Li Jian-Jun, Wu Su-Fang, Bai Feng-Xi
Department of Tuberculosis Ⅱ,Henan Provincial Chest Hospital,Zhengzhou 450008,China.
Zhongguo Yi Xue Ke Xue Yuan Xue Bao. 2022 Aug;44(4):555-562. doi: 10.3881/j.issn.1000-503X.14923.
Objective To explore the therapeutic effect of ethambutol tablets (EMB) on pulmonary tuberculosis (PTB) in rats and whether the action mechanism of EMB is related to Janus kinase (JAK)/signal transducer and activator of transcription (STAT) signaling pathway. Methods Sixty SD rats were assigned into a control group,a PTB group,a PTB+EMB group (30 mg/kg),and a PTB+EMB+Colivelin (JAK/STAT pathway activator) group (30 mg/kg+1 mg/kg) via the random number table method,with 15 rats in each group.The rats in other groups except the control group were injected with 0.2 ml of 5 mg/ml suspension to establish the PTB model.After the modeling,the rats were administrated with corresponding drugs for 4 consecutive weeks (once a day).On days 1,14,and 28 of administration,the body weights of rats were measured and the colonies were counted.Hematoxylin-eosin staining was carried out to detect the pathological changes in the lung tissue.Enzyme-linked immunosorbent assay was employed to measure the levels of interleukin(IL)-6,tumor necrosis factor-α (TNF-α),IL-1β,and interferon-γ (IFN-γ) in the serum.Flow cytometry was used to determine the levels of T lymphocyte subsets CD3+,CD4+,CD8+,and CD4+/CD8+.The 16S rRNA sequencing was performed to detect the relative abundance of the intestinal microorganisms.Western blotting was employed to determine the expression of the proteins in the JAK/STAT pathway. Results Compared with the control group,the modeling of PTB reduced the rat body weight (on days 14 and 28),increased colonies,caused severe pathological changes in the lung tissue,and elevated the levels of IL-6,TNF-α,and IL-1β in serum and CD8+.Moreover,the modeling increased the relative abundance of ,,,,,,and in the intestine,up-regulated the protein levels of phosphorylated JAK2 and phosphorylated STAT3 in the lung tissue,and lowered the levels of CD3+,CD4+,CD4+/CD8+,and IFN-γ levels (all <0.001).Compared with the PTB group,PTB+EMB increased the rat body weight (on days 14 and 28),reduced colonies,alleviated the pathological damage in lung tissue,lowered the levels of IL-6,TNF-α,and IL-1β in serum and CD8+.Moreover,the treatment decreased the relative abundance of ,,,,,, in the intestine,down-regulated the protein levels of phosphorylated JAK2 and phosphorylated STAT3 in the lung tissue,and elevated the levels of CD3+,CD4+,CD4+/CD8+,and IFN-γ (all <0.001).Colivelin weakened the alleviation effect of EMB on PTB (all <0.001). Conclusion EMB can inhibit the JAK/STAT signaling pathway to alleviate the PTB in rat.
目的 探讨乙胺丁醇片(EMB)对大鼠肺结核(PTB)的治疗作用以及EMB的作用机制是否与Janus激酶(JAK)/信号转导子和转录激活子(STAT)信号通路有关。方法 将60只SD大鼠通过随机数字表法分为对照组、PTB组、PTB+EMB组(30 mg/kg)和PTB+EMB+可利韦林(JAK/STAT通路激活剂)组(30 mg/kg+1 mg/kg),每组15只。除对照组外,其他组大鼠均注射0.2 ml 5 mg/ml菌悬液以建立PTB模型。造模后,大鼠连续4周每天给予相应药物。在给药第1、14和28天,测量大鼠体重并计数菌落。进行苏木精-伊红染色以检测肺组织的病理变化。采用酶联免疫吸附测定法检测血清中白细胞介素(IL)-6、肿瘤坏死因子-α(TNF-α)、IL-1β和干扰素-γ(IFN-γ)水平。采用流式细胞术测定T淋巴细胞亚群CD3+、CD4+、CD8+和CD4+/CD8+水平。进行16S rRNA测序以检测肠道微生物的相对丰度。采用蛋白质印迹法测定JAK/STAT通路中蛋白的表达。结果 与对照组相比,PTB造模降低了大鼠体重(在第14和28天),增加了菌落数,导致肺组织出现严重病理变化,并升高了血清中IL-6、TNF-α和IL-1β水平以及CD8+水平。此外,造模增加了肠道中……、……、……和……的相对丰度,上调了肺组织中磷酸化JAK2和磷酸化STAT3的蛋白水平,并降低了CD3+、CD4+、CD4+/CD8+和IFN-γ水平(均<0.001)。与PTB组相比,PTB+EMB增加了大鼠体重(在第14和28天),减少了菌落数,减轻了肺组织的病理损伤,降低了血清中IL-6、TNF-α和IL-1β水平以及CD8+水平。此外,该治疗降低了肠道中……、……、……和……的相对丰度,下调了肺组织中磷酸化JAK2和磷酸化STAT3的蛋白水平,并升高了CD3+、CD4+、CD4+/CD8+和IFN-γ水平(均<0.001)。可利韦林减弱了EMB对PTB的缓解作用(均<0.001)。结论 EMB可抑制JAK/STAT信号通路以减轻大鼠PTB。