Defective Brain Energy Metabolism Shown by in vivo 31 P MR Spectroscopy in 28 Patients with Mitochondrial Cytopathies
Author(s) -
Barbiroli Bruno,
Montagna Pasquale,
Martinelli Paolo,
Lodi Raffaele,
Iotti Stefano,
Cortelli Pietro,
Funicello Rosanna,
Zaniol Paolo
Publication year - 1993
Publication title -
journal of cerebral blood flow and metabolism
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 2.167
H-Index - 193
eISSN - 1559-7016
pISSN - 0271-678X
DOI - 10.1038/jcbfm.1993.61
Subject(s) - phosphocreatine , creatine , high energy phosphate , energy metabolism , metabolism , medicine , cytosol , mitochondrial myopathy , creatine kinase , endocrinology , in vivo , mitochondrion , chemistry , biochemistry , biology , mitochondrial dna , enzyme , gene , genetics
We studied brain energy metabolism by phosphorus magnetic resonance spectroscopy ( 31 P MRS) in 28 patients with mitochondrial cytopathies, and 20 normal control subjects. Fourteen patients had myopathy alone, six had only mild brain symptoms, and eight showed different degrees of brain involvement. Brain 31 P MRS showed a low phosphocreatine content in all patients, accompanied by a high inorganic phosphate in 14 of 28 patients. The average value of the P i concentration in the patient group was significantly (p = 0.009) different from the control group. The cytosolic pH was normal. From these data were derived a high concentration of ADP (calculated from the creatine kinase equilibrium), a high percent value of V/V max for ATP biosynthesis, and a low phosphorylation potential, all features showing a derangement of brain energy metabolism, in all patients with mitochondrial cytopathies. 31 P MRS proved to be sensitive enough to disclose a deficit of mitochondrial functionality not only in the affected patients, but also in those without clinically evident brain symptoms.
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