CHOLESTERYL-CONJUGATED PHOSPHOROTHIOATE OLIGODEOXYNUCLEOTIDES MODULATE CYP2B1 EXPRESSION IN-VIVO

被引:26
作者
DESJARDINS, J
MATA, J
BROWN, T
GRAHAM, D
ZON, G
IVERSEN, P
机构
[1] UNIV NEBRASKA,MED CTR,DEPT PHARMACOL,OMAHA,NE 68198
[2] UNIV NEBRASKA,MED CTR,EPPLEY INST RES CANC,OMAHA,NE 68198
[3] UNIV EDINBURGH,DEPT CHEM,EDINBURGH,MIDLOTHIAN,SCOTLAND
[4] LYNX THERAPEUT INC,HAYWARD,CA 94545
关键词
CHOLESTERYL-CONJUGATED; CYP2B1; CYP450; OLIGODEOXYNUCLEOTIDES; PHOSPHOROTHIOATE;
D O I
10.3109/10611869509015917
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
5' cholesteryl-conjugated phosphorothioate oligodeoxynucleotides with sequence complementary to the rat CYP2B1 mRNA were evaluated in adult male Sprague-Dawley rats for their pharmacokinetic properties, toxicity, and ability to modulate CYP2B1 expression in vivo. Following intraperitoneal administration of S-35-labelled oligodeoxynucleotides, volume of distribution for the phosphorothioate was 0.33 1/kg while the 5' cholesteryl-conjugate oligodeoxynucleotide was 0.12 1/kg. The elimination half-life was 23.2 and 55.4 hrs for cholesteryl modified and unmodified oligodeoxynucleotides, respectively. Cholesteryl-conjugate oligodeoxynucleotide toxicity was detected at a dose of 1.0 mg/kg and consisted primarily of midzonal liver cell enlargement and increased total RNA. Hexobarbital sleep times, a measure of CYP2B1 enzyme activity in vivo, increased from 21.9 minutes in saline-treated animals to 29.5 minutes in cholesterol oligodeoxynucleotide-treated animals. A significant decrease in liver microsomal pentoxyresorufin O-dealkylase enzyme activity, a CYP2B1/2 specific assay, was observed but not a change in p-nitrophenol hydroxylase activity, a specific CYP2E1 assay. These data indicate that in vivo modulation of the CYP2B1 gene can be accomplished with synthetic phosphorothioate oligodeoxynucleotides in a sequence-specific manner. Further, cholesteryl conjugation to the 5' end of the oligodeoxynucleotide enhanced potency despite lesser bioavailability.
引用
收藏
页码:477 / 485
页数:9
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