北京大学学报(医学版) ›› 2020, Vol. 52 ›› Issue (2): 269-274. doi: 10.19723/j.issn.1671-167X.2020.02.012

• 论著 • 上一篇    下一篇

绿原酸对高脂饲料诱导的肥胖大鼠糖耐量及其曲线特征的影响

郭成成,张晓圆,玉应香,谢岚,常翠青()   

  1. 北京大学第三医院运动医学研究所,北京 100191
  • 收稿日期:2019-01-28 出版日期:2020-04-18 发布日期:2020-04-18
  • 通讯作者: 常翠青 E-mail:changcuiqing@126.com
  • 基金资助:
    国家重点研发计划(2016YFD0400603)

Effects of chlorogenic acid on glucose tolerance and its curve characteristics in high-fat diet-induced obesity rats

Cheng-cheng GUO,Xiao-yuan ZHANG,Ying-xiang YU,Lan XIE,Cui-qing CHANG()   

  1. Institute of Sports Medicine, Peking University Third Hospital, Beijing 100191, China
  • Received:2019-01-28 Online:2020-04-18 Published:2020-04-18
  • Contact: Cui-qing CHANG E-mail:changcuiqing@126.com

摘要:

目的 观察绿原酸(chlorogenic acid,CGA)对高脂饲料诱导的肥胖(diet-induced-obesity,DIO)大鼠糖耐量及其曲线特征的作用, 为开发利用CGA早期预防和延缓糖尿病的发生提供依据.方法: 46只雄性Sprague-Dawley(SD)大鼠随机选择8只作为普通饲料组(normal control group,CON), 其余大鼠饲喂高脂饲料.4周后按标准筛选高脂诱导的肥胖大鼠24只并随机分为高脂饲料组(high fat diet group,HFD),50%(质量分数)CGA组和98%(质量分数)CGA组,每组8只,分别给予磷酸缓冲盐溶液(phosphate buffer saline,PBS),50%CGA和98%CGA灌胃8周,每周检测体质量,每4周进行一次口服糖耐量试验(oral glucose tolerance test,OGTT),实验期末检测空腹胰岛素及胰岛素释放,计算稳态模型胰岛素抵抗指数(homeostasis model assessment insulin resistance,HOMA-IR)和内脏脂肪百分比,苏木精和伊红(hematoxylin and eosin,HE)染色检测胰腺组织病理变化.结果: CGA干预前,与CON组相比,HFD组OGTT第120分时(OGTT-120min)血糖值(P<0.05)和葡萄糖曲线下面积(area under curve-glucose,AUC-G)(P<0.05)均显著升高;干预4周后葡萄糖峰值时间延迟(P<0.05);干预8周 HOMA-IR指数显著升高且OGTT-0min,OGTT-30min,OGTT-60min,OGTT-120min胰岛素水平和胰岛素曲线下面积(area under curve-insulin,AUC-I)显著升高(P<0.05), 胰腺胰岛显著增生(P<0.05).与HFD组相比,干预4周末,50%CGA和98%CGA组大鼠糖耐量及其葡萄糖峰值时间均无显著变化;干预8周后,50%CGA组大鼠OGTT-60min,OGTT-120min血糖值,HOMA-IR指数,OGTT-0min,OGTT-30min,OGTT-120min血清胰岛素水平显著降低(P<0.05);98%CGA组大鼠OGTT-60min,OGTT-120min血糖值,HOMA-IR指数,OGTT-0min,OGTT-120min血清胰岛素水平显著降低(P<0.05);50%和98%CGA组大鼠的葡萄糖峰值时间均显著前移(P<0.05), 胰岛异常增生改善(P<0.05).结论: OGTT葡萄糖峰值时间延迟是DIO大鼠糖耐量异常表现之一,50%和98%CGA均可改善DIO大鼠的糖耐量和葡萄糖峰值时间延迟.

关键词: 绿原酸, 肥胖, 糖耐量异常, OGTT葡萄糖峰值时间

Abstract:

