Alteration of Nitric Oxide Gas on Gene Expression of Endothelin-1 and Endothelial Nitric Oxide Synthase by a Time- and Dose-Dependent Manner in Human Endothelial Cells

被引:12
作者
Weng, Yi-Hao [1 ]
Kuo, Chii-Yuh [1 ]
Chiu, Ya-Wen [2 ]
Kuo, Ming-Ling [1 ]
Liao, Sui-Ling [1 ]
机构
[1] Univ Coll Med, Div Neonatol, Dept Pediat, Chang Gung Childrens Hosp, Guishan 333, Taoyuan County, Taiwan
[2] Natl Hlth Res Inst, Ctr Hlth Policy Res & Dev, Miaoli, Taiwan
来源
CHINESE JOURNAL OF PHYSIOLOGY | 2009年 / 52卷 / 02期
关键词
endothelial nitric oxide synthase; endothelin-1; nitric oxide; REBOUND PULMONARY-HYPERTENSION; NEGATIVE-FEEDBACK-REGULATION; NO SYNTHASE; INHIBITION; MECHANISMS; INHALATION; SECRETION; DELIVERY; CYCLASE;
D O I
10.4077/CJP.2009.AMG085
中图分类号
Q4 [生理学];
学科分类号
071003 ;
摘要
Our purpose was to investigate the gene expression of endothelin-1 (ET-1) and endothelial nitric oxide synthase (eNOS) in human umbilical vein endothelial cells (HUVECs) under various concentrations and periods of exogenous nitric oxide (NO) gas exposure. Cultured HUVECs were exposed to 0, 20, and 80 ppm NO for 0, 24, and 48 h. With NO exposure for 24 h, ET-1 peptide levels decreased in both the 20 and 80 ppm groups. Thereafter, at 48 h, ET-1 peptide levels persistently decreased in the 20 ppm group, but significantly increased in the 80 ppm group. Furthermore, there was a significant decrease in the expression levels of eNOS protein and mRNA in the 80 ppm 48 h group. The data suggest a time- and dose-dependent effect of NO gas exposure on the gene expression of ET-1 and eNOS in HUVECs. A high concentration and long period of NO exposure induces an inhibition of eNOS and enhancement of ET-1, which could lead to vasoconstriction. These findings may have clinical implications in NO therapy regarding the optimal dose and period.
引用
收藏
页码:59 / 64
页数:6
相关论文
共 28 条
[11]   Inhaled nitric oxide - A selective pulmonary vasodilator - Current uses and therapeutic potential [J].
Ichinose, F ;
Roberts, JD ;
Zapol, WM .
CIRCULATION, 2004, 109 (25) :3106-3111
[12]   Nitric oxide decreases endothelin-1 secretion through the activation of soluble guanylate cyclase [J].
Kelly, LK ;
Wedgwood, S ;
Steinhorn, RH ;
Black, SM .
AMERICAN JOURNAL OF PHYSIOLOGY-LUNG CELLULAR AND MOLECULAR PHYSIOLOGY, 2004, 286 (05) :L984-L991
[13]   Long-term inhalation of nitric oxide for a patient with primary pulmonary hypertension [J].
Koh, E ;
Niimura, J ;
Nakamura, T ;
Yamakage, H ;
Takahashi, H .
JAPANESE CIRCULATION JOURNAL-ENGLISH EDITION, 1998, 62 (12) :940-942
[14]   NITRIC-OXIDE REGULATES THE EXPRESSION OF VASOCONSTRICTORS AND GROWTH-FACTORS BY VASCULAR ENDOTHELIUM UNDER BOTH NORMOXIA AND HYPOXIA [J].
KOUREMBANAS, S ;
MCQUILLAN, LP ;
LEUNG, GK ;
FALLER, DV .
JOURNAL OF CLINICAL INVESTIGATION, 1993, 92 (01) :99-104
[15]   Nitric oxide: Cytotoxicity versus cytoprotection - How, why, when, and where? [J].
Kroncke, KD ;
Fehsel, K ;
Kolb-Bachofen, V .
NITRIC OXIDE-BIOLOGY AND CHEMISTRY, 1997, 1 (02) :107-120
[16]   MECHANISMS OF DISEASE - ENDOTHELINS [J].
LEVIN, ER .
NEW ENGLAND JOURNAL OF MEDICINE, 1995, 333 (06) :356-363
[17]   Physiological mechanisms regulating the expression of endothelial-type NO synthase [J].
Li, HG ;
Wallerath, T ;
Förstermann, U .
NITRIC OXIDE-BIOLOGY AND CHEMISTRY, 2002, 7 (02) :132-147
[18]   Highlights on endothelins: A review [J].
Mateo, AO ;
de Artinano, AA .
PHARMACOLOGICAL RESEARCH, 1997, 36 (05) :339-351
[19]   Inhaled nitric oxide-induced rebound pulmonary hypertension: role for endothelin-1 [J].
McMullan, DM ;
Bekker, JM ;
Johengen, MJ ;
Hendricks-Munoz, K ;
Gerrets, R ;
Black, SM ;
Fineman, JR .
AMERICAN JOURNAL OF PHYSIOLOGY-HEART AND CIRCULATORY PHYSIOLOGY, 2001, 280 (02) :H777-H785
[20]   Effects of endogenous and exogenous nitric oxide on endothelin-1 production in cultured vascular endothelial cells [J].
Mitsutomi, N ;
Akashi, C ;
Odagiri, J ;
Matsumura, Y .
EUROPEAN JOURNAL OF PHARMACOLOGY, 1999, 364 (01) :65-73