ACETYLSALICYLIC-ACID, AT HIGH-CONCENTRATIONS, INHIBITS VASCULAR SMOOTH-MUSCLE CELL-PROLIFERATION

被引:22
作者
BERNHARDT, J
ROGALLA, K
LUSCHER, TF
BUHLER, FR
RESINK, TJ
机构
[1] UNIV BASEL HOSP, DEPT RES, BASEL, SWITZERLAND
[2] UNIV BASEL HOSP, DEPT CLIN PHARMACOL, BASEL, SWITZERLAND
[3] BAYER DEPT RES & DEV, WUPPERTAL, GERMANY
关键词
VASCULAR SMOOTH MUSCLE CELL; ACETYLSALICYLIC ACID; PROLIFERATION;
D O I
10.1097/00005344-199306000-00019
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
The growth of human smooth muscle cells in culture is inhibited by acetylsalicylic acid (ASA). In comparison to control, the proliferation of cells treated with 270 mg/L lysinmono(acetytsalicylate)/30 mg/L glycine was inhibited by 50-90% under different culture conditions. Cell numbers per well (control vs. treated) were as follows: (a) 470,500 +/- 55,890 vs. 24,750 +/- 4,030 (p < 0.002) after 6 days in the presence of 10% fetal calf serum (FCS), (b) 160,500 +/- 9,920 vs. 74,000 (p < 0.001) after 8 days in the presence of 10% human serum; and (c) 387,000 +/- 29,420 vs. 35,250 +/- 1,110 (p < 0.001) after 8 days in the presence of 5% FCS. Significant inhibition of growth by lysinmono(acetylsalicylate) at 90 mg/L was noted only for cultures grown with 10% FCS. Lower concentrations of this drug were ineffective under all culture conditions. Higher dosages of ASA, which would prevent not only platelet aggregation but also smooth muscle cell growth, may therefore be indicated in therapy of patients who undergo percutaneous transluminal coronary angio (PTCA) or coronary artery transplantation.
引用
收藏
页码:973 / 976
页数:4
相关论文
共 11 条
[1]   RELEASE OF NITRIC-OXIDE FROM HUMAN VASCULAR SMOOTH-MUSCLE CELLS [J].
BERNHARDT, J ;
TSCHUDI, MR ;
DOHI, Y ;
GUT, I ;
URWYLER, B ;
BUHLER, FR ;
LUSCHER, TF .
BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 1991, 180 (02) :907-912
[2]   INOSITOL TRISPHOSPHATE AND DIACYLGLYCEROL AS 2ND MESSENGERS [J].
BERRIDGE, MJ .
BIOCHEMICAL JOURNAL, 1984, 220 (02) :345-360
[3]   INHIBITION OF PLATELET PROSTAGLANDIN SYNTHETASE BY ORAL ASPIRIN [J].
BURCH, JW ;
STANFORD, N ;
MAJERUS, PW .
JOURNAL OF CLINICAL INVESTIGATION, 1978, 61 (02) :314-319
[4]   ROLE OF PLATELETS IN SMOOTH-MUSCLE CELL-PROLIFERATION AND MIGRATION AFTER VASCULAR INJURY IN RAT CAROTID-ARTERY [J].
FINGERLE, J ;
JOHNSON, R ;
CLOWES, AW ;
MAJESKY, MW ;
REIDY, MA .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1989, 86 (21) :8412-8416
[5]  
FRESHNEY RI, 1987, CULTURE ANIMAL CELLS, P246
[6]   FACTORS DETERMINING EFFICACY OF NSAIDS [J].
PORTER, RS .
DRUG INTELLIGENCE & CLINICAL PHARMACY, 1984, 18 (01) :42-51
[7]   HISTAMINE-INDUCED PHOSPHOINOSITIDE METABOLISM IN CULTURED HUMAN UMBILICAL VEIN ENDOTHELIAL-CELLS - ASSOCIATION WITH THROMBOXANE AND PROSTACYCLIN RELEASE [J].
RESINK, TJ ;
GRIGORIAN, GY ;
MOLDABAEVA, AK ;
DANILOV, SM ;
BUHLER, FR .
BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 1987, 144 (01) :438-446
[8]   PLATELET INHIBITOR AGENTS IN CARDIOVASCULAR-DISEASE - AN UPDATE [J].
STEIN, B ;
FUSTER, V ;
ISRAEL, DH ;
COHEN, M ;
BADIMON, L ;
BADIMON, JJ ;
CHESEBRO, JH .
JOURNAL OF THE AMERICAN COLLEGE OF CARDIOLOGY, 1989, 14 (04) :813-836
[9]   THE EFFECTS OF VARYING DOSES OF ASPIRIN ON HUMAN PLATELET ACTIVATION INDUCED BY PAF, COLLAGEN AND ARACHIDONIC-ACID [J].
TAYLOR, ML ;
MISSO, NLA ;
STEWART, GA ;
THOMPSON, PJ .
BRITISH JOURNAL OF CLINICAL PHARMACOLOGY, 1992, 33 (01) :25-31
[10]   INHIBITION OF PROSTAGLANDIN SYNTHESIS AS A MECHANISM OF ACTION FOR ASPIRIN-LIKE DRUGS [J].
VANE, JR .
NATURE-NEW BIOLOGY, 1971, 231 (25) :232-&