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类黄酮可减轻清醒豚鼠雾化卵白蛋白暴露后即刻和迟发性哮喘反应。

Flavonols attenuate the immediate and late-phase asthmatic responses to aerosolized-ovalbumin exposure in the conscious guinea pig.

机构信息

Division of pathophysiology and Pharmacology, College of Pharmacy, Chung-Ang University, Seoul 156-756, South Korea.

出版信息

Fitoterapia. 2010 Oct;81(7):803-12. doi: 10.1016/j.fitote.2010.04.011. Epub 2010 May 10.

Abstract

We previously reported that quercetin and rutin have potent, anti-asthmatic activity, but the structure-activity relationships of flavonoids and anti-asthmatic agents are still poorly understood. In the current study, the effects of kaempferol, fisetin, and morin on the immediate-phase response (IAR) and late-phase response (LAR) caused by exposure to aerosolized-ovalbumin (OA) in OA-sensitized guinea pigs were evaluated by determining the specific airway resistance (sRaw), recruitment of leukocytes and chemical mediators in bronchoalveolar lavage fluid (BALF), histopathological surveys, and determination of neutrophil chemotaxis. Fisetin and kaempherol (30 mg/kg, p.o.) significantly (P<0.01) inhibited sRaw by 47.93% and 30.05% in IAR, and 54.45% and 40.50% in LAR, when compared to vehicle control, respectively. Furthermore, all three studied flavonols (30 mg/kg, p.o.) significantly (P<0.05) inhibited the recruitment of total, as well as subtypes of, leukocytes into the lung BALF. This recruitment inhibition corresponded to the inhibition of leukocyte infiltration, particularly of eosinophils and neutrophils, into the lung in pathological surveys and formly-methionyl-leucyl-phenylalanine (FMLP)-induced neutrophil chemotaxis studies. Kaempferol inhibited FMLP-induced neutrophil chemotaxis in a concentration-dependent manner in a tested range of 1-100 μM. Fisetin inhibited histamine content and peroxidase (EPO) activity in BALF in a dose-dependent manner. All three tested flavonols significantly (P<0.01) inhibited histamine content at 10 mg/kg, and phospholipase A(2) (PLA(2)) and EPO activities at 30 mg/kg (p.o.) in BALF. Kaempherol had a greater anti-asthmatic effect than other flavonols. Fisetin demonstrated the greatest inhibition of sRaw, whereas morin had lesser effects. These results indicate that the lower the molecular weight, the greater the anti-asthmatic activities of these compounds.

摘要

我们之前报道过槲皮素和芦丁具有很强的抗哮喘活性,但黄酮类化合物和抗哮喘药物的构效关系仍知之甚少。在本研究中,通过测定气道阻力(sRaw)、支气管肺泡灌洗液(BALF)中白细胞和化学介质的募集、组织病理学检查以及中性粒细胞趋化性,评估了山奈酚、非瑟酮和桑色素对卵白蛋白(OA)致敏豚鼠雾化 OA 引起的即刻相反应(IAR)和迟发相反应(LAR)的影响。非瑟酮和山奈酚(30mg/kg,po)分别显著(P<0.01)抑制 IAR 中的 sRaw47.93%和 30.05%,以及 LAR 中的 54.45%和 40.50%,与载体对照相比。此外,三种研究的类黄酮(30mg/kg,po)均显著(P<0.05)抑制总白细胞以及肺 BALF 中白细胞亚型的募集。这种募集抑制与白细胞浸润的抑制相对应,特别是在病理学检查和甲酰基-甲硫氨酸-亮氨酸-苯丙氨酸(FMLP)诱导的中性粒细胞趋化性研究中对嗜酸性粒细胞和中性粒细胞的浸润抑制。在 1-100μM 的测试范围内,山奈酚以浓度依赖的方式抑制 FMLP 诱导的中性粒细胞趋化性。非瑟酮以剂量依赖的方式抑制 BALF 中的组胺含量和过氧化物酶(EPO)活性。三种测试的类黄酮均显著(P<0.01)抑制 10mg/kg 时的组胺含量,以及 30mg/kg(po)时的磷脂酶 A2(PLA2)和 EPO 活性。山奈酚的抗哮喘作用强于其他类黄酮。非瑟酮显示出最强的 sRaw 抑制作用,而桑色素的作用较小。这些结果表明,这些化合物的分子量越低,其抗哮喘活性越强。

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