| Literature DB >> 27612165 |
Ricardo Basto Souza1, Annyta Fernandes Frota2, Rayane Siqueira Sousa2, Nayara Araújo Cezario2, Tarcizio Brito Santos2, Luziana Mara Frota Souza2, Chistiane Oliveira Coura1, Valdécio Silvano Monteiro1, Gerardo Cristino Filho2, Silvânia Maria Mendes Vasconcelos3, Rodrigo Maranguape Silva da Cunha4, Lissiana Magna Vasconcelos Aguiar2, Norma Maria Barros Benevides1.
Abstract
Parkinson's disease (PD) is a multifactorial disease associated with the degeneration of dopaminergic neurons and behavioural alterations. Natural bioactive compounds may provide new therapeutic alternatives for neurodegenerative disorders, such as PD. The sulphated polysaccharides isolated from marine algae are heterogenic molecules that show different biological activities. The red marine alga Gracilaria cornea has a sulphated polysaccharide (SA-Gc) with structure and anti-inflammatory and antinociceptive activities reported in the literature. Therefore, this study aimed to evaluate the neuroprotective effects of SA-Gc in rat model PD induced by 6-hydroxydopamine (6-OHDA). Firstly, we established the PD model in rats, induced by an intrastriatal injection (int.) of 6-OHDA, followed by a single administration of SA-Gc (15, 30 or 60 μg; int.). On the 14th day, behavioural tests were performed. After killing, brain areas were dissected and used for neurochemical and/or transcriptional analyses. The results showed that SA-Gc (60 μg, int.) promoted neuroprotective effects in vivo through reducing the oxidative/nitroactive stress and through alterations in the monoamine contents induced by 6-OHDA. Furthermore, SA-Gc modulated the transcription of neuroprotective and inflammatory genes, as well as returning behavioural activities and weight gain to normal conditions. Thus, this study reports the neuroprotective effects of SA-Gc against 6-OHDA in rats.Entities:
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Year: 2016 PMID: 27612165 DOI: 10.1111/bcpt.12669
Source DB: PubMed Journal: Basic Clin Pharmacol Toxicol ISSN: 1742-7835 Impact factor: 4.080