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北京中医医院顺义医院脾胃病科,北京 101300
张立宏,女,37岁,硕士,副主任医师。研究方向:中西医结合治疗脾胃疾病。
谭海成,E-mail:zleehom417@163.com
收稿日期:2024-07-31,
纸质出版日期:2025-05-25
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张立宏,常雄飞,谭海成.基于Notch信号通路探讨芍药汤治疗溃疡性结肠炎的作用机制[J].北京中医药,2025,44(5):575-583.
ZHANG Lihong,CHANG Xiongfei,TAN Haicheng.Mechanism of Shaoyao Decoction in the treatment of ulcerative colitis based on Notch signaling pathway[J]. Beijing Journal of Traditional Chinese Medicine,2025,44(05):575-583.
张立宏,常雄飞,谭海成.基于Notch信号通路探讨芍药汤治疗溃疡性结肠炎的作用机制[J].北京中医药,2025,44(5):575-583. DOI: 10.16025/j.1674-1307.2025.05.008.
ZHANG Lihong,CHANG Xiongfei,TAN Haicheng.Mechanism of Shaoyao Decoction in the treatment of ulcerative colitis based on Notch signaling pathway[J]. Beijing Journal of Traditional Chinese Medicine,2025,44(05):575-583. DOI: 10.16025/j.1674-1307.2025.05.008.
目的
2
基于Notch信号通路探讨芍药汤治疗溃疡性结肠炎(UC)小鼠的作用机制。
方法
2
将50只雄性C57BL/6小鼠用随机数字表法分为正常组、模型组、中药低剂量组、中药中剂量组、中药高剂量组,各10只。采用葡聚糖硫酸钠盐(DSS)诱导造模,造模开始第4天中药低、中、高剂量组分别给予7.74、15.47、30.94 g/(kg·d)芍药汤水煎剂灌胃,正常组、模型组均每天8:00给予0.3 mL等容积生理盐水灌胃,均连续7 d。计算小鼠疾病活动指数(DAI)。于造模第10天将全部小鼠摘眼球取血,处死,分离肛门以上至盲肠末端获取结肠段,测量其长度;苏木精-伊红染色(HE)染色观察小鼠结肠上皮组织病理变化,进行病理炎症评分;酶联免疫吸附试验(ELISA)检测血清白细胞介素(IL)6、IL-1β、肿瘤坏死因子(TNF)α;爱先蓝-糖原(AB-PAS)染色观察小鼠结肠组织杯状细胞;实时荧光定量多聚核苷酸链式反应(qPCR)法检测小鼠结肠组织中Notch-1、Hes-1 mRNA表达;Western blotting法检测小鼠结肠组织中Notch-1、Hes-1、ATOH-1蛋白表达;免疫组织化学染色法检测小鼠结肠组织黏蛋白(MUC)2蛋白表达;免疫荧光法观察小鼠结肠组织嗅觉调节素4(OLFM4)蛋白表达。
结果
2
造模第2天开始,除正常组外,其余小鼠DAI评分均缓慢升高,模型组小鼠DAI评分高于正常组(
P
<
0.01),并于第10天达到峰值;第10天的中药中、高剂量组小鼠DAI评分低于模型组(
P
<
0.05,
P
<
0.01)。与正常组比较,模型组小鼠结肠长度短(
P
<
0.01);与模型组比较,中药低、中、高剂量组小鼠结肠长度长(
P
<
0.05)。与模型组比较,中药组小鼠结肠组织病理特征明显改善,肠道厚度均匀正常,偶见肠绒毛形态、固有膜形态不规则,黏膜层细胞大小正常密度均匀,中药中剂量组、中药高剂量组病理炎症评分低(
P
<
0.01)。与正常组比较,模型组小鼠血清IL-6、IL-1β、TNF-α水平高(
P
<
0.01);与模型组比较,各中药组小鼠血清IL-6、IL-1β、TNF-α水平低(
P
<
0.05,
P
<
0.01)。与正常组比较,模型组小鼠结肠组织杯状细胞数量少;与模型组比较,各中药组小鼠结肠组织杯状细胞数量多。与正常组比较,模型组小鼠结肠组织中Notch-1、Hes-1 mRNA表达高(
P
<
0.05,
P
<
0.01)。与模型组比较,中药中、高剂量组小鼠结肠组织中Notch-1、Hes-1 mRNA表达低(
P
<
0.05,
P
<
0.01)。与正常组比较,模型组小鼠结肠组织中Notch-1、Hes-1蛋白表达高(
P
<
0.01),ATOH-1蛋白表达低(
P
<
0.01);与模型组比较,中药中、高剂量组小鼠结肠组织中Notch-1蛋白表达低(
P
<
0.05),中药低、高剂量组小鼠结肠组织中Hes-1蛋白表达低(
P
<
0.05),中药各组ATOH-1蛋白表达均高(
P
<
0.01)。与正常组比较,模型组小鼠结肠组织中MUC2蛋白表达的平均光密度值低(
P
<
0.01);与模型组比较,中药中、高剂量组小鼠结肠组织中MUC2蛋白表达的平均光密度值高(
P
<
0.05)。与正常组比较,模型组小鼠结肠组织中OLFM4蛋白表达高;与模型组比较,各中药组结
肠组织中OLFM4蛋白表达低。
结论
2
芍药汤对DSS诱导的UC小鼠有明显的降低肠道炎症反应,及改善肠道黏膜屏障功能的治疗作用,其作用机制与Notch信号通路相关。
Objective
2
To investigate the mechanism of
Shaoyao Decoction
in treating ulcerative colitis (UC) in mice based on the Notch signaling pathway.
