Aristolochia trilobata: Identification of the Anti-Inflammatory and Antinociceptive Effects

被引:8
作者
Salome, Dayana Costa [1 ]
Cordeiro, Natalia de Morais [1 ]
Valerio, Tayna Sequeira [1 ]
Santos, Darlisson de Alexandria [2 ,3 ]
Alves, Pericles Barreto [2 ]
Alviano, Celuta Sales [4 ]
Alviano Moreno, Daniela Sales [4 ]
Fernandes, Patricia Dias [1 ]
机构
[1] Univ Fed Rio de Janeiro, Inst Ciencias Biomed, Lab Farmacol Dor & Inflamacao, BR-21941902 Rio De Janeiro, Brazil
[2] Univ Fed Sergipe, Dept Quim, BR-49100000 Sergipe, Brazil
[3] Univ Fed Sul & Sudeste Para, Fac Quim, Inst Ciencias Exatas, BR-68507590 Maraba, Brazil
[4] Univ Fed Rio de Janeiro, Inst Microbiol Prof Paulo de Goes, Lab Superficie Fungos, BR-21941902 Rio De Janeiro, Brazil
关键词
Aristolochia trilobata; sulcatyl acetate; antinociceptive effect; anti-inflammatory activity; ACTIVATED PROTEIN-KINASE; NITRIC-OXIDE SYNTHASE; FORMALIN TEST; MURINE MODEL; LIPOPOLYSACCHARIDE; INFLAMMATION; INVOLVEMENT; CARRAGEENAN; INDUCTION; PATHWAYS;
D O I
10.3390/biomedicines8050111
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
Aristolochia trilobata, popularly known as "mil-homens," is widely used for treatment of stomach aches, colic, asthma, pulmonary diseases, diabetes, and skin affection. We evaluated the antinociceptive and anti-inflammatory activities of the essential oil (EO) and the main constituent, 6-methyl-5-hepten-2-yl acetate (sulcatyl acetate, SA). EO and SA (1, 10, and 100 mg/kg, p.o.) were evaluated using chemical (formalin-induced licking) and thermal (hot-plate) models of nociception or inflammation (carrageenan-induced cell migration into the subcutaneous air pouch, SAP). The mechanism of antinociceptive activity was evaluated using opioid, cholinergic receptor antagonists (naloxone and atropine), or nitric oxide synthase inhibitor (L-NAME). EO and SA presented a central antinociceptive effect (the hot-plate model). In formalin-induced licking response, higher doses of EO and SA also reduced 1st and 2nd phases. None of the antagonists and enzyme inhibitor reversed antinociceptive effects. EO and SA reduced the leukocyte migration into the SAP, and the cytokines tumor necrosis factor and interleukin-1 (TNF-alpha and IL-1 beta, respectively) produced in the exudate. Our results are indicative that EO and SA present peripheral and central antinociceptive and anti-inflammatory effects.
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页数:18
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