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Caloric restrictions affect some factors involved in age‐related hypercholesterolemia
Author(s) -
Martini Chiara,
Pallottini Valentina,
Cavallini Gabriella,
Donati Alessio,
Bergamini Ettore,
Trentalance Anna
Publication year - 2007
Publication title -
journal of cellular biochemistry
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.028
H-Index - 165
eISSN - 1097-4644
pISSN - 0730-2312
DOI - 10.1002/jcb.21158
Subject(s) - ldl receptor , cholesterol , sterol regulatory element binding protein , ageing , familial hypercholesterolemia , endocrinology , receptor , medicine , caloric theory , hmg coa reductase , biology , reductase , lipoprotein , homeostasis , sterol , biochemistry , enzyme
Ageing has been defined as a progressive decrease in physiological capacity and a reduced ability to respond to environmental stresses. It has been observed that diet‐restricted animals show a minor morbidity in age‐related disease. Among these age‐related diseases, hypercholesterolemia is the most recurring one and it is often associated with cardiac failure. Several studies have been published indicating age‐dependent changes in circulating levels of cholesterol in both humans and in rodents; recently changes have also been reported in the proteins involved in cholesterol homeostasis, that is, 3‐hydroxy‐3‐methylglutaryl coenzyme A reductase (HMG‐CoAR), Insig‐induced gene (Insig) protein, SREBP cleavage activating protein (SCAP), sterol regulatory element binding protein (SREBP), and low density lipoprotein receptor (LDLr). Most age‐related modifications of biochemical parameters are normalized or very improved in food‐restricted animals, so the aim of this work is to examine whether or not alterations of the factors involved in cholesterol homeostasis which occur during ageing could be counteracted by caloric restriction (CR). The data show that the diet restrictions used attenuate the age‐related effects on the factors involved in the synthesis and the degradation rate of HMG‐CoAR; in spite of this, CRs have a good effect on the age‐related hypercholesterolemia whose reduction seems to depend both on the correct membrane LDLr localization and on the proper restored HMG‐CoAR activity. J. Cell. Biochem. 101: 235–243, 2007. © 2007 Wiley‐Liss, Inc.