Membrane receptors for estrogen, progesterone, and testosterone in the rat brain: Fantasy or reality

Cellular and Molecular Neurobiology

Volumn 16, Issue 2, 1996, Pages 175-198

  Ramirez, Victor D ^a,b   Zheng, Jianbiao ^b   Siddique, Khawar M ^a  

^a Department of Molecular and Integrative Physiology ^*

^b UNIVERSITY OF ILLINOIS AT URBANA CHAMPAIGN   (United States)

Author keywords

affinity chromatography; brain; radioligand binding assay; steroid bovine serum albumin conjugates; Western blot analysis

Indexed keywords

ESTROGEN; MEMBRANE RECEPTOR; PROGESTERONE; TESTOSTERONE;

AFFINITY CHROMATOGRAPHY; ANIMAL EXPERIMENT; ANIMAL MODEL; BINDING SITE; BRAIN METABOLISM; CELL FUNCTION; CONTROLLED STUDY; IMMUNOBLOTTING; LIGAND BINDING; NONHUMAN; PRIORITY JOURNAL; PROGESTERONE METABOLISM; RADIOIODINATION; RAT; RECEPTOR AFFINITY; REVIEW; STEROID BINDING; SYNAPTOSOME;

ANIMALS; BINDING SITES; BINDING, COMPETITIVE; BRAIN CHEMISTRY; FEMALE; IODINE RADIOISOTOPES; KINETICS; MALE; MEMBRANE PROTEINS; PROTEIN STRUCTURE, TERTIARY; RATS; RATS, SPRAGUE-DAWLEY; RECEPTORS, ANDROGEN; RECEPTORS, ESTROGEN; RECEPTORS, PROGESTERONE; SEPHAROSE; SERUM ALBUMIN, BOVINE; STEROIDS;

EID: 0029890498     PISSN: 02724340     EISSN: None     Source Type: Journal    
DOI: 10.1007/BF02088175     Document Type: Review

References (28)

