Department of Pharmacology, University of Health Sciences, khyaban e Jamia Punjab, Lahore, Pakistan.
Department of Pharmacy, The University of Lahore-Gujrat campus, Gujrat, Pakistan.
Inflammation. 2019 Dec;42(6):2037-2047. doi: 10.1007/s10753-019-01066-2.
Curcumin is well known for possessing anti-inflammatory properties and for its beneficial effects in the treatment of asthma. Current study investigates the immunomodulatory and anti-inflammatory effects of curcumin using mouse model of ovalbumin-induced allergic asthma. BALB/c mice were immunized with ovalbumin on day 0 and 14 to induce allergic asthma. Animals were treated with two different doses of curcumin (20 mg/kg and 100 mg/kg) and methylprednisolone from day 21 to 28. Mice were also daily challenged intranasally with ovalbumin during treatment period, and all groups were sacrificed at day 28. Histopathological examination showed amelioration of allergic asthma in treated groups as evident by the attenuation of infiltration of inflammatory cells, goblet cell hyperplasia, alveolar thickening, and edema and vascular congestion. Curcumin significantly reduced total and differential leukocyte counts in both bronchoalveolar lavage fluid and blood. Reverse transcription polymerase chain reaction analysis showed significantly suppressed mRNA expression levels of IL-4 and IL-5 (pro-inflammatory cytokines), TNF-α, TGF-β (pro-fibrotic cytokines), eotaxin (chemokine), and heat shock protein 70 (marker of airway obstruction) in treated groups. Attenuation of these pro-inflammatory markers might have led to the suppression of airway inflammation. The expression levels of aquaporin-1 (AQP) and AQP-5 were found significantly elevated in experimental groups which might be responsible for reduction of pulmonary edema. In conclusion, curcumin significantly ameliorated allergic asthma. The anti-asthmatic effect might be attributed to the suppression of pro-inflammatory cytokines, and elevation of aquaporin expression levels, suggesting further studies and clinical trials to establish its candidature in the treatment of allergic asthma.
姜黄素以具有抗炎特性和在治疗哮喘方面的有益作用而闻名。本研究使用卵清蛋白诱导的过敏性哮喘小鼠模型来研究姜黄素的免疫调节和抗炎作用。BALB/c 小鼠在第 0 天和第 14 天用卵清蛋白免疫以诱导过敏性哮喘。动物用两种不同剂量的姜黄素(20mg/kg 和 100mg/kg)和甲泼尼龙从第 21 天到第 28 天治疗。在治疗期间,小鼠还每天接受卵清蛋白鼻腔内挑战,所有组均在第 28 天处死。组织病理学检查显示治疗组过敏性哮喘得到改善,表现为炎症细胞浸润、杯状细胞增生、肺泡增厚、水肿和血管充血减轻。姜黄素显著降低了支气管肺泡灌洗液和血液中的总白细胞和分类白细胞计数。逆转录聚合酶链反应分析显示,治疗组 IL-4 和 IL-5(促炎细胞因子)、TNF-α、TGF-β(促纤维化细胞因子)、嗜酸性粒细胞趋化因子(趋化因子)和热休克蛋白 70(气道阻塞标志物)的 mRNA 表达水平显著降低。这些促炎标志物的衰减可能导致气道炎症的抑制。实验各组中发现水通道蛋白-1(AQP1)和 AQP-5 的表达水平显著升高,这可能是肺水肿减少的原因。总之,姜黄素显著改善了过敏性哮喘。其抗哮喘作用可能归因于对促炎细胞因子的抑制以及水通道蛋白表达水平的升高,提示进一步的研究和临床试验以确定其在治疗过敏性哮喘方面的候选地位。