L-carnitine and isovaleryl L-carnitine fumarate positively affect human osteoblast proliferation and differentiation in vitro

被引:55
作者
Colucci, S
Mori, G
Vaira, S
Brunetti, G
Greco, G
Mancini, L
Simone, GM
Sardelli, F
Koverech, A
Zallone, A
Grano, M [1 ]
机构
[1] Univ Bari, Dept Human Anat & Histol, I-70121 Bari, Italy
[2] Sigma Tau Pharmaceut Co, Dept Unit Carnitine, Rome, Italy
关键词
carnitine; carnitine derivatives; osteoblast; proliferation; differentiation;
D O I
10.1007/s00223-004-0147-4
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Age-related bone loss is characterized by decreased osteoblast activity, possibly related to the reduction of energy production. Carnitine promotes energy availability and its concentration declines with age; Therefore,. two Carnitine derivatives, L-carnitine fumarate (LC) and isovaleryl L-carnitine fumarate (Iso-V-LC), have been tested on several parameters of human osteoblasts in vitro. Both compounds significantly increased osteoblast activity, but the new compound Iso-V-LC was more efficient than LC at lower concentrations. They both significantly enhanced cell proliferation, [(3)H]-proline incorporation and the expression of collagen type I (COLLI), and the bone sialoproteins (BSPs) and osteopontin (OPN). The percentage of alkaline phosphatase (ALP)-positive cells and the secretion of osteocalcin were not modified by LC and Iso-V-LC. Both molecules increased the formation of mineralized nodules, but Iso-V-LC reached the maximum effect at a concentration 10-fold lower than that of LC. Furthermore, we showed that insulin-like growth factor (IGF)-I and IGF-II mRNA levels were not modified by the treatment. However, the two compounds induced an increase of insulin-like growth factor binding protein (IGFBP)-3 and a decrease of IGFBP-5 in both osteoblast lysates and the extracellular matrix (ECM). In conclusion these data suggest that carnitine and, in particular, its new derivative, Iso-V-LC supplementation in the elderly may stimulate osteoblast activity and decrease age-related bone loss.
引用
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页码:458 / 465
页数:8
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