Objective: To observe the effect of chlorogenic acid (chlorogenic acid,CGA) on the glucose tolerance and its curve characteristics in high fat diet-induced obesity (diet-induced-obesity,DIO) rats, so as to provide scientific grounds for the development and utilization of CGA in early prevention and reversal of prediabetes.Methods: Eight of forty-six male Sprague-Dawley rats were randomly selected as the normal diet group (CON group), and the rest were fed with high-fat diet. After 4 weeks, 24 high-fat-induced obese rats were screened according to the criteria and then randomly divided into high fat diet group (HFD group), 50% CGA group and 98% CGA group. The CGA groups received intragastric administrations of 50% CGA and 98% CGA orally via a gavage needle once a day for 8 weeks, respectively, while the CON and HFD groups received a carrier solution (phosphate buffer saline, PBS). Their body weights were measured weekly and oral glucose tolerance test (OGTT) was performed every 4 weeks. Fasting insulin and insulin release were measured at the end of the study. Meanwhile, HOMA-IR and visceral fat percentage were calculated. Histopathological examination by hematoxylin and eosin staining method were evaluated in the pancreatic tissues.Results: Before the intervention of chlorogenic acid, blood glucose levels 120 min after glucose loading (P<0.05) and AUC-G (P<0.05) were increased in the HFD group when compared with the CON group, and the time to glucose peak was delayed after 4 weeks of chlorogenic acid intervention (P<0.05). After 8 weeks of intervention, the HOMA-IR index, the insulin levels at 0 min, 30 min, 60 min, and 120 min after glucose loading and AUC-I increased (P<0.05), and the histopathological examination showed obvious hyperplasia of pancreatic islets (P<0.05). Compared with the HFD group, there was no significant change in glucose tolerance and glucose peak time in 50%CGA and 98%CGA groups at the end of 4 weeks of intervention. How-ever, after 8 weeks of intervention, OGTT-60min,OGTT-120min blood glucose (P<0.05) were lower, HOMA-IR index and OGTT-0min, OGTT-120min serum insulin level decreased (P<0.05), the time to glucose peak shifted to an earlier timepoint (P<0.05), abnormal islet hyperplasia attenuated (P<0.05) in 50% CGA and 98% CGA groups. Also, the OGTT-30min serum insulin level was decreased (P<0.05) in 50% CGA group.Conclusion: Delay in time to glucose peak during the OGTT was one of the manifestations of impaired glucose tolerance in DIO rats, and 50% and 98% CGA could improve the glucose tolerance and delay in glucose peak time.

Key words: Chlorogenic acid, Obesity, Impaired glucose tolerance, Oral glucose tolerance test glucose peak time

中图分类号: 

  • R587.1

表1

CGA对DIO大鼠体质量,Lee's指数和内脏脂肪百分比的影响($\bar{x}±s$)"

Items n Body weight/g Lee's index Visceral fat
percentage/%
CON 8 498.9±29.3 26.9±0.5 3.0±0.4
HFD 8 674.4±62.2* 29.1±0.7* 9.0±1.6*
50%CGA 8 649.1±50.3 28.8±0.6 8.9±2.6
98%CGA 8 655.0±66.3 29.1±0.8 7.2±2.0

图1

CGA对DIO大鼠糖耐量的影响"

图2

CGA对DIO大鼠OGTT胰岛素分泌的影响"

图3

DIO大鼠胰腺病理学变化(HE ×100)"

