中国组织工程研究 ›› 2026, Vol. 30 ›› Issue (12): 3058-3065.doi: 10.12307/2026.662

• 组织构建实验造模 experimental modeling in tissue construction • 上一篇    下一篇

穿心莲内酯干预妊娠糖尿病模型大鼠胰岛素抵抗的作用机制

王  鹏,陆  欢,刘海凤,李  峰   

  1. 成都医学院第二附属医院·核工业四一六医院妇产科,四川省成都市  610000

  • 收稿日期:2025-03-07 接受日期:2025-07-31 出版日期:2026-04-28 发布日期:2025-09-29
  • 通讯作者: 刘海凤,硕士,副主任医师,成都医学院第二附属医院·核工业四一六医院妇产科,四川省成都市 610000
  • 作者简介:王鹏,男,1979年生,四川省成都市人,汉族,主治医师,主要从事妇产科相关研究。
  • 基金资助:
    成都市医学科研课题立项项目(2018065),项目负责人:李峰

Mechanism by which andrographolide intervenes in insulin resistance in rats with gestational diabetes mellitus 

Wang Peng, Lu Huan, Liu Haifeng, Li Feng   

  1. Department of Obstetrics and Gynecology, The Second Affiliated Hospital of Chengdu Medical College, Nuclear Industry 416 Hospital, Chengdu 610000, Sichuan Province, China
  • Received:2025-03-07 Accepted:2025-07-31 Online:2026-04-28 Published:2025-09-29
  • Contact: Liu Haifeng, MS, Associate chief physician, Department of Obstetrics and Gynecology, The Second Affiliated Hospital of Chengdu Medical College, Nuclear Industry 416 Hospital, Chengdu 610000, Sichuan Province, China
  • About author:Wang Peng, Attending physician, Department of Obstetrics and Gynecology, The Second Affiliated Hospital of Chengdu Medical College, Nuclear Industry 416 Hospital, Chengdu 610000, Sichuan Province, China
  • Supported by:
    Chengdu Medical Research Project, No. 2018065 (to LF)

摘要:


文题释义:
空腹血糖:指空腹(除饮水外)8 h未进食采集静脉血检测的血糖值。空腹血糖为糖尿病最常用的检测指标,空腹血糖水平高低可反映胰岛β细胞功能,一般代表基础胰岛素的分泌功能。
胰岛素抵抗:指机体对胰岛素的敏感性降低,正常剂量的胰岛素产生低于正常生物学效应的一种状态。简单来说,胰岛素不能很好地将血液中的葡萄糖转运到细胞内进行利用和储存,从而导致血糖升高,危害人体正常功能。

背景:妊娠期糖尿病可能会引起胚胎发育不良和胎儿畸形等,严重威胁胎儿及孕妇健康,目前尚无完善的治疗措施。穿心莲内酯可降低糖尿病大鼠血糖水平、胰岛素抵抗和氧化应激,减轻神经损伤。
目的:探究穿心莲内酯对妊娠糖尿病大鼠胰岛素抵抗的影响。
方法:取50只雌性SD大鼠,通过高脂饲料喂养联合腹腔注射链脲佐菌素的方式建立妊娠糖尿病模型,选取造模成功的40只大鼠,采用随机数字表法分4组干预:模型组(n=10)给予生理盐水灌胃,穿心莲内酯低剂量组(n=10)给予2.5 mg/kg穿心莲内酯灌胃,穿心莲内酯高剂量组(n=10)给予5 mg/kg穿心莲内酯灌胃,穿心莲内酯高剂量+Colivelin组(n=10)给予5 mg/kg穿心莲内酯灌胃+腹腔注射酪氨酸激酶2/信号转导和转录激活因子3(janus kinase 2/signal transducer and activator of transcription 3,JAK2/STAT3)信号通路激活剂Colivelin,1次/d,连续给药2周;另取10只妊娠SD大鼠作为对照组,给予生理盐水灌胃,1次/d,连续给药2周。给药结束后,检测各组大鼠体质量、空腹血糖与胰岛素水平、胰岛素抵抗指数及血清炎症因子(白细胞介素6、肿瘤坏死因子α、白细胞介素1β)、血脂水平,胰腺组织超氧化物歧化酶、过氧化物酶和丙二醛水平,苏木精-伊红染色观察胰腺组织形态,Western blot检测胰腺组织Bcl-2、Bax、半胱氨酸蛋白酶3、JAK2/STAT3信号通路蛋白表达。
结果与结论:①与对照组相比,模型组大鼠胰腺组织结构明显被破坏,体质量、空腹血糖与胰岛素水平、胰岛素抵抗指数以及血清炎症因子、三酰甘油、总胆固醇、低密度脂蛋白胆固醇、丙二醛水平均升高,Bax、半胱氨酸蛋白酶3、p-JAK2/JAK2、p-STAT3/STAT3蛋白表达升高,高密度脂蛋白胆固醇水平与超氧化物歧化酶、过氧化物酶活性、Bcl-2蛋白表达均降低(P < 0.05);②与模型组相比,穿心莲内酯高、低剂量组上述指标均明显改善,并且以穿心莲内酯高剂量组改善作用更显著;腹膜注射Colivelin可部分逆转穿心莲内酯对妊娠糖尿病大鼠胰岛素抵抗的改善作用;③结果表明,穿心莲内酯可能通过抑制JAK2/STAT3信号通路降低妊娠期糖尿病大鼠血糖、胰岛素抵抗、炎症和氧化应激,改善血糖代谢和胰腺组织损伤。
https://orcid.org/0009-0009-5308-9356(王鹏)

