The prodrug DHED selectively delivers 17β-estradiol to the brain for treating estrogen-responsive disorders.

Abstract

Many neurological and psychiatric maladies originate from the deprivation of the human brain from estrogens. However, current hormone therapies cannot be used safely to treat these conditions commonly associated with menopause because of detrimental side effects in the periphery. The latter also prevents the use of the hormone for neuroprotection. We show that a small-molecule bioprecursor prodrug, 10β,17β-dihydroxyestra-1,4-dien-3-one (DHED), converts to 17β-estradiol in the brain after systemic administration but remains inert in the rest of the body. The localized and rapid formation of estrogen from the prodrug was revealed by a series of in vivo bioanalytical assays and through in vivo imaging in rodents. DHED treatment efficiently alleviated symptoms that originated from brain estrogen deficiency in animal models of surgical menopause and provided neuroprotection in a rat stroke model. Concomitantly, we determined that 17β-estradiol formed in the brain from DHED elicited changes in gene expression and neuronal morphology identical to those obtained after direct 17β-estradiol treatment. Together, complementary functional and mechanistic data show that our approach is highly relevant therapeutically, because administration of the prodrug selectively produces estrogen in the brain independently from the route of administration and treatment regimen. Therefore, peripheral responses associated with the use of systemic estrogens, such as stimulation of the uterus and estrogen-responsive tumor growth, were absent. Collectively, our brain-selective prodrug approach may safely provide estrogen neuroprotection and medicate neurological and psychiatric symptoms developing from estrogen deficiency, particularly those encountered after surgical menopause, without the adverse side effects of current hormone therapies.

• Authors: Laszlo Prokai, Vien Nguyen, Szabolcs Szarka, Puja Garg, Gauri Sabnis, Heather A Bimonte-Nelson, Katie J McLaughlin, Joshua S Talboom, Cheryl D Conrad, Paul J Shughrue, Todd D Gould, Angela Brodie, Istvan Merchenthaler, Peter Koulen, Katalin Prokai-Tatrai
• Journal: Science translational medicine (Sci Transl Med) Vol. 7 Issue 297 Pg. 297ra113 (Jul 22 2015) ISSN: 1946-6242 [Electronic] United States
• PMID: 26203081 (Publication Type: Journal Article)
• Copyright: Copyright © 2015, American Association for the Advancement of Science.

Chemical References

• Androstenediols
• Antidepressive Agents
• Biomarkers
• Estrogens
• Prodrugs
• 3,16-dihydroxyandrost-5-ene-17,19-dione
• Estradiol

Topics

• Androstenediols (pharmacology, therapeutic use)
• Animals
• Antidepressive Agents (pharmacology, therapeutic use)
• Biomarkers (metabolism)
• Brain (drug effects, metabolism)
• Brain Ischemia (complications, drug therapy)
• Breast Neoplasms (drug therapy, pathology)
• Cell Proliferation (drug effects)
• Disease Models, Animal
• Estradiol (chemistry, metabolism)
• Estrogens (chemistry, metabolism)
• Female
• Humans
• MCF-7 Cells
• Neuroprotection (drug effects)
• Prodrugs (metabolism, pharmacology)
• Stroke (complications, drug therapy)
• Uterus (drug effects)