.

MeSH terms

  • Aminoisobutyric Acids / blood
  • Aminoisobutyric Acids / cerebrospinal fluid
  • Aminoisobutyric Acids / chemistry
  • Aminoisobutyric Acids / metabolism*
  • Aminoisobutyric Acids / urine
  • Brain Diseases, Metabolic, Inborn / enzymology
  • Brain Diseases, Metabolic, Inborn / genetics
  • Brain Diseases, Metabolic, Inborn / metabolism
  • Dihydropyrimidine Dehydrogenase Deficiency*
  • Dihydrouracil Dehydrogenase (NADP) / genetics
  • Fluorouracil / pharmacokinetics
  • Homeostasis
  • Humans
  • Inactivation, Metabolic / genetics
  • Neurotransmitter Agents / metabolism
  • Purine-Pyrimidine Metabolism, Inborn Errors / enzymology
  • Purine-Pyrimidine Metabolism, Inborn Errors / genetics
  • Purine-Pyrimidine Metabolism, Inborn Errors / metabolism*
  • Stereoisomerism
  • Thymine / metabolism*
  • Uracil / metabolism
  • Valine / metabolism*
  • beta-Alanine / blood
  • beta-Alanine / cerebrospinal fluid
  • beta-Alanine / metabolism*
  • beta-Alanine / urine

Substances

  • Aminoisobutyric Acids
  • Neurotransmitter Agents
  • beta-Alanine
  • Uracil
  • Dihydrouracil Dehydrogenase (NADP)
  • Valine
  • Thymine
  • 3-aminoisobutyric acid
  • Fluorouracil