Chinese Materia Medica College, Tianjin University of Traditional Chinese Medicine, Tianjin 300193, China.
Tianjin Academy of Traditional Chinese Medicine, Tianjin 300120, China.
Molecules. 2018 Jun 19;23(6):1477. doi: 10.3390/molecules23061477.
Cutaneous eruption is a common drug-adverse reaction, characterised by keratinocytes inflammation and apoptosis. Shuanghuanglian injeciton (SHLI) is a typical Chinese medicine injection, which is used to treat influenza. It has been reported that SHLI has the potential to induce cutaneous adverse eruptions. However, the mechanisms remain unclear. Since desmoglein 1 (DSG1) shows a crucial role in maintaining skin barrier function and cell susceptibility, we assume that DSG1 plays a critical role in the cutaneous eruptions induced by SHLI. In our study, retinoic acid (RA) was selected to downregulate the DSG1 expression, and lipopolysaccharide (LPS) was first used to identify the susceptibility of the DSG1-deficiency Hacat cells. Then, SHLI was administrated to normal or DSG1-deficient Hacat cells and mice. The inflammatory factors and apoptosis rate were evaluated by RT-PCR and flow cytometry. The skin pathological morphology was observed by hematoxylin and eosin (HE) staining. Our results show that treated only with SHLI could not cause IL-4 and TNF-α mRNA increases in normal Hacat cells. However, in the DSG1-deficient Hacat cells or mice, SHLI induced an extreme increase of IL-4 and TNF-α mRNA levels, as well as in the apoptosis rate. The skin tissue showed a local inflammatory cell infiltration when treated with SHIL in the DSG1-deficient mice. Thus, we concluded that DSG1 deficiency was a potential causation of SHLI induced eruptions. These results indicated that keratinocytes with DSG1 deficiency were likely to induce the cutaneous eruptions when stimulated with other medicines.
皮肤发疹是一种常见的药物不良反应,其特征为角质形成细胞炎症和凋亡。双黄连注射液(SHLI)是一种典型的中药注射液,用于治疗流感。据报道,SHLI 有可能引起皮肤不良反应。然而,其机制尚不清楚。由于桥粒芯糖蛋白 1(DSG1)在维持皮肤屏障功能和细胞易感性方面起着至关重要的作用,我们假设 DSG1 在 SHLI 引起的皮肤发疹中起着关键作用。在我们的研究中,选择维 A 酸(RA)下调 DSG1 的表达,并首先使用脂多糖(LPS)鉴定 DSG1 缺陷的 Hacat 细胞的易感性。然后,将 SHLI 施用于正常或 DSG1 缺陷的 Hacat 细胞和小鼠。通过 RT-PCR 和流式细胞术评估炎症因子和细胞凋亡率。通过苏木精和伊红(HE)染色观察皮肤病理形态。我们的结果表明,单独用 SHLI 处理不能引起正常 Hacat 细胞中 IL-4 和 TNF-α mRNA 的增加。然而,在 DSG1 缺陷的 Hacat 细胞或小鼠中,SHLI 诱导了 IL-4 和 TNF-α mRNA 水平以及细胞凋亡率的极度增加。当在 DSG1 缺陷的小鼠中用 SHIL 处理时,皮肤组织显示出局部炎症细胞浸润。因此,我们得出结论,DSG1 缺乏是 SHLI 引起发疹的潜在原因。这些结果表明,当受到其他药物刺激时,缺乏 DSG1 的角质形成细胞可能会引起皮肤发疹。