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Malaysian macroalga Hauck attenuates high dose corticosterone-mediated oxidative damage in PC12 cells mimicking the effects of depression. | LitMetric

AI Article Synopsis

  • - Oxidative damage plays a role in depression, and Malaysian macroalgae have natural antioxidant properties that may help combat this damage.
  • - Researchers extracted different compounds from macroalgae and found that the ethanol extract was the most effective in reducing oxidative damage caused by high levels of corticosterone in cell models.
  • - The ethanol extract improved cell health by reversing oxidative stress effects similarly to the antidepressant desipramine, indicating its potential as an antioxidant for mitochondrial protection in depression treatment.

Article Abstract

Oxidative damage has been associated with the pathophysiology of depression. Macroalgae are equipped with antioxidant defense system to counteract the effects of free radicals We explored the use of Malaysian to attenuate high dose corticosterone-mediated oxidative damage in a cellular model mimicking depression. Fresh specimen of was freeze-dried and extracted sequentially with hexanes, ethyl acetate and ethanol. The extracts were screened for their phytochemical contents and antioxidant activities. Ethanol extract demonstrated the most potent antioxidant capacity and was selected for subsequent assays against high dose corticosterone of 600 µM-mediated oxidative damage in the rat pheochromocytoma (PC12) cells. The corticosterone reduced the cell viability, glutathione (GSH) level, aconitase activity, and mitochondrial membrane potential (MMP); and increased the lactate dehydrogenase (LDH) release, intracellular reactive oxygen species (ROS) level and apoptosis. However, the extent of oxidative damage was reversed by 0.25-0.5 mg/mL ethanol extract suggesting a possible role of -based antioxidants in the mitochondrial defense against constant ROS generation and regulation of antioxidant pathway. The effects were similar to that of desipramine, a tricyclic antidepressant. Our findings indicate that can be developed as a mitochondria-targeted antioxidant to mitigate antidepressant-like effects.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC7254034PMC
http://dx.doi.org/10.1016/j.sjbs.2020.04.042DOI Listing

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