Gender differences in hypertrophy, insulin resistance and ischemic injury in the aging type 2 diabetic rat heart

被引:59
作者
Desrois, M
Sidell, RJ
Gauguier, D
Davey, CL
Radda, GK
Clarke, K
机构
[1] Univ Oxford, Physiol Lab, Oxford OX1 3PT, England
[2] Univ Oxford, Wellcome Trust Ctr Human Genet, Oxford OX3 7BN, England
关键词
aging; gender; type; 2; diabetes; Goto-Kakizaki rat; insulin resistance; glucose transporters; ischemic injury; protein kinase B;
D O I
10.1016/j.yjmcc.2004.05.014
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Aging and diabetes in women increase their susceptibility to myocardial ischemic injury, but the cellular mechanisms involved are not understood. Consequently, we studied the influence of gender on cardiac insulin resistance and ischemic injury in the aging of Goto-Kakizaki (GK) rat, a model of type 2 diabetes. Male and female GK rats had heart/body weight ratios 29% (P < 0.0001) and 53% (P < 0.0001) higher, respectively, than their sex-matched controls, with the female GK rat hearts significantly more hypertrophied than the male (P < 0.001). Glucose transporter (GLUT) 1 protein levels were the same in all hearts, but GLUT4 protein levels were 28% lower (P < 0.01) in all GK rat hearts compared with their sex-matched controls. In isolated, perfused hearts, insulin-stimulated 3 H-glucose uptake rates were decreased by 23% (P < 0.05) and 40% (P < 0.05) in male and female GK rat hearts, respectively, compared with their controls, with the female significantly more insulin resistant than the male GK rat hearts (P < 0.05). Protein kinase B protein levels and insulin-stimulated phosphorylation were the same in all hearts. During low-flow ischemia, glucose uptake was 59% lower (P < 0.001) in female, but the same as controls in male, GK rat hearts. Consequently, recovery of contractile function during reperfusion was 30% lower (P < 0.05) in female, but the same as controls in male GK rat hearts. We conclude that the aging female type 2 diabetic rat heart has increased insulin resistance and greater susceptibility to ischernic injury, than non-diabetic or male type 2 diabetic rat hearts. (C) 2004 Elsevier Ltd. All rights reserved.
引用
收藏
页码:547 / 555
页数:9
相关论文
共 54 条
  • [1] Age-dependent changes in metabolism, contractile function, and ischemic sensitivity in hearts from db/db mice
    Aasum, E
    Hafstad, AD
    Severson, DL
    Larsen, TS
    [J]. DIABETES, 2003, 52 (02) : 434 - 441
  • [2] Cardiac function and metabolism in Type 2 diabetic mice after treatment with BM 17.0744, a novel PPAR-α activator
    Aasum, E
    Belke, DD
    Severson, DL
    Riemersma, RA
    Cooper, M
    Andreassen, M
    Larsen, TS
    [J]. AMERICAN JOURNAL OF PHYSIOLOGY-HEART AND CIRCULATORY PHYSIOLOGY, 2002, 283 (03): : H949 - H957
  • [3] Left ventricular diastolic dysfunction in type 2 diabetes mellitus model rats
    Abe, T
    Ohga, Y
    Tabayashi, N
    Kobayashi, S
    Sakata, S
    Misawa, H
    Tsuji, T
    Kohzuki, H
    Suga, H
    Taniguchi, S
    Takaki, M
    [J]. AMERICAN JOURNAL OF PHYSIOLOGY-HEART AND CIRCULATORY PHYSIOLOGY, 2002, 282 (01): : H138 - H148
  • [4] Cardiac hypertrophy with preserved contractile function after selective deletion of GLUT4 from the heart
    Abel, ED
    Kaulbach, HC
    Tian, R
    Hopkins, JCA
    Duffy, J
    Doetschman, T
    Minnemann, T
    Boers, ME
    Hadro, E
    Oberste-Berghaus, C
    Quist, W
    Lowell, BB
    Ingwall, JS
    Kahn, BB
    [J]. JOURNAL OF CLINICAL INVESTIGATION, 1999, 104 (12) : 1703 - 1714
  • [5] Hypertrophied rat hearts are less responsive to the metabolic and functional effects of insulin
    Allard, MF
    Wambolt, RB
    Longnus, SL
    Grist, M
    Lydell, CP
    Parsons, HL
    Rodrigues, B
    Hall, JL
    Stanley, WC
    Bondy, GP
    [J]. AMERICAN JOURNAL OF PHYSIOLOGY-ENDOCRINOLOGY AND METABOLISM, 2000, 279 (03): : E487 - E493
  • [6] Effects of adenoviral gene transfer of wild-type, constitutively active, and kinase-defective protein kinase C-λ on insulin-stimulated glucose transport in L6 myotubes
    Bandyopadhyay, G
    Kanoh, Y
    Sajan, MP
    Standaert, ML
    Farese, RV
    [J]. ENDOCRINOLOGY, 2000, 141 (11) : 4120 - 4127
  • [7] WHY IS DIABETES-MELLITUS A STRONGER RISK FACTOR FOR FATAL ISCHEMIC-HEART-DISEASE IN WOMEN THAN IN MEN - THE RANCHO-BERNARDO STUDY
    BARRETTCONNOR, EL
    COHN, BA
    WINGARD, DL
    EDELSTEIN, SL
    [J]. JAMA-JOURNAL OF THE AMERICAN MEDICAL ASSOCIATION, 1991, 265 (05): : 627 - 631
  • [8] No-flow ischemia inhibits insulin signaling in heart by decreasing intracellular pH
    Beauloye, C
    Bertrand, L
    Krause, U
    Marsin, AS
    Dresselaers, T
    Vanstapel, F
    Vanoverschelde, JL
    Hue, L
    [J]. CIRCULATION RESEARCH, 2001, 88 (05) : 513 - 519
  • [9] Activation of protein kinase C-ζ by insulin and phosphatidylinositol-3,4,5-(PO4)3 is defective in muscle in type 2 diabetes and impaired glucose tolerance -: Amelioration by rosiglitazone and exercise
    Beeson, M
    Sajan, MP
    Dizon, M
    Grebenev, D
    Gomez-Daspet, J
    Miura, A
    Kanoh, Y
    Powe, J
    Bandyopadhyay, G
    Standaert, ML
    Farese, RV
    [J]. DIABETES, 2003, 52 (08) : 1926 - 1934
  • [10] Altered metabolism causes cardiac dysfunction in perfused hearts from diabetic (db/db) mice
    Belke, DD
    Larsen, TS
    Gibbs, EM
    Severson, DL
    [J]. AMERICAN JOURNAL OF PHYSIOLOGY-ENDOCRINOLOGY AND METABOLISM, 2000, 279 (05): : E1104 - E1113