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纸质出版日期:2015
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唐锋, 梁少瑜, 田元新, 等. 细辛挥发油抗过敏性鼻炎有效成分及靶点预测的研究[J]. 中国实验方剂学杂志, 2015,21(24):126-131.
TANG Feng, LIANG Shao-yu, TIAN Yuan-xin, et al. Predicting Effective Components and Targets of Essential Oil of Asari Radix et Rhizoma on Allergic Rhinitis[J]. Chinese journal of experimental traditional medical formulae, 2015, 21(24): 126-131.
唐锋, 梁少瑜, 田元新, 等. 细辛挥发油抗过敏性鼻炎有效成分及靶点预测的研究[J]. 中国实验方剂学杂志, 2015,21(24):126-131. DOI: 10.13422/j.cnki.syfjx.2015240126.
TANG Feng, LIANG Shao-yu, TIAN Yuan-xin, et al. Predicting Effective Components and Targets of Essential Oil of Asari Radix et Rhizoma on Allergic Rhinitis[J]. Chinese journal of experimental traditional medical formulae, 2015, 21(24): 126-131. DOI: 10.13422/j.cnki.syfjx.2015240126.
目的:采用血清药物化学-血清药理学与网络药理学方法
预测细辛挥发油抗过敏性鼻炎的有效成分及潜在靶点。方法:36只Wistar大鼠随机分为空白组、细辛挥发油0.5
1 h组(3 g·kg-1生药量)、盐酸西替利嗪片1 h组(10 mg·kg-1)、醋酸泼尼松片1 h组(12 mg·kg-1)和辛芩颗粒1 h组(15 g·kg-1)
每组6只。灌胃后腹主动脉采血
血样3000 r·min-1离心10 min
无菌分离血清
-20℃冷冻保存。酶联免疫吸附测定法(ELISA)测定各时间点含药血清(血清容积10%)对抗原刺激1.5 h后大鼠嗜碱性细胞白血病细胞株(RBL-2H3)细胞(细胞密度2.5×105/mL)释放组胺、氨基己糖苷酶的影响(n=6);采用气相色谱-质谱联用(GC-MS)技术检测各时间点含药血清中的成分
比较细辛挥发油、灌胃0.5
1 h后含药血清和空白血清的色谱图
寻找细辛挥发油的移行成分;对移行成分进行靶点预测
构建和分析其"成分-靶点"网络。结果:与空白血清组相比
细辛挥发油0.5
1 h含药血清组均能抑制抗原诱导RBL-2H3肥大细胞释放组胺和脱颗粒(P<0.05)。含药血清中检测到12个移行成分
分别为α-蒎烯
莰烯
2-β-蒎烯
δ-3-蒈烯
柠檬油精
1
8-桉叶素
优香芹酮
龙脑
3
5-二甲氧基甲苯
黄樟脑
甲基丁香酚
2
3
5-三甲氧基甲苯
它们可能通过调控环氧合酶-2
毒蕈碱乙酰胆碱受体M3
alpha 1肾上腺素能受体
一氧化氮合酶等靶点发挥抗过敏性鼻炎的作用。结论:该方法初步揭示细辛挥发油抗过敏性鼻炎的有效成分及其潜在靶点。
Objective: To predict the effective components and potential targets of essential oil of Asari Radix et Rhizoma on allergic rhinitis based on serum pharmacochemistry-serum pharmacology and network pharmacology methods. Method: Thirty-six Wistar rats were randomly divided into blank group
essential oil of Asari Radix et Rhizoma 0.5
1 h groups(3 g·kg-1 crude drug)
cetirizine tablets 1 h group(10 mg·kg-1)
prednisone tablets 1 h group(12 mg·kg-1) and Xinqin granules 1 h group(15 g·kg-1)
n=6 in each group. Abdominal aortic blood samples were collected after ig. Sterile separation of serum was done at 3000 r·min-1 and centrifuged for 10 min
then cryopreservedat-20℃. The effect of drug-containing serum sampled at different time points(10% serum volume) on histamine release and hexosaminidase of RBL-2H3(cell density of 2.5×105/mL) was measured by enzyme-linked immunosorbent assay(ELISA)after 1.5 h of antigen stimulation(n=6). Components of drug-containing serum at different time points were detected by gas chromatography-mass spectrometry(GC-MS)
and the transitional components of essential oil of Asari Radix et Rhizoma were determined by comparing the GC-MS fingerprints of essential oil of Asari Radix et Rhizoma
drug-containing serum after 0.5 h
1 h ig as well as blank serum. Then the potential targets of transitional components were predicted to construct and analyze compound-target network. Result: Compared with blank serum group
drug-containing serum sampled at different time points after 0.5
1 h ig of essential oil of Asari Radix et Rhizoma can reduce the total release of histamine and degranulation from RBL-2H3 cells induced by antigen(P<0.05). 12 transitional components in drug-containing serum were detected
ie α-pinene
camphene
2-β-pinene
δ-3-carene
l-limonene
1
8-cineole
eucarvone
borneoll
3
5-dimethoxytoluene
safrole
methyleugenol
and 2
3
5-toluene three oxygen radicals. They may have effects on allergic rhinitis by controlling the targets including prostaglandin G/H synthase 2
muscrinic acetylcholine receptor M3
alpha-1A adrenergic receptor
endothelial nitric-oxide synthase and so on. Conclusion: This method initially reveals the effective components and potential targets of essential oil of Asari Radix et Rhizoma on allergic rhinitis.
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