The effect of caloric restriction on the aortic tissue of aging rats

被引:23
作者
Fornieri, C
Taparelli, F
Quaglino, D
Contri, MB
Davidson, JM
Algeri, S
Ronchetti, IP
机构
[1] Univ Modena & Reggio Emilia, Dept Biomed Sci, Div Gen Pathol, I-41100 Modena, Italy
[2] Vanderbilt Univ, Dept Pathol, Nashville, TN USA
[3] Inst Res Senescence, Rome, Italy
关键词
aorta; caloric restriction; collagen; elastase; elastin; lipoprotein; proteoglycans;
D O I
10.3109/03008209909029109
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Connective tissue shows peculiar and complex age-related modifications, which can be, at least in part, responsible for altered functions and increased susceptibility to diseases. Food restriction has long been known to prolong life in rodents, having antiaging effects on a variety of physiologic and pathologic processes. Therefore, the aorta has been investigated in rats fed normal or hypocaloric diet, from weaning to senescence. Compared with controls, caloric-restricted animals showed less pronounced age-dependent alterations such as elastic fiber degradation, collagen accumulation and cellular modifications. Immunocytochemical analyses revealed that elastic fibers were positively labelled for biglycan, decorin, ApoB100 (LDL), ApoAl (HDL) and elastase and that the intensity of the reactions was time- and diet-dependent, With age, the major changes affecting aortic elastic fibers were increased positivity for decorin, LDL and elastase, Compared with age-matched normal fed rats, caloric restricted animals revealed lower content of LDL, decorin and elastase and higher positivity for HDL. These data suggest that a caloric restricted diet might influence the aging process of the arterial wall in rats, delaying the appearance of age-related degenerative features, such as structural alterations of cells and matrix and modified interactions of elastin with cells and with other extracellular matrix molecules.
引用
收藏
页码:131 / 143
页数:13
相关论文
共 67 条
[11]  
DESANTI MM, 1989, EXP MOL PATHOL, V51, P18
[12]  
DREHER KL, 1990, EUR J CELL BIOL, V53, P296
[13]  
FISHER LW, 1987, J BIOL CHEM, V262, P9702
[14]   PHYSIOLOGY OF CARDIOVASCULAR AGING [J].
FOLKOW, B ;
SVANBORG, A .
PHYSIOLOGICAL REVIEWS, 1993, 73 (04) :725-764
[15]  
Fornieri C, 1989, Aging (Milano), V1, P127
[16]   ROLE OF THE EXTRACELLULAR-MATRIX IN AGE-RELATED MODIFICATIONS OF THE RAT AORTA - ULTRASTRUCTURAL, MORPHOMETRIC, AND ENZYMATIC EVALUATIONS [J].
FORNIERI, C ;
QUAGLINO, D ;
MORI, G .
ARTERIOSCLEROSIS AND THROMBOSIS, 1992, 12 (09) :1008-1016
[17]   LYSYL OXIDASE ACTIVITY AND ELASTIN GLYCOSAMINOGLYCAN INTERACTIONS IN GROWING CHICK AND RAT AORTAS [J].
FORNIERI, C ;
BACCARANICONTRI, M ;
QUAGLINO, D ;
PASQUALIRONCHETTI, I .
JOURNAL OF CELL BIOLOGY, 1987, 105 (03) :1463-1469
[18]   PLASMA AND URINARY LIPIDS AND LIPOPROTEINS DURING THE DEVELOPMENT OF NEPHROTIC SYNDROME INDUCED IN THE RAT BY PUROMYCIN AMINONUCLEOSIDE [J].
GHERARDI, E ;
CALANDRA, S .
BIOCHIMICA ET BIOPHYSICA ACTA, 1982, 710 (02) :188-196
[19]   INTERACTIONS OF HUMAN AND BOVINE ELASTINS WITH LIPIDS - THEIR PROTEOLYSIS BY ELASTASE [J].
GUANTIERI, V ;
TAMBURRO, AM ;
GORDINI, DD .
CONNECTIVE TISSUE RESEARCH, 1983, 12 (01) :79-83
[20]   OXIDIZED LIPOPROTEINS IN ATHEROSCLEROSIS AND THROMBOSIS [J].
HOLVOET, P ;
COLLEN, D .
FASEB JOURNAL, 1994, 8 (15) :1279-1284