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1. 南方医科大学中医药学院中药药理教研室
2. 南方医科大学中医药学院广东省中药制剂重点实验室
纸质出版日期:2012
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[1]赵杰,余林中,方芳,徐文杰,罗佳波.麻黄-甘草药对的抗炎作用及机制研究[J].中国实验方剂学杂志,2012,18(15):163-166.
ZHAO Jie1, YU Lin-zhong1, FANG Fang1, et al. Anti-inflammatory Effects and Mechanism of Ephedra sinica-Glycyrrhiza uralensis Herbal Compatibility[J]. Chinese journal of experimental traditional medical formulae, 2012, 18(15): 163-166.
[1]赵杰,余林中,方芳,徐文杰,罗佳波.麻黄-甘草药对的抗炎作用及机制研究[J].中国实验方剂学杂志,2012,18(15):163-166. DOI: 10.13422/j.cnki.syfjx.2012.15.053.
ZHAO Jie1, YU Lin-zhong1, FANG Fang1, et al. Anti-inflammatory Effects and Mechanism of Ephedra sinica-Glycyrrhiza uralensis Herbal Compatibility[J]. Chinese journal of experimental traditional medical formulae, 2012, 18(15): 163-166. DOI: 10.13422/j.cnki.syfjx.2012.15.053.
目的:观察麻黄-甘草药对的抗炎作用
探讨抗炎机制。方法:ICR小鼠随机分为模型对照组
地塞米松组(0.01g·kg-1)
麻黄-甘草药对组(22.4
11.2
5.6 g·kg-1)
每天1次
连续ig给药5 d
末次给药30 min后采用醋酸致腹腔毛细血管通透性增加实验观察抗炎作用;取SD大鼠随机分为正常对照组
模型对照组
地塞米松组(0.01 g·kg-1)
麻黄-甘草药对组(22.4
11.2
5.6 g·kg-1)
每天1次
连续ig给药5 d
末次给药30 min后采用角叉菜胶诱导胸膜炎实验观察抗炎作用
测定胸膜炎大鼠胸腔渗出液前列腺素E2(PGE2)、肿瘤坏死因子-α(TNF-α)和白细胞介素-1β(IL-1β)含量以及肺组织TNF-α
IL-1β和丙二醛(MDA)含量
探讨抗炎机制。结果:与模型对照组比较
麻黄-甘草药对(22.4
11.2 g·kg-1)可显著抑制醋酸致小鼠腹腔毛细血管通透性增加
抑制角叉菜胶诱导的胸膜炎大鼠胸腔液渗出(P<0.01)
抑制渗出液白细胞数量增多(P<0.01);22.4 g·kg-1能抑制中性粒细胞比率升高;麻黄-甘草药对3个剂量组对淋巴细胞比率没有明显影响;麻黄-甘草药对(22.4
11.2 g·kg-1)抑制胸腔液PGE2
TNF-α
IL-1β含量升高(P<0.05);药对22.4 g·kg-1能抑制肺组织TNF-α
IL-1β
MDA含量升高(P<0.01)
11.2 g·kg-1能抑制肺组织IL-1β含量升高(P<0.01)。结论:麻黄-甘草药对有抗炎作用
抗炎机制可能与影响炎症介质产生和抗氧化作用有关。
Objective: To observe the anti-inflammatory effects of Ephedra sinica-Glycyrrhiza uralensis herbal compatibility and explore its mechanism.Method: ICR mice were divided into 5 groups randomly
namely the model group
dexameathone group(0.01 g·kg-1)
E.sinica-G.uralensis herbal compatibility groups(22.4
11.2
5.6 g·kg-1).Each drug was administrated to mice orally once a day for 5 days.After 30 min of the last administration
anti-inflammatory effect was observed by the method of acetic acid-induced permeability accentuation.SD rats were divided into 6 groups randomly
namely the control group
model group
dexameathone group(0.01 g·kg-1)
E.sinica-G.uralensis herbal compatibility groups(22.4
11.2
5.6 g·kg-1).Each drug was administrated to mice orally once a day for 5 days.After 30 min of the last administration
the rat model of carrageenan-induced acute pleurisy was also selected to observe the anti-inflamatory activity.The anti-inflammatory mechanisms were investigated by detecting the contents of prostaglandins(PGE2)
tumor necrosis factor-alpha(TNF-α)
interleukin-lβ(IL-1β) in exudates
and the contents of TNF-α
IL-1β
malondialdehyde(MDA) in lung tissue were also detected.Result: Compared with the model group
E.sinica-G.uralensisherbal compatibility(22.4
11.2 g·kg-1)produced significant inhibitory effects on acetic acid-induced permeability accentuation in mice
and inhibited the increase of the volume of exudates(P<0.01)
as well as the total leukocytes in the exudates(P<0.01) induced by carrageenan
22.4 g·kg-1 inhibited the increase of the percentage of neutrophil
and three doses of herbal compatibility had no significant effects on the percentage of lymphocytes
E.sinica-G.uralensis drug pair(22.4
11.2 g·kg-1)significantly reduced the levels of PGE2
TNF-α
IL-1β in exudates(P<0.05)
drug pair 22.4 g·kg-1 also reduced the contents of TNF-α
IL-1β
MDA in lung tissue in carrageenan treated rats(P<0.01)
11.2 g·kg-1 reduced the contents of IL-1β in lung tissue(P<0.01).Conclusion: E.sinica-G.uralensis herbal compatibility possess significant anti-inflammatory effects
which can be related with the inhibition of the generation of mediators of inflammation and its antioxidation.
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