1. 1 ATPase from bovine heart mitochondria. Nature 370:621-628.
2. Aronica, S. M., Kraus, W. L., and Katzenellenbogen, B. S. (1994). Estrogen action via the cAMP signalling pathway: Stimulation of adenylate cyclase and cAMP-regulated gene transcription. Proc. Natl. Acad. Sci. USA 91:8517-8521.
3. Becker, J. B. (1990a), Estrogen rapidly potentiates amphetamine-induced striatal dopamine release and rotational behavior during microdialysis. Neurosci. Lett. 118:169-171.
4. Becker, J. B. (1990b). Direct effect of 17β-estradiol on striatum: Sex difference in dopamine release. Synapse 5:157-164.
5. Blackmore, P. F., and Lattanzio, F. A. (1991a). Cell surface localization of a novel nongenomic progesterone receptor on the head of human sperm. Biochem. Biophys. Res. Commun. 181:331-336.
6. Blackmore, P. F., Neulen, J., Lattanzio, F., and Beebe, S. J. (1991b). Cell surface-binding sites for progesterone mediate calcium uptake in human sperm. J. Biol. Chem. 266:18655-18659.
7. Bradford, M. M. (1976). A rapid and sensitive method for the quantitation of microgram quantities of protein utilizing the principle of protein-dye binding. Anal. Biochem. 72:248-252.
8. Clark, J. H., and Shailaja, K. M. (1994). Actions of ovarian steroid hormones. In The Physiology of Reproduction, 2nd ed. (E. Kuobil and J. N. Neil, Eds.), Raven Press, New York, pp. 1011-1059.
9. Di Paolo, T., Rouillard, D. C., and Bedard, P. (1985). 17β-Estradiol at a physiological dose acutely increases dopamine turnover in rat brain. Eur. J. Pharmacol. 117:197-203.
10. Dluzen, D. E., and Ramirez, V. D. (1991). Modulatory effects of progesterone upon dopamine release from the corpus striatum of ovariectomized estrogen-treated rats are stereospecific. Brain Res. 538:176-179
11. Dluzen D. E., and Ramirez, V. D. (1990). In vitro progesterone modulation of amphetamine-stimulated dopamine release from the corpus striatum of overiectomized estrogen-treated female rats: Response characteristics. Brain Res. 517:117-122.
12. Dluzen, D. E., and Ramirez, V. D. (1989). Progesterone effects upon dopamine release from the corpus striatum of female rats. II. Evidence for a membrane site of action and the role of albumin. Brain Res. 476:338-344.
13. El-Ashry, D., Onate, S. A., Nordeen, S. K., and Edwards, D. P. (1989). Human progesterone receptor complexed with the antagonist R4486 binds to hormone response elements in a structurally altered form. Mol. Endocrinol. 3:1545-1558.
14. Evans, R. M. (1988). The steroid and thyroid hormone receptor super family. Science 240:889-895.
15. Frye, C. A., and DeBold, J. F. (1993). P-3-BSA, but not P-11-BSA, implants in the VTA rapidly facilitate receptivity in hamsters after progesterone priming to the VMH. Behavioral Brain Res. 53:167-175.
16. Frye, C. A., Mermelstein, P. G., and DeBold, J. F. (1992). Evidence for a non-genomic action of progestins on sexual receptivity in hamster ventral tegmental area but not hypothalamus. Brain Res. 578:87-93.
17. Garcia-Segura, L. M., Chowen, J. A., Duenas, M., and Naftolin, F. (1995). Hypothalamic syanptic plasticity. Part II: Gliol actions of estrogen. Cellular and Molecular Neurobiology (in press).
18. Garcia-Segura, L. M., Olmos, G., Tranque, P., and Naftolin, F. (1987). Rapid effects of gonadal steroids upon hypothalamic neuronal membrane ultrastructure. J. Steroid Biochem. 27: 615-623.
19. +-ATP synthase in rat mitochondria. Biochim. Biophys. Acta 1172:311-314.
20. Kawakami, M., and Sawyer, C. H. (1959). Neuroendocrine correlates of changes in brain activity thresholds by sex steroids and pituitary hormones. Endocrinology 65:652-658.
21. Ke, F.-C., and Ramirez, V. D. (1987). Membrane mechanism mediates progesterone stimulatory effect on LHRH release from superfused rat hypothalami in vitro. Neuroendocrinology 45:514-517.
22. 125I-BSA as a ligand. J. Neurochem. 54:467-472.
23. Kelly, M. J., Moss, R. L., and Dudley, C. A. (1976). Differential sensitivity of preoptic-septal neurons to microelectrophoresed estrogen during the estrous cycle. Brain Res. 114:152-157.
24. Kelly, M. J., Moss, R. L., Dudley, C. A., and Fawcett, C. P. (1977a). The specificity of the response of preoptic-septal area neurons to estrogen: 17α-Estradiol versus 17β-estradiol and the response of extrahypothalamie neurons. Exp. Brain Res. 30:43-52.
25. Kelly, M. J., Moss, R. L., and Dudley, C. A. (1977b). The effects of microelectrophoretically applied estrogen, cortisol and acetylcholine on medial preoptic-septal unit activity throughout the estrous cycle of the female rat. Exp. Brain Res. 30:53-64.
26. Kubli-Garfias, C. (1987). Modulatory action of 5-reduced androgens and progestins on the excitability of CNS and smooth muscle. J. Steroid Biochem. 27:631-634.
27. Laemmli, U. K. (1970). Cleavage of structural proteins during the assembly of the head of bacteriophage T4. Nature 227:680-685.
28. Lieberherr, M., Grosse, B., Kachkache, M., and Balsan, S. (1993). Cell signaling and estrogens in female rat osteoblasts: A possible involvement of unconventional nonnuclear receptors. J. Bone Mineral Res. 8:1365-1376.