中国组织工程研究杂志出版内容重点:干细胞;骨髓干细胞;造血干细胞;脂肪干细胞;肿瘤干细胞;胚胎干细胞;脐带脐血干细胞;干细胞诱导;干细胞分化;组织工程

关键词: 穿心莲内酯, JAK2/STAT3信号通路, 妊娠糖尿病, 胰岛素抵抗, 空腹血糖, 空腹胰岛素
缩略语:酪氨酸激酶2/信号转导和转录激活因子3:janus kinase 2/signal transducer and activator of transcription 3,
JAK2/STAT3

Abstract: BACKGROUND: Gestational diabetes mellitus may cause embryonic dysplasia and fetal malformations, which seriously threaten the health of fetus and pregnant women; however, there is no perfect treatment measures. Andrographolide reduces blood glucose level, insulin resistance and oxidative stress, and attenuates nerve damage in diabetic rats.
OBJECTIVE: To investigate the effect of andrographolide on insulin resistance in gestational diabetes mellitus rats. 
METHODS: Fifty female Sprague-Dawley rats were enrolled. Animal models of gestational diabetes mellitus were established by high-fat feed combined with intraperitoneal injection of streptozotocin. Forty rats with successful modeling were selected and randomly divided into four intervention groups by using the randomized numerical table method: saline gavage was given to the model group (n=10), and 2.5 mg/kg andrographolide was given to the low-dose andrographolide group (n=10), and 5 mg/kg andrographolide was given to the high-dose andrographolide group (n=10), and intragastric injection of 5 mg/kg andrographolide and peritoneal injection of janus kinase 2/signal transducer and activator of transcription 3 (JAK2/STAT3) signaling pathway activator Colivelin were given to the high-dose andrographolide+Colivelin group (n=10). The administration was given once a day, for 2 continuous weeks. Another 10 pregnant Sprague-Dawley rats were taken as the control group and given saline by gavage once a day for 2 weeks. After administration, body mass, fasting blood glucose and insulin levels, insulin resistance index and serum inflammatory factors (interleukin 6, tumor necrosis factor α, interleukin 1β), blood lipid levels, pancreatic tissue superoxide dismutase, peroxidase and malondialdehyde levels were detected in each group. The morphology of pancreatic tissue was observed by hematoxylin-eosin staining. Western blot was used to detect Bcl-2, Bax, cysteine proteinase 3, JAK2/STAT3 signaling pathway protein expression in pancreatic tissue.
RESULTS AND CONCLUSION: (1) Compared with the control group, in the model group, the pancreatic tissue structure of rats was significantly damaged, and the body mass, fasting blood glucose and insulin levels, insulin resistance index, levels of serum inflammatory factors, triglyceride, total cholesterol, low-density lipoprotein cholesterol, and malondialdehyde, and protein expression levels of Bax, cysteine protease 3, p-JAK2/JAK2, and p-STAT3/STAT3 increased, while the levels of serum high-density lipoprotein cholesterol and superoxide dismutase, peroxidase activity, and Bcl-2 protein expression decreased (P < 0.05). (2) Compared with the model group, the above indexes were significantly improved in both the high-and low-dose andrographolide groups, and the improvement was more significant in the high-dose andrographolide group. Peritoneal injection of Colivelin could partially reverse the improvement effect of andrographolide on insulin resistance of rats with gestational diabetes mellitus. To conclude, andrographolide can reduce blood glucose, insulin resistance, inflammation, and oxidative stress in rats with gestational diabetes mellitus, improve blood glucose metabolism and pancreatic tissue damage, which may be related to the inhibition of the JAK2/STAT3 signaling pathway.

Key words: andrographolide, JAK2/STAT3 signaling pathway, gestational diabetes mellitus, insulin resistance, fasting blood glucose, fasting insulin

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