A high fat/high carbohydrate diet induces aortic valve disease in C57BL/6J mice

被引:97
作者
Drolet, MC [1 ]
Roussel, E [1 ]
Deshaies, Y [1 ]
Couet, J [1 ]
Arsenault, M [1 ]
机构
[1] Univ Laval, Ctr Rech, Dept Anat & Physiol, Fac Med,Hop Laval, Ste Foy, PQ G1V 4G5, Canada
关键词
D O I
10.1016/j.jacc.2005.09.049
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
OBJECTIVES The purpose of this study was to compare aortic valve function and morphology in adult-wild-type (WT) mice and in low-density lipoprotein receptor-deficient (LDLr-/-) mice fed or not fed a high -fat/high-carbohydrate (HF/HC) diet. BACKGROUND Observations suggest a link between degenerative aortic valve stenosis (AS) and atherosclerosis. Aortic valve stenosis has been successfully induced in animal models of extreme hypercholesterolemia, but these models are less relevant to humans. It is nor known if a proatherogenic HF/HC diet without added cholesterol could have the same negative impacts. METHODS Forty C57BL/6J mice were divided into four groups: WT + normal diet, WT + HF/HC diet, LDLr-/- with a normal diet, and LDLr-/- with a HF/HC diet. Aortic valve function and histology were evaluated by echocardiography after four months. RESULTS Wild-type mice on a HF/HC diet became mildly hypercholesterolemic, obese, and hyperglycemic. As expected, LDLr-/- mice became severely hypercholesterolemic. Both WT and LDLr-/- mice on a HF/HC diet displayed smaller valve areas and higher transvalvular velocities (p < 0.01) after four months. Aortic valve leaflets were thicker and infiltrated with lipids and macrophages in both HF/HC groups. CONCLUSIONS A HF/HC diet in mice results in significant aortic valve abnormalities. Putting WT mice on a HF/HC diet reproduced a combination of atherogenic factors (obesity, mild dyslipidemia, and hyperglycemia) more commonly encountered in humans than isolated severe hypercholesterolemia. Severe hypercholesterolemia was not a prerequisite in our model. This experimental model suggests that AS development is multifactorial and that hyercholesterolemia should not be the only target in this disease.
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页码:850 / 855
页数:6
相关论文
共 26 条
  • [1] Amsterdam Ezra A, 2002, Prev Cardiol, V5, P50, DOI 10.1111/j.1520-037X.2002.00553.x
  • [2] Association of coronary risk factors and use of statins with progression of mild valvular aortic stenosis in older persons
    Aronow, WS
    Ahn, C
    Kronzon, I
    Goldman, ME
    [J]. AMERICAN JOURNAL OF CARDIOLOGY, 2001, 88 (06) : 693 - 695
  • [3] Aortic valve sclerosis as a marker of active atherosclerosis
    Branch K.R.
    O'Brien K.D.
    Otto C.M.
    [J]. Current Cardiology Reports, 2002, 4 (2) : 111 - 117
  • [4] Association between calcific aortic stenosis and hypercholesterolemia: Is there a need for a randomized controlled trial of cholesterol-lowering therapy?
    Chui, MCK
    Newby, DE
    Panarelli, M
    Bloomfield, P
    Boon, NA
    [J]. CLINICAL CARDIOLOGY, 2001, 24 (01) : 52 - 55
  • [5] Cimini M, 2005, J HEART VALVE DIS, V14, P365
  • [6] A randomized trial of intensive lipid-lowering therapy in calcific aortic stenosis
    Cowell, SJ
    Newby, DE
    Prescott, RJ
    Bloomfield, P
    Reid, J
    Northridge, DB
    Boon, NA
    [J]. NEW ENGLAND JOURNAL OF MEDICINE, 2005, 352 (23) : 2389 - 2397
  • [7] DIABETES AND HYPERCHOLESTEROLEMIA AMONG PATIENTS WITH CALCIFIC AORTIC-STENOSIS
    DEUTSCHER, S
    ROCKETTE, HE
    KRISHNASWAMI, V
    [J]. JOURNAL OF CHRONIC DISEASES, 1984, 37 (05): : 407 - 415
  • [8] Experimental aortic valve stenosis in rabbits
    Drolet, MC
    Arsenault, M
    Couet, J
    [J]. JOURNAL OF THE AMERICAN COLLEGE OF CARDIOLOGY, 2003, 41 (07) : 1211 - 1217
  • [9] Definition of metabolic syndrome - Report of the National Heart, Lung, and Blood Institute/American Heart Association conference on scientific issues related to definition
    Grundy, SM
    Brewer, HB
    Cleeman, JI
    Smith, SC
    Lenfant, C
    [J]. ARTERIOSCLEROSIS THROMBOSIS AND VASCULAR BIOLOGY, 2004, 24 (02) : E13 - E18
  • [10] Can serum lipid and CRP levels predict the "severity" of aortic valve stenosis?
    Gunduz, H
    Akdemir, R
    Binak, E
    Tanier, A
    Keser, N
    Uyan, G
    [J]. ACTA CARDIOLOGICA, 2003, 58 (04) : 321 - 326