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穿心莲内酯衍生物在实验动物中的镇痛、解热、抗炎及毒性作用。

Analgesic, antipyretic, anti-inflammatory and toxic effects of andrographolide derivatives in experimental animals.

作者信息

Suebsasana Supawadee, Pongnaratorn Panicha, Sattayasai Jintana, Arkaravichien Tarinee, Tiamkao Siriporn, Aromdee Chantana

机构信息

Pharmaceutical Chemistry, Faculty of Pharmaceutical Sciences, Khon Kaen University, Khon Kaen, Thailand.

出版信息

Arch Pharm Res. 2009 Sep;32(9):1191-200. doi: 10.1007/s12272-009-1902-x. Epub 2009 Sep 26.

Abstract

Andrographolide (1) and 14-deoxy-11,12-didehydroandrographolide (2) are active constituents of Andrographis paniculata (Burm. f.), family Acanthaceae. A. paniculata extracts are reported to have antiviral, antipyretic, immunostimulant and anticancer activities. In this study, 1 and its 14-acetyl- (4) and 3,19-isopropylidenyl- (3) derivatives, as well as 2 and its 3,19-dipalmitoyl-derivative (5), were intraperitoneally tested for their analgesic, antipyretic, anti-inflammatory and acute toxicity effects in animal models. Analgesic effects were tested in mice using hot plate and writhing tests to distinguish the central and peripheral effects, respectively. The results showed that, at 4 mg/kg, all tested substances have significant analgesic effects, and the highest potency was seen with 3, 4 and 5. Increasing the dose of 3 and 5 to 8 mg/kg did not increase the analgesic effect. In the writhing test, 3 and 5, but not 1, showed significant results. In a baker's yeast-induced fever model, 3 and 5 significantly reduced rats' rectal temperature (p < 0.05). In a carrageenan-induced inflammation model, 1, 3 and 5 significantly reduced rats' paw volume. Doses of 3 and 5 up to 100 mg/kg did not show any serious toxic effects. From this study, 3 and 5 are the most interesting derivatives, showing much greater potency than their parent compounds. These could be further developed as analgesic, antipyretic and anti-inflammatory agents, without any serious toxicity.

摘要

穿心莲内酯(1)和14-去氧-11,12-二脱氢穿心莲内酯(2)是爵床科植物穿心莲的活性成分。据报道,穿心莲提取物具有抗病毒、解热、免疫刺激和抗癌活性。在本研究中,对1及其14-乙酰基衍生物(4)和3,19-异亚丙基衍生物(3),以及2及其3,19-二棕榈酰衍生物(5)进行了腹腔注射,以测试它们在动物模型中的镇痛、解热、抗炎和急性毒性作用。在小鼠中使用热板法和扭体法分别测试镇痛效果,以区分中枢和外周作用。结果表明,在4mg/kg时,所有测试物质均具有显著的镇痛作用,其中3、4和5的效力最高。将3和5的剂量增加到8mg/kg并未增强镇痛效果。在扭体试验中,3和5显示出显著效果,而1则未显示。在面包酵母诱导的发热模型中,3和5显著降低了大鼠的直肠温度(p<0.05)。在角叉菜胶诱导的炎症模型中,1、3和5显著降低了大鼠的爪体积。高达100mg/kg的3和5剂量未显示出任何严重的毒性作用。从本研究来看,3和5是最具吸引力的衍生物,其效力比母体化合物大得多。它们可进一步开发为镇痛、解热和抗炎药物,且无任何严重毒性。

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