Glucose and oxygen hypometabolism in aceruloplasminemia brains.
Glucose and oxygen hypometabolism in aceruloplasminemia brains.
复制标题
铜蓝蛋白血症大脑中的葡萄糖和氧代谢低下。
DOI：
10.2169/internalmedicine.41.186
复制
发表时间：
2002
影响因子：
1.2
通讯作者：
Y. Ouchi
中科院分区：
文献类型：
--
作者：
H. Miyajima;Yoshitomo Takahashi;S. Kono;M. Sugimoto;Yoji Suzuki;A. Hishida;M. Sakamoto;Y. Ouchi
客观的
OBJECTIVE
Aceruloplasminemia is an iron metabolic disorder caused by mutations in the ceruloplasmin gene. It is characterized by progressive neurodegeneration in association with iron accumulation. Excess iron functions as a potent catalyst of biologic oxidation. Previously we showed that an increased iron concentration is associated with the products of lipid peroxidation in the serum, cerebrospinal fluid, and brain tissues. To clarify the free radical-mediated tissue injury caused by intracellular iron accumulation through mitochondrial dysfunction.
PATIENTS AND METHODS
We have measure brain oxygen and glucose metabolisms using positron emission tomography (PET) and examined brains at autopsy for iron contents and activities of the mitochondrial respiratory chain in two affected patients who had different truncation mutations of the ceruloplasmin gene.
RESULTS
PET showed a marked decrease in glucose and oxygen consumption in the entire brain of aceruloplasminemia patients, with a preponderance of metabolic reduction in basal ganglia. Enzyme activities in the mitochondrial respiratory chain of the basal ganglia were reduced to approximately 45% and 42% respectively for complexes I and IV. An inverse relationship was shown between the amounts of iron accumulated and the levels of mitochondrial enzyme activities in all the brain regions examined.
CONCLUSION
Iron-mediated free radicals may contribute to the impairment of mitochondrial energy metabolism in aceruloplasminemia.