Chymase-dependent angiotensin II formation in the saphenous vein versus the internal thoracic artery

被引:38
作者
Nishimoto, M
Takai, S
Sawada, Y
Yuda, A
Kondo, K
Yamada, M
Jin, D
Sakaguchi, M
Asada, K
Sasaki, S
Miyazaki, M
机构
[1] Osaka Med Coll, Dept Pharmacol, Takatsuki, Osaka 5698686, Japan
[2] Osaka Med Coll, Dept Cardiovasc & Thorac Surg, Takatsuki, Osaka 5698686, Japan
关键词
D O I
10.1067/mtc.2001.112467
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Objectives: The great saphenous vein graft is known to be less patent than the internal thoracic artery graft. Recently, we reported that chymase-dependent angiotensin II formation plays an important role in the development of intimal hyperplasia in dog grafted veins. In this study we investigated the levels of angiotensin II-forming enzymes, angiotensin-converting enzyme, and chymase in human saphenous veins and internal thoracic arteries. Methods: The saphenous vein and internal thoracic artery specimens were obtained from coronary artery bypass grafts of patients during surgical procedures (saphenous vein, n = 16, internal thoracic artery, n = 16). Activities of angiotensin-converting enzyme and chymase were determined by using the extract from the saphenous vein or internal thoracic artery. Sections of the saphenous vein or internal thoracic artery were stained with van Gieson's elastin stain and were immunostained with anti-human chymase antibody. Results: The activities of angiotensin-converting enzyme in the saphenous vein and internal thoracic artery were 0.34 +/- 0.12 and 0.32 +/- 0.17 mU/mg protein, respectively, and the difference was not significant. The chymase activity in the saphenous vein was significantly higher than that in the internal thoracic artery (saphenous vein, 10.1 +/- 0.81 mU/mg protein; internal thoracic artery, 6.21 +/- 1.86 mU/mg protein). Chymase-positive cells in the saphenous vein were located in both the media and adventitia, and those in the internal thoracic artery were located only in the adventitia. The number of chymase-positive cells in the saphenous vein was about 2.6 times that in the internal thoracic artery. Conclusion: The chymase activity, but not the angiotensin-converting enzyme activity, was significantly higher in the saphenous vein, suggesting that the high levels of chymase activity may be related to the poorer performance of the saphenous vein for use as a bypass conduit.
引用
收藏
页码:729 / 734
页数:6
相关论文
共 30 条
[1]   PHARMACOLOGICAL PROPERTIES OF N-(3',4'-DIMETHOXYCINNAMOYL) ANTHRANILIC ACID (N-5'), A NEW ANTI-ATOPIC AGENT [J].
AZUMA, H ;
BANNO, K ;
YOSHIMURA, T .
BRITISH JOURNAL OF PHARMACOLOGY, 1976, 58 (04) :483-488
[2]   Differential action of angiotensin II and activity of angiotensin-converting enzyme in human bypass grafts [J].
Borland, JAA ;
Chester, AH ;
Crabbe, S ;
Parkerson, JB ;
Catravas, JD ;
Yacoub, MH .
JOURNAL OF THORACIC AND CARDIOVASCULAR SURGERY, 1998, 116 (02) :206-212
[3]   Alternative pathways of angiotensin II production in the human saphenous vein [J].
Borland, JAA ;
Chester, AH ;
Morrison, KA ;
Yacoub, MH .
BRITISH JOURNAL OF PHARMACOLOGY, 1998, 125 (03) :423-428
[4]   ANGIOTENSIN-II INDUCES SMOOTH-MUSCLE CELL-PROLIFERATION IN THE NORMAL AND INJURED RAT ARTERIAL-WALL [J].
DAEMEN, MJAP ;
LOMBARDI, DM ;
BOSMAN, FT ;
SCHWARTZ, SM .
CIRCULATION RESEARCH, 1991, 68 (02) :450-456
[5]   SURGICAL PROGRESS - POST-OPERATIVE CHANGES IN AUTOLOGOUS VEIN GRAFTS [J].
FUCHS, JCA ;
MITCHENER, JS ;
HAGEN, PO .
ANNALS OF SURGERY, 1978, 188 (01) :1-15
[6]  
Green G E, 1968, Ann Thorac Surg, V5, P443
[7]  
HANSON SR, 1991, HYPERTENSION S2, V18, P1170
[8]   Roles of vascular angiotensin converting enzyme and chymase in two-kidney, one clip hypertensive hamsters [J].
Jin, D ;
Takai, S ;
Shiota, N ;
Miyazaki, M .
JOURNAL OF HYPERTENSION, 1998, 16 (05) :657-664
[9]   ANGIOTENSIN-II TYPE-1 RECEPTOR BLOCKADE INHIBITS THE EXPRESSION OF IMMEDIATE-EARLY GENES AND FIBRONECTIN IN RAT INJURED ARTERY [J].
KIM, SK ;
KAWAMURA, M ;
WANIBUCHI, H ;
OHTA, K ;
HAMAGUCHI, A ;
OMURA, T ;
YUKIMURA, T ;
MIURA, K ;
IWAO, H .
CIRCULATION, 1995, 92 (01) :88-95
[10]   STUDY OF THE MECHANISM OF INHIBITORY-ACTION OF TRANILAST ON CHEMICAL MEDIATOR RELEASE [J].
KOMATSU, H ;
KOJIMA, M ;
TSUTSUMI, N ;
HAMANO, S ;
KUSAMA, H ;
UJIIE, A ;
IKEDA, S ;
NAKAZAWA, M .
JAPANESE JOURNAL OF PHARMACOLOGY, 1988, 46 (01) :43-51