Summary: Mouse study identifies specific neurons and a signaling pathway to regions of the hindbrain that mediate sexual reproductive activity and physical activity that appear to influence activity behaviors during ovulation. The findings may provide valuable insights into how estrogen loss during menopause disrupts this activity.
Scientists have known for a century that female animals become more active just as they are about to ovulate, a behavior that evolved to enhance their chances of mating when they are fertile.
Now, a team at UC San Francisco has identified the specific neurons and signaling pathway that make sexually receptive females of many species run around at this critical time. The work was done in mice, but researchers expect it will bear out in humans, since the behavior is related to such a fundamental aspect of life.
“Why do you want to get up and move?” asked Holly Ingraham, PhD, the Herzstein Professor of Molecular Physiology at UCSF and senior author of the study published in Nature. “Well, if you activate the circuit in these neurons, maybe that’s why.”
The discovery also illuminates what happens in menopause as the loss of estrogen disrupts this activity circuit, and both mouse and human females become more sedentary, gain weight, and develop metabolic disorders like type 2 diabetes. And it offers the possibility of a new kind of treatment for menopause that sidesteps estrogen and reactivates the circuit with CRISPRa technology.
“As we discover what estrogen does in the brain, we’re probably going to discover more of its benefits,” Ingraham said. “This is just one area in the brain, and it has a powerful effect. We’d also like to know more about other circuits in the brain that affect well-being and cognition.”
When estrogen bathes the brain, it interacts with estrogen receptor α (ERα) to activate a gene called Mc4r. This produces melanocortin-4 receptors (MC4R) on the surface of estrogen-sensitive neurons in a part of the brain called the ventrolateral ventromedial hypothalamic nucleus (VMHvl) that regulates how energy is used in adult females.
The study team created a precise map of where proteins attach to DNA, using technology established in the living mouse brain by co-senior author Jessica Tollkuhn, PhD, an assistant professor at Cold Spring Harbor Laboratory in New York. The technique, called CUT&RUN or cleavage under targets and release using nuclease, identified two sites where ERα binds to Mc4r to regulate its activity, thus establishing a clear link between the hormone receptor and the gene.
To their surprise, the team also discovered that the VMHvl neurons activated by this circuit project into a part of the hippocampus equipped with “speed cells” that control how fast the mouse moves. The neurons also project into a region of the hindbrain that mediates sexual receptivity and physical activity.
The gene at the center of this circuit, Mc4r, is well known for its role in regulating energy, appetite, and weight in adult females, and mutated forms of the gene cause obesity that are particularly severe in women.
The MC4R receptor is also the target of bremelanotide, which is marketed under the brand name Vyleesi to treat a condition called acquired, generalized hypoactive sexual desire disorder (HSDD) in premenopausal women.
To be sure the neurons really were making the mice more active, the researchers used a chemogenetic technique called DREADDs (Designer Receptors Exclusively Activated by Designer Drugs) to make the VMHvl neurons express a receptor that could only be activated by a harmless chemical added to their water.
When their VMHvl neurons were stimulated that way, both male and female mice became more active, and the females lost nearly 10 percent of their body weight after 24-hours of continuous administration. Inhibiting these neurons had the opposite effect, making females more sedentary.
The same thing happened in female mice that lacked ovaries and had been put on a high-fat diet. A single instance of DREADD stimulation reversed the harmful metabolic effects of both estrogen depletion and diet-induced obesity. Long-term administration caused obese mice to slim down dramatically, and it improved their overall metabolic health.
The team also used CRISPRa, a technique that upregulates gene expression without changing the gene itself, to increase the activity of Mc4r. Both male and female mice became more active, but the effects were stronger in females, and their bones grew thicker. They did not lose weight, however, most likely because they also ate more.
“These data are exciting not only because they highlight the key role of Mc4r in these activity-promoting neurons, but because they also suggest how gene therapy tools might be adapted to target advantageous factors downstream of estrogen signaling,” said first author William Krause, PhD, a researcher in the Department of Cellular and Molecular Pharmacology at UCSF.
The beneficial results add to the debate over hormone replacement therapy for symptoms of menopause. Many doctors stopped prescribing it after an influential 2002 study found it slightly increased the risk of endometrial and breast cancer, as well as blood clots and stroke.
But Ingraham said it’s worth another look.
“Estrogen has a profound effect on behavior and can make a difference to your well-being,” she said. “Let’s at least find out what it’s doing, so maybe we can bypass it and get those positive effects of estrogen another way, by another drug, another target. Until we have that, women are just stuck with, ‘You’re not going to have what makes you feel better.’ That’s why I’m so passionate about this research.”
Other authors of the study include Ruben Rodriguez, