Barbiroli B, Montagna P, Cortelli P, Martinelli P, Sacquegna T, Zaniol P, Lugaresi E
Istituto di Clinica Neurologica, Università di Bologna, Italy.
Cephalalgia. 1990 Oct;10(5):263-72. doi: 10.1046/j.1468-2982.1990.1005263.x.
The brain and skeletal muscle of eight adult patients with migraine with prolonged auras or migraine strokes leaving a permanent hemianopic defect were studied by phosphorus magnetic resonance spectroscopy. Biochemical assays performed on muscle biopsy and platelets had revealed abnormal mitochondrial enzyme activities. Brain magnetic resonance spectroscopy showed an abnormally low phosphocreatine to inorganic phosphate ratio in all patients, apparently due to decreased phosphocreatine and increased inorganic phosphate contents. Muscle phosphorus magnetic resonance spectroscopy showed low recovery from exercise in seven patients. Three patients had an increased phosphocreatine/inorganic phosphate ratio at rest, and the exercise transfer characteristics were abnormal in four patients for relatively low levels of exercise. The mitochondrial metabolic defects present in platelets and muscle of complicated migraine patients are therefore also expressed in the brain.
通过磷磁共振波谱对8例伴有长时间先兆的偏头痛成年患者或遗留永久性偏盲缺损的偏头痛性卒中患者的大脑和骨骼肌进行了研究。对肌肉活检和血小板进行的生化分析显示线粒体酶活性异常。脑磁共振波谱显示所有患者磷酸肌酸与无机磷酸盐的比率异常低,这显然是由于磷酸肌酸减少和无机磷酸盐含量增加所致。肌肉磷磁共振波谱显示7例患者运动后恢复缓慢。3例患者静息时磷酸肌酸/无机磷酸盐比率升高,4例患者在运动量相对较低时运动转换特征异常。因此,复杂性偏头痛患者血小板和肌肉中存在的线粒体代谢缺陷在大脑中也有表现。