Jiang Feng, Zhou Jin-Yong, Wu Jian, Tian Fang, Zhu Xuan-Xuan, Zhu Chang-Le, Yang Bo-Lin, Chen Yu-Gen
No. 1 Clinical Medical College, Nanjing University of Chinese Medicine, Nanjing, Jiangsu 210023, China.
Jiangsu Province Hospital of TCM, The Affiliated Hospital of Nanjing University of TCM, Nanjing 210029, China.
Evid Based Complement Alternat Med. 2017;2017:4249016. doi: 10.1155/2017/4249016. Epub 2017 Dec 18.
This study assessed the efficacy and mechanism of action of Yangyin Runchang decoction (YRD) in the treatment of slow-transit constipation (STC). ICR mice were randomly divided into four groups ( = 10/group) and treated with saline (normal control; NC), atropine/diphenoxylate (model control; MC; 20 mg/kg), or atropine/diphenoxylate plus low-dose YRD (L-YRD; 29.6 g/kg) or high-dose YRD (H-YRD; 59.2 g/kg). Intestinal motility was assessed by evaluating feces and the intestinal transit rate (ITR). The serum level of stem cell factor (SCF) and changes in interstitial cells of Cajal (ICCs) were also evaluated. Additionally, the expression of SCF and c-kit and the intracellular Ca concentration [Ca] were investigated. Fecal volume and ITR were greater in the L-YRD and H-YRD groups than in the MC group. The serum SCF level was lower in the MC group than in the NC group; this effect was ameliorated in the YRD-treated mice. Additionally, YRD-treated mice had more ICCs and elevated expression of c-kit and membrane-bound SCF, and YRD also increased [Ca] in isolated ICCs. YRD treatment in this STC mouse model was effective, possibly via the restoration of the SCF/c-kit pathway, increase in the ICC count, and enhancement of ICC function by increasing [Ca] .
本研究评估了养阴润肠汤(YRD)治疗慢传输型便秘(STC)的疗效及作用机制。将ICR小鼠随机分为四组(每组n = 10),分别用生理盐水(正常对照组;NC)、阿托品/地芬诺酯(模型对照组;MC;20 mg/kg)或阿托品/地芬诺酯加低剂量YRD(L - YRD;29.6 g/kg)或高剂量YRD(H - YRD;59.2 g/kg)进行处理。通过评估粪便和肠道传输率(ITR)来评价肠道动力。还评估了干细胞因子(SCF)的血清水平以及Cajal间质细胞(ICC)的变化。此外,研究了SCF和c - kit的表达以及细胞内钙离子浓度[Ca]。L - YRD组和H - YRD组的粪便量和ITR均高于MC组。MC组血清SCF水平低于NC组;YRD处理的小鼠中这种效应得到改善。此外,YRD处理的小鼠有更多的ICC,c - kit和膜结合SCF的表达升高,YRD还增加了分离的ICC中的[Ca]。在该STC小鼠模型中,YRD治疗是有效的,可能是通过恢复SCF/c - kit途径、增加ICC数量以及通过增加[Ca]增强ICC功能来实现的。