Key Laboratory of Zoonosis, Ministry of Education, Institute of Zoonosis, College of Veterinary Medicine, Jilin University, Xi'an Road 5333#, Changchun 130062, China.
Int Immunopharmacol. 2013 Apr;15(4):780-8. doi: 10.1016/j.intimp.2013.01.010. Epub 2013 Jan 26.
Protocatechuic acid (PCA) has been isolated from the leaves of ilex chinenses and has numerous pharmacologic effects, including anti-inflammatory and antitumoral activities. This study aims to evaluate the antiasthma activity of PCA and investigate its possible molecular mechanisms. BALB/c mice were sensitized and challenged to ovalbumin (OVA).Then mice were intraperitoneally (i.p.) injected with PCA 1h before OVA challenge. We found that PCA treatment at 15 or 30 mg/kg significantly decreased OVA-induced airway hyper-responsiveness (AHR) to inhaled methacholine. Type 2 helper T cell (Th2) cytokines in bronchoalveolar lavage (BAL) fluid, such as interleukin-4 (IL-4), interleukin 5 (IL-5) and interleukin-13 (IL-13), and serum OVA-specific immunoglobulin E (IgE) levels, were also reduced by PCA. Moreover treatment with PCA markedly decreased the number of inflammatory cells in BALF and attenuated OVA-induced mRNA expression of CCl11, CCR3, Muc5ac, acidic mammalian chitinase (AMCase), chitinase 3-like protein 4 (Ym2) and E-selectin in lung tissues, lung histopathological studies showed that PCA inhibited inflammatory cell infiltration and mucus hypersecretion compared with the OVA-induced mice group. We then investigated the possible molecular mechanisms which might be implicated in PCA activity. Our results suggested that the protective effect of PCA might be mediated by the inhibition of the extracellular signal-regulated protein kinase (ERK), p38 Mitogen-activated protein kinase (MAPK) phosphorylation and the nuclear factor-κB (NF-κB) activation.
原儿茶酸(PCA)已从冬青叶中分离出来,具有多种药理作用,包括抗炎和抗肿瘤活性。本研究旨在评估 PCA 的抗哮喘活性,并探讨其可能的分子机制。BALB/c 小鼠用卵清蛋白(OVA)致敏和攻毒。然后,在 OVA 攻毒前 1 小时,将 PCA 通过腹腔内(i.p.)注射给小鼠。我们发现,15 或 30mg/kg 的 PCA 处理可显著降低 OVA 诱导的气道高反应性(AHR)对吸入性乙酰甲胆碱的反应。BAL 液中的 2 型辅助 T 细胞(Th2)细胞因子,如白细胞介素-4(IL-4)、白细胞介素 5(IL-5)和白细胞介素 13(IL-13)以及血清 OVA 特异性免疫球蛋白 E(IgE)水平也被 PCA 降低。此外,PCA 治疗还显著减少了 BALF 中的炎症细胞数量,并减弱了 OVA 诱导的肺组织 CCl11、CCR3、Muc5ac、酸性哺乳动物几丁质酶(AMCase)、几丁质酶 3 样蛋白 4(Ym2)和 E-选择素的 mRNA 表达。肺组织病理研究表明,与 OVA 诱导的小鼠组相比,PCA 抑制了炎症细胞浸润和粘液分泌过度。然后,我们研究了可能涉及 PCA 活性的可能分子机制。我们的结果表明,PCA 的保护作用可能是通过抑制细胞外信号调节蛋白激酶(ERK)、p38 丝裂原活化蛋白激酶(MAPK)磷酸化和核因子-κB(NF-κB)激活来介导的。