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首页> 外文期刊>Biological & pharmaceutical bulletin >Further antinociceptive properties of extracts and phenolic compounds from Plinia glomerata (Myrtaceae) leaves.
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Further antinociceptive properties of extracts and phenolic compounds from Plinia glomerata (Myrtaceae) leaves.

机译:从Plinia glomerata(桃金娘科)叶片中提取物和酚类化合物的进一步抗伤害感受特性。

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This study describes the antinociceptive activity of extracts (methanolic (ME) and acetonic (AE)) and two phenolic compounds, 3,4,3'-trimethoxyflavellagic acid (1) and 3,4,3'-trimethoxy flavellagic acid 4'-O-glucoside (2), from Plinia glomerata leaves, against different experimental models of pain in mice. When evaluated against writhing test, by i.p. route, ME and AE presented calculated ID(50) values (and respective confidence interval) of 3.28 (1.63-6.61) and 24.79 (16.57-37.09) mg/kg, respectively. Given by the oral route at 500 mg/kg, AE and ME extracts inhibited the abdominal constrictions by 60.5% and 35.3%, respectively. In the formalin test (10 mg/kg, i.p.), AE inhibited both phases of pain (45.6% in the first phase; 99.8% in the second phase) whereas ME inhibited 47.8% the first phase, and 92.6% the second phase. In the capsaicin test both extracts showed activity, with calculated ID(50) values of 6.56 (5.69-7.56) and 7.68 (4.94-11.93) mg/kg for AE and ME, respectively. When evaluated againstthe hot-plate test, both extracts demonstrated activity, but only in high doses. Compound 2, when evaluated against the formalin test (10 mg/kg, i.p.), inhibited both phases of pain (77.6%, first phase; 62%, second phase) whereas 1 inhibited only the first phase, with inhibition of 70%. When tested in the capsaicin and glutamate tests, at 10 mg/kg, i.p., 1 and 2 caused inhibitions of 41.5% and 37.9%, and 37.7% and 54.5%, respectively. These results confirm previous studies carried out by our research group regarding the antinociceptive properties of P. glomerata, stimulating other studies on mechanism of action as well as the determination of additional active principles in this plant.
机译:这项研究描述了提取物(甲醇(ME)和丙酮(AE))和两种酚类化合物3,4,3'-三甲氧基黄酮酸(1)和3,4,3'-三甲氧基黄酮酸4'-的抗伤害感受活性。来自Plinia glomerata叶片的O-葡萄糖苷(2)可以抵抗小鼠不同的疼痛实验模型。当通过扭力测试进行评估时,由i.p.路线中,ME和AE的计算得出的ID(50)值(以及相应的置信区间)分别为3.28(1.63-6.61)和24.79(16.57-37.09)mg / kg。通过500 mg / kg的口服途径,AE和ME提取物分别抑制了60.5%和35.3%的腹部收缩。在福尔马林试验中(10 mg / kg,腹腔注射),AE抑制了两个阶段的疼痛(第一阶段为45.6%;第二阶段为99.8%),而ME在第一阶段为47.8%,第二阶段为92.6%。在辣椒素测试中,两种提取物均显示出活性,AE和ME的ID(50)计算值分别为6.56(5.69-7.56)和7.68(4.94-11.93)mg / kg。当根据热板测试进行评估时,两种提取物均显示出活性,但仅在高剂量时才显示活性。根据福尔马林试验评估化合物2(10 mg / kg,腹膜内),可抑制两个阶段的疼痛(77.6%,第一阶段; 62%,第二阶段),而化合物1仅抑制第一阶段的疼痛,抑制率为70%。当在辣椒素和谷氨酸测试中测试时,以10mg / kg的i.p.,1和2分别引起41.5%和37.9%,37.7%和54.5%的抑制。这些结果证实了我们的研究小组先前对球果假单胞菌的抗伤害感受特性进行的研究,这刺激了其他有关作用机理的研究以及确定该植物中其他活性成分的研究。

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