Campos Cristina, de Castro Alexandre Luz, Tavares Angela Maria Vicente, Fernandes Rafael Oliveira, Ortiz Vanessa Duarte, Barboza Tatiane Evelyn, Pereira Cláudio, Apel Miriam, da Silva Onilda Santos, Llesuy Susana, Araujo Alex Sander da Rosa, Belló-Klein Adriane
*Universidade Federal Do Rio Grande Do Sul, Porto Alegre, Brasil; †Centro Universitário Ritter dos Reis, Porto Alegre, Brasil; ‡Tecnano, Porto Alegre, Brasil; and §Universidad de Buenos Aires, Argentina.
J Cardiovasc Pharmacol. 2017 Feb;69(2):79-85. doi: 10.1097/FJC.0000000000000442.
Copaiba oil comes from an Amazonian tree and has been used as an alternative medicine in Brazil. However, it has not been investigated yet in the treatment of cardiovascular diseases. This study was designed to test whether copaiba oil or nanocapsules containing this oil could modulate monocrotaline (MCT)-induced pulmonary arterial hypertension (PAH). Male Wistar rats (170 ± 20 g) received oil or nanocapsules containing this oil (400 mg/kg) by gavage daily for 1 week. At the end of this period, a single injection of MCT (60 mg/kg i.p.) was administered and measurements were performed after 3 weeks. The animals were divided into 6 groups: control, copaiba oil, nanocapsules with copaiba oil, MCT, oil + MCT, and nanocapsules + MCT. Afterward, echocardiographic assessments were performed, and rats were killed to collect hearts for morphometry and oxidative stress. MCT promoted a significant increase in pulmonary vascular resistance, right ventricle (RV) hypertrophy, and RV oxidative stress. Both oil and copaiba nanocapsules significantly reduced RV hypertrophy and oxidative stress. Pulmonary vascular resistance was reduced by copaiba oil in natura but not by nanocapsules. In conclusion, copaiba oil seems to offer protection against MCT-induced PAH. Our preliminary results suggest that copaiba oil may be an important adjuvant treatment for PAH.
苦配巴油来自一种亚马逊树木,在巴西已被用作替代药物。然而,其在心血管疾病治疗方面尚未得到研究。本研究旨在测试苦配巴油或含该油的纳米胶囊是否能调节野百合碱(MCT)诱导的肺动脉高压(PAH)。雄性Wistar大鼠(170±20克)每天经口灌胃给予油或含该油的纳米胶囊(400毫克/千克),持续1周。在此期间结束时,单次腹腔注射MCT(60毫克/千克),3周后进行测量。动物被分为6组:对照组、苦配巴油组、含苦配巴油的纳米胶囊组、MCT组、油+MCT组和纳米胶囊+MCT组。之后,进行超声心动图评估,并处死大鼠以收集心脏进行形态计量学和氧化应激分析。MCT显著增加了肺血管阻力、右心室(RV)肥大和RV氧化应激。油和苦配巴纳米胶囊均显著减轻了RV肥大和氧化应激。天然苦配巴油降低了肺血管阻力,但纳米胶囊未降低。总之,苦配巴油似乎对MCT诱导的PAH具有保护作用。我们的初步结果表明,苦配巴油可能是PAH的一种重要辅助治疗药物。