ANG-(1-7) IMPROVES ISLET B CELL FUNCTION BY UP-REGULATING THE ACTIVITY OF ANG-(1-7)-MAS AXIS/PDX-1

被引:0
|
作者
Zhang, Zeng [1 ]
He, Yanming [1 ]
Zheng, Min [1 ]
Fan, Zhaohua [1 ]
Zhang, Dan [1 ]
Li, Yunhao [1 ]
Zhang, Qiang [1 ]
Yuan, Shasha [1 ]
Wang, Yanyan [1 ]
Liu, Chenghao [1 ]
Yang, Hongjie [1 ]
机构
[1] Shanghai Univ Tradit Chinese Med, Yueyang Hosp Integrated Tradit Chinese & Western, Dept Endocrinol, Shanghai, Peoples R China
来源
ACTA MEDICA MEDITERRANEA | 2020年 / 36卷 / 06期
关键词
Ang-(1-7); Ang-(1-7)-Mas axis; islet beta cell; diabetes; MIMETIC AVE0991;
D O I
10.19193/0393-6384_2020_6_530
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Objective: To study the function of islet beta cells improved by Ang-(1-7) by up-regulating Ang-(1-7)-Mas axis/PDX-1 activity. Methods: Thirty clean-grade male Wistar rats were used. Twelve rats were randomly selected to be the normal control group, and 20 rats were selected and fed a high-fat, high-calorie diet, and the DM rat model was established with 30 mg/kg STZ. Rats with successful modelling were randomly divided into a DM model group (9 rats) and an Ang-(1-7) intervention group (9 rats). The body weight and general condition of rats in each group were observed and recorded. The fasting blood glucose (FBG) of each rat was detected with the glucose oxidase method, and serum insulin and angiotensin 11 (Ang 11) levels were detected with an enzyme-linked immunosorbent assay. The expression level of pancreatic duodenal honzeobox factor-1 (PDX-1) protein was detected using Western blotting, and the insulin resistance index (Homa-IR) was calculated. Results: The rats in the normal control group showed normal growth and development, good spirit, rapid response and normal body weight. The rats in the model group gradually lost weight, showing polyphagia, polyuria, poor mental function and unresponsiveness. Food consumption of the rats in the intervention group gradually decreased, the number of second stools decreased, and the spirit and reaction rate improved after intervention. Additionally, the body weight and insulin concentration of the model group were significantly lower than those of the control group, and the FBG level was significantly higher than that of the control group (P<0.05). Body weight was not significantly different between the intervention group and the model group (P>0.05). The insulin concentration of the intervention group was significantly higher than that of the model group, and the FBG level was significantly lower than that of the model group (P<0.05). The AngII concentration and Homa-IR value in the model group were significantly higher than those in the control group (P<0.05) and that in the intervention group were significantly lower than those in the model group (P<0.05). The PDX-1 expression level in the model group was significantly lower than that of the control group (P<0.05), but the PDX-1 expression level of the intervention group was significantly higher than that of the control group (P<0.05). Conclusion: Ang-(1-7) can improve the function of islet beta cells by upregulating the Ang-(1-7)-Mas axis and PDX-1 activity to delay the progression of diabetes.
引用
收藏
页码:3359 / +
页数:5
相关论文
共 50 条
  • [31] Characterization of angiotensin-(1-7) [Ang-(1-7)] receptor subtype in mesenteric resistance arteries
    Neves, LA
    Averill, DB
    Walkup, MP
    Aschner, JL
    Ferrario, CM
    Brosnihan, KB
    FASEB JOURNAL, 2002, 16 (04): : A95 - A95
  • [32] ANGIOTENSIN-(1-7) [ANG-(1-7)] INHIBITS VASCULAR SMOOTH-MUSCLE CELL-GROWTH
    FREEMAN, EJ
    CHISOLM, GM
    FERRARIO, CM
    TALLANT, EA
    HYPERTENSION, 1993, 22 (03) : 414 - 414
  • [33] Physiological and pathological roles of Ang II and Ang- (1-7) in the female reproductive system
    Liu, Yuanyuan
    Hao, Haomeng
    Lan, Tingting
    Jia, Rui
    Cao, Mingya
    Zhou, Liang
    Zhao, Zhiming
    Pan, Wensen
    FRONTIERS IN ENDOCRINOLOGY, 2022, 13
  • [34] Increased Plasma Ang II/ Ang-(1-7) Ratio In Pulmonary Arterial Hypertension
    Johnson, J. A.
    Hemnes, A.
    Robbins, I.
    West, J. D.
    AMERICAN JOURNAL OF RESPIRATORY AND CRITICAL CARE MEDICINE, 2011, 183
  • [35] Vascular smooth muscle cells transfected with the AT1b receptor exhibit high affinity for Ang-(1-7) and D-Ala7-Ang-(1-7)
    Diz, DI
    Chappell, MC
    Ferrario, CM
    Gallagher, PE
    Tallant, EA
    HYPERTENSION, 2003, 42 (03) : 430 - 430
  • [36] Ang-(1-7) acts as a weak agonist to downregulate AT1 receptors
    Clark, MA
    Tallant, EA
    Diz, DI
    FASEB JOURNAL, 1999, 13 (04): : A481 - A481
  • [37] Liposomes as Ang-(1-7) Carriers to the CNS for Ischemic Stroke Therapy
    Fernandes, L. F.
    Soares, I. N.
    Ferreira-Vieira, T. H.
    Fernandes, S. O. A.
    Cardoso, V. N.
    Frezard, F. J. G.
    Massensini, A. R.
    CELL TRANSPLANTATION, 2017, 26 : 708 - 709
  • [38] Ang-(1-7) Induced MAS1 Receptor-Mediated Angiogenesis in the Rat Microvasculature
    Hoffmann, Brian Robert
    Stodola, Timothy J.
    Wagner, Jordan R.
    Greene, Andrew S.
    FASEB JOURNAL, 2013, 27
  • [39] Neprilysin and endothelin converting enzyme contribute to the processing of Ang I and Ang-(1-9) to Ang-(1-7) in human endothelial cells
    Pirro, NT
    Ferrario, CM
    Chappell, MC
    FASEB JOURNAL, 2001, 15 (05): : A778 - A778
  • [40] ACE2/Ang-(1-7) improves insulin resistance in hepatic cells
    Cao, Xi
    Xie, Rongrong
    Xin, Zhong
    Yang, Jinkui
    DIABETES-METABOLISM RESEARCH AND REVIEWS, 2014, 30 : 46 - 46