Ethyl-acetate fraction of Trichilia catigua restores long-term retrograde memory and reduces oxidative stress and inflammation after global cerebral ischemia in rats

[Display omitted] •Transient global cerebral ischemia (TGCI) induced persistent retrograde memory loss.•Protein carbonylation and myeloperoxidase activity increased after TGCI.•Trichilia catigua prevented the cognitive and biochemical outcomes of TGCI.•The antiamnesic effect of T. catigua occurred i...

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Veröffentlicht in:Behavioural brain research 2018-01, Vol.337, p.173-182
Hauptverfasser: Godinho, Jacqueline, de Oliveira, Rúbia Maria Weffort, de Sa-Nakanishi, Anacharis Babeto, Bacarin, Cristiano Correia, Huzita, Claudia Hitomi, Longhini, Renata, Mello, João Carlos P., Nakamura, Celso Vataru, Previdelli, Isolde Santos, Dal Molin Ribeiro, Matheus Henrique, Milani, Humberto
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Sprache:eng
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Zusammenfassung:[Display omitted] •Transient global cerebral ischemia (TGCI) induced persistent retrograde memory loss.•Protein carbonylation and myeloperoxidase activity increased after TGCI.•Trichilia catigua prevented the cognitive and biochemical outcomes of TGCI.•The antiamnesic effect of T. catigua occurred in absence of neuronal rescue.•T. catigua may represent a source of substances with neuroprotective properties. We originally reported that an ethyl-acetate fraction (EAF) of Trichilia catigua prevented the impairment of water maze learning and hippocampal neurodegeneration after transient global cerebral (TGCI) in mice. We extended that previous study by evaluating whether T. catigua (i) prevents the loss of long-term retrograde memory assessed in the aversive radial maze (AvRM), (ii) confers hippocampal and cortical neuroprotection, and (iii) mitigates oxidative stress and neuroinflammation in rats that are subjected to the four vessel occlusion (4-VO) model of TGCI. In the first experiment, naive rats were trained in the AvRM and then subjected to TGCI. The EAF was administered orally 30min before and 1h after TGCI, and administration continued once per day for 7days post-ischemia. In the second experiment, the EAF was administered 30min before and 1h after TGCI, and protein carbonylation and myeloperoxidase (MPO) activity were assayed 24h and 5days later, respectively. Retrograde memory performance was assessed 8, 15, and 21days post-ischemia. Ischemia caused persistent retrograde amnesia, and this effect was prevented by T. catigua. This memory protection (or preservation) persisted even after the treatment was discontinued, despite the absence of histological neuroprotection. Protein carbonyl group content and MPO activity increased around 43% and 100%, respectively, after TGCI, which were abolished by the EAF of T. catigua. The administration of EAF did not coincide with the days of memory testing. The data indicate that antioxidant and/or antiinflammatory actions in the early phase of ischemia/reperfusion contribute to the long-term antiamnesic effect of T. catigua.
ISSN:0166-4328
1872-7549
DOI:10.1016/j.bbr.2017.08.050