Increased expression of endothelin-1 and inducible nitric oxide synthase isoform II in aging arteries in vivo:: Implications for atherosclerosis

被引:75
作者
Goettsch, W [1 ]
Lattmann, T
Amann, K
Szibor, M
Morawietz, H
Münter, K
Müller, SP
Shaw, S
Barton, M
机构
[1] Univ Halle Wittenberg, Fac Med, Inst Pathophysiol, D-06097 Halle, Germany
[2] Univ Halle Wittenberg, Inst Environm Toxicol, D-06097 Halle, Germany
[3] Univ Erlangen Nurnberg, Dept Pathol, D-91054 Erlangen, Germany
[4] Knoll AG, Cardiovasc Res, D-67061 Ludwigshafen, Germany
[5] Univ Bern, Dept Clin Res, CH-3010 Bern, Switzerland
[6] Univ Zurich Hosp, Dept Med, CH-8091 Zurich, Switzerland
[7] Univ Zurich Hosp, Med Policlin, CH-8091 Zurich, Switzerland
基金
瑞士国家科学基金会;
关键词
aorta; atherosclerosis; blood pressure; carotid artery; gene; in situ hybridization; kidney; messenger RNA; renal artery; risk factors; reverse transcriptase polymerase chain reaction;
D O I
10.1006/bbrc.2000.4180
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
We here report that aging increases expression of endothelin-l and NO synthases in the vasculature and kidney of normotensive rats in vivo. Expression of preproendothelin-1 mRNA was quantified by RT-PCR and in situ hybridization, and endothelin-l protein was determined by radioimmunoassay/HPLC. Vascular mRNA expression of NO synthase isoforms LI and III was analyzed by RT-PCR. In young animals, vascular endothelin-l protein was differentially expressed (aorta < renal artery < carotid artery) and increased with aging in all vascular beds (P < 0.05). In the intact aorta of aged rats, mRNA expression of preproendothelin-l, "inducible" NO synthase II, and endothelial cell NO synthase III gene was up-regulated (P < 0.05). Moreover, preproendothelin-l mRNA expression increased in glomeruli and tubulointerstitial cells (P < 0.05). To our knowledge this is the first study demonstrating local vascular up-regulation of the trophic factor endothelin under physiological conditions. Activation of vascular endothelin and NO synthases may be important, pressure-independent factors contributing to structural and functional abnormalities of age dependent diseases, including atherosclerosis. (C) 2001 Academic Press.
引用
收藏
页码:908 / 913
页数:6
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