Increased membrane sphingomyelin and arachidonic acid in stroke-prone spontaneously hypertensive rats

被引:15
作者
Dorrance, AM
Graham, D
Webb, RC
Fraser, R
Dominiczak, A
机构
[1] Med Coll Georgia, Dept Physiol, Augusta, GA 30912 USA
[2] Univ Glasgow, Western Infirm, Dept Med & Therapeut, Glasgow, Lanark, Scotland
[3] Univ Glasgow, MRC Blood Pressure Grp, Glasgow, Lanark, Scotland
关键词
genetic hypertension; membrane lipids; erythrocytes;
D O I
10.1016/S0895-7061(01)02188-4
中图分类号
R6 [外科学];
学科分类号
1002 ; 100210 ;
摘要
Background: Cell membrane composition and fluidity are altered in hypertension. Previous reports suggest arachidonic acid, a metabolically active fatty acid, is increased in the membranes of hypertensive animals compared to control. This increase in unsaturated fatty acids does not explain the observed reduction in fluidity in hypertensive rats, suggesting some other factors affecting fluidity may be present. It has been suggested that the metabolism of sphingomyelin is altered in genetic hypertension. We hypothesized that membrane sphingomyelin content is increased in hypertensive animals. Procedures: Stroke-prone spontaneously hypertensive rats (n = 8) were compared with Wistar-Kyoto rats (n = 8). Erythrocyte membranes were prepared and the lipids extracted and separated. Fatty acid methyl esters were produced, identified, and quantified by gas chromatography-mass spectrometry; membrane lipid content was also assessed. Results: The concentration of sphingomyelin was higher in the membrane of the hypertensive rats (45.7 +/- 6 v 22.4 +/- 2 mug/mg of protein) compared to control. The previously observed increase in membrane arachidonic acid content was observed in hypertensive animals when compared to control (130 +/- 32 v 40 +/- 3 mug/mg of protein). However, this difference was confined to the phosphatidylinositol (18 +/- 4 v 6.5 +/- 1.5 mug/mg of protein) and free fatty acid (2.1 +/- 0.4 v 0.6 +/- 0.1 mug/mg of protein) fractions. Conclusion: We hypothesize that reports of reduced membrane fluidity observed in hypertension may be due to an increase in the proportion of sphingomyelin in the cell membrane. Am J Hypertens 2001;14:1149-1153 (C) 2001 American Journal of Hypertension, Ltd.
引用
收藏
页码:1149 / 1153
页数:5
相关论文
共 24 条
[1]   ARACHIDONIC-ACID SUPPRESSION OF FATTY-ACID SYNTHASE GENE-EXPRESSION IN CULTURED RAT HEPATOCYTES [J].
ARMSTRONG, MK ;
BLAKE, WL ;
CLARKE, SD .
BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 1991, 177 (03) :1056-1061
[2]   SUPPRESSION OF RAT HEPATIC FATTY-ACID SYNTHASE AND S-14 GENE-TRANSCRIPTION BY DIETARY POLYUNSATURATED FAT [J].
BLAKE, WL ;
CLARKE, SD .
JOURNAL OF NUTRITION, 1990, 120 (12) :1727-1729
[3]   EFFECT OF PHOSPHATIDYLCHOLINE TO SPHINGOMYELIN MOLE RATIO ON DYNAMIC PROPERTIES OF SHEEP ERYTHROCYTE-MEMBRANE [J].
BOROCHOV, H ;
ZAHLER, P ;
WILBRANDT, W ;
SHINITZKY, M .
BIOCHIMICA ET BIOPHYSICA ACTA, 1977, 470 (03) :382-388
[4]   Alterations in membrane fatty acid unsaturation and chain length in hypertension as observed by 1H NMR spectroscopy [J].
Chi, YL ;
Gupta, RK .
AMERICAN JOURNAL OF HYPERTENSION, 1998, 11 (03) :340-348
[5]   Polyunsaturated fatty acid regulation of hepatic gene transcription [J].
Clarke, SD ;
Jump, DB .
JOURNAL OF NUTRITION, 1996, 126 (04) :S1105-S1109
[6]  
CLARKE SD, 1994, ANNU REV NUTR, V14, P83, DOI 10.1146/annurev.nu.14.070194.000503
[7]   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
[8]   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
[9]   Inhibition of nitric oxide synthesis increases erythrocyte membrane fluidity and unsaturated fatty acid content [J].
Dorrance, AM ;
Graham, D ;
Dominiczak, A ;
Fraser, R .
AMERICAN JOURNAL OF HYPERTENSION, 2000, 13 (11) :1194-1202
[10]  
FOLCH J, 1957, J BIOL CHEM, V226, P497