Anticonvulsant and Antioxidant Effects of Cyano-carvone and Its Action on Acetylcholinesterase Activity in Mice Hippocampus

被引:28
作者
Costa, Dayane Alves [3 ]
Lopes de Oliveira, Guilherme Antonio [3 ]
Lima, Tamires Cardoso [2 ]
dos Santos, Pauline Sousa [3 ]
de Sousa, Damio Pergentino [2 ]
de Freitas, Rivelilson Mendes [1 ,3 ]
机构
[1] Univ Fed Piaui, Programa Posgrad Ciencias Farmaceut, Nucleo Tecnol Farmaceut, Ctr Ciencias Saude, BR-64049550 Teresina, Piaui, Brazil
[2] Univ Fed Sergipe, Dept Physiol, BR-49100000 Sao Cristovao, Sergipe, Brazil
[3] Univ Fed Piaui, Lab Res Expt Neurochem, Postgrad Program Pharmaceut Sci, BR-64049550 Teresina, Piaui, Brazil
关键词
Acetylcholinesterase; Cyano-carvone; Oxidative stress; Pilocarpine; Seizures; INDUCED STATUS EPILEPTICUS; LIPID-PEROXIDATION; OXIDATIVE STRESS; NITRITE FORMATION; ALPHA-TOCOPHEROL; INDUCED SEIZURES; WISTAR RATS; KAINIC ACID; LIPOIC ACID; PILOCARPINE;
D O I
10.1007/s10571-012-9812-8
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
The anticonvulsant effect of cyano-carvone, a monoterpene monocyclic, was investigated in epilepsy model induced by pilocarpine. Cyano-carvone at doses of 25, 50 or 75 mg/kg promoted a reduction of 16.7, 33 and 66.7%, respectively, against pilocarpine-induced seizures, and it was efficacious in increasing both the latency to first seizures and the survival percentage, resulting in 33.3, 67 and 91.7% of protection against death induced by seizures, respectively (P < 0.05). The reference drug atropine (25 mg/kg) also produced a significant protection (100%). Its monoterpene, at 25, 50 and 75 mg/kg, was also capable to increase the latency for installation of status epilepticus induced by pilocarpine, and presented a significant protection against lipid peroxidation and nitrite formation in mice hippocampus (P < 0.05). In addition, it was observed that the cyano-carvone pretreatment increased the acetylcholinesterase activity in mice hippocampus after pilocarpine-induced seizures. The present results clearly indicate the anticonvulsant ability of cyano-carvone, which can be, at least in part, explained by the increased activity of the acetylcholinesterase enzyme. Our data suggest that the action mechanism can also be due to a direct activation of the antioxidant enzymes that could be associated with a reduction observed in oxidative stress in mice hippocampus, probably involving an inhibition of free radical production.
引用
收藏
页码:633 / 640
页数:8
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