Effect of Melatonin Administration on Mitochondrial Activity and Oxidative Stress Markers in Patients with Parkinson's Disease

被引:34
|
作者
Jimenez-Delgado, Alicia [1 ]
Gabriel Ortiz, Genaro [2 ]
Delgado-Lara, Daniela L. [2 ]
Alberto Gonzalez-Usigli, Hector [3 ]
Javier Gonzalez-Ortiz, Luis [1 ]
Cid-Hernandez, Margarita [1 ]
Antonio Cruz-Serrano, Jose [4 ]
Paul Pacheco-Moises, Fermin [1 ]
机构
[1] Univ Guadalajara, Univ Ctr Exact Sci & Engn, Dept Chem, Guadalajara, Jalisco, Mexico
[2] Univ Guadalajara, Univ Ctr Hlth Sci, Dept Philosoph & Methodol Disciplines, Guadalajara, Jalisco, Mexico
[3] Mexican Inst Social Secur, Western Natl Med Ctr, Dept Neurol, Subspecialty Med Unit, Guadalajara, Jalisco, Mexico
[4] Kurago Biotek, Guadalajara, Jalisco, Mexico
关键词
NITRIC-OXIDE SYNTHASE; RESPIRATORY-CHAIN ACTIVITY; COMPLEX-I DEFICIENCY; SKELETAL-MUSCLE; DYSFUNCTION; PROTECTS; CYCLOOXYGENASE-2; PREVENTS; PLASMA; BRAIN;
D O I
10.1155/2021/5577541
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Mitochondrial dysfunction and oxidative stress are extensively linked to Parkinson's disease (PD) pathogenesis. Melatonin is a pleiotropic molecule with antioxidant and neuroprotective effects. The aim of this study was to evaluate the effect of melatonin on oxidative stress markers, mitochondrial complex 1 activity, and mitochondrial respiratory control ratio in patients with PD. A double-blind, cross-over, placebo-controlled randomized clinical trial study was conducted in 26 patients who received either 25 mg of melatonin or placebo at noon and 30 min before bedtime for three months. At the end of the trial, in patients who received melatonin, we detected a significant diminution of lipoperoxides, nitric oxide metabolites, and carbonyl groups in plasma samples from PD patients compared with the placebo group. Conversely, catalase activity was increased significantly in comparison with the placebo group. Compared with the placebo group, the melatonin group showed significant increases of mitochondrial complex 1 activity and respiratory control ratio. The fluidity of the membranes was similar in the melatonin group and the placebo group at baseline and after three months of treatment. In conclusion, melatonin administration was effective in reducing the levels of oxidative stress markers and restoring the rate of complex I activity and respiratory control ratio without modifying membrane fluidity. This suggests that melatonin could play a role in the treatment of PD.
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页数:7
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