Programa de Pós-Graduação em Ciências Farmacêuticas, Universidade Federal do Pará, 66075-900 Belém, Pará, Brazil.
J Ethnopharmacol. 2011 Nov 18;138(2):479-86. doi: 10.1016/j.jep.2011.09.037. Epub 2011 Sep 29.
Peperomia serpens (Piperaceae), popularly known as "carrapatinho", is an epiphyte herbaceous liana grown wild on different host trees in the Amazon rainforest. Its leaves are largely used in Brazilian folk medicine to treat inflammation, pain and asthma.
This study investigated the effects of essential oil of Peperomia serpens (EOPs) in standard rodent models of pain and inflammation.
The antinociceptive activity was evaluated using chemical (acetic acid and formalin) and thermal (hot plate) models of nociception in mice whereas the anti-inflammatory activity was evaluated by carrageenan- and dextran-induced paw edema tests in rats croton oil-induced ear edema, as well as cell migration, rolling and adhesion induced by carrageenan in mice. Additionally, phytochemical analysis of the EOPs has been also performed.
Chemical composition of the EOPs was analyzed by gas chromatography and mass spectrometry (GC/MS). Twenty-four compounds, representing 89.6% of total oil, were identified. (E)-Nerolidol (38.0%), ledol (27.1%), α-humulene (11.5%), (E)-caryophyllene (4.0%) and α-eudesmol (2.7%) were found to be the major constituents of the oil. Oral pretreatment with EOPs (62.5-500 mg/kg) significantly reduced the writhing number evoked by acetic acid injection, with an ED(50) value of 188.8 mg/kg that was used thereafter in all tests. EOPs had no significant effect on hot plate test but reduced the licking time in both phases of the formalin test, an effect that was not significantly altered by naloxone (0.4 mg/kg, s.c.). EOPs inhibited the edema formation induced by carrageenan and dextran in rats. In mice, EOPs inhibited the edema formation by croton oil as well as the leukocyte and neutrophil migration, the rolling and the adhesion of leukocytes.
These data show for the first time that EOPs has a significant and peripheral antinociceptive effect that seems unrelated to interaction with the opioid system. EOPs also displays a significant anti-inflammatory effect in acute inflammation models. This effect seems to be related to components which inhibit the production of several inflammatory mediators. These results support the widespread use of Peperomia serpens in popular medicine to treat inflammation and pain.
Peperomia serpens(胡椒科),俗称“carrapatinho”,是一种附生草本藤本植物,野生于亚马逊雨林中不同的宿主树上。其叶子在巴西民间医学中被广泛用于治疗炎症、疼痛和哮喘。
本研究旨在研究 Peperomia serpens 精油(EOPs)在标准啮齿动物疼痛和炎症模型中的作用。
采用醋酸和福尔马林化学(化学)和热(热板)疼痛模型评估 EOPs 的镇痛活性,而采用角叉菜胶和葡聚糖诱导的爪肿胀试验评估抗炎活性在大鼠中,用巴豆油诱导的耳肿胀以及由角叉菜胶诱导的细胞迁移、滚动和粘附来评价。此外,还对 EOPs 的植物化学进行了分析。
通过气相色谱和质谱联用(GC/MS)分析了 EOPs 的化学成分。鉴定出 24 种化合物,占总油量的 89.6%。(E)-橙花叔醇(38.0%)、愈创木酚(27.1%)、α-葎草烯(11.5%)、(E)-石竹烯(4.0%)和α-桉叶醇(2.7%)被发现是该油的主要成分。口服 EOPs(62.5-500mg/kg)预处理可显著减少醋酸注射引起的扭体次数,ED50 值为 188.8mg/kg,此后用于所有试验。EOPs 对热板试验没有显著影响,但减少了福尔马林试验两个阶段的舔舐时间,纳洛酮(0.4mg/kg,sc)对该作用无明显改变。EOPs 抑制角叉菜胶和葡聚糖诱导的大鼠水肿形成。在小鼠中,EOPs 抑制了巴豆油引起的水肿以及白细胞和中性粒细胞的迁移、滚动和粘附。
这些数据首次表明,EOPs 具有显著的外周镇痛作用,似乎与与阿片系统的相互作用无关。EOPs 还在急性炎症模型中表现出显著的抗炎作用。这种作用似乎与抑制几种炎症介质产生的成分有关。这些结果支持了在民间医学中广泛使用 Peperomia serpens 来治疗炎症和疼痛的做法。