Endothelial dysfunction in the klotho mouse and downregulation of klotho gene expression in various animal models of vascular and metabolic diseases

被引:167
作者
Nagai, R
Saito, Y
Ohyama, Y
Aizawa, H
Suga, T
Nakamura, T
Kurabayashi, M
Kuro-o, M
机构
[1] Gunma Univ, Sch Med, Dept Internal Med 2, Gunma 3718511, Japan
[2] Univ Tokyo, Dept Cardiovasc Med, Bunkyo Ku, Tokyo 1138865, Japan
[3] Univ Texas, SW Med Ctr, Dallas, TX USA
关键词
klotho; endothelial function; nitric oxide production; hypertension; renal failure; cytokine;
D O I
10.1007/s000180050038
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
The human aging process is associated with vascular endothelial dysfunction. However, humoral factors which might protect against endothelial dysfunction during aging have not yet been identified. We recently identified the klotho gene as a possible regulator of human aging. In the present study using the klotho-deficient heterozygous mouse, we examined whether the Klotho protein is a humoral factor protecting against endothelial dysfunction. We further clotted rat klotho cDNA and investigated whether klotho mRNA expression in rat kidney is altered under pathological conditions such as hypertension, hyperlipidemia, renal failure, and inflammatory stress. The Klotho protein itself, or its metabolites, promotes endothelial NO production in aorta as well as arterioles, and klotho mRNA in kidney is downregulated under sustained circulatory stress.
引用
收藏
页码:738 / 746
页数:9
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