Methods
2
Fifty male C57BL/6 mice were randomly divided into five groups (
n
=10 for each group): normal,model,low-dose,medium-dose,and high-dose
Shaoyao Decoction
groups. UC was induced by administration of DSS. Starting on day 4 of modeling,the low-,medium-,and high-dose groups were given
Shaoyao Decoction
by gavage at doses of 7.74,15.47,and 30.94 g/(kg·d),respectively. The normal and model groups received equal volumes of saline by gavage daily at 8:00 a.m. for 7 consecutive days. The disease activity index (DAI) was recorded. On day 10,all mice were euthanized. Blood was collected via eyeball extraction,and colon segments from the anus to the end of the cecum were isolated and measured for length. Colon tissue pathology was observed by hematoxylin-eosin (HE) staining for histological inflammation scoring. Serum levels of IL-6,IL-1β,and TNF-α were measured by ELISA. Alcian blue-periodic acid-Schiff (AB-PAS) staining assessed goblet cells. The mRNA expression of Notch-1 and Hes-1 in colon tissue was measured by qPCR. Protein expression of Notch-1,Hes-1,and ATOH-1 was detected by Western blot. Mucin 2 (MUC2) protein expression was assessed by immunohistochemistry,and olfactomedin 4 (OLFM4) protein expression was observed by immunofluorescence.
Results
2
From day 2 of modeling,DAI scores increased gradually in all groups except the normal group,and the model group showed significantly higher DAI scores than the normal group (
P
<
0.01),peaking at day 10. On day 10,the medium- and high-dose
Shaoyao Decoction
gr
oups had significantly lower DAI scores than the model group (
P
<
0.05,
P
<
0.01). Colon length was shorter in the model group than the normal group (
P
<
0.01),and longer in the low-,medium-,and high-dose groups compared with the model group (
P
<
0.05). Histopathological analysis showed marked improvement in the
Shaoyao Decoction
groups compared with the model group,with normal and uniform intestinal thickness,occasional irregular villi and lamina propria morphology,and normal cell size and density. Inflammation scores in medium- and high-dose groups were significantly lower than those in the model group (
P
<
0.01). Serum IL-6,IL-1β,and TNF-α levels were significantly higher in the model group than in the normal group (
P
<
0.01),but significantly lower in all
Shaoyao Decoction
groups compared with the model group (
P
<
0.05,
P
<
0.01). The number of goblet cells in colon tissue was reduced in the model group compared with the normal group,but increased in all
Shaoyao Decoction
groups compared with the model group. Notch-1 and Hes-1 mRNA expression was significantly higher in the model group than in the normal group (
P
<
0.05,
P
<
0.01),whereas medium- and high-dose groups showed significant decreases compared with the model group (
P
<
0.05,
P
<
0.01). Notch-1 and Hes-1 protein expression in the model group was higher (
P
<
0.01),and ATOH-1 protein expression was lower than in the normal group (
P
<
0.01). Compared with the results in the model group,Notch-1 protein expression was lower in the medium- and high-dose groups (
P
<
0.05),Hes-1 protein expression was lower in low- and high-dose groups (
P
<
0.05),and ATOH-1 protein expression was higher in all
Shaoyao Decoction
groups (
P
<
0.01). MUC2 protein expression optical density was lower in the model group than in the normal group (
P
<
0.01),but higher in the medium- and high-dose groups compared with the model group (
P
<
0.05). OLFM4 protein expression was elevated in the model group compared with the normal group and significantly reduced in all
Shaoyao Decoction
groups compared with the model group.
Conclusions
2
Shaoyao Decoction
significantly reduces intestinal inflammation and improves mucosal barrier function in DSS-induced UC mice. Its therapeutic effect is related to modulation of the Notch signaling pathway.
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