Mixture of Phlorotannin and Fucoidan from Ecklonia cava Prevents the Aβ-Induced Cognitive Decline with Mitochondrial and Cholinergic Activation.
Hye Ju HanSeon Kyeong ParkJin Yong KangJong Min KimSeul Ki YooDae-Ok KimHwan Hee LeeHo-Jin HeoPublished in: Marine drugs (2021)
The anti-amnesic effect of a mixture (4:6 = phlorotannin:fucoidan from Ecklonia cava, P4F6) was evaluated on amyloid-beta peptide (Aβ)-induced cognitive deficit mice. The cognitive function was examined by Y-maze, passive avoidance, and Morris water maze tests, and the intake of the mixture (P4F6) showed an ameliorating effect on Aβ-induced learning and memory impairment. After the behavioral tests, superoxide dismutase (SOD) activity and thiobarbituric acid-reactive substances (TBARS) contents were confirmed in brain tissue, and in the results, the mixture (P4F6) attenuated Aβ-induced oxidative stress. In addition, mitochondrial activity was evaluated by mitochondrial reactive oxygen species (ROS) content, mitochondrial membrane potential (MMP), adenosine triphosphate (ATP) content, and mitochondria-mediated apoptotic signaling pathway, and the mixture (P4F6) enhanced mitochondrial function. Furthermore, the mixture (P4F6) effectively regulated tau hyperphosphorylation by regulating the protein kinase B (Akt) pathway, and promoted brain-derived neurotrophic factor (BDNF) in brain tissue. Moreover, in the cholinergic system, the mixture (P4F6) ameliorated acetylcholine (ACh) content by regulating acetylcholinesterase (AChE) activity and choline acetyltransferase (ChAT) expression in brain tissue. Based on these results, we suggest that this mixture of phlorotannin and fucoidan (P4F6) might be a substance for improving cognitive function by effectively regulating cognition-related molecules.
Keyphrases
- reactive oxygen species
- cognitive decline
- oxidative stress
- signaling pathway
- white matter
- cell death
- diabetic rats
- high glucose
- mild cognitive impairment
- protein kinase
- resting state
- hydrogen peroxide
- drug induced
- cell proliferation
- transcription factor
- risk assessment
- multiple sclerosis
- type diabetes
- metabolic syndrome
- dna damage
- nitric oxide
- functional connectivity
- weight gain
- brain injury
- body mass index
- adipose tissue
- cerebral ischemia
- binding protein
- stress induced
- subarachnoid hemorrhage
- insulin resistance
- endoplasmic reticulum stress
- anti inflammatory
- cell migration