Huang Pan, Wang Yu-Xiang, Zhang Qing-Qing, Ma You-Gang, Wei Min-Min, Wang Ya-Ting, Ma Lan
Qinghai University Xining 810001, China Research Center for High Altitude Medicine, Medical College, Qinghai University Xining 810001, China.
Qinghai University Xining 810001, China Research Center for High Altitude Medicine, Medical College, Qinghai University Xining 810001, China Department of Respiratory, Affiliated Hospital of Qinghai University Xining 810001, China.
Zhongguo Zhong Yao Za Zhi. 2024 Oct;49(19):5297-5306. doi: 10.19540/j.cnki.cjcmm.20240611.703.
This study aims to investigate the effect of Zhishi Xiebai Guizhi Decoction on the phenotypic transformation of pulmonary artery smooth muscle cells(PASMCs) in rats with hypoxic pulmonary hypertension(HPH). Healthy SPF SD rats were randomly assigned to five groups: control group, hypoxia model group, hypoxia + low-dose Zhishi Xiebai Guizhi Decoction group(440 mg·kg(-1)·d(-1)), hypoxia + high-dose Zhishi Xiebai Guizhi Decoction group(880 mg·kg(-1)·d(-1)), and hypoxia + sildenafil group(30 mg·kg(-1)·d(-1)), with right rats in each group. Rats in the hypoxia model and hypoxia + drug groups were exposed to a hypobaric oxygen chamber with a simulated altitude of 5 000 m to induce the PH model. The control group was fed under standard conditions. The hypoxia + drug groups received Zhishi Xiebai Guizhi Decoction and sildenafil once daily for 28 days. After the experiment, the ratio of pulmonary acceleration time to pulmonary ejection time(PAT/PET) was measured in rats from each group using echocardiography. Additionally, the mean pulmonary artery pressure(mPAP) in rats from each group was determined through right heart catheterization. Hematoxylin-eosin(HE) staining was employed to observe pathological changes in lung tissue, while Western blot was utilized to detect the expression levels of proteins associated with the phenotypic transformation of pulmonary artery tissue. At the in vitro level, primary PASMCs were cultured using the type Ⅱ collagenase digestion method and identified through immunocytochemistry staining. SPF SD rats were administered Zhishi Xiebai Guizhi Decoction, and drug-containing serum was collected. Cell counting kit-8(CCK-8) was utilized to determine the optimal intervention concentration of drug-containing serum on PASMCs under hypoxic conditions. The cells were categorized into the normoxia control group, hypoxia control group, and hypoxia + drug-containing serum groups(10% and 15% drug-containing serum). 5-ethynyl-2'-deoxyuridine(EdU) was employed to assess cell proliferation in each group. Cell migration was evaluated through Transwell and cell scratch experiments, while Western blot was used to analyze the expression levels of proteins associated with the phenotypic transformation of PASMCs in each group. In vivo results indicated that the expression of PAT/PET and contraction-rela-ted proteins of pulmonary artery tissue was significantly decreased in the hypoxia model group compared to the control group, while the expression of mPAP, pulmonary vessel wall thickness, and synthetic-related proteins was significantly increased. Furthermore, compared to the hypoxia model group, the expression of PAT/PET and contraction-related proteins of the pulmonary artery tissue of rats in the drug groups increased, along with a significant decrease in mPAP, pulmonary vessel wall thickness, and synthetic-related proteins. In vitro results demonstrated that hypoxia induction significantly up-regulated the proliferation and migration abilities of PASMCs, as well as the expression of synthetic-related proteins while decreasing the expression of contraction-related proteins compared to the normoxia control group. Additionally, compared to the hypoxia control group, serum with Zhishi Xiebai Guizhi Decoction was found to inhibit the proliferation and migration of PASMCs induced by hypoxia, reduce the expression of synthetic-related proteins, and up-regulate the expression of contraction-related proteins. In conclusion, Zhishi Xiebai Guizhi Decoction could inhibit the excessive proliferation and migration of PASMCs in a hypoxic environment, providing a protective effect on rats with HPH. This mechanism may involve the regulation of protein expression levels associated with the phenotypic transformation of PASMCs.
本研究旨在探讨枳实薤白桂枝汤对缺氧性肺动脉高压(HPH)大鼠肺动脉平滑肌细胞(PASMCs)表型转化的影响。将健康的SPF级SD大鼠随机分为五组:对照组、缺氧模型组、缺氧+低剂量枳实薤白桂枝汤组(440 mg·kg⁻¹·d⁻¹)、缺氧+高剂量枳实薤白桂枝汤组(880 mg·kg⁻¹·d⁻¹)和缺氧+西地那非组(30 mg·kg⁻¹·d⁻¹),每组各10只大鼠。缺氧模型组和缺氧+药物组的大鼠置于模拟海拔5000 m的低压氧舱中以诱导肺动脉高压模型。对照组在标准条件下饲养。缺氧+药物组每日分别给予枳实薤白桂枝汤和西地那非,连续给药28天。实验结束后,采用超声心动图测量各组大鼠的肺动脉加速时间与射血时间之比(PAT/PET)。此外,通过右心导管术测定各组大鼠的平均肺动脉压(mPAP)。采用苏木精-伊红(HE)染色观察肺组织病理变化,利用蛋白质印迹法检测肺动脉组织中与表型转化相关蛋白的表达水平。在体外水平,采用Ⅱ型胶原酶消化法培养原代PASMCs,并通过免疫细胞化学染色进行鉴定。给SPF级SD大鼠灌胃枳实薤白桂枝汤,收集含药血清。利用细胞计数试剂盒-8(CCK-8)测定缺氧条件下含药血清对PASMCs的最佳干预浓度。将细胞分为常氧对照组、缺氧对照组和缺氧+含药血清组(10%和15%含药血清)。采用5-乙炔基-2'-脱氧尿苷(EdU)评估各组细胞增殖情况。通过Transwell实验和细胞划痕实验评估细胞迁移情况,利用蛋白质印迹法分析各组中与PASMCs表型转化相关蛋白的表达水平。体内实验结果表明,与对照组相比,缺氧模型组大鼠的PAT/PET及肺动脉组织收缩相关蛋白表达显著降低,而mPAP、肺血管壁厚度及合成相关蛋白表达显著升高。此外,与缺氧模型组相比,药物组大鼠肺动脉组织的PAT/PET及收缩相关蛋白表达增加,同时mPAP、肺血管壁厚度及合成相关蛋白显著降低。体外实验结果表明,与常氧对照组相比,缺氧诱导显著上调了PASMCs的增殖和迁移能力,以及合成相关蛋白的表达,同时降低了收缩相关蛋白的表达。此外,与缺氧对照组相比,发现枳实薤白桂枝汤含药血清可抑制缺氧诱导的PASMCs增殖和迁移,降低合成相关蛋白的表达,并上调收缩相关蛋白的表达。综上所述,枳实薤白桂枝汤可抑制缺氧环境下PASMCs的过度增殖和迁移,对HPH大鼠具有保护作用。其机制可能涉及对PASMCs表型转化相关蛋白表达水平的调控。