Butylated hydroxyl-toluene, 2,4-Di-tert-butylphenol, and phytol of Chlorella sp. protect the PC12 cell line against H 2 O 2 -induced neurotoxicity

• Published in: Biomedicine & pharmacotherapy Vol. 145; p. 112415
• Main Authors: Vahdati, Saeed Niazi, Lashkari, Ali, Navasatli, Sepideh Aliniaye, Ardestani, Susan Kabudanian, Safavi, Maliheh
• Format: Journal Article
• Language: English
• Published: France 01.01.2022
• Subjects: Animals; Antioxidants - isolation & purification; Antioxidants - pharmacology; Apoptosis - drug effects; Butylated Hydroxytoluene - isolation & purification; Butylated Hydroxytoluene - pharmacology; Cell Survival - drug effects; Chlorella - chemistry; Free Radical Scavengers - isolation & purification; Free Radical Scavengers - pharmacology; Hydrogen Peroxide - toxicity; Membrane Potential, Mitochondrial - drug effects; Neurodegenerative Diseases - physiopathology; Neurodegenerative Diseases - prevention & control; Neuroprotective Agents - isolation & purification; Neuroprotective Agents - pharmacology; Oxidative Stress - drug effects; PC12 Cells; Phenols - isolation & purification; Phenols - pharmacology; Phytol - isolation & purification; Phytol - pharmacology; Rats; Reactive Oxygen Species - metabolism; Neuroprotective; Chlorella sp; PC12 cell; Microalgae; Antioxidant; Anti-inflammatory
• ISSN: 1950-6007

Oxidative stress is considered the main cause of cellular damage in a number of neurodegenerative disorders. One suitable ways to prevent cell damage is the use of the exogenous antioxidant capacity of natural products, such as microalgae. In the present study, four microalgae extracts, isolated from the Persian Gulf, were screened to analyze their potential antioxidant activity and free radical scavenging using ABTS, DPPH, and FRAP methods. The methanolic extracts (D1M) of green microalgae derived from Chlorella sp. exhibited potent free radical scavenging activity. In order to characterize microalgae species, microscopic observations and analysis of the expression of 18S rRNA were performed. The antioxidant and neuroprotective effects of D1M on H O -induced toxicity in PC12 cells were investigated. The results demonstrated that D1M significantly decreased the release of nitric oxide (NO), formation of intracellular reactive oxygen species (ROS), and the level of malondialdehyde (MDA), whereas it enhanced the content of glutathione (GSH), and activity of heme oxygenase 1 (HO-1), NAD(P)H: quinone oxidoreductase 1 (NQO1), and catalase (CAT) in PC12 cells exposed to H O . The pretreatment of D1M improved cell viability as measured by the MTT assay and invert microscopy, reduced cell apoptosis as examined by flow cytometry analysis, increased mitochondrial membrane potential (MMP), and diminished caspase-3 activity. The GC/MS analysis revealed that D1M ingredients have powerful antioxidant and anti-inflammatory compounds, such as butylated hydroxytoluene (BHT), 2,4-di-tert-butyl-phenol (2,4-DTBP), and phytol. These results suggested that Chlorella sp. extracts have strong potential to be applied as neuroprotective agents, for the treatment of neurodegenerative disorders.