EFFECT OF SQUALESTATIN-1 ON THE BIOSYNTHESIS OF THE MEVALONATE PATHWAY LIPIDS

被引:28
作者
THELIN, A
PETERSON, E
HUTSON, JL
MCCARTHY, AD
ERICSSON, J
DALLNER, G
机构
[1] GLAXO GRP RES LTD,GREENFORD UB6 0HE,MIDDX,ENGLAND
[2] KAROLINSKA INST,NOVUM,CLIN RES CTR,S-14186 HUDDINGE,SWEDEN
来源
BIOCHIMICA ET BIOPHYSICA ACTA-LIPIDS AND LIPID METABOLISM | 1994年 / 1215卷 / 03期
关键词
SQUALESTATIN; 1; SQUALENE SYNTHASE; UBIQUINONE; DOLICHOL; CHOLESTEROL; PROTEIN ISOPRENYLATION;
D O I
10.1016/0005-2760(94)90049-3
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
The effects of squalestatin 1 on rat brain and liver homogenates and on Chinese hamster ovary tissue culture cells have been investigated. This compound effectively inhibits squalene biosynthesis in a highly selective manner. Cytoplasmic farnesyl pyrophosphate and geranylgeranyl pyrophosphate synthases are not affected, which is also the case for microsomal cis-prenyltransferase. In tissue culture cells, squalestatin 1 inhibits cholesterol biosynthesis completely, but does not alter dolichol synthesis or protein isoprenylation to a great extent. Incorporation of [H-3]mevalonate into ubiquinone-9 and -10 increases 3-4-fold, probably as a result of increased synthesis of this lipid. Squalestatin 1 appears not only to be an effective inhibitor of cholesterol biosynthesis, but also to be more specific than other inhibitors used earlier in various in vitro and in vivo systems.
引用
收藏
页码:245 / 249
页数:5
相关论文
共 30 条
  • [1] RATES OF CHOLESTEROL, UBIQUINONE, DOLICHOL AND DOLICHYL-P BIOSYNTHESIS IN RAT-BRAIN SLICES
    ANDERSSON, M
    ELMBERGER, PG
    EDLUND, C
    KRISTENSSON, K
    DALLNER, G
    [J]. FEBS LETTERS, 1990, 269 (01) : 15 - 18
  • [2] BAXTER A, 1992, J BIOL CHEM, V267, P11705
  • [3] BEYER RE, 1990, HIGHLIGHTS IN UBIQUINONE RESEARCH, P191
  • [4] CARSON DD, 1981, J BIOL CHEM, V256, P4679
  • [5] CHOJNACKI T, 1984, ACTA BIOCHIM POL, V31, P115
  • [7] THE SQUALESTATINS, NOVEL INHIBITORS OF SQUALENE SYNTHASE PRODUCED BY A SPECIES OF PHOMA .1. TAXONOMY, FERMENTATION, ISOLATION, PHYSICOCHEMICAL PROPERTIES AND BIOLOGICAL-ACTIVITY
    DAWSON, MJ
    FARTHING, JE
    MARSHALL, PS
    MIDDLETON, RF
    ONEILL, MJ
    SHUTTLEWORTH, A
    STYLLI, C
    TAIT, RM
    TAYLOR, PM
    WILDMAN, HG
    BUSS, AD
    LANGLEY, D
    HAYES, MV
    [J]. JOURNAL OF ANTIBIOTICS, 1992, 45 (05) : 639 - 647
  • [8] EGGENS I, 1990, J EXP PATHOL, V71, P219
  • [9] ENDO A, 1992, J LIPID RES, V33, P1569
  • [10] ERICSSON J, 1992, J BIOL CHEM, V267, P18708