Vitamin D and aging: old concepts and new insights

被引:86
作者
Lanske, Beate [1 ]
Razzaque, M. Shawkat [1 ]
机构
[1] Harvard Univ, Sch Dent Med, Dept Dev Biol, Boston, MA 02115 USA
关键词
vitamin D; aging; Fgf-23; klotho; calcification; survival;
D O I
10.1016/j.jnutbio.2007.02.002
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Aging is a complex biological process driven by a selective class of molecules and pathways that affect overall deterioration of physiological functions to increase the risk of age-related diseases. A role of vitamin D in mammalian aging is well documented. Since vitamin D has an essential role in bone formation and mineralization, its deficiency results in impaired bone mineralization, such as rickets in children, osteomalacia in adults and osteoporosis in the aged population. Vitamin D replacement therapy therefore is one of the most commonly prescribed treatments for the elderly. Recent studies using genetically altered mouse models, such as in Fgf-23(-/-) and klotho mutant mice, that exhibit altered mineral ion metabolism due to high vitamin D activities showed features of premature aging that include atherosclerosis, emphysema, osteopenia/osteoporosis, hypogonadism, soft tissue calcifications and generalized atrophy of organs; the pathologic effects of vitamin D in these mouse models are obvious, as diminution or genetic ablation of the vitamin D pathway ameliorated most of the above-mentioned phenotypes, by reversing mineral ion metabolism, and the resultant effect being prolonged survival of the mutant mice. These in vivo mouse studies, although Subject to further molecular characterization, add new insights into the role of vitamin D in aging. (c) 2007 Elsevier Inc. All rights reserved.
引用
收藏
页码:771 / 777
页数:7
相关论文
共 55 条
[1]   Gains in bone mineral density with resolution of vitamin D intoxication [J].
Adams, JS ;
Lee, G .
ANNALS OF INTERNAL MEDICINE, 1997, 127 (03) :203-206
[2]   Rescue of the skeletal phenotype of vitamin D receptor-ablated mice in the setting of normal mineral ion homeostasis: Formal histomorphometric and biomechanical analyses [J].
Amling, M ;
Priemel, M ;
Holzmann, T ;
Chapin, K ;
Rueger, JM ;
Baron, R ;
Demay, MB .
ENDOCRINOLOGY, 1999, 140 (11) :4982-4987
[3]   Association between a functional variant of the KLOTHO gene and high-density lipoprotein cholesterol, blood pressure, stroke, and longevity [J].
Arking, DE ;
Atzmon, G ;
Arking, A ;
Barzilai, N ;
Dietz, HC .
CIRCULATION RESEARCH, 2005, 96 (04) :412-418
[4]   Targeted inactivation of Npt2 in mice leads to severe renal phosphate wasting, hypercalciuria, and skeletal abnormalities [J].
Beck, L ;
Karaplis, AC ;
Amizuka, N ;
Hewson, AS ;
Ozawa, H ;
Tenenhouse, HS .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1998, 95 (09) :5372-5377
[5]   An FGF23 missense mutation causes familial tumoral calcinosis with hyperphosphatemia [J].
Benet-Pagès, A ;
Orlik, P ;
Strom, TM ;
Lorenz-Depiereux, B .
HUMAN MOLECULAR GENETICS, 2005, 14 (03) :385-390
[6]   Effect of fish oil on bone mineral density in aging C57BL/6 female mice [J].
Bhattacharya, Arunabh ;
Rahman, Mizanur ;
Sun, Dongxu ;
Fernandes, Gabriel .
JOURNAL OF NUTRITIONAL BIOCHEMISTRY, 2007, 18 (06) :372-379
[7]   Regulation of 25-hydroxyvitamin D3 1α-hydroxylase gene expression by parathyroid hormone and 1,25-dihydroxyvitamin D3 [J].
Brenza, HL ;
DeLuca, HF .
ARCHIVES OF BIOCHEMISTRY AND BIOPHYSICS, 2000, 381 (01) :143-152
[8]   Vitamin D [J].
Brown, AJ ;
Dusso, A ;
Slatopolsky, E .
AMERICAN JOURNAL OF PHYSIOLOGY-RENAL PHYSIOLOGY, 1999, 277 (02) :F157-F175
[9]   Subliminal ultraviolet-B irradiation for the prevention of vitamin D deficiency in the elderly: a feasibility study [J].
Chuck, A ;
Todd, J ;
Diffey, B .
PHOTODERMATOLOGY PHOTOIMMUNOLOGY & PHOTOMEDICINE, 2001, 17 (04) :168-171
[10]  
Cofan F, 1999, J RHEUMATOL, V26, P379