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Article type: Research Article
Authors: Qadri, Rizwanaa; b | Namdeo, Manjuc | Behari, Madhurib | Goyal, Vinayb | Sharma, Subhadraa | Mukhopadhyay, Asok Kumar a; *
Affiliations: [a] Department of Laboratory Medicine, All India Institute of Medical Sciences, New Delhi, India | [b] Department of Neurology, All India Institute of Medical Sciences, New Delhi, India | [c] Department of Transplant Immunology and Immunogenetics, All India Institute of Medical Sciences, New Delhi, India
Correspondence: [*] Corresponding author: Prof. A.K. Mukhopadhyay, Room No 7, Department of Laboratory Medicine, All India Institute of Medical Sciences, New Delhi, 110029, India. Tel.: +91 011 26594407; E-mail: mukhoak1953@gmail.com.
Abstract: Background:Progressive apoptosis in the dopaminergic neurons of substantia nigra lead to Parkinson’s disease. Since neurons require substantially higher supply of energy, their mitochondria have a pivotal status in neuronal survival. These organelles have a key role to play in apoptosis and any impairment thereof may lead to apoptosis mediated cell death. Objectives:To evaluate and compare the mitochondrial membrane potential (Δψ) in Parkinson’s disease patients and healthy controls. Methods:We evaluated the mitochondrial membrane potential (Δψ) in the peripheral blood mononuclear cells by Flow cytometry using a lipophillic cationic dye JC-1 in Parkinson’s disease patients (N = 61) and healthy controls (N = 37). Results:JC-1 fluorescence was measured and represented as percentage positivity i.e., Mean±SEM in FL-2 (representing non-apoptotic aggregates) and FL-1 (indicating apoptotic cell population having depolarized or damaged mitochondria) channels. The ratio of % FL-2 and % FL-1, which is an indicator of cellular mitochondrial membrane potential, was found to be significantly higher in healthy controls (Mean±SEM = 60.48±18.42) as compared to patients (Mean±SEM = 24.30±4.671) in both stimulated and unstimulated conditions. Conclusions:Mitochondrial membrane potential is altered and hence its evaluation in peripheral blood mononuclear cells may serve as an early marker of apoptosis in PD and, therefore, may pave way for early interventions. Since Δψ has a role in the maintenance of electrochemical gradient, the disruption of which may lead to neuronal apoptosis, Δψ is intricately nested within etiopathogenesis of PD and may prove to be useful in design of diagnostics, prognostics and therapeutics for PD.
Keywords: Mitochondrial membrane potential, apoptosis, Parkinson’s disease, movement disorder
DOI: 10.3233/RNN-180852
Journal: Restorative Neurology and Neuroscience, vol. 36, no. 6, pp. 719-727, 2018
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