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本文引用的文献

1
Leaves extract of murraya koenigii linn for anti-inflammatory and analgesic activity in animal models.九里香叶提取物在动物模型中的抗炎和镇痛活性。
J Adv Pharm Technol Res. 2010 Jan;1(1):68-77.
2
Antinociceptive activity of chronic administration of different extracts of Terminalia bellerica Roxb. and Terminalia chebula Retz. fruits.长期服用诃子(Terminalia bellerica Roxb.)和余甘子(Terminalia chebula Retz.)果实不同提取物的抗伤害感受活性。
Indian J Exp Biol. 2010 Sep;48(9):925-30.
3
Antinociceptive activity of methanolic extract of leaves of Achyranthes aspera Linn. (Amaranthaceae) in animal models of nociception.牛膝草(苋科)叶甲醇提取物在伤害感受动物模型中的抗伤害感受活性。
Indian J Exp Biol. 2010 Aug;48(8):817-21.
4
Beneficial effects of Murraya koenigii leaves on antioxidant defense system and ultra structural changes of pancreatic beta-cells in experimental diabetes in rats.九里香叶对实验性糖尿病大鼠抗氧化防御系统及胰腺β细胞超微结构变化的有益作用。
Chem Biol Interact. 2007 Jan 30;165(2):155-64. doi: 10.1016/j.cbi.2006.10.014. Epub 2006 Dec 2.
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The inhibitory effect of fentanyl and other morphine-like analgesics on the warm water induced tail withdrawl reflex in rats.芬太尼及其他吗啡类镇痛药对大鼠温水诱导甩尾反射的抑制作用。
Arzneimittelforschung. 1963 Jun;13:502-7.
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Release of prostaglandins E and F in an algogenic reaction and its inhibition.致痛反应中前列腺素E和F的释放及其抑制作用。
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Gangliosides antinociceptive effects in rodents.
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Tetrahedron. 1970 Mar;26(6):1475-82. doi: 10.1016/s0040-4020(01)92976-x.

急性和慢性给予九里香叶片在实验动物模型中的抗伤害作用。

Antinociceptive activity of acute and chronic administration of Murraya koenigii L. leaves in experimental animal models.

机构信息

Department of Pharmacology, MGV's Pharmacy College, Panchavati, Nasik, Maharashtra, India.

出版信息

Indian J Pharmacol. 2012 Jan;44(1):15-9. doi: 10.4103/0253-7613.91860.

DOI:10.4103/0253-7613.91860
PMID:22345863
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3271532/
Abstract

AIM

To evaluate the antinociceptive activity of acute and chronic administration of petroleum ether extract of Murraya koenigii L. leaves (PMK) and total alkaloids separated from petroleum ether extract of Murraya koenigii leaves (AMK) in mice.

MATERIALS AND METHODS

PMK was subjected for isolation of total alkaloid fraction AMK. The antinociceptive activity of PMK (100 and 300 mg/kg, p.o.) and AMK (100 and 300 mg/kg, p.o.), after acute and chronic administration (for 15 days), was evaluated using peripheral model like acetic acid-induced writhing method and central model like hot plate method and tail immersion method. Statistical analysis was carried out by one-way ANOVA followed by Dunnett's test.

RESULT

In acute studies, PMK and AMK significantly and dose-dependently reduced the number of acetic acid-induced writhing, significantly increased the latency of paw licking in hot plate method, and significantly increased the basal reaction time in tail immersion method. With chronic administration of PMK and AMK, highest activity was observed on day 9 in acetic acid-induced writhing model. In hot plate and tail immersion method, chronic administration of PMK and AMK initially showed fluctuating responses but produced highest degree of antinociception on day 9 of the study.

CONCLUSION

The degree of antinociception produced by PMK and AMK at the end of 15 days study suggest that Murraya koenigii has potential to use as an analgesic.

摘要

目的

评价急性和慢性给予九里香叶石油醚提取物(PMK)和从九里香叶石油醚提取物中分离得到的总生物碱(AMK)对小鼠的镇痛活性。

材料和方法

PMK 用于分离总生物碱部分 AMK。通过外周模型(醋酸诱导扭体法)和中枢模型(热板法和尾浸法)评估 PMK(100 和 300mg/kg,po)和 AMK(100 和 300mg/kg,po)在急性和慢性给药(15 天)后的镇痛活性。统计分析采用单因素方差分析,然后进行 Dunnett 检验。

结果

在急性研究中,PMK 和 AMK 显著且剂量依赖性地减少了醋酸诱导的扭体次数,显著增加了热板法中舔爪的潜伏期,显著增加了尾浸法中的基础反应时间。在慢性给予 PMK 和 AMK 的研究中,在醋酸诱导的扭体模型中,第 9 天观察到最高的活性。在热板和尾浸法中,PMK 和 AMK 的慢性给药最初表现出波动的反应,但在研究的第 9 天产生了最高程度的镇痛作用。

结论

在 15 天研究结束时,PMK 和 AMK 产生的镇痛程度表明九里香具有作为镇痛药的潜力。