The expression of heme oxygenase-1 and inducible nitric oxide synthase in aorta during the development of hypertension in spontaneously hypertensive rats

被引:28
作者
Cheng, PY
Chen, JJ
Yen, MH
机构
[1] Natl Def Med Ctr, Dept Pharmacol, Taipei, Taiwan
[2] Natl Def Med Ctr, Grad Inst Life Sci, Taipei, Taiwan
[3] Natl Taiwan Univ Hosp, Taipei, Taiwan
[4] Acad Sinica, Inst Biomed Sci, Taipei, Taiwan
关键词
blood pressure; heme oxygenase; nitric oxide synthase; spontaneously hypertensive rats;
D O I
10.1016/j.amjhyper.2004.07.018
中图分类号
R6 [外科学];
学科分类号
1002 ; 100210 ;
摘要
Background: The aim of this study was to observe the time-course changes of heme oxygenase-1 (HO-1) and inducible nitric oxide synthase (iNOS) induction in aorta during the development of hypertension, as well as the relationship of HO-1/carbon monoxide (CO) system and iNOS/nitric oxide (NO) system in spontaneously hypertensive rats (SHR). Methods: The systolic blood pressure (SBP) was determined in conscious rats by the tail-cuff method. The tissue HO-I and iNOS mRNA and protein levels were estimated with reverse transcription polymerase chain reaction and Western blot method. Results: The expression of HO-1 and iNOS in aorta increased with the SBP elevation during the development of SHR and was attenuated when the hypertension was lowered with the vasodilator hydralazine. At 8 weeks, only HO-1 was induced, whereas at 12 and 16 weeks, both HO-1 and iNOS were observed. The level of plasma nitrite/nitrate was associated with the change in iNOS expression in SHR. In addition, the SBP of 8-week-old SHR was significantly increased after pretreatment with zinc protoporphyrin IX for 7 consecutive days. Chronic blockade of iNOS activity by aminoguanidine resulted in significant up-regulation of HO-1, but the pressor effect was blunt. Conclusions: These results suggest that the up-regulation of HO-1 and iNOS in aorta is a compensatory mechanism for the elevation of SBP during the development of hypertension in SHR. The expression of HO-I is earlier than that of iNOS. Our data suggest that the HO-1/CO system takes over and acts as a major modulator for the regulation of SBP when the iNOS/NO system is suppressed. (C) 2004 American Journal of Hypertension, Ltd.
引用
收藏
页码:1127 / 1134
页数:8
相关论文
共 29 条
[21]   Age-related alterations in soluble guanylyl cyclase and cGMP pathway in spontaneously hypertensive rats [J].
Ndisang, JF ;
Wang, R .
JOURNAL OF HYPERTENSION, 2003, 21 (06) :1117-1124
[22]   Selective regulation of blood pressure by heme oxygenase-1 in hypertension [J].
Ndisang, JF ;
Zhao, W ;
Wang, R .
HYPERTENSION, 2002, 40 (03) :315-321
[23]  
OHRUI T, 1992, J PHARMACOL EXP THER, V261, P1268
[24]   Carbon monoxide has anti-inflammatory effects involving the mitogen-activated protein kinase pathway [J].
Otterbein, LE ;
Bach, FH ;
Alam, J ;
Soares, M ;
Lu, HT ;
Wysk, M ;
Davis, RJ ;
Flavell, RA ;
Choi, AMK .
NATURE MEDICINE, 2000, 6 (04) :422-428
[25]   AN NADPH OXIDASE SUPEROXIDE-GENERATING SYSTEM IN THE RABBIT AORTA [J].
PAGANO, PJ ;
ITO, Y ;
TORNHEIM, K ;
GALLOP, PM ;
TAUBER, AI ;
COHEN, RA .
AMERICAN JOURNAL OF PHYSIOLOGY-HEART AND CIRCULATORY PHYSIOLOGY, 1995, 268 (06) :H2274-H2280
[26]   Human heme oxygenase-1 gene transfer lowers blood pressure and promotes growth in spontaneously hypertensive rats [J].
Sabaawy, HE ;
Zhang, F ;
Nguyen, XD ;
ElHosseiny, A ;
Nasjletti, A ;
Schwartzman, M ;
Dennery, P ;
Kappas, A ;
Abraham, NG .
HYPERTENSION, 2001, 38 (02) :210-215
[27]   CARBON-MONOXIDE - A PUTATIVE NEURAL MESSENGER [J].
VERMA, A ;
HIRSCH, DJ ;
GLATT, CE ;
RONNETT, GV ;
SNYDER, SH .
SCIENCE, 1993, 259 (5093) :381-384
[28]   Exacerbation of chronic renovascular hypertension and acute renal failure in heme oxygenase-1-deficient mice [J].
Wiesel, P ;
Patel, AP ;
Carvajal, IM ;
Wang, ZY ;
Pellacani, A ;
Maemura, K ;
DiFonzo, N ;
Rennke, HG ;
Layne, MD ;
Yet, SF ;
Lee, ME ;
Perella, MA .
CIRCULATION RESEARCH, 2001, 88 (10) :1088-1094
[29]   Vascular NADH/NADPH oxidase is involved in enhanced superoxide production in spontaneously hypertensive rats [J].
Zalba, G ;
Beaumont, FJ ;
San José, G ;
Fortuño, A ;
Fortuño, MA ;
Etayo, JC ;
Díez, J .
HYPERTENSION, 2000, 35 (05) :1055-1061