Induction of lipid peroxidation and decrease of antioxidant defenses in symptomatic and asymptomatic patients with X‐linked adrenoleukodystrophy

无症状的 肾上腺脑白质营养不良 氧化应激 脂质过氧化 抗氧化剂 内科学 病理生理学 内分泌学 医学 化学 生物化学 过氧化物酶体 受体
作者
Marion Deon,Ângela Sitta,Alethéa Gatto Barschak,Daniela M. Coelho,Maiara Cássia Pigatto,Graziela O. Schmitt,Laura Bannach Jardim,Roberto Giugliani,Moacır Wajner,Carmen Regla Vargas
出处
期刊:International Journal of Developmental Neuroscience [Wiley]
卷期号:25 (7): 441-444 被引量:43
标识
DOI:10.1016/j.ijdevneu.2007.08.008
摘要

Abstract Patients affected by X‐linked adrenoleukodystrophy (X‐ALD) present a progressive brain and peripheral demyelination and adrenal cortex insufficiency, associated with accumulation of the very long chain fatty acids (VLCFA) hexacosanoic acid (C26:0) and tetracosanoic acid (C24:0) in different tissues and biological fluids. X‐ALD is characterized by heterogeneous clinical phenotypes. Seven clinical variants have been described for this genetic disorder, being the childhood cerebral form (CCER), adrenomyeloneuropathy (AMN) and asymptomatic the most common clinical forms. In a previous work, we showed evidence that oxidative stress is involved in the pathophysiology of X‐ALD symptomatic patients. In the present study, we compared oxidative stress parameters, namely thiobarbituric acid reactive substances (TBA‐RS) and total antioxidant status (TAS), in plasma from patients with CCER, AMN and in asymptomatic X‐ALD patients. It was observed that symptomatic and asymptomatic X‐ALD patients presented a significant increase of plasma TBA‐RS measurement, indicating a stimulation of lipid peroxidation. Furthermore, lipid peroxidation was higher in AMN, as compared to CCER and asymptomatic patients. We also observed that the total antioxidant defenses (TAS) were decreased in symptomatic but not in asymptomatic X‐ALD patients. Therefore, it may be presumed that asymptomatic patients seem to be protected against oxidative stress because of their normal antioxidant defenses and that other factors besides oxidative damage may be responsible for the severity of the symptoms in X‐ALD and need to be investigated.
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