| Literature DB >> 32779097 |
Guilherme Lopes Dornelles1, Juliana Sorraila de Oliveira2, Erin John Rieger de Almeida3, Camila Benaduce Emanuelli Mello4, Bernardo Rodrigues E Rodrigues4, Cássia Bagolin da Silva4, Letícia Dos Santos Petry5, Micheli Mainardi Pillat2, Taís Vidal Palma2, Cinthia Melazzo de Andrade4,2.
Abstract
Neuroinflammation is a predisposing factor for the development of cognitive impairment and dementia. Among the new molecules that are currently being studied, ellagic acid (EA) has stood out for its neuroprotective properties. The present study investigated the effects of ellagic acid in the object recognition test, oxidative stress, cholinergic neurotransmission, glial cell expression, and phosphorylated Tau protein expression. For this, 32 male Wistar rats received an intraperitoneal (IP) application of lipopolysaccharides (LPS) at a dose of 250 µg/kg or 0.9% saline solution (SAL) for 8 days. Two hours after the IP injections, the animals received 100 mg/kg of EA or SAL via intragastric gavage. Behavioral parameters (open field test and object recognition) were performed on days 5, 6, and 7 of the experimental periods. The results showed that the treatment with EA in the LPS group was able to inhibit cognitive impairment, modulate the immune system response by significantly reducing glial cell expression, attenuating phosphorylated Tau and oxidative damage with consequent improvement in the antioxidant system, as well as preventing the increase of acetylcholinesterase activity. Thus, the neuroprotective effects of EA and its therapeutic potential in cognitive disorders secondary to neuroinflammation were demonstrated.Entities:
Keywords: Acetylcholinesterase; Astrocytes; Ellagic acid; Microglia; Oxidative stress; Rats
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Year: 2020 PMID: 32779097 DOI: 10.1007/s11064-020-03105-z
Source DB: PubMed Journal: Neurochem Res ISSN: 0364-3190 Impact factor: 3.996