HIGH-FRUCTOSE FEEDING ELICITS INSULIN-RESISTANCE, HYPERINSULINISM, AND HYPERTENSION IN NORMAL MONGREL DOGS

被引:103
作者
MARTINEZ, FJ
RIZZA, RA
ROMERO, JC
机构
[1] MAYO CLIN & MAYO FDN, MAYO MED SCH, DEPT PHYSIOL & BIOPHYS, DIV HYPERTENS, ROCHESTER, MN USA
[2] MAYO CLIN & MAYO FDN, MAYO MED SCH, DEPT ENDOCRINOL, ROCHESTER, MN USA
关键词
FRUCTOSE; INSULIN; TRIGLYCERIDES; HYPERTENSION; EXPERIMENTAL; ATRIAL NATRIURETIC FACTOR; ENDOTHELINS; DOGS;
D O I
10.1161/01.HYP.23.4.456
中图分类号
R6 [外科学];
学科分类号
1002 ; 100210 ;
摘要
To determine whether chronic high-fructose feeding causes insulin resistance and hypertension in normal dogs, we fed 10 male dogs a normosodic diet containing 60% of the calories as fructose for 20 to 28 days; a control group of 8 dogs was fed a similar diet containing dextrose instead of fructose. In the fructose-fed group, (1) fasting triglyceridemia increased from 35.3+/-0.63 to 91.9+/-11.55 mg/dL after 25 days (P<.001); (2) fasting insulinemia increased from 19.0+/-1.9 to 58.9+/-7.22 mu U/mL after 25 days (P<.001); (3) insulin resistance, which was estimated by steady-state glycemia during an insulin suppression test, increased from 105.8+/-21.5 to 187.8+/-32.6 mg/dL after 15 days (P<.001), whereas steady-state insulinemia did not change; (4) mean arterial pressure increased from 100.4+/-1.6 to 122.6+/-2.3 mm Hg after 28 days (P<.01); and (5) cumulative sodium balance was increased on days 7 through 11 (111.60+/-4.44 mEq on day 8, P<.01), returning to normal for the rest of the experiment. All these parameters were similar between the fructose-fed and dextrose-fed groups before the diets were started and remained constant in the dextrose-fed group. Neither group showed any change in body weight, fasting plasma glucose, atrial natriuretic factor, or endothelin-1 levels. We conclude that chronic high-fructose feeding elicits hypertriglyceridemia, insulin resistance, hyperinsulinemia, hypertension, and a transient sodium retention in dogs without fostering fasting hyperglycemia or weight gain. Endothelin and atrial natriuretic factor do not appear to play a role in the development of hypertension in this model.
引用
收藏
页码:456 / 463
页数:8
相关论文
共 50 条
[1]   HIGH-CARBOHYDRATE DIET - ANTINATRIURETIC AND BLOOD-PRESSURE RESPONSE IN NORMAL MEN [J].
AFFARAH, HB ;
HALL, WD ;
HEYMSFIELD, SB ;
KUTNER, M ;
WELLS, JO ;
TUTTLE, EP .
AMERICAN JOURNAL OF CLINICAL NUTRITION, 1986, 44 (03) :341-348
[2]   CHARACTERIZATION OF INDUCTION OF PROTOONCOGENE C-MYC AND CELLULAR GROWTH IN HUMAN VASCULAR SMOOTH-MUSCLE CELLS BY INSULIN AND IGF-I [J].
BANSKOTA, NK ;
TAUB, R ;
ZELLNER, K ;
OLSEN, P ;
KING, GL .
DIABETES, 1989, 38 (01) :123-129
[3]   EFFECTS OF DIET ON CELLULAR INSULIN BINDING AND INSULIN SENSITIVITY IN YOUNG HEALTHY SUBJECTS [J].
BECKNIELSEN, H ;
PEDERSEN, O ;
SORENSEN, NS .
DIABETOLOGIA, 1978, 15 (04) :289-296
[4]   ASSESSMENT OF INSULIN SENSITIVITY INVIVO [J].
BERGMAN, RN ;
FINEGOOD, DT ;
ADER, M .
ENDOCRINE REVIEWS, 1985, 6 (01) :45-86
[5]   TOWARD PHYSIOLOGICAL UNDERSTANDING OF GLUCOSE-TOLERANCE - MINIMAL-MODEL APPROACH [J].
BERGMAN, RN .
DIABETES, 1989, 38 (12) :1512-1527
[6]  
BLACK HR, 1990, J CARDIOVASC PHARM, V15, pS26
[7]   SODIUM IONS, CALCIUM-IONS, BLOOD-PRESSURE REGULATION, AND HYPERTENSION - REASSESSMENT AND A HYPOTHESIS [J].
BLAUSTEIN, MP .
AMERICAN JOURNAL OF PHYSIOLOGY, 1977, 232 (05) :C165-C173
[8]   The physiology of the liver XIX. The utilization of fructose following complete removal of the liver [J].
Bollman, JL ;
Mann, FC .
AMERICAN JOURNAL OF PHYSIOLOGY, 1931, 96 (03) :683-695
[9]   CHRONIC SUCROSE INGESTION INDUCES MILD HYPERTENSION AND TACHYCARDIA IN RATS [J].
BUNAG, RD ;
TOMITA, T ;
SASAKI, S .
HYPERTENSION, 1983, 5 (02) :218-225
[10]   Is levulose converted to dextrose in the process of absorption from the intestine? [J].
Burget, GE ;
Moore, P ;
Lloyd, R .
AMERICAN JOURNAL OF PHYSIOLOGY, 1932, 101 (03) :570-572