Li Hongzeng, Wang Yitong, Tian Yuxin, Tian Feiyue, Xing Zhiyang, Wang Yunfei, Yan Meixing, Gong Yanling
Department of Pharmacy, College of Chemical Engineering, Qingdao University of Science and Technology, Qingdao, China.
These authors contributed equally to this work.
Iran J Basic Med Sci. 2022 Apr;25(4):520-526. doi: 10.22038/IJBMS.2022.60126.13339.
Diabetic gastroparesis (DGP) is one of the main complications of diabetes, and more than half of diabetes cases are accompanied by gastroparesis. This study aims to explore the effect of volatile oil (ACVO) on DGP rats.
The rats were injected with STZ combined with a high-sugar and high-fat diet in an irregular manner to establish the DGP model. ACVO at different doses (9.11 mg/kg, 18.23 mg/kg, and 36.45 mg/kg) were given by intragastric administration. A mixture of cisapride and metformin was used as the positive control. At the end of the experiment, gastric emptying and intestinal propulsion were determined. Then the tissue samples and blood were taken from each group for serum analysis, western blot and immunopathological examination.
After treatment with ACVO, body weight increased and blood glucose decreased when compared with rats in the DGP group. Gastric emptying and intestinal propulsion were accelerated, and gastric acid secretion increased. The serum insulin-like growth factor-1 (IGF-1) level was increased. Protein expressions and positive cells of IGF-1 receptor (IGF-1R), acetylcholine transferase (CHAT), and stem cell factors (SCF) in the stomach were significantly increased determined by western blot and immunofluorescence staining. The morphology and the number of interstitial cells of Cajal (ICCs) in the stomach were restored, determined by hematoxylin and eosin staining and immunohistochemical staining, respectively.
ACVO effectively alleviated DGP in rats, and its mechanism may be related to the up-regulation of IGF-1/IGF-1R signaling.
糖尿病胃轻瘫(DGP)是糖尿病的主要并发症之一,超过半数的糖尿病患者伴有胃轻瘫。本研究旨在探讨挥发油(ACVO)对DGP大鼠的影响。
通过不规则注射链脲佐菌素(STZ)并结合高糖高脂饮食建立DGP模型。以不同剂量(9.11mg/kg、18.23mg/kg和36.45mg/kg)的ACVO进行灌胃给药。使用西沙必利和二甲双胍的混合物作为阳性对照。实验结束时,测定胃排空和肠推进情况。然后从每组采集组织样本和血液进行血清分析、蛋白质印迹法和免疫病理学检查。
与DGP组大鼠相比,ACVO治疗后体重增加,血糖降低。胃排空和肠推进加快,胃酸分泌增加。血清胰岛素样生长因子-1(IGF-1)水平升高。通过蛋白质印迹法和免疫荧光染色测定,胃中IGF-1受体(IGF-1R)、乙酰胆碱转移酶(CHAT)和干细胞因子(SCF)的蛋白表达和阳性细胞显著增加。分别通过苏木精-伊红染色和免疫组织化学染色测定,胃中Cajal间质细胞(ICC)的形态和数量得以恢复。
ACVO可有效减轻大鼠的DGP,其机制可能与上调IGF-1/IGF-1R信号通路有关。