Reduced up-regulation of the nitric oxide pathway and impaired endothelial and smooth muscle functions in the female type 2 diabetic goto-kakizaki rat heart

被引:9
作者
Desrois, Martine [1 ,3 ]
Lan, Carole [1 ]
Movassat, Jamileh [2 ]
Bernard, Monique [1 ]
机构
[1] Aix Marseille Univ, CNRS, CRMBM, Marseille, France
[2] Univ Paris Diderot, Lab Biol & Pathol Pancreas Endocrine B2PE, Unite BFA, CNRS,UMR 8251, Paris, France
[3] Aix Marseille Univ, CRMBM, CNRS, UMR 7339,Fac Med, 27 Bd Jean Moulin, F-13385 Marseille 05, France
来源
NUTRITION & METABOLISM | 2017年 / 14卷
关键词
Type 2 diabetic heart; Gender differences; Cardiac function; Energy metabolism; Endothelial function; ISCHEMIA-REPERFUSION INJURY; GENDER-DIFFERENCE; SEX-DIFFERENCES; INSULIN-RESISTANCE; METABOLIC SYNDROME; GK RAT; CARDIOVASCULAR-DISEASE; ENERGY-METABOLISM; RHO KINASE; WOMEN;
D O I
10.1186/s12986-016-0157-z
中图分类号
R15 [营养卫生、食品卫生]; TS201 [基础科学];
学科分类号
100403 ;
摘要
Background: Type 2 diabetes is associated with greater relative risk of cardiovascular diseases in women than in men, which is not well understood. Consequently, we have investigated if male and female displayed differences in cardiac function, energy metabolism, and endothelial function which could contribute to increased cardiovascular complications in type 2 diabetic female. Methods: Male and female Control and type 2 diabetic Goto-Kakizaki (GK) isolated rat hearts were perfused during 28 min with a physiological buffer before freeze-clamping for biochemical assays. High energy phosphate compounds and intracellular pH were followed using P-31 magnetic resonance spectroscopy with simultaneous measurement of contractile function. Nitric oxide (NO) pathway and endothelium-dependent and independent vasodilatations were measured as indexes of endothelial function. Results were analyzed via two-way ANOVA, p < 0.05 was considered as statistically significant. Results: Myocardial function was impaired in male and female diabetic versus Control groups (p < 0.05) without modification of energy metabolism. Coronary flow was decreased in both diabetic versus Control groups but to a higher extent in female GK versus male GK rat hearts (p < 0.05). NO production was up-regulated in diabetic groups but to a less extent in female GK rat hearts (p < 0.05). Endothelium-dependent and independent vasodilatations were impaired in female GK rat compared with male GK (p < 0.05) and female Control (p < 0.05) rat hearts. Conclusions: We reported here an endothelial damage characterized by a reduced up-regulation of the NO pathway and impaired endothelial and smooth muscle functions, and coronary flow rates in the female GK rat hearts while energy metabolism was normal. Whether these results are related to the higher risk of cardiovascular complications among type 2 diabetic female needs to be further elicited in the future.
引用
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页码:1 / 11
页数:11
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[1]   Temporal changes in vascular reactivity in early diabetes mellitus in rats: role of changes in endothelial factors and in phosphodiesterase activity [J].
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Ghali-Ghoul, R. ;
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[2]   Impaired TGF-β signaling and a defect in resolution of inflammation contribute to delayed wound healing in a female rat model of type 2 diabetes [J].
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Leibovich, Samuel J. ;
Francis, Issam M. ;
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[3]   INSULIN-RESISTANCE IN THE GK RAT - DECREASED RECEPTOR NUMBER BUT NORMAL KINASE-ACTIVITY IN LIVER [J].
BISBIS, S ;
BAILBE, D ;
TORMO, MA ;
PICARELBLANCHOT, F ;
DEROUET, M ;
SIMON, J ;
PORTHA, B .
AMERICAN JOURNAL OF PHYSIOLOGY, 1993, 265 (05) :E807-E813
[4]   Nitric oxide dynamics and endothelial dysfunction in type II model of genetic diabetes [J].
Bitar, MS ;
Wahid, S ;
Mustafa, S ;
Al-Saleh, E ;
Dhaunsi, GS ;
Al-Mulla, F .
EUROPEAN JOURNAL OF PHARMACOLOGY, 2005, 511 (01) :53-64
[5]   Molecular mechanisms for myocardial mitochondrial dysfunction in the metabolic syndrome [J].
Bugger, Heiko ;
Abel, E. Dale .
CLINICAL SCIENCE, 2008, 114 (3-4) :195-210
[6]   PPAR-α activation protects the type 2 diabetic myocardium against ischemia-reperfusion injury: involvement of the PI3-Kinase/Akt and NO pathway [J].
Bulhak, Aliaksandr A. ;
Jung, Christian ;
Ostenson, Claes-Goran ;
Lundberg, Jon O. ;
Sjoquist, Per-Ove ;
Pernow, John .
AMERICAN JOURNAL OF PHYSIOLOGY-HEART AND CIRCULATORY PHYSIOLOGY, 2009, 296 (03) :H719-H727
[7]   Ratio of 5,6,7,8- tetrahydrobiopterin to 7,8- dihydrobiopterin in endothelial cells determines glucose- elicited changes in NO vs. superoxide production by eNOS (vol 294, H1530, 2008) [J].
Crabtree, M. J. ;
Smith, C. L. ;
Lam, G. ;
Goligorsky, M. S. ;
Gross, S. S. .
AMERICAN JOURNAL OF PHYSIOLOGY-HEART AND CIRCULATORY PHYSIOLOGY, 2010, 299 (02) :H576-H576
[8]   Ca2+ loading and adrenergic stimulation reveal male/female differences in susceptibility to ischemia-reperfusion injury [J].
Cross, HR ;
Murphy, E ;
Steenbergen, C .
AMERICAN JOURNAL OF PHYSIOLOGY-HEART AND CIRCULATORY PHYSIOLOGY, 2002, 283 (02) :H481-H489
[9]   Endothelial dysfunction in diabetes [J].
De Vriese, AS ;
Verbeuren, TJ ;
Van de Voorde, J ;
Lameire, NH ;
Vanhoutte, PM .
BRITISH JOURNAL OF PHARMACOLOGY, 2000, 130 (05) :963-974
[10]   Gender differences in hypertrophy, insulin resistance and ischemic injury in the aging type 2 diabetic rat heart [J].
Desrois, M ;
Sidell, RJ ;
Gauguier, D ;
Davey, CL ;
Radda, GK ;
Clarke, K .
JOURNAL OF MOLECULAR AND CELLULAR CARDIOLOGY, 2004, 37 (02) :547-555