Endothelial cellular senescence is inhibited by nitric oxide: Implications in atherosclerosis associated with menopause and diabetes

被引:176
作者
Hayashi, Toshio
Matsui-Hirai, Hisako
Miyazaki-Akita, Asaka
Fukatsu, Akiko
Funami, Jun
Ding, Qun-Fang
Kamalanathan, Sumitra
Hattori, Yuichi
Ignarro, Louis J.
Iguchi, Akihisa
机构
[1] Nagoya Univ, Dept Geriatr, Grad Sch Med, Showa Ku, Nagoya, Aichi 4668550, Japan
[2] Toyama Univ, Sch Med, Dept Pharmacol, Toyama 9300194, Japan
[3] Univ Calif Los Angeles, Ctr Hlth Sci, David Geffen Sch Med, Dept Mol & Med Pharmacol, Los Angeles, CA 90095 USA
关键词
diabetes mellitus; endothelial nitric oxide synthase; estrogen; aging;
D O I
10.1073/pnas.0607873103
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Senescence may contribute to the pathogenesis of atherosclerosis. Although the bioavailability of nitric oxide (NO) is limited in senescence, the effect of NO on senescence and its relationship to cardiovascular risk factors have not been investigated fully. We studied these factors by investigating senescence-associated beta-galactosidase (SA-beta-gal) and human telomerase activity in human umbilical venous endothelial cells (HUVECs). Treatment with NO donor (Z)-1-[2-(2-aminoethyl)-N-(2-aminoethyl)amino]diazen-ium-1,2-diolate (DETA-NO) and transfection with endothelial NO synthase (eNOS) into HUVECs each decreased the number of SA-beta-gal positive cells and increased telomerase activity. The NOS inhibitor N-G-nitro-L-arginine methyl ester (L-NAME) abolished the effect of eNOS transfection. The physiological concentration of 17 beta-estradiol activated hTERT, decreased SA-beta-gal-positive cells, and caused cell proliferation. However, ICI 182780, an estrogen receptor-specific antagonist, and L-NAME each inhibited these effects. Finally, we investigated the effect of NO bioavailability on high glucose-promoted cellular senescence of HUVECs. Inhibition by eNOS transfection of this cellular senescence under high glucose conditions was less pronounced. Treatment with L-arginine or L-citrulline of eNOS-transfected cells partially inhibited, and combination of L-arginine and L-citrulline with antioxidants strongly prevented, high glucose-induced cellular senescence. These data demonstrate that NO can prevent endothelial senescence, thereby contributing to the anti-senile action of estrogen. The ingestion of NO-boosting substances, including L-arginine, L-citrulline, and antioxidants, can delay endothelial senescence under high glucose. We suggest that the delay in endothelial senescence through NO and/or eNOS activation may have clinical utility in the treatment of atherosclerosis in the elderly.
引用
收藏
页码:17018 / 17023
页数:6
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