Research Topics
Species | B AttardiSummaryAffiliation: BIOQUAL Inc Country: USA Publications
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Publications
Development of dimethandrolone 17beta-undecanoate (DMAU) as an oral male hormonal contraceptive: induction of infertility and recovery of fertility in adult male rabbitsBarbara J Attardi
Division of Reproductive Endocrinology and Toxicology, BIOQUAL Inc, 9600 Medical Center Dr, Rockville, MD 20850, USA
J Androl 32:530-40. 2011..Collectively, these data indicate that DMAU has the potential to be an orally active single-agent male hormonal contraceptive at an appropriate dose level and should be tested for contraceptive efficacy in nonhuman primates...
Long-term effects of dimethandrolone 17?-undecanoate and 11?-methyl-19-nortestosterone 17?-dodecylcarbonate on body composition, bone mineral density, serum gonadotropins, and androgenic/anabolic activity in castrated male ratsBarbara J Attardi
Molecular Endocrinology Laboratory, Division of Reproductive Endocrinology and Toxicology, BIOQUAL Inc, 9600 Medical Center Drive, Rockville, MD 20850, USA
J Androl 32:183-92. 2011..05). Collectively, our data indicate that androgen replacement with DMAU or 11?-MNTDC in Cx rats resulted in favorable changes in body composition and maintenance of BMD comparable to those of T...
The potent synthetic androgens, dimethandrolone (7?,11?-dimethyl-19-nortestosterone) and 11?-methyl-19-nortestosterone, do not require 5?-reduction to exert their maximal androgenic effectsBarbara J Attardi
Division of Reproductive Endocrinology and Toxicology, BIOQUAL, Inc, 9600 Medical Center Dr, Rockville, MD 20850, United States
J Steroid Biochem Mol Biol 122:212-8. 2010..These results indicate that inhibition of 5?-reductase activity in vivo does not affect the androgenic potency of DMA, MNT, or MENT...
Relative progestational and androgenic activity of four progestins used for male hormonal contraception assessed in vitro in relation to their ability to suppress LH secretion in the castrate male ratBarbara J Attardi
BIOQUAL, Inc Division of Reproductive Endocrinology and Toxicology, 9600 Medical Center Dr, Rockville, MD 20850, USA
Mol Cell Endocrinol 328:16-21. 2010..2mg/kg/day; and NES and CPA showed no or minimal LH suppression at doses up to 3.2mg/kg/day. We concluded, therefore, that suppression of LH is correlated with androgenic, rather than progestational, potency of the synthetic progestins...
Dimethandrolone undecanoate: a new potent orally active androgen with progestational activityBarbara J Attardi
Molecular Endocrinology Laboratory, BIOQUAL, Inc, Rockville, Maryland 20850, USA
Endocrinology 147:3016-26. 2006....
Facilitation or inhibition of the oestradiol-induced gonadotrophin surge in the immature female rat by progesterone: effects on pituitary responsiveness to gonadotrophin-releasing hormone (GnRH), GnRH self-priming and pituitary mRNAs for the progesterone B Attardi
Department of Neurobiology and Behavior, The Rockefeller University, New York, NY, USA
J Neuroendocrinol 19:988-1000. 2007..The differences between progesterone-facilitation and progesterone-inhibition are not due to differences in regulation of pituitary PR-B mRNA...
Dimethandrolone (7alpha,11beta-dimethyl-19-nortestosterone) and 11beta-methyl-19-nortestosterone are not converted to aromatic A-ring products in the presence of recombinant human aromataseBarbara J Attardi
Division of Reproductive Endocrinology and Toxicology, BIOQUAL Inc, 9600 Medical Center Drive, Rockville, MD 20850, USA
J Steroid Biochem Mol Biol 110:214-22. 2008....
Mechanism of action of bolandiol (19-nortestosterone-3beta,17beta-diol), a unique anabolic steroid with androgenic, estrogenic, and progestational activitiesBarbara J Attardi
BIOQUAL, Inc, 9600 Medical Center Dr, Rockville, MD 20850, USA
J Steroid Biochem Mol Biol 118:151-61. 2010..As bolandiol exhibits tissue selectivity in vivo, it may act via AR, PR, and/or ER, utilize alternative signaling pathway(s) or transcriptional coregulators, and/or be metabolized to a more potent selective steroid...
Mechanism of action of l-CDB-4022, a potential nonhormonal male contraceptive, in the seminiferous epithelium of the rat testisSailaja Koduri
Division of Reproductive Endocrinology and Toxicology, BIOQUAL Inc, 9600 Medical Center Drive, Rockville, MD 20850 3336, USA
Endocrinology 149:1850-60. 2008....
CDB-4124 and its putative monodemethylated metabolite, CDB-4453, are potent antiprogestins with reduced antiglucocorticoid activity: in vitro comparison to mifepristone and CDB-2914Barbara J Attardi
Molecular Endocrinology Laboratory, BIOQUAL, Inc, 9600 Medical Center Drive, Rockville, MD 20850, USA
Mol Cell Endocrinol 188:111-23. 2002..In agreement with our in vivo results, CDB-4124 and CDB-4453, as well as CDB-2914, are potent antiprogestins in vitro, but show considerably less antiglucocorticoid activity than mifepristone...
Development of l-CDB-4022 as a nonsteroidal male oral contraceptive: induction and recovery from severe oligospermia in the adult male cynomolgus monkey (Macaca fascicularis)Sheri Ann Hild
Division of Reproductive Endocrinology and Toxicology, BIOQUAL, Inc, 9600 Medical Center Drive, Rockville, Maryland 20850, USA
Endocrinology 148:1784-96. 2007....
Steroid hormonal regulation of growth, prostate specific antigen secretion, and transcription mediated by the mutated androgen receptor in CWR22Rv1 human prostate carcinoma cellsBarbara J Attardi
Molecular Endocrinology Laboratory, BIOQUAL Inc, 9600 Medical Center Drive, Rockville, MD 20850, USA
Mol Cell Endocrinol 222:121-32. 2004....
In vitro antiprogestational/antiglucocorticoid activity and progestin and glucocorticoid receptor binding of the putative metabolites and synthetic derivatives of CDB-2914, CDB-4124, and mifepristoneBarbara J Attardi
Molecular Endocrinology Laboratory, BIOQUAL Inc, 9600 Medical Center Drive, Rockville, MD 20850, USA
J Steroid Biochem Mol Biol 88:277-88. 2004..Furthermore, the reduced antiglucocorticoid activity of CDB-2914 and CDB-4124 compared to mifepristone in vivo may be due in part to decreased activity of their putative proximal metabolites...
The ability of a gonadotropin-releasing hormone antagonist, acyline, to prevent irreversible infertility induced by the indenopyridine, CDB-4022, in adult male rats: the role of testosteroneSheri Ann Hild
BIOQUAL, Inc, Rockville, Maryland 20850, USA
Biol Reprod 71:348-58. 2004..Continued development of CDB-4022 as a potential male contraceptive will depend largely on its safety profile and whether its antispermatogenic activity is reversible in primates...
Comparison of progesterone and glucocorticoid receptor binding and stimulation of gene expression by progesterone, 17-alpha hydroxyprogesterone caproate, and related progestinsBarbara J Attardi
Molecular Endocrinology Laboratory, BIOQUAL, Inc, Rockville, MD, USA
Am J Obstet Gynecol 197:599.e1-7. 2007....
