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迷迭香通过调节基质重塑发挥其在新生大鼠中的抗哮喘活性。

Myrcene exerts anti-asthmatic activity in neonatal rats via modulating the matrix remodeling.

机构信息

Department of Pediatrics, Shandong Provincial Third Hospital, Cheeloo College of Medicine, Shandong University, Jinan, Shandong, China.

出版信息

Int J Immunopathol Pharmacol. 2020 Jan-Dec;34:2058738420954948. doi: 10.1177/2058738420954948.

DOI:10.1177/2058738420954948
PMID:32962470
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC7517990/
Abstract

Myrcene (MC), an organic hydrocarbon, was found to exert anti-inflammatory, analgesic, antimutagenic and antioxidant properties. However, the protective role of MC has not been reported against neonatal asthma. Wistar rats induced with asthma were administered with MC; while asthma control and vehicle control were maintained without MC administration. At the end of the experimental period, lung histology, inflammatory cell counts, cytokine analysis, matrix protein expressions were elucidated. Rats administered with MC exerted significant ( < 0.05) defense in protecting the lung tissue with the evidenced restoration of alveolar thickening of the lung tissues. Also, the present study elicited the anti-asthmatic activity of MC, especially via modulating the extracellular matrix protein expression in the asthma-induced animals, while a significant reduction ( < 0.05) in the fibrotic markers were found in MC treated animals. Moreover, the protective effect of MC was evidenced with reduced leukocyte infiltration in BALF, hypersensitive specific IgE levels with a profound decrease in the inflammatory cytokines such as IL-2, IL-4, IL-18, and IL-21 in MC administered animals compared to the asthma-induced group. To an extent, the markers of asthmatic inflammation such as CD14, MCP-1, and TARC were also found to be attenuated in MC exposed animals. The possible application of MC is a promising drug for the treatment of asthma-mediated complications.

摘要

迷迭香烯(MC)是一种有机烃类化合物,具有抗炎、镇痛、抗突变和抗氧化特性。然而,MC 对新生儿哮喘的保护作用尚未见报道。将哮喘诱导的 Wistar 大鼠给予 MC;而哮喘对照组和载体对照组则不给予 MC 给药。在实验期末,对肺组织学、炎症细胞计数、细胞因子分析、基质蛋白表达进行了阐明。给予 MC 的大鼠在保护肺组织方面表现出显著(<0.05)的防御作用,证据表明肺组织的肺泡增厚得到了恢复。此外,本研究表明 MC 具有抗哮喘活性,特别是通过调节哮喘诱导动物的细胞外基质蛋白表达,而在 MC 治疗动物中发现纤维化标志物显著减少(<0.05)。此外,与哮喘诱导组相比,MC 给药动物的 BALF 白细胞浸润减少,过敏特异性 IgE 水平降低,IL-2、IL-4、IL-18 和 IL-21 等炎症细胞因子水平显著降低,这证明了 MC 的保护作用。在 MC 暴露的动物中,哮喘炎症的标志物如 CD14、MCP-1 和 TARC 也被发现有所减弱。MC 的可能应用是治疗哮喘介导的并发症的有前途的药物。

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