[1] Wang L, Gao P, Zhang M , et al. Prevalence and ethnic pattern of diabetes and prediabetes in China in 2013[J]. JAMA, 2017,317(24):2515-2523.
[2] Li G, Zhang P, Wang J , et al. Cardiovascular mortality, all-cause mortality, and diabetes incidence after lifestyle intervention for people with impaired glucose tolerance in the da qing diabetes prevention study: a 23-year follow-up study[J]. Lancet Diabetes Endocrinol, 2014,2(6):474-480.
[3] Unwin N, Shaw J, Zimmet P , et al. Impaired glucose tolerance and impaired fasting glycaemia: the current status on definition and intervention[J]. Diabet Med, 2002,19(9):708-723.
[4] Hulman A, Witte DR, Vistisen D , et al. Pathophysiological characteristics underlying different glucose response curves: a latent class trajectory analysis from the prospective EGIR-RISC study[J]. Diabetes Care, 2018,41(8):1740-1748.
[5] Tura A, Morbiducci U, Sbrignadello S , et al. Shape of glucose, insulin, C-peptide curves during a 3-h oral glucose tolerance test: any relationship with the degree of glucose tolerance[J]. Am J Physiol Regul Integr Comp Physiol, 2011,300(4):R941-R948.
[6] Abdul-Ghani MA, Williams K, Defronzo R , et al. Risk of progression to type 2 diabetes based on relationship between postload plasma glucose and fasting plasma glucose[J]. Diabetes Care, 2006,29(7):1613-1618.
[7] Hayashi T, Boyko EJ, Sato KK , et al. Patterns of insulin concentration during the OGTT predict the risk of type 2 diabetes in Japanese Americans[J]. Diabetes Care, 2013,36(5):1229-1235.
[8] Kramer CK, Vuksan V, Choi H , et al. Emerging parameters of the insulin and glucose response on the oral glucose tolerance test: reproducibility and implications for glucose homeostasis in individuals with and without diabetes[J]. Diabetes Res Clin Pract, 2014,105(1):88-95.
[9] Wang X, Zhao X, Zhou R , et al. Delay in glucose peak time during the oral glucose tolerance test as an indicator of insulin resistance and insulin secretion in type 2 diabetes patients[J]. J Diabetes Investig, 2018,9(6):1288-1295.
[10] Kramer CK, Ye C, Hanley AJ , et al. Delayed timing of post-challenge peak blood glucose predicts declining beta cell function and worsening glucose tolerance over time: insight from the first year postpartum[J]. Diabetologia, 2015,58(6):1354-1362.
[11] Kanauchi M, Kimura K, Kanauchi K , et al. Beta-cell function and insulin sensitivity contribute to the shape of plasma glucose curve during an oral glucose tolerance test in non-diabetic individuals[J]. Int J Clin Pract, 2005,59(4):427-432.
[12] Chung ST, Ha J, Onuzuruike AU , et al. Time to glucose peak during an oral glucose tolerance test identifies prediabetes risk[J]. Clin Endocrinol (Oxf), 2017,87(5):484-491.
[13] Li G, Zhang P, Wang J , et al. The long-term effect of lifestyle interventions to prevent diabetes in the China da qing diabetes prevention study: a 20-year follow-up study[J]. Lancet, 2008,371(9626):1783-1789.
[14] Zuniga LY , Aceves-de LMM, Gonzalez-Ortiz M, et al. Effect of chlorogenic acid administration on glycemic control, insulin secretion, and insulin sensitivity in patients with impaired glucose tolerance[J]. J Med Food, 2018,21(5):469-473.
[15] Ma Y, Gao M, Liu D . Chlorogenic acid improves high fat diet-induced hepatic steatosis and insulin resistance in mice[J]. Pharm Res, 2015,32(4):1200-1209.
[16] Jin S, Chang C, Zhang L , et al. Chlorogenic acid improves late diabetes through adiponectin receptor signaling pathways in db/db mice[J]. PLoS One, 2015,10(4):e120842.
[17] Panchal SK, Poudyal H, Waanders J , et al. Coffee extract attenuates changes in cardiovascular and hepatic structure and function without decreasing obesity in high-carbohydrate, high-fat diet-fed male rats[J]. J Nutr, 2012,142(4):690-697.
[18] Hariri N, Thibault L . High-fat diet-induced obesity in animal models[J]. Nutr Res Rev, 2010,23(2):270-299.
[19] Le Floch JP, Escuyer P, Baudin E , et al. Blood glucose area under the curve. Methodological aspects[J]. Diabetes Care, 1990,13(2):172-175.
[20] Tschritter O, Fritsche A, Shirkavand F , et al. Assessing the shape of the glucose curve during an oral glucose tolerance test[J]. Diabetes Care, 2003,26(4):1026-1033.
[21] Wong SK, Chin KY, Suhaimi FH , et al. The effects of a modified high-carbohydrate high-fat diet on metabolic syndrome parameters in male rats[J]. Exp Clin Endocrinol Diabetes, 2018,126(4):205-212.
[22] Joung KH, Ju SH, Kim JM , et al. Clinical implications of using post-challenge plasma glucose levels for early diagnosis of type 2 diabetes mellitus in older individuals[J]. Diabetes Metab J, 2018,42(2):147-154.
[1] 朱忆颖,闵赛南,俞光岩. 局部注射环孢素A对非肥胖糖尿病小鼠下颌下腺分泌功能及炎症的影响[J]. 北京大学学报(医学版), 2021, 53(4): 750-757.
[2] 张晓圆,郭成成,玉应香,谢岚,常翠青. 高脂饲料诱导肥胖胰岛素抵抗大鼠模型的建立[J]. 北京大学学报(医学版), 2020, 52(3): 557-563.
[3] 那晓娜,朱珠,陈阳阳,王东平,王浩杰,宋阳,马晓川,王培玉,刘爱萍. 身体活动、静坐行为的时间分布与肥胖的关系[J]. 北京大学学报(医学版), 2020, 52(3): 486-491.
[4] 董彦会,宋逸,董彬,邹志勇,王政和,杨招庚,王西婕,李艳辉,马军. 2014年中国7~18岁学生血压状况与营养状况的关联分析——基于中国儿童青少年血压评价标准[J]. 北京大学学报(医学版), 2018, 50(3): 422-428.
[5] 吴宇佳,迟晓培,陈峰,邓旭亮. 肥胖者唾液微生物宏基因组学特点[J]. 北京大学学报(医学版), 2018, 50(1): 5-12.
[6] 杜依青,刘慧鑫,刘春雷,顿耀军,李清,于路平,刘士军,陈黎黎,王晓峰,徐涛. 代谢相关因素与肾细胞癌分级、分期的相关研究[J]. 北京大学学报(医学版), 2016, 48(4): 612-617.
[7] 程兰,李钦,宋逸,马军,王海俊. 中国9~11岁小学生体育锻炼、静态行为和#br# 超重与肥胖的关系[J]. 北京大学学报(医学版), 2016, 48(3): 436-441.
[8] 付连国, 王海俊, 阳益德, 李晓卉, 王烁, 孟祥坤, 王政和, 马军. 儿童青少年对肥胖危险因素知晓的现状分析[J]. 北京大学学报(医学版), 2015, 47(3): 410-413.
[9] 温萌萌, 朱广荣, 王海雪. 中国11~18岁汉族男生肥胖与首次遗精年龄的相关性分析[J]. 北京大学学报(医学版), 2015, 47(3): 406-409.
[10] 崔馨月, 陈天娇, 马军. 社会生态模式在儿童青少年肥胖防控中对体格指标的干预效果[J]. 北京大学学报(医学版), 2015, 47(3): 400-405.
[11] 刘严, 齐丽彤, 马为, 杨颖, 孟磊, 张宝娓, 霍勇. 中老年人体测量学指标与动脉硬化指标的关系[J]. 北京大学学报(医学版), 2014, 46(3): 455-459.
[12] 刘芳宏, 宋洁云, 马军, 尚晓瑞, 孟祥睿, 王海俊. SREBP2基因rs2228314多态性与儿童青少年血脂水平和肥胖的关系[J]. 北京大学学报(医学版), 2014, 46(3): 355-359.
[13] 徐昊, 吴峥昊, 许雅君. 孕期和哺乳期槲皮素干预对肥胖母鼠后代的体重及胰岛素样生长因子-1 mRNA表达的影响[J]. 北京大学学报(医学版), 2014, 46(3): 347-354.
[14] 马军. 我国儿童青少年面临的主要健康问题及应对策略[J]. 北京大学学报(医学版), 2013, 45(03): 337-342.
[15] 付连国, 马军, 王海俊, 董彬, 王晶晶, 尚晓瑞, 张子龙, 刘芳宏, 蔡赐河, 文晗. 儿童青少年超重、肥胖对其身体机能影响的
多水平分析
[J]. 北京大学学报(医学版), 2012, 44(3): 359-363.
Viewed
Full text


