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Neuroprotective effect of melatonin against hypoxia‐induced retinal ganglion cell death in neonatal rats
Author(s) -
Kaur Charanjit,
Sivakumar Viswanathan,
Robinson Remya,
Foulds Wallace S.,
Luu Chi D.,
Ling EngAng
Publication year - 2013
Publication title -
journal of pineal research
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.881
H-Index - 131
eISSN - 1600-079X
pISSN - 0742-3098
DOI - 10.1111/jpi.12016
Subject(s) - melatonin , endocrinology , medicine , neuroprotection , biology , glutathione , apoptosis , retina , retinal , pharmacology , biochemistry , neuroscience , enzyme
The purpose of this study was to determine whether melatonin treatment would mitigate retinal ganglion cell ( RGC ) death in the developing retina following a hypoxic insult. Lipid peroxidation ( LPO ), glutathione ( GSH ), tumor necrosis factor‐α ( TNF ‐α) and interleukin‐1β ( IL ‐1β) concentrations, expression of vascular endothelial growth factor receptors, F lt‐1 and F lk‐1, release of cytochrome c from mitochondria, and caspase‐3 expression were examined in the retinas of 1‐day‐old rats at 3 hr to 14 days after a hypoxic exposure. The m RNA and protein expression of F lt‐1 and F lk‐1 and the tissue concentration of LPO , TNF ‐α, and IL ‐1β were upregulated significantly after the hypoxic exposure, whereas the content of GSH was decreased significantly. RGC cultures also showed increased LPO and decreased GSH levels after hypoxic exposure but these effects were reversed in cells treated with melatonin. TNF ‐α and IL ‐1β expression was specifically located on microglial cells, whereas F lt‐1 and F lk‐1 was limited to RGC s as confirmed by double immunofluorescence labeling. Cultures of hypoxic microglial cells treated with melatonin showed a significant reduction in the release of these cytokines as compared to untreated hypoxic cells. Hypoxia induced increase in the cytosolic cytochrome c and caspase‐3 in RGC s was attenuated with melatonin treatment. The results suggest that, in hypoxic injuries, melatonin is neuroprotective to RGC s in the developing retina through its antioxidative, anti‐inflammatory, and anti‐apoptotic effects. Melatonin suppressed F lt‐1 and F lk‐1 expression in retinal blood vessels, which may result in reduced retinal vascular permeability and it also preserved mitochondrial function as shown by a reduction in cytochrome c leakage into the cytosol. The results may have therapeutic implications for the management of retinopathy of prematurity.