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首页> 外文期刊>Pharmaceutical Biology >Water Extract of Leaves and Stems of Preflowering but not Flowering Plants of Anisomeles indica Possesses Analgesic and Antihyperalgesic Activities in Rats
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Water Extract of Leaves and Stems of Preflowering but not Flowering Plants of Anisomeles indica Possesses Analgesic and Antihyperalgesic Activities in Rats

机译:An仁无花果叶片和茎的水提取物具有大鼠镇痛和抗痛觉过敏作用

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According to Sri Lankan traditional medicine, a decoction made from stems and leaves of Anisomeles indica Kuntze (Lamiaceae) possesses analgesic activity. However, the validity of this claim has not been scientifically tested. The aim of this study was to investigate analgesic and antihyperal-gesic activities of this plant using a water extract made from the leaves and stems. The water extracts were made from leaves and stems of both preflowering (El) and flowering plants (E2). El showed a dose-dependent analgesic effect up to 6h of treatment when tested in rats using the hot plate and the tail flick techniques. Further, the analgesic effect of El was not accompanied by toxic effects. This effect was neither gender dependent nor dependent on the stage of the estrous cycle. El also showed a dose-dependent antihyperalgesic activity in the hot plate test. In contrast, E2 did not show any analgesic effect (500mg/kg). The analgesic effect produced by El was not abolished by naloxone. El dose-dependently retarded the amplitude of the spontaneous contractions of isolated dioestrous rat uterus. Further, El induced a dose-dependent plasma membrane stabilisation effect on rat ery-throcytes. Collectively, these observations suggest that the analgesic and antihyperalgesic effects of El are mediated from inhibition of COX-1, thus impairing the synthesis of prostaglandins. A change in chemical contents that accompanies flowering could be one possible reason for the inability of E2 to demonstrate analgesic effect.
机译:根据斯里兰卡的传统医学,由印度无芒茴香(菊科)的茎和叶制成的汤具有镇痛作用。但是,该声明的有效性尚未经过科学检验。这项研究的目的是使用由叶和茎制成的水提取物研究这种植物的镇痛和抗痛觉过敏活性。水提取物是从预花(E1)和开花植物(E2)的叶子和茎上制成的。当使用热板和甩尾技术在大鼠中进行测试时,E1在长达6小时的治疗中显示出剂量依赖性镇痛作用。此外,E1的镇痛作用不伴有毒性作用。这种影响既不依赖性别也不依赖于发情周期的阶段。 El在热板测试中还显示出剂量依赖性的抗痛觉过敏活性。相反,E2没有显示出任何镇痛作用(500mg / kg)。 El产生的镇痛作用并未被纳洛酮所消除。 El剂量依赖性地延迟了离体的雌雄同体大鼠子宫自发收缩的幅度。此外,E1对大鼠红细胞诱导了剂量依赖性的质膜稳定作用。总体而言,这些观察结果表明,E1的镇痛和抗痛觉过敏作用是由抑制COX-1介导的,从而损害了前列腺素的合成。开花时化学含量的变化可能是E2无法显示镇痛作用的可能原因之一。

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