17β-Estradiol synthesis in the adult male rat retina

被引:62
作者
Cascio, C.
Russo, D.
Drago, G.
Gaizzi, G.
Passantino, R.
Guarneri, R.
Guarneri, P.
机构
[1] CNR, Ist Biomed & Immunol Mol, I-90146 Palermo, Italy
[2] CNR, Ist Metodol Diagnost Avanzata, Lab Elettromicroscopia, Palermo, Italy
关键词
P450scc; 3; beta-HSD; P450c17; P450aromatase; 17; beta-estradiol; ER alpha; ER beta; retina;
D O I
10.1016/j.exer.2007.02.008
中图分类号
R77 [眼科学];
学科分类号
100212 ;
摘要
17 beta-Estradiol (E2) exerts neurotrophic and neuroprotective effects in the retina as well as in other CNS structures, independently of sex. Retinal effects, however, have not been supported by evidence on local synthesis, and whether CNS 17 beta-estradiol is formed in a neurosteroidogenic pathway starting from cholesterol conversion into pregnenolone is a question still left unanswered. In the adult male rat retina, we have previously showed localization and activity of the P450 side chain cleavage (P450scc) enzyme, which is involved in pregnenolone synthesis. Here, we demonstrate both the mRNA and protein expression of 3 beta-hydroxy steroid dehydrogenase (3 beta-HSD), P450aromatase and also of P450scc, but only the protein expression of P450 17 alpha-hydroxylase/lyase (P450c17). Using radiolabeled pregnenolone and testosterone as precursors, in the isolated and intact retina of adult male rats, E2 is produced in a large amount by each precursor within 1-4 h, suggesting a highly active metabolic pathway towards its formation. The immunolocalization pattern shows enzymes and estrogen receptor subtypes (ER alpha, ER beta.) scattered in the retina with different intensities throughout the layers. The results point to the adult male rat retina as a neurosteroidogenic structure where E2 synthesis via a progesterone pathway and the presence of estrogen receptors provide important clues for understanding the neurotrophic and neuroprotective effects of the steroid hormone. (c) 2007 Elsevier Ltd. All rights reserved.
引用
收藏
页码:166 / 172
页数:7
相关论文
共 35 条
[1]   Effects of neurosteroids on ischemia-reperfusion injury in the rat retina:: role of σ1 recognition sites [J].
Bucolo, C ;
Drago, F .
EUROPEAN JOURNAL OF PHARMACOLOGY, 2004, 498 (1-3) :111-114
[2]   A caspase-3-dependent pathway is predominantly activated by the excitotoxin pregnenolone sulfate and requires early and late cytochrome c release and cell-specific caspase-2 activation in the retinal cell death [J].
Cascio, C ;
Guarneri, R ;
Russo, D ;
De Leo, G ;
Guarneri, M ;
Piccoli, F ;
Guarneri, P .
JOURNAL OF NEUROCHEMISTRY, 2002, 83 (06) :1358-1371
[3]   Detection of P450c17-independent pathways for dehydroepiandrosterone (DHEA) biosynthesis in brain glial tumor cells [J].
Cascio, C ;
Prasad, VVK ;
Lin, YY ;
Lieberman, S ;
Papadopoulos, V .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1998, 95 (06) :2862-2867
[4]   Pregnenolone sulfate, a naturally occurring excitotoxin involved in delayed retinal cell death [J].
Cascio, C ;
Guarneri, R ;
Russo, D ;
De Leo, G ;
Guarneri, M ;
Piccoli, F ;
Guarneri, P .
JOURNAL OF NEUROCHEMISTRY, 2000, 74 (06) :2380-2391
[5]   Sex steroid hormone metabolism takes place in human ocular cells [J].
Coca-Prados, M ;
Ghosh, S ;
Wang, YG ;
Escribano, J ;
Herrala, A ;
Vihko, P .
JOURNAL OF STEROID BIOCHEMISTRY AND MOLECULAR BIOLOGY, 2003, 86 (02) :207-216
[6]   Neurosteroids: Biosynthesis and function of these novel neuromodulators [J].
Compagnone, NA ;
Mellon, SH .
FRONTIERS IN NEUROENDOCRINOLOGY, 2000, 21 (01) :1-56
[7]   STEROIDOGENIC ENZYME P450C17 IS EXPRESSED IN THE EMBRYONIC CENTRAL-NERVOUS-SYSTEM [J].
COMPAGNONE, NA ;
BULFONE, A ;
RUBENSTEIN, JLR ;
MELLON, SH .
ENDOCRINOLOGY, 1995, 136 (11) :5212-5223
[8]   Aromatase: a neuroprotective enzyme [J].
Garcia-Segura, LM ;
Veiga, S ;
Sierra, A ;
Melcangi, RC ;
Azcoitia, I .
PROGRESS IN NEUROBIOLOGY, 2003, 71 (01) :31-41
[9]   Induction of neurosteroid synthesis by NMDA receptors in isolated rat retina: a potential early event in excitotoxicity [J].
Guarneri, P ;
Russo, D ;
Cascio, C ;
De Leo, G ;
Piccoli, F ;
Guarneri, R .
EUROPEAN JOURNAL OF NEUROSCIENCE, 1998, 10 (05) :1752-1763
[10]  
GUARNERI P, 1994, J NEUROCHEM, V63, P86