机构地区:[1]济宁医学院临床医学院,山东济宁272067 [2]济宁医学院附属医院,山东济宁272067 [3]济宁医学院行为医学教育研究所,山东济宁272067 [4]济宁医学院基础医学院,山东济宁272067
出 处:《药学学报》2018年第10期1652-1659,共8页Acta Pharmaceutica Sinica
基 金:国家自然科学基金青年基金资助项目(81603143);济宁医学院博士基金资助项目(JY2015BS08);山东省高等学校国家级大学生创新创业训练计划项目(201710443013)
摘 要:本研究旨在探讨N-对氯苯磺酰基-4-氨基水杨酸对葡聚糖硫酸钠(dextran sodium sulfate, DSS)诱导的溃疡性结肠炎的治疗作用。将60只BALB/c小鼠随机分为空白组、DSS模型组、5-氨基水杨酸(5-amino salicylic acid, 5-ASA)组、给药组,每组10只,空白组正常饮水,其他各组均饮用质量浓度(w/v)为0.04的DSS, 5-ASA组(40 mg·kg^(-1))、N-对氯苯磺酰基-4-氨基水杨酸(10、20、40mg·kg^(-1))采用灌胃给药方式。实验期间每日测量小鼠体重,观察各组小鼠大便形态(大便是否成形)和肉眼血便情况以及精神状态等。建模10天,取血后处死小鼠,解剖并摘取重要脏器以及结肠组织,称取脏器重量,测量结肠长度。通过苏木精-伊红(hematoxylinand eosin,HE)染色对各组小鼠的重要脏器(心、肝、肺、肾)和结肠组织进行病理学评分。通过ELISA检测血清中肿瘤坏死因子α(tumor necrosis factor alpha, TNF-α)、白细胞介素1(interleukin 1 beta, IL-1)、白细胞介素6(interleukin6,IL-6)、巨噬细胞炎性蛋白2(macrophageinflammatoryprotein2,MIP-2)、髓过氧化物酶(myeloperoxidase, MPO)等炎症因子的表达。实验结果显示,建模第4天, DSS模型组小鼠出现便血的情况,第7日模型组便血小鼠数量上升至10只,造模后5-ASA组及给药组小鼠出现便血和腹泻。DSS模型组小鼠从建模第4天起出现精神状态差,体重下降明显,给药组和5-ASA组小鼠精神状态较好,体重接近于空白组小鼠(P <0.01)。给药组的结肠长度明显大于DSS模型组。HE染色结果显示, DSS模型组小鼠结肠黏膜层出现重度炎症细胞浸润,局部出现不同程度的坏死,坏死处已有成纤维细胞增生,黏膜肌层组织出现炎症细胞浸润;中剂量组(20mg·kg^(-1))结肠黏膜表现为轻度慢性炎症和少量炎性细胞浸润,情况略有改善;高剂量组(40mg·kg^(-1))小鼠结肠黏膜结构基本恢复正常,上皮结构较完整,少量炎症细胞浸润。ELISA结果显示,给药组小�The study aims to explore the effects of N-p-chlorobenzenesulfonyl-4-amino salicylic acid on the dextran sodium sulfate(DSS)-induced ulcerative colitis in mouse. A total of 60 BALB/c mice were randomly divided into 6 groups(n = 10): control group, DSS model group, 5-amino salicylic acid(5-ASA) group, and administration groups(N-p-chlorobenzenesulfonyl-4-aminosalicylic acid) 10, 20, 40 mg·kg^(-1). Model group were induced by drinking 4%(w/v) DSS solution for 7 days and normal water for the next 3 days. The positive group and drug group mouse were given 5-ASA(40 mg·kg^(-1)) and N-p-chlorobenzene sulfonyl-4-amino salicylic acid(10, 20, 40 mg·kg^(-1)) by gavage respectively. During the experiment, changes in body weight, bloody stool, fecal character and mental status were observed daily. Damage and repair of the colon mucosa and the pathological changes of important organs were observed by hematoxylin and eosin(HE) staining. Expression of inflammatory factors such as tumor necrosis factor alpha(TNF-α), interleukin 1 beta(IL-1), interleukin 6(IL-6), macrophage inflammatory protein 2(MIP-2), myeloperoxidase(MPO) in serum were detected by ELISA. The results showed that bloody stools and diarrhea emerged on the 4 th day after model establishment in model mice. The number of bloody mice rose to ten, and blood and diarrhea began to appear in the administration group on the 7 th day. Mental status was poor and body weight decreased significantly in model group since the 4 th day, and the situation was improved in the administration group and 5-ASA group. Colons in the administration groups(10, 20, 40 mg·kg^(-1)) were longer than those in the DSS model group. In the DSS model group, the colonic mucosa and submucosa of mice exhibited severe inflammatory cell infiltration, various degrees of necrosis, proliferation. In the middle dose group(20 mg·kg^(-1)), the situation has improved slightly and the colonic mucosa showed mildly chronic
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