Response of tyrosine hydroxylase and GTP cyclohydrolase I gene expression to estrogen in brain catecholaminergic regions varies with mode of administration

被引:72
作者
Serova, LI
Maharjan, S
Huang, A
Sun, D
Kaley, G
Sabban, EL [1 ]
机构
[1] New York Med Coll, Dept Biochem & Mol Biol, Valhalla, NY 10595 USA
[2] New York Med Coll, Dept Physiol, Valhalla, NY 10595 USA
关键词
estradiol; tyrosine hydroxylase; GTP cyclohydrolase I; mRNA; tetrahydrobiopterin;
D O I
10.1016/j.brainres.2004.04.002
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
The effect of different dose, mode and duration of estradiol administration was examined in the different brain catecholaminergic areas in ovariectomized (OVX) female rats. We determined changes in mRNA levels of tyrosine hydroxylase (TH), rate-limiting enzyme in catecholamine (CA) biosynthesis, and of GTP cyclohydrolase I (GTPCH), rate-limiting enzyme in biosynthesis of tetrahydrobiopterm (BH4), as well as concentration of BH4, which is an essential cofactor for TH, tryptophan hydroxylase and nitric oxide synthase. Short-term administration of estradiol benzoate (EB) by five injections of 15 or 40 mug/kg 12 h apart led to increase in TH and GTPCH mRNA levels in dopaminergic and noradrenergic cell bodies of the ventral tegmental area (VTA), substantia nigra (SN), locus coeruleus (LC) and the nucleus of solitary tract (NTS) depending on dose of administration. Estrogen-elicited alterations in BH4 concentrations were mostly correlated with changes in GTPCH mRNA levels, except in SN. Long-term administration of estradiol by injections (EB: 25 mug/kg, 16 injections 24 h apart; 50 mug/kg, 16 injections 48 h apart) or pellets (0.1 mg 17 beta-estradiol, 14 days) were not very effective in modulating mRNA levels for both genes in most locations except the NTS. Long-term injections of EB elevated GTPCH mRNA levels throughout the NTS and in microvessels. Administration of estradiol by pellets led to decline of TH mRNA in rostral-medial and elevation in caudal parts of the NTS. Thus, estradiol has a complex and differential effect on TH and GTPCH gene expression in a tissue specific manner and depends on the mode of administration. (C) 2004 Elsevier B.V. All rights reserved.
引用
收藏
页码:1 / 8
页数:8
相关论文
共 50 条
[1]   Nitric oxide synthases: structure, function and inhibition [J].
Alderton, WK ;
Cooper, CE ;
Knowles, RG .
BIOCHEMICAL JOURNAL, 2001, 357 (03) :593-615
[2]   Estradiol attenuates the forskolin-induced increase in hypothalamic tyrosine hydroxylase activity [J].
Arbogast, LA ;
Hyde, JF .
NEUROENDOCRINOLOGY, 2000, 71 (04) :219-227
[3]  
Behl C, 2002, ADV EXP MED BIOL, V513, P475
[4]   Estrogen receptor α and endothelial nitric oxide synthase are organized into a functional signaling module in caveolae [J].
Chambliss, KL ;
Yuhanna, IS ;
Mineo, C ;
Liu, PS ;
German, Z ;
Sherman, TS ;
Mendelsohn, ME ;
Anderson, RGW ;
Shaul, PW .
CIRCULATION RESEARCH, 2000, 87 (11) :E44-E52
[5]   SPATIALLY AND TEMPORALLY DIFFERENTIATED PATTERNS OF C-FOS EXPRESSION IN BRAIN-STEM CATECHOLAMINERGIC CELL GROUPS INDUCED BY CARDIOVASCULAR CHALLENGES IN THE RAT [J].
CHAN, RKW ;
SAWCHENKO, PE .
JOURNAL OF COMPARATIVE NEUROLOGY, 1994, 348 (03) :433-460
[6]   Estrogen receptor α mediates the nongenomic activation of endothelial nitric oxide synthase by estrogen [J].
Chen, Z ;
Yuhanna, IS ;
Galcheva-Gargova, Z ;
Karas, RH ;
Mendelsohn, RE ;
Shaul, PW .
JOURNAL OF CLINICAL INVESTIGATION, 1999, 103 (03) :401-406
[7]  
DAHLSTROM A, 1964, ACTA PHYSIOL SCAND, V62, P1
[8]   Systemic hypertension in postmenopausal women: A clinical approach [J].
Fisman, EZ ;
Tenenbaum, A ;
Pines, A .
CURRENT HYPERTENSION REPORTS, 2002, 4 (06) :464-470
[9]   Perspectives on the Women's Health Initiative trial of hormone replacement therapy [J].
Grimes, DA ;
Lobo, RA .
OBSTETRICS AND GYNECOLOGY, 2002, 100 (06) :1344-1353
[10]   Understanding the divergent data on postmenopausal hormone therapy [J].
Grodstein, F ;
Clarkson, TB ;
Manson, JE .
NEW ENGLAND JOURNAL OF MEDICINE, 2003, 348 (07) :645-650