Lipids: potential regulators of nitric oxide generation

被引:23
作者
Chikani, G [1 ]
Zhu, WF [1 ]
Smart, EJ [1 ]
机构
[1] Univ Kentucky, Sch Med, Dept Pediat, Lexington, KY 40536 USA
来源
AMERICAN JOURNAL OF PHYSIOLOGY-ENDOCRINOLOGY AND METABOLISM | 2004年 / 287卷 / 03期
关键词
caveolae; cholesterol; oxidized low-density lipoprotein; caveolin;
D O I
10.1152/ajpendo.00106.2004
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
The endothelium is a dynamic organ that secretes several biologically active substances and plays a major functional role in the health of an organism in both physiological and pathological conditions. For instance, the endothelium is involved in control of the exchange of plasma and tissue biomolecules, regulation of vessel tone, inflammation, lipid metabolism, vessel growth and remodeling, and modulation of coagulation and fibrinolysis (6, 12, 15). The endothelium generates nitric oxide, which is a key regulator of vasodilation and plays important roles in preventing, or in some cases promoting, numerous cardiovascular diseases (41). Several recent studies have examined the interplay between lipids and nitric oxide generation, especially in relation to atherosclerosis (14, 29, 34, 36, 40). The endothelium is continuously exposed to circulating lipids in the form of lipoproteins and protein carriers that may have a direct impact on nitric oxide synthesis and function. The purpose of this review is to illustrate some of the recent findings that link lipids (plasma and cellular) to nitric oxide generation (see Fig. 1).
引用
收藏
页码:E386 / E389
页数:4
相关论文
共 42 条
[1]  
ACTON SL, 1994, J BIOL CHEM, V269, P21003
[2]   Murine SR-BI, a high density lipoprotein receptor that mediates selective lipid uptake, is N-glycosylated and fatty acylated and colocalizes with plasma membrane caveolae [J].
Babitt, J ;
Trigatti, B ;
Rigotti, A ;
Smart, EJ ;
Anderson, RGW ;
Xu, SZ ;
Krieger, M .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1997, 272 (20) :13242-13249
[3]   Oxidized low density lipoprotein displaces endothelial nitric-oxide synthase (eNOS) from plasmalemmal caveolae and impairs eNOS activation [J].
Blair, A ;
Shaul, PW ;
Yuhanna, IS ;
Conrad, PA ;
Smart, EJ .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1999, 274 (45) :32512-32519
[4]   LIPOPROTEIN METABOLISM IN THE MACROPHAGE - IMPLICATIONS FOR CHOLESTEROL DEPOSITION IN ATHEROSCLEROSIS [J].
BROWN, MS ;
GOLDSTEIN, JL .
ANNUAL REVIEW OF BIOCHEMISTRY, 1983, 52 :223-261
[5]  
CaulinGlaser T, 1997, CIRC RES, V81, P885
[6]   Endothelial dysfunction: Does it matter? Is it reversible? [J].
Celermajer, DS .
JOURNAL OF THE AMERICAN COLLEGE OF CARDIOLOGY, 1997, 30 (02) :325-333
[7]   Estrogen receptor α and endothelial nitric oxide synthase are organized into a functional signaling module in caveolae [J].
Chambliss, KL ;
Yuhanna, IS ;
Mineo, C ;
Liu, PS ;
German, Z ;
Sherman, TS ;
Mendelsohn, ME ;
Anderson, RGW ;
Shaul, PW .
CIRCULATION RESEARCH, 2000, 87 (11) :E44-E52
[8]   Estrogen modulation of endothelial nitric oxide synthase [J].
Chambliss, KL ;
Shaul, PW .
ENDOCRINE REVIEWS, 2002, 23 (05) :665-686
[9]   Rapid activation of endothelial NO synthase by estrogen: Evidence for a steroid receptor fast-action complex (SRFC) in caveolae [J].
Chambliss, KL ;
Shaul, PW .
STEROIDS, 2002, 67 (06) :413-419
[10]   ERβ has nongenomic action in caveolae [J].
Chambliss, KL ;
Yuhanna, IS ;
Anderson, RGW ;
Mendelsohn, ME ;
Shaul, PW .
MOLECULAR ENDOCRINOLOGY, 2002, 16 (05) :938-946