2020
DOI: 10.20944/preprints202005.0342.v1
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Neuroprotective Potentials of Marine Algae and Their Bioactive Metabolites: Pharmacological Insights and Therapeutic Advances

Abstract: Beyond their significant contribution to the dietary and industrial supplies, marine algae are considered to be a potential source of some unique metabolites with diverse health benefits. The pharmacological properties, such as antioxidant, anti-inflammatory, cholesterol homeostasis, protein clearance and anti-amyloidogenic potentials of algal metabolites endorse their protective efficacy against oxidative stress, neuroinflammation, mitochondrial dysfunction, and impaired proteostasis which are known t… Show more

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Cited by 48 publications
(30 citation statements)
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“…Another source of marine compounds with antioxidant activity is seaweeds, which have been the target of numerous studies (extensively reviewed in [ 121 ]), standing out as major producers of bioactive molecules with high antioxidant ability. Another research group tested the effects of different seaweed extracts ( S. muticum.…”
Section: Marine Drugs In Parkinson’s Diseasementioning
confidence: 99%
“…Another source of marine compounds with antioxidant activity is seaweeds, which have been the target of numerous studies (extensively reviewed in [ 121 ]), standing out as major producers of bioactive molecules with high antioxidant ability. Another research group tested the effects of different seaweed extracts ( S. muticum.…”
Section: Marine Drugs In Parkinson’s Diseasementioning
confidence: 99%
“…Algae metabolites are known to have cytostatic, antiviral, anthelmintic, antifungal and antibacterial activity [ 1 , 2 ]. High biological activity of algae is often associated with the presence of powerful and non-toxic natural antioxidants.…”
Section: Introductionmentioning
confidence: 99%
“…Recently, it was reported that the downstream phosphorylation of ERK, which is a mitogen-activated protein kinase (MAPK), activated CREB transcription, regulating the expression of BDNF [ 35 , 36 ]. In contrast, the phosphorylation of JNK and p38, which are also MAPKs, leads to apoptosis and cell death [ 37 , 38 ]. Based on these results, we suggest that ERK may promote the expression of BDNF and TrkB in oxidative stress-induced HT-22 cells.…”
Section: Discussionmentioning
confidence: 99%