Delwing Daniela, Bavaresco Caren Serra, Chiarani Fábria, Wannmacher Clóvis Milton Duval, Wajner Moacir, Dutra-Filho Carlos Severo, de Souza Wyse Angela Terezinha
Departamento de Bioquímica, Instituto de Ciências Básicas da Saúde, Universidade Federal do Rio Grande do Sul, Rua Ramiro Barcelos, 2600-Anexo, CEP 90035-003, Porto Alegre, RS, Brazil.
Brain Res. 2003 Nov 21;991(1-2):180-6. doi: 10.1016/j.brainres.2003.08.014.
Hyperprolinemia type II is an autosomal recessive disorder caused by the severe deficiency of delta(1)-pyrroline-5-carboxylate dehydrogenase activity leading to tissue accumulation of proline (Pro). Most patients detected so far show neurological manifestations including epilepsy and mental retardation, whose pathophysiology is not yet fully established. In the present study, we determined the in vivo and in vitro effects of Pro on some parameters of oxidative stress, namely chemiluminescence, total radical-trapping antioxidant potential (TRAP) and the activity of the antioxidant enzymes catalase (CAT), glutathione peroxidase (GSH-Px) and superoxide dismutase (SOD) from cerebral cortex of 29-day-old Wistar rats. Results showed that acute administration of Pro provoked a significant increase of chemiluminescence and a decrease of TRAP, whereas chronic administration of the metabolite did not alter these parameters. Furthermore, in vitro brain exposure to Pro resulted in increased chemiluminescence and decreased TRAP at Pro concentrations similar to those observed in tissues of hyperprolinemic patients (0.5-1.0 mM). As regards to the antioxidant enzymes, acute injection of Pro significantly decreased CAT activity and did not alter SOD and GSH-Px activities, whereas chronic Pro administration provoked a significant increase of CAT activity, a decrease of GSH-Px activity and did not modify SOD activity. Furthermore, CAT, GSH-Px and SOD activities were not affected by the presence of Pro in the incubation medium. The data indicate that Pro induces oxidative stress in vivo and in vitro, which may be involved in the brain dysfunction observed in hyperprolinemic patients.
II型高脯氨酸血症是一种常染色体隐性疾病,由δ(1)-吡咯啉-5-羧酸脱氢酶活性严重缺乏导致脯氨酸(Pro)在组织中蓄积引起。到目前为止,检测到的大多数患者表现出包括癫痫和智力迟钝在内的神经学症状,其病理生理学尚未完全明确。在本研究中,我们测定了脯氨酸对29日龄Wistar大鼠大脑皮质氧化应激的一些参数的体内和体外影响,这些参数即化学发光、总自由基捕获抗氧化能力(TRAP)以及抗氧化酶过氧化氢酶(CAT)、谷胱甘肽过氧化物酶(GSH-Px)和超氧化物歧化酶(SOD)的活性。结果显示,急性给予脯氨酸会引起化学发光显著增加和TRAP降低,而长期给予该代谢物则不会改变这些参数。此外,体外将大脑暴露于脯氨酸中,在与高脯氨酸血症患者组织中观察到的浓度相似(0.5 - 1.0 mM)的脯氨酸浓度下,会导致化学发光增加和TRAP降低。至于抗氧化酶,急性注射脯氨酸会显著降低CAT活性,而不改变SOD和GSH-Px活性,而长期给予脯氨酸会引起CAT活性显著增加、GSH-Px活性降低且不改变SOD活性。此外,孵育培养基中脯氨酸的存在不影响CAT、GSH-Px和SOD的活性。数据表明,脯氨酸在体内和体外均可诱导氧化应激,这可能与高脯氨酸血症患者中观察到的脑功能障碍有关。