Jin Ming, Wu Yan, Wang Lin, Zang Baoxia, Tan Li
Department of Pharmacology, Beijing Anzhen Hospital, Beijing Institute of Heart Lung and Blood Vessel Disease, Capital Medical University, No. 2, Anzhen Road, Chaoyang District, Beijing, 100029, China.
Phytother Res. 2016 Apr;30(4):577-87. doi: 10.1002/ptr.5560. Epub 2016 Jan 18.
Hydroxysafflor yellow A (HSYA) is an active component of Carthamus tinctorius L., and we want to investigate whether HSYA attenuates pulmonary fibrosis induced by bleomycin (BLM) in mice. The mice received a BLM via oropharyngeal aspiration, and HSYA was intraperitoneally injected. Arterial blood gas analysis was performed. Morphological changes and hydroxyproline content were measured. mRNA expression of transforming growth factor-β1 (TGF-β1), connective tissue growth factor, α-smooth muscle actin (α-SMA), and collagen I was measured by real-time polymerase chain reaction. α-SMA-positive cells in lung tissues were detected by immunohistochemical staining. A549 cell was cultured, and morphological changes were observed after TGF-β1 and HSYA treatment. mRNA expression was detected by real-time polymerase chain reaction. Phosphorylation of Smad3 was evaluated by western blotting. HSYA decreased the lung consolidation area and collagen deposition in mice with pulmonary fibrosis. The blood gas changes due to BLM were attenuated by HSYA. HSYA also alleviated the BLM-induced increase of TGF-β1, connective tissue growth factor, α-SMA, and collagen I mRNA levels. HSYA treatment inhibited the increase of α-SMA expression, Smad3 phosphorylation, the morphological changes in lung tissue. HSYA inhibits Smad3 phosphorylation and elevated expression of collagen I mRNA in epithelial-mesenchymal transition induced by TGF-β1.
羟基红花黄色素A(HSYA)是红花的一种活性成分,我们想要研究HSYA是否能减轻博来霉素(BLM)诱导的小鼠肺纤维化。通过经口咽吸入给予小鼠BLM,并腹腔注射HSYA。进行动脉血气分析。测量形态学变化和羟脯氨酸含量。通过实时聚合酶链反应测量转化生长因子-β1(TGF-β1)、结缔组织生长因子、α-平滑肌肌动蛋白(α-SMA)和I型胶原的mRNA表达。通过免疫组织化学染色检测肺组织中α-SMA阳性细胞。培养A549细胞,观察TGF-β1和HSYA处理后的形态学变化。通过实时聚合酶链反应检测mRNA表达。通过蛋白质印迹法评估Smad3的磷酸化。HSYA减少了肺纤维化小鼠的肺实变面积和胶原沉积。HSYA减轻了BLM引起的血气变化。HSYA还减轻了BLM诱导的TGF-β1、结缔组织生长因子、α-SMA和I型胶原mRNA水平的升高。HSYA处理抑制了α-SMA表达的增加、Smad3磷酸化以及肺组织的形态学变化。在TGF-β1诱导的上皮-间质转化中,HSYA抑制Smad3磷酸化和I型胶原mRNA表达的升高。