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首页> 外文期刊>BMC Pharmacology >Antinociceptive effect of geranylgeraniol and 6α,7β-dihydroxyvouacapan-17β-oate methyl ester isolated from Pterodon pubescens Benth
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Antinociceptive effect of geranylgeraniol and 6α,7β-dihydroxyvouacapan-17β-oate methyl ester isolated from Pterodon pubescens Benth

机译:香叶蕨中的香叶基香叶醇和6α,7β-二羟基vouacapan-17β-oate甲酯的抗伤害作用

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Background Pterodon pubescens Benth seeds are commercially available in the Brazilian medicinal plant street market. The crude alcoholic extracts of this plant are used in folk medicine as anti-inflammatory, analgesic, and anti-rheumatic preparations. The aim of this study was to evaluate the contribution of geranylgeraniol (C1) and 6α, 7β-dihydroxyvouacapan-17β-oate methyl ester (C2) isolated from Pterodon pubescens Benth. to the antinociceptive activity of the crude extract. Results Compounds C1 and C2 demonstrated activity against writhing with intraperitoneal (i.p.) and oral (p.o.) routes, capsaicin (i.p. and p.o.), glutamate (i.p.), and in the hot-plate (p.o.) tests, demonstrating their contribution to the antinociceptive activity of crude Pterodon pubescens Benth extracts. The observed activity of compounds C1 and C2 may be related to vanilloid receptors VR1, and/or glutamate peripheral receptors. In hot-plate model, the antinociceptive activity was maintained when naloxone chloride (opioid antagonist) was administered prior to treatment with compounds suggesting that C1 and C2 (p.o.) do not exert their antinociceptive effects in the hot-plate test via opioid receptors. The findings presented herein also suggest that compounds within the crude Pterodon pubescens Benth. extract may exert a synergistic interactive effect, since the crude extract (300 mg.kg-1) containing lower concentrations of compounds C1 (11.5%- 34.6 mg. kg-1) and C2 (1.5% - 4.7 mg.kg-1) gave statistically the same effect to the pure compounds when tested separately (C1 = C2 = 300 mg.kg-1) in writhing experimental model with p.o. administration. Further studies will be undertaken to establish more specifically the mechanisms of action for compounds C1 and C2. Possible synergistic interactions will be evaluated employing the Isobole method. Conclusion These results allowed us to establish a relationship between the popular use of Pterodon pubescens seeds for pain relief and the activity of two major compounds isolated from this species which demonstrated antinociceptive activity. Various "in vivo" experimental models corroborate the folk use of this species for different pain and inflammation disorders.
机译:背景技术翼龙蕨(Pterodon pubescens)Benth种子可在巴西药用植物街市购得。该植物的粗酒精提取物在民间医学中用作抗炎,止痛和抗风湿制剂。这项研究的目的是评估香叶基香叶醇(C1)和从耻骨蕨(Pterodon pubescens Benth)分离出的6α,7β-二羟基vouacapan-17β-oate甲酯(C2)的贡献。对粗提物的抗伤害感受活性。结果化合物C1和C2在腹膜内(ip)和口服(po)途径,辣椒素(ip和po),谷氨酸(ip)和热板试验(po)中表现出抗扭体作用,证明了它们对抗伤害感受药的作用毛蕨(Pterodon pubescens Benth)提取物的活性。观察到的化合物C1和C2的活性可能与类香草酸受体VR1和/或谷氨酸外围受体有关。在热板模型中,在用纳洛酮氯化物(阿片类药物拮抗剂)治疗之前给予纳洛酮氯化物(阿片类药物拮抗剂)可维持抗伤害感受活性,表明C1和C2(p.o。)在热板试验中不通过阿片样物质受体发挥其抗伤害感受作用。本文介绍的发现还表明,粗制的翼手蕨中存在化合物。提取物可能发挥协同作用,因为粗提取物(300 mg.kg -1 )含有较低浓度的化合物C1(11.5%-34.6 mg。kg -1 ) )和C2(1.5%-4.7 mg.kg -1 )在单独测试时对纯化合物具有统计学上相同的作用(C1 = C2 = 300 mg.kg -1 )用po扭曲实验模型行政。将进行进一步的研究以更具体地建立化合物C1和C2的作用机理。可能的协同相互作用将使用Isobole方法进行评估。结论这些结果使我们能够建立在广泛使用的紫檀种子减轻疼痛方面与从该物种中分离出的两种主要化合物的活性之间的关系,该化合物具有抗伤害感受活性。各种“体内”实验模型证实了该物种在不同疼痛和炎症疾病中的民间使用。

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