4.5 Article

Polygala sabulosa AW Bennett extract mitigates motor and cognitive deficits in a mouse model of acute ischemia

Journal

METABOLIC BRAIN DISEASE
Volume 36, Issue 3, Pages 453-462

Publisher

SPRINGER/PLENUM PUBLISHERS
DOI: 10.1007/s11011-020-00660-w

Keywords

Polygala sabulosa; Ischemic stroke; Neuroprotection; Cognition; Motor rehabilitation

Funding

  1. Fundacao de Amparo a Pesquisa do Espirito Santo (FAPES), Brazil
  2. Coordenacao de Aperfeicoamento de Pessoal de Nivel Superior (CAPES), Brazil
  3. Conselho Nacional de Desenvolvimento Cientifico e Tecnologico (CNPq), Brazil
  4. Fundacao de Amparo a Pesquisa e Inovacao do Estado de Santa Catarina (FAPESC), Brazil
  5. Programa INCT-INOVAMED, Brazil [465430/2014-7]

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Stroke is a leading cause of death worldwide, with limited treatment options. Studies have shown that the medicinal plant Polygala sabulosa W. Bennett has potential therapeutic properties for stroke. Research suggests that HEPs treatment can prevent motor and cognitive impairments caused by ischemic stroke, making it a promising therapy option.
Stroke is considered one of the leading causes of death worldwide. The treatment is limited; however, the Brazilian flora has a great source of natural products with therapeutic potentials. Studies with the medicinal plant Polygala sabulosa W. Bennett provided evidence for its use as an anti-inflammatory and neuroprotective drug. In the case of ischemic stroke due to lack of oxygen, both acute and chronic inflammatory processes are activated. Thus, we hypothesized that P. sabulosa (HEPs) has the potential to treat the motor and cognitive deficits generated by ischemic stroke. Male mice were subjected to global ischemia for 60 min, followed by reperfusion and orally treated with HEPs (100 mg/kg in saline + 3% tween 20) twice a day (12 h apart) for 48 h starting 3 h after surgery. Motor skills were assessed using grip force and open field tasks. Hippocampi were then collected for mRNA quantification of the cytokines IL-1-beta and TNF-alpha levels. After 48 h of acute treatment, spatial reference memory was evaluated in a Morris water maze test for another group of animals. We show that HEPs treatment significantly prevented motor weakness induced by ischemia. Brain infarct area was reduced by 22.25% with downregulation of the levels of IL-1 beta and TNF-alpha mRNA. Learning performance and memory ability on Morris water maze task were similar to the sham group. Our data demonstrates the neuroprotective properties of HEPs through its anti-inflammatory activities, which prevent motor and cognitive impairments, suggesting that HEPs may be an effective therapy for ischemic stroke.

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