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
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