US study of mice finds alternative to condoms and vasectomies
Salk Institute scientists discover new target for reversible, non-hormonal male birth control
Women who want to control their reproduction generally complain that they, and not men, are responsible for avoiding pregnancy, except when males use condoms or undergo invasive vasectomy surgery.
With unintended pregnancies costing billions of dollars a year in the US alone and the growing limits on abortion, the socioeconomic and health benefits of improved birth control are very important to many couples.
Ironically, surveys show that most American men are interested in using male contraceptives, yet they have almost no options. Recent attempts to develop drugs that block sperm production, maturation, or fertilization have had limited success, providing incomplete protection or severe side effects. New approaches to male contraception are needed, but because sperm development is so complex, researchers have struggled to identify parts of the process that can be safely and effectively tinkered with.
Now, scientists at the Salk Institute in California have found a new method of interrupting sperm production that is both non-hormonal and reversible. The study, just published in Proceedings of the National Academy of Sciences under the title “Targeting nuclear receptor corepressors for reversible male contraception,” has found a new protein complex in regulating gene expression during sperm production.
The researchers demonstrate that treating male mice with an existing class of drugs called HDAC (histone deacetylase) inhibitors can interrupt the function of this protein complex and block fertility without affecting libido.
“Most experimental male birth control drugs use a hammer approach to blocking sperm production, but ours is much more subtle,” said senior author Prof. Ronald Evans, director of the Gene Expression Laboratory, and head of molecular and developmental biology at Salk. “This makes it a promising therapeutic approach, which we hope to see in development for human clinical trials soon.”
A MAN’S body produces several million new sperm per day. To do this, sperm stem cells in the testes continuously make more of themselves until a signal tells them it’s time to turn into sperm – a process called spermatogenesis. This signal comes in the form of retinoic acid, a product of vitamin A. Pulses of retinoic acid bind to retinoic acid receptors in the cells, and when the system is positioned just right, this initiates a complex genetic program that turns the stem cells into mature sperm.
Salk scientists found that for this to work, retinoic acid receptors must bind with a protein called SMRT (Silencing Mediator of Retinoid and Thyroid hormone receptors) that then recruits HDACs; this complex of proteins then goes on to synchronize the expression of genes that produce sperm.
Previous groups have tried to stop sperm production by directly blocking retinoic acid or its receptor, but this acid is important to several systems in the body, so interrupting it throughout the body can lead to various side effects. This is the reason why many previous studies and trials have failed to produce a viable drug.
Evans and his colleagues instead asked whether they could modulate one of the molecules downstream of retinoic acid to produce a more targeted effect.
The researchers first looked at a line of genetically engineered lab mice that had previously been developed in which the SMRT protein was mutated and could no longer bind to retinoic acid receptors. Without this SMRT-retinoic acid receptor interaction, the mice weren’t able to produce mature sperm, but they displayed normal testosterone levels and mounting behavior, indicating that their desire to mate was not affected.
To see whether they could replicate these genetic results with pharmacological intervention, the researchers treated normal mice with MS-275, an oral HDAC inhibitor with FDA breakthrough status. By blocking the activity of the SMRT-retinoic acid receptor-HDAC complex, the drug successfully stopped sperm production without producing obvious side effects.
ANOTHER REMARKABLE thing also happened once the treatment was stopped: within 60 days of going off the pill, the animals’ fertility was completely restored, and all subsequent offspring were developmentally healthy. The researchers said their strategy of inhibiting molecules downstream of retinoic acid is key to achieving this reversibility.
“Think of retinoic acid and the sperm-producing genes as two dancers in a waltz. Their rhythm and steps need to be coordinated with each other for the dance to work,” they said. But if you throw something in that makes the genes miss a step, the two are suddenly out of sync and the dance falls apart. In this case, the HDAC inhibitor causes the genes’ misstep, halting the dance of sperm production.”
However, if the dancer can find its footing and get back in step with its partner, the waltz can resume. In the same way, the authors say that removing the HDAC inhibitor allows the sperm-producing genes to get back in sync with the pulses of retinoic acid, turning sperm production back on as desired.
“It’s all about timing,” says co-author Michael Downes, a senior staff scientist in Evans’ lab. “When we add the drug, the stem cells fall out of sync with the pulses of retinoic acid, and sperm production is halted, but as soon as we take the drug away, the stem cells can reestablish their coordination with retinoic acid and sperm production will start up again.”
The authors say the drug doesn’t damage the sperm stem cells or their genomic integrity. While the drug was present, the sperm stem cells simply continued regenerating as stem cells, and when the drug was later removed, the cells could regain their ability to differentiate into mature sperm.
“We weren’t necessarily looking to develop male contraceptives when we discovered SMRT and generated this mouse line, but when we saw that their fertility was interrupted, we were able to follow the science and discover a potential therapeutic,” concluded first author Suk-Hyun Hong, a staff researcher in Evans’ lab. “It’s a great example of how Salk’s foundational biological research can lead to major translational impact.”