Antinociceptive Activity and Toxicity Evaluation of the Fatty Oil from Plukenetia polyadenia Mull. Arg. (Euphorbiaceae)

被引:9
|
作者
Mota, Amanda S. [1 ]
de Lima, Anderson B. [1 ,2 ]
Albuquerque, Thayana Lucy F. [1 ]
Silveira, Tiago S. [2 ]
do Nascimento, Jose Luiz M. [3 ]
da Silva, Joyce Kelly R. [2 ]
Ribeiro, Alcy F. [4 ]
Maia, Jose Guilherme S. [5 ,6 ]
Bastos, Gilmara N. T. [1 ]
机构
[1] Univ Fed Para UFPA, Lab Neuroinflamacao, BR-66075900 Belem, Para, Brazil
[2] Univ Fed Para UFPA, Programa Posgrad Biotecnol, BR-66075900 Belem, Para, Brazil
[3] Univ Fed Para UFPA, Lab Neuroquim Mol & Celular, BR-66075900 Belem, Para, Brazil
[4] Univ Fed Sul & Sudeste Para UNIFESSPA, Inst Ciencias Exatas & Nat, BR-68507590 Maraba, PA, Brazil
[5] Univ Fed Para UFPA, Programa Posgrad Quim, BR-66075900 Belem, Para, Brazil
[6] Univ Fed Oeste Para UFOPA, Programa Posgrad Recursos Nat, BR-68035110 Santarem, PA, Brazil
来源
MOLECULES | 2015年 / 20卷 / 05期
关键词
Plukenetia polyadenia; Euphorbiaceae; fatty oil; linoleic and -linolenic acids; antinociception activity; toxicity; AQUEOUS EXTRACT; ACIDS; PROFILE;
D O I
10.3390/molecules20057925
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Seed oil (Pp-oil) of Plukenetia polyadenia is used by native people of the Brazilian Amazon against arthritis and rheumatism, spreading it on the arms and legs to reduce the pain and inflammation. Pp-oil was obtained by pressing dried seeds at room temperature to give a 47.0% yield of oil. It was then subjected to fatty acid composition analysis. The principal fatty acids were linoleic acid (46.5%), -linolenic acid (34.4%) and oleic acid (13.9%). Then, it was evaluated for its antinociceptive activity in mice, using the acetic acid-induced abdominal writhing, hot plate and formalin test models. Additionally, its toxicity was determined. The Pp-oil proved to have no toxicological effects, showing dose-dependent antinociceptive effect under chemical stimulation. At oral doses of 25-100 mg/kg, Pp-oil significantly reduced the abdominal writhes in the writhing test. A higher oral dose of 200 mg/kg did not induce alterations in the latency time of the hot plate test when compared to the control, suggesting an analgesic activity of peripheral origin. At oral doses of 50 and 100 mg/kg, the Pp-oil significantly reduced the second phase of the algic stimulus in the formalin test. In addition, the antinociception of Pp-oil was reversed by naloxone in the evaluation of its mechanism of action. Therefore, the Pp-oil proved to be safe at very high doses and to show significant analgesic properties. The role of Pp-oil is still being investigated with respect the mechanism of action, but the results suggest that opiod receptors could be involved in the antinociception action observed for the oil of P. polyadenia.
引用
收藏
页码:7925 / 7939
页数:15
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