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Dyslipidemia is not associated with cardiovascular disease risk in an animal model of mild chronic suboptimal nutrition
Authors:Fima Lifshitz,Patricia M. Pintos,Christian E. Lezó  n,Elisa V. Macri,Silvia M. Friedman,Patricia M. Boyer
Affiliation:1. Pediatric Sunshine Academics and Sansum Diabetes Research Institute, Santa Barbara, CA 93105, USA;2. Department of Physiology, School of Dentistry, University of Buenos Aires, Argentina, Marcelo T. de Alvear 2142 3 A. (C1122 AAH), Buenos Aires, Argentina;3. Department of General and Oral Biochemistry, School of Dentistry, University of Buenos Aires, Argentina, Marcelo T. de Alvear 2142 12 B. (C1122 AAH), Buenos Aires, Argentina
Abstract:Previous studies performed in an experimental model of nutritional growth retardation (NGR) have observed metabolic adaptation. We hypothesized that changes in lipid-lipoprotein profile, glucose, and insulin levels occur, whereas overall body growth is reduced.The aim of this study was to assess serum lipid-lipoprotein profile, hepatogram, insulinemia and glycemia, and CVD risk markers in rats fed a suboptimal diet. Weanling male rats were assigned either to control (C) or NGR group. In this 4-week study, C rats were fed ad libitum a standard diet, and NGR rats received 80% of the amount of food consumed by C. Zoometric parameters, body fat content, serum lipid-lipoprotein profile, hepatogram, insulinemia, and glycemia were determined, and the cardiovascular disease (CVD) risk markers homeostasis model assessment–insulin resistance and homeostasis model assessment and β-cell function were calculated. Suboptimal food intake induced a significant decrease in body weight and length, which were accompanied by a reduction of 50% in body fat mass. Serum lipoproteins were significantly higher in NGR rats, with the exception of high-density lipoprotein cholesterol, which remained unchanged. Nutritional growth retardation rats had decreased triglycerides compared with C rats. No significant differences were detected in liver function parameters. The CVD risk markers homeostasis model assessment (HOMA)–insulin resistance and homeostasis model assessment and β-cell function were significantly lower in NGR rats. Mild chronic suboptimal nutrition in weanling male rats led to growth retardation and changes in the lipid-lipoprotein profile, glucose, and insulin levels while preserving the integrity of liver function. These data suggest a metabolic adaptation during suboptimal food intake, which ensures substrates flux to tissues that require constant energy—in detriment to body growth. The CVD risk markers suggested that mild chronic food restriction of approximately 20% could provide protection against this degenerative disease.
Keywords:Alb, albumin   ALP, alkaline phosphatase   ALT, alanine aminotransferase   AST, aspartate aminotransferase   CVD, cardiovascular disease   Chol, cholesterol   D-Bil, direct bilirubin   FFA, free fatty acids   G, glucose   GF, fasting glucose   GGT, γ-glutamyl transferase   HDL-Chol, high-density lipoprotein cholesterol   HOMA, homeostasis model assessment   IF, fasting insulin   LDL-Chol, low-density lipoprotein cholesterol   NGR, nutritional growth retardation   T-Bil, total bilirubin   T-Chol, total cholesterol   TG, triglycerides   T-Pro, total proteins   VLDL-Chol, very low density lipoprotein cholesterol
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