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Human Primary Trophoblast Cell Culture Model to Study the Protective Effects of Melatonin Against Hypoxia/reoxygenation-induced Disruption
Published on: July 30, 2016
Melatonin protects against common deletion of mitochondrial DNA-augmented mitochondrial oxidative stress and
Mei-Jie Jou1, Tsung-I Peng, Pai-Zu Yu
1Department of Physiology and Pharmacology, School of Medicine, College of Medicine, Chang Gung University, Tao-Yuan, and Department of Neurology, Kee-Lung Medical Center, Chang Gung Memorial Hospital, Taiwan. mjjou@mail.cgu.edu.tw
Abstract:
Defected mitochondrial respiratory chain (RC), in addition to causing a severe ATP deficiency, often augments reactive oxygen species (ROS) generation in mitochondria (mROS) which enhances pathological conditions and diseases. Previously, we demonstrated a potent endogenously RC defect-augmented mROS associated dose-dependently with a commonly seen large-scale deletion of 4977 base pairs of mitochondrial DNA (mtDNA), i.e. the common deletion (CD). As current treatments for CD-associated diseases are rather supplementary and ineffective, we investigated whether melatonin, a potential mitochondrial protector, provides beneficial protection for CD-augmented mitochondrial oxidative stress and apoptosis particularly upon the induction of a secondary oxidative stress. Detailed mechanistic investigations were performed by using laser scanning dual fluorescence imaging microscopy to provide precise spatial and temporal resolution of mitochondrial events at single cell level. We demonstrate, for the first time, that melatonin significantly prevents CD-augmented mROS formation under basal conditions as well as at early time-points upon secondary oxidative stress induced by H2O2 exposure. Thus, melatonin prevents mROS-mediated depolarization of mitochondrial membrane potential (DeltaPsim) and subsequent opening of the mitochondrial permeability transition pore (MPTP) and cytochrome c release. Moreover, melatonin prevents depletion of cardiolipin which appears to be crucial for postponing later MPTP opening, disruption of the mitochondrial membrane and apoptosis. Finally, the protection provided by melatonin is superior to those caused by the suppression of mitochondrial Ca2+ regulators including the mitochondrial Na+-Ca2) exchanger, the MPTP, and the mitochondrial Ca2+ uniporter and by antioxidants including vitamin E and mitochondria-targeted coenzyme Q, MitoQ. As RC defect-augmented endogenous mitochondrial oxidative stress is centrally involved in a variety of pathological conditions and diseases, melatonin thus may serve as a therapeutic drug to benefit many clinical conditions that involve malfunction of the mitochondria.
Insights
Melatonin protects against mitochondrial damage caused by a common DNA deletion and oxidative stress. This finding suggests melatonin as a potential therapeutic for mitochondrial dysfunction diseases.
Area of Science:
- Mitochondrial biology
- Cellular biochemistry
- Oxidative stress research
Background:
- Defects in the mitochondrial respiratory chain (RC) lead to ATP deficiency and increased mitochondrial reactive oxygen species (mROS).
- A common 4977 base pair deletion in mitochondrial DNA (mtDNA), known as the common deletion (CD), is linked to RC defects and augmented mROS.
- Existing treatments for CD-associated diseases are largely supportive and lack efficacy.
Purpose of the Study:
- To investigate the protective effects of melatonin against CD-augmented mitochondrial oxidative stress and apoptosis.
- To determine if melatonin can prevent mROS generation under basal conditions and upon induced secondary oxidative stress.
- To compare the efficacy of melatonin with other interventions like Ca2+ regulators and antioxidants.
Main Methods:
- Utilized laser scanning dual fluorescence imaging microscopy for high-resolution, single-cell analysis of mitochondrial events.
- Assessed mROS production, mitochondrial membrane potential (DeltaPsim), mitochondrial permeability transition pore (MPTP) opening, and cytochrome c release.
- Evaluated cardiolipin levels and apoptosis markers.
Main Results:
- Melatonin significantly inhibited CD-augmented mROS formation under basal and H2O2-induced oxidative stress conditions.
- Melatonin prevented DeltaPsim depolarization, MPTP opening, and subsequent cytochrome c release.
- Melatonin preserved cardiolipin levels, delayed MPTP opening, and inhibited apoptosis, outperforming other tested agents.
Conclusions:
- Melatonin demonstrates potent protective effects against mitochondrial oxidative stress and apoptosis linked to the common deletion.
- Melatonin's mechanism involves preventing mROS overproduction, maintaining mitochondrial membrane integrity, and inhibiting apoptotic pathways.
- Melatonin shows therapeutic potential for a range of clinical conditions associated with mitochondrial dysfunction.
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