Abnormalities of membrane function and lipid metabolism in hypertension - A review

被引:186
作者
Zicha, J [1 ]
Kunes, J
Devynck, MA
机构
[1] Acad Sci Czech Republ, Inst Physiol, Videnska 1083, CZ-14220 Prague 4, Czech Republic
[2] Fac Med Necker Enfants Malad, URA 1482, CNRS, Dept Pharmacol, Paris, France
关键词
plasma lipids; membrane microviscosity; Na+ and K+ transport; cytosolic calcium; cytosolic pH; cholesterol; triglycerides; phospholipids; LDL; HDL;
D O I
10.1016/S0895-7061(98)00178-2
中图分类号
R6 [外科学];
学科分类号
1002 ; 100210 ;
摘要
Hypertension, which is characterized by multiple alterations in the structure and function of the cell membrane, is often associated with important metabolic abnormalities including those concerning lipid metabolism. Dyslipidemia accompanying essential hypertension consists of elevated plasma triglycerides, low HDL cholesterol, and increased levels of atherogenic LDL cholesterol particles. The altered membrane microviscosity seen in hypertensive subjects reflects the changes of membrane lipid composition resulting from intensive exchange between circulating and membrane lipids, as well as from abnormal cellular lipid synthesis and metabolism The changes of membrane microviscosity are known to modulate the activity of proteins involved in ion transport, signal transduction, cell Ca2+ handling, intracellular pH regulation, etc. Alterations in plasma or membrane lipids are indeed closely associated with ion transport abnormalities as well as with impaired control of cytosolic Ca2+ and pH in various forms of hypertension in both humans and rats. Such lipid-dependent modifications of membrane properties in cells participating in the cardiovascular regulation might be a part of pathogenetic mechanisms responsible for chronic blood pressure elevation. Thus nutritional and pharmacologic interventions aiming to normalize abnormal lipid metabolism could be useful for amelioration of membrane abnormalities and lowering of high blood pressure. Future studies of functional membrane alterations in hypertension or dyslipidemia will therefore require the detailed determination of membrane lipid composition and the measurement of microviscosity in particular membrane domains. Am J Hypertens 1999; 12:315-331(C) 1999 American Journal of Hypertension, Ltd.
引用
收藏
页码:315 / 331
页数:17
相关论文
共 217 条
[41]   Membrane microviscosity and plasma triacylglycerols in the rat [J].
Devynck, MA ;
Kunes, J ;
Le Quan Sang, KH ;
Zicha, J .
CLINICAL SCIENCE, 1998, 94 (01) :79-85
[42]   DIFFUSE STRUCTURAL ALTERATIONS IN CELL-MEMBRANES OF SPONTANEOUSLY HYPERTENSIVE RATS [J].
DEVYNCK, MA ;
PERNOLLET, MG ;
NUNEZ, AM ;
ARAGON, I ;
MONTENAYGARESTIER, T ;
HELENE, C ;
MEYER, P .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA-BIOLOGICAL SCIENCES, 1982, 79 (16) :5057-5060
[43]  
DIEZ J, 1992, J HYPERTENS, V10, P579
[44]   AN NMR INVESTIGATION OF THE CHANGES IN PLASMA-MEMBRANE TRIGLYCERIDE AND PHOSPHOLIPID PRECURSORS DURING THE ACTIVATION OF LYMPHOCYTES-T [J].
DINGLEY, AJ ;
KING, NJC ;
KING, GF .
BIOCHEMISTRY, 1992, 31 (37) :9098-9106
[45]   LATERAL DIFFUSION AND FATTY-ACID COMPOSITION IN VASCULAR SMOOTH-MUSCLE MEMBRANE FROM STROKE-PRONE SPONTANEOUSLY HYPERTENSIVE RATS [J].
DOMINICZAK, AF ;
MCLAREN, Y ;
KUSEL, JR ;
BALL, DL ;
GOODFRIEND, TL ;
BOHR, DF ;
REID, JL .
AMERICAN JOURNAL OF HYPERTENSION, 1993, 6 (12) :1003-1008
[46]   CELL-MEMBRANE ABNORMALITIES AND THE REGULATION OF INTRACELLULAR CALCIUM-CONCENTRATION IN HYPERTENSION [J].
Dominiczak, AF ;
Bohr, DF .
CLINICAL SCIENCE, 1990, 79 (05) :415-423
[47]   LIPID BILAYER IN GENETIC-HYPERTENSION [J].
DOMINICZAK, AF ;
LAZAR, DF ;
DAS, AK ;
BOHR, DF .
HYPERTENSION, 1991, 18 (06) :748-757
[48]  
Dominiczak AF, 1994, HYPERTENS RES, V17, P79
[49]   INCREASED HUMAN ERYTHROCYTE SODIUM-LITHIUM COUNTERTRANSPORT IN HYPERLIPEMIC PATIENTS MAY INDICATE INCREASED MEMBRANE LIPID FLUIDITY [J].
DOWD, A ;
THOMAS, TH ;
WILKINSON, R .
EUROPEAN JOURNAL OF CLINICAL INVESTIGATION, 1993, 23 (02) :102-107
[50]   ACCELERATED MAXIMAL VELOCITY OF THE RED-BLOOD-CELL NA+/K+ PUMP IN HYPERLIPIDEMIA IS RELATED TO INCREASE IN 1-PALMITOYL,2-ARACHIDONOYL-PLASMALOGEN PHOSPHATIDYLETHANOLAMINE [J].
DUHM, J ;
ENGELMANN, B ;
SCHONTHIER, UM ;
STREICH, S .
BIOCHIMICA ET BIOPHYSICA ACTA, 1993, 1149 (01) :185-188