Administration of Danhong Injection to diabetic db/db mice inhibits the development of diabetic retinopathy and nephropathy

被引:41
|
作者
Liu, Mengyang [1 ,2 ]
Pan, Quan [1 ,2 ]
Chen, Yuanli [1 ,3 ]
Yang, Xiaoxiao [1 ,2 ]
Zhao, Buchang [4 ]
Jia, Lifu [4 ]
Zhu, Yan [5 ]
Zhang, Boli [5 ]
Gao, Xiumei [5 ]
Li, Xiaoju [2 ]
Han, Jihong [1 ,3 ]
Duan, Yajun [1 ,3 ]
机构
[1] Nankai Univ, State Key Lab Med Chem Biol, Tianjin 300071, Peoples R China
[2] Nankai Univ, Coll Life Sci, Tianjin 300071, Peoples R China
[3] Nankai Univ, Collaborat Innovat Ctr Biotherapy, Tianjin 300071, Peoples R China
[4] Buchang Pharmaceut Co Ltd, Xian 712000, Peoples R China
[5] Tianjin Univ Tradit Chinese Med, Tianjin 300193, Peoples R China
来源
SCIENTIFIC REPORTS | 2015年 / 5卷
基金
美国国家科学基金会;
关键词
GLYCATION END-PRODUCTS; GROWTH-FACTOR; INSULIN-SENSITIVITY; SALVIANOLIC ACID; LITHOSPERMATE-B; HIGH GLUCOSE; ACTIVATION; RECEPTOR; LIVER; CELLS;
D O I
10.1038/srep11219
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Danhong Injection (DHI), a Chinese medicine for treatment of patients with coronary heart disease, inhibits primary abdominal aortic aneurysms in apoE deficient (apoE(-/-)) mice. Formation of microaneurysms plays an important role in the development of diabetic retinopathy and nephropathy. It remains unknown if DHI can reduce these diabetic complications. In this study, diabetic db/db mice in two groups were injected with saline and DHI, respectively, for 14 weeks. Blood and tissue samples were collected to determine serum glucose, lipids and tissue structure. DHI reduced diabetes-induced body weight gain, serum cholesterol and glucose levels. In retinas, DHI blocked the shrink of whole retina and retinal sub-layers by inhibiting expression of caspase 3, matrix metalloproteinase 2 (MMP-2) and MMP-9, accumulation of carbohydrate macromolecules and formation of acellular capillaries. DHI improved renal functions by inhibiting mesangial matrix expansion, expression of vascular endothelial growth factor A, fibronectin and advanced glycation end products in kidneys. Mechanistically, DHI induced expression of glucokinase, AMPK alpha/phosphorylated AMPK alpha, insulin receptor substrate 1, fibroblast growth factor 21 and peroxisome proliferator-activated.. Expression of genes responsible for energy expenditure was also activated by DHI. Therefore, DHI inhibits diabetic retinopathy and nephropathy by ameliorating glucose metabolism and demonstrates a potential application in clinics.
引用
收藏
页数:14
相关论文
共 50 条
  • [41] Analyzing and cloning of diabetic nephropathy relative gene from db/db mice
    Zheng, JM
    Liu, ZH
    Zhang, X
    Li, LS
    PROGRESS IN BIOCHEMISTRY AND BIOPHYSICS, 2003, 30 (03) : 406 - 411
  • [42] Telmisartan Attenuates Diabetic Nephropathy by Suppressing Oxidative Stress in db/db Mice
    Sato-Horiguchi, Chikage
    Ogawa, Daisuke
    Wada, Jun
    Tachibana, Hiromi
    Kodera, Ryo
    Eguchi, Jun
    Nakatsuka, Atsuko
    Terami, Naoto
    Shikata, Kenichi
    Makino, Hirofumi
    NEPHRON EXPERIMENTAL NEPHROLOGY, 2012, 121 (3-4): : E97 - E108
  • [43] Combined therapy of rhein and benazepril on the treatment of diabetic nephropathy in db/db mice
    Jia, Z. H.
    Liu, Z. H.
    Zheng, J. M.
    Zeng, C. H.
    Li, L. S.
    EXPERIMENTAL AND CLINICAL ENDOCRINOLOGY & DIABETES, 2007, 115 (09) : 571 - 576
  • [44] The effect of dietary iron restriction against diabetic nephropathy in db/db mice
    Ikeda, Yasumasa
    Enomoto, Hideaki
    Tajima, Soichiro
    Izawa-Ishizawa, Yuki
    Kihira, Yoshitaka
    Ishizawa, Keisuke
    Tomita, Shuhei
    Tsuchiya, Koichiro
    Tamaki, Toshiaki
    FASEB JOURNAL, 2013, 27
  • [45] Therapeutic potential of NaoXinTong Capsule on the developed diabetic nephropathy in db/db mice
    Yang, Shu
    Chen, Yuanli
    Duan, Yajun
    Ma, Chuanrui
    Liu, Lipei
    Li, Qi
    Yan, Jie
    Li, Xiaoju
    Zhao, Buchang
    Wang, Yong
    Qian, Ke
    Liu, Mengyang
    Zhu, Yan
    Yang, Xiaoxiao
    Han, Jihong
    BIOMEDICINE & PHARMACOTHERAPY, 2019, 118
  • [46] Differential expression of AL023001 in db/db diabetic nephropathy mice
    Zheng, JM
    Liu, ZH
    Zhang, X
    Chen, S
    Li, LS
    PROGRESS IN BIOCHEMISTRY AND BIOPHYSICS, 2004, 31 (09) : 834 - 840
  • [47] Epiretinal membranes in a db/db model of diabetic retinopathy
    Bonet, A.
    Valenca, A.
    Catita, J.
    Nacher, V.
    Navarro, M.
    Carretero, A.
    Mendes-Jorge, L.
    Ramos, D.
    Ruberte, J.
    ACTA OPHTHALMOLOGICA, 2018, 96 : 15 - 15
  • [48] Arginase Isoforms and Diabetic Retinopathy in the db/db Mouse
    Bunch, Katharine Leilani
    Caldwell, Ruth B.
    Caldwell, Robert W.
    INVESTIGATIVE OPHTHALMOLOGY & VISUAL SCIENCE, 2021, 62 (08)
  • [49] Mechanism of the onset of diabetic nephropathy in type 2 diabetic db/db mice (1st report)
    Hosoyamada, M
    Suzuki, M
    Yasuda, H
    Takiue, Y
    Suzuki, T
    Kimura, M
    Shibasaki, T
    JOURNAL OF PHARMACOLOGICAL SCIENCES, 2006, 100 : 210P - 210P
  • [50] Prevention of diabetic nephropathy by treatment with astaxanthin in diabetic db/db mice (vol 20, pg 49, 2004)
    Naitoa, Yuji
    Uchiyama, Kazuhiko
    Aoi, Wataru
    Hasegawa, Goji
    Nakamura, Naoto
    Yoshida, Norimasa
    Maoka, Takashi
    Takahashi, Jiro
    Yoshikawa, Toshikazu
    BIOFACTORS, 2013, 39 (05) : 590 - 590