Abstract

Cited

  Shared   
  Discussed   
[1] 张三. 中文标题测试[J]. 北京大学学报(医学版), 2010, 42(1): 1 -10 .
[2] 赵磊, 王天龙 . 右心室舒张末期容量监测用于肝移植术中容量管理的临床研究[J]. 北京大学学报(医学版), 2009, 41(2): 188 -191 .
[3] 万有, , 韩济生, John E. Pintar. 孤啡肽基因敲除小鼠电针镇痛作用增强[J]. 北京大学学报(医学版), 2009, 41(3): 376 -379 .
[4] 张燕, 韩志慧, 钟延丰, 王盛兰, 李玲玲, 郑丹枫. 骨骼肌活组织检查病理诊断技术的改进及应用[J]. 北京大学学报(医学版), 2009, 41(4): 459 -462 .
[5] 林红, 王玉凤, 吴野平. 学校生活技能教育对小学三年级学生行为问题影响的对照研究[J]. 北京大学学报(医学版), 2007, 39(3): 319 -322 .
[6] 丰雷, 程嘉, 王玉凤. 注意缺陷多动障碍儿童的运动协调功能[J]. 北京大学学报(医学版), 2007, 39(3): 333 -336 .
[7] 李岳玲, 钱秋瑾, 王玉凤. 儿童注意缺陷多动障碍成人期预后及其预测因素[J]. 北京大学学报(医学版), 2007, 39(3): 337 -340 .
[8] . 书讯[J]. 北京大学学报(医学版), 2007, 39(3): 225 -328 .
[9] 牟向东, 王广发, 刁小莉, 阙呈立. 肺黏膜相关淋巴组织型边缘区B细胞淋巴瘤一例[J]. 北京大学学报(医学版), 2007, 39(4): 346 -350 .
[10] 张宏文, 丁洁, 王芳, 杨惠霞. 一例X连锁Alport综合征女性妊娠期随访[J]. 北京大学学报(医学版), 2007, 39(4): 351 -354 .