AI Article Synopsis

  • - The study investigated the effects of astaxanthin (ASX) from shrimp shells on Wistar rats with Alzheimer’s disease caused by amyloid-β (1-42) peptides, using eight different treatment groups over 30 days.
  • - Behavioral tests showed that the Aβ group had significantly impaired cognitive abilities and increased memory loss, while oxidative stress markers in the brain worsened.
  • - ASX powder at 10 mg/kg body weight effectively reduced cognitive and memory issues and oxidative stress more than both ASX extract and vitamin E, highlighting its potential benefits for neurodegeneration.

Article Abstract

This study aimed to investigate the effect of astaxanthin (ASX) extracted and ASX powder from shrimp () shells on Wistar rats with Alzheimer's disease, induced by amyloid-β (1-42) peptides. In this task, the rats were divided into eight groups: (1) Control, (2) sham operate, (3) negative control (vehicle) + Aβ, (4) ASX extract+Aβ, (5) commercial ASX + Aβ, (6) ASX powder + Aβ, (7) blank powder + Aβ, and (8) vitamin E + Aβ. All treatments were orally administrated for 30 days. At 14- and 29-days post injection, animals were observed in behavioral tests. On the 31st day, animals were sacrificed; the hippocampus and cortex were collected. Those two brain areas were then homogenized and stored for biochemical and histological analysis. The results showed that the Aβ infused group significantly reduced cognitive ability and increased memory loss, as assessed by the Morris water maze test, novel object recognition test, and novel object location test. Moreover, the Aβ infused group exhibited a deterioration of oxidative markers, including glutathione peroxidase enzymes (GPx), lipid peroxidation (MDA), products of protein oxidation, and superoxide anion in the cortex and the hippocampus. Meanwhile, ASX powder (10 mg/kg body weight) showed a significant reduction in cognitive and memory impairments and oxidative stress which is greater than ASX extract in the same dose of compound or vitamin E (100 mg/kg body weight). Our study indicates the beneficial properties of ASX in alleviation of cognitive functions and reducing neurodegeneration in Wistar rats induced by amyloid-β (1-42) peptides.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC6891431PMC
http://dx.doi.org/10.3390/md17110628DOI Listing

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