Imatinib mesylate (Gleevec) protects against streptozotocin-induced diabetes and islet cell death in vitro

被引:46
|
作者
Hagerkvist, Robert
Makeeva, Natalia
Elliman, Stephen
Welsh, Nils
机构
[1] Univ Uppsala, Biomedicum, Dept Med Cell Biol, S-75123 Uppsala, Sweden
[2] Novartis Inst BioMed Res, Diabet & Metab Dis Area, Cambridge, MA 02139 USA
关键词
imatinib; pancreatic islet; diabetes; JNK; apoptosis;
D O I
10.1016/j.cellbi.2006.08.006
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
The tyrosine kinase inhibitor imatinib mesylate (Gleevec) has been demonstrated to protect various cell types from death by inhibition of Abelson tyrosine kinase (c-Abl). The aim of the present study was to establish whether imatinib protects the insulin producing P-cell from the different apoptosis promoting agents it? vitro and whether imatinib counteracts streptozotocin-induced diabetes in NMRI mice. We observe that imatinib attenuated the actions of several different death promoting substances. In addition, mice injected with streptozotocin did not develop diabetes when given imatinib. The beneficial effects of imatinib may be related to inhibition of the pro-apoptotic MAP kinase JNK. We conclude that imatinib protects against beta-cell death and that this may contribute to the previously reported anti-diabetic actions of imatinib. (c) 2006 International Federation for Cell Biology. Published by Elsevier Ltd. All rights reserved.
引用
收藏
页码:1013 / 1017
页数:5
相关论文
共 50 条
  • [31] Nicorandil improves diabetes and rat islet β-cell damage induced by streptozotocin in vivo and in vitro
    Kasono, K
    Yasu, T
    Kakehashi, A
    Kinoshita, N
    Tamemoto, H
    Namai, K
    Ohn, R
    Ueba, H
    Kuroki, M
    Ishikawa, S
    Kawakami, M
    EUROPEAN JOURNAL OF ENDOCRINOLOGY, 2004, 151 (02) : 277 - 285
  • [32] Loss of Pancreatic Mitogen-inducible Gene 6 Protects Mice Against Streptozotocin-induced Diabetes
    Fong, Kimberley
    Chen, Yi-Chun
    Fueger, Patrick
    FASEB JOURNAL, 2015, 29
  • [33] Loss of CB1R Protects against Streptozotocin-Induced β-Cell Dysfunction in Mice
    Aseer, Kanikkai Raja
    O'Connell, Jennifer F.
    Egan, Josephine M.
    DIABETES, 2020, 69
  • [34] Dihydromyricetin Protects against Diabetic Cardiomyopathy in Streptozotocin-Induced Diabetic Mice
    Wu, Bin
    Lin, Jie
    Luo, Jian
    Han, Dong
    Fan, Miaomiao
    Guo, Tao
    Tao, Ling
    Yuan, Ming
    Yi, Fu
    BIOMED RESEARCH INTERNATIONAL, 2017, 2017
  • [35] CTRP3 protects against streptozotocin-induced diabetic cardiomyopathy
    Yuan, Yupei
    Tang, Qizhu
    JOURNAL OF THE AMERICAN COLLEGE OF CARDIOLOGY, 2016, 68 (16) : C47 - C47
  • [36] Spironolactone Protects against Diabetic Cardiomyopathy in Streptozotocin-Induced Diabetic Rats
    Liu, Wenjuan
    Gong, Wei
    He, Min
    Liu, Yemei
    Yang, Yeping
    Wang, Meng
    Wu, Meng
    Guo, Shizhe
    Yu, Yifei
    Wang, Xuanchun
    Sun, Fei
    Li, Yiming
    Zhou, Linuo
    Qin, Shengmei
    Zhang, Zhaoyun
    JOURNAL OF DIABETES RESEARCH, 2018, 2018
  • [37] Cilostazol protects against changes caused by streptozotocin-induced diabetic retinopathy
    Schebelski, Diego Jose
    Lipinski, Leandro
    Moreira, Carlos Augusto
    Koga, Adriana Yuriko
    Carletto, Bruna
    Montemor, Mario M.
    Farago, Paulo Vitor
    Gomes, Ricardo Zanetti
    ARQUIVOS BRASILEIROS DE OFTALMOLOGIA, 2024, 87 (01)
  • [38] Perindopril protects against streptozotocin-induced hyperglycemic myocardial damage/alterations
    Patel, B. M.
    Agarwal, S. S.
    Bhadada, S. V.
    HUMAN & EXPERIMENTAL TOXICOLOGY, 2012, 31 (11) : 1132 - 1143
  • [39] ALTERATIONS IN IMMUNOLOGICAL FUNCTION IN STREPTOZOTOCIN-INDUCED MURINE DIABETES-MELLITUS - CORRECTION BY ISLET CELL TRANSPLANTATION
    HANDWERGER, BS
    FERNANDES, G
    RIEHM, T
    SUTHERLAND, DER
    BROWN, DM
    CLINICAL IMMUNOLOGY AND IMMUNOPATHOLOGY, 1984, 32 (03): : 275 - 284
  • [40] Different effects of islet transplantation and Detemir treatment on the reversal of streptozotocin-induced diabetes associated with β-cell regeneration
    Inada A.
    Inada O.
    Fujii H.
    Akashi T.
    Sueishi K.
    Fukatsu A.
    Nagafuchi S.
    Diabetology International, 2010, 1 (1) : 49 - 59