Hydroxysafflor Yellow A Phytosomes Administered via Intervaginal Space Injection Ameliorate Pulmonary Fibrosis in Mice.

Tingting Li, Dong Han, Zhongxian Li, Mengqi Qiu, Yuting Zhu, Kai Li, Jiawei Xiang, Huizhen Sun, Yahong Shi, Tun Yan, Xiaoli Shi, Qiang Zhang
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引用次数: 1

Abstract

Idiopathic pulmonary fibrosis is a fatal interstitial disease characterized by fibroblast proliferation and differentiation and abnormal accumulation of extracellular matrix, with high mortality and an increasing annual incidence. Since few drugs are available for the treatment of pulmonary fibrosis, there is an urgent need for high-efficiency therapeutic drugs and treatment methods to reduce the mortality associated with pulmonary fibrosis. The interstitium, a highly efficient transportation system that pervades the body, plays an important role in the occurrence and development of disease, and can be used as a new route for disease diagnosis and treatment. In this study, we evaluated the administration of hydroxysafflor yellow A phytosomes via intervaginal space injection (ISI) as an anti-pulmonary fibrosis treatment. Our results show that this therapeutic strategy blocked the activation of p38 protein in the MAPK-p38 signaling pathway and inhibited the expression of Smad3 protein in the TGF-β/Smad signaling pathway, thereby reducing secretion of related inflammatory factors, deposition of collagen in the lungs of mice, and destruction of the alveolar structure. Use of ISI in the treatment of pulmonary fibrosis provides a potential novel therapeutic modality for the disease.

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阴道间隙注射羟红花黄A磷脂复合物改善小鼠肺纤维化。
特发性肺纤维化是一种以成纤维细胞增殖分化和细胞外基质异常积聚为特征的致死性间质性疾病,病死率高,年发病率呈上升趋势。由于肺纤维化的治疗药物很少,因此迫切需要高效的治疗药物和治疗方法来降低肺纤维化的死亡率。间质是一个遍布全身的高效运输系统,在疾病的发生发展中起着重要作用,可以作为疾病诊断和治疗的新途径。在这项研究中,我们通过阴道间隙注射(ISI)评估羟基红花黄A磷脂复合物作为抗肺纤维化治疗的管理。我们的研究结果表明,这种治疗策略阻断了MAPK-p38信号通路中p38蛋白的激活,抑制了TGF-β/Smad信号通路中Smad3蛋白的表达,从而减少了相关炎症因子的分泌,减少了小鼠肺部胶原的沉积,破坏了肺泡结构。使用ISI治疗肺纤维化提供了一种潜在的新型治疗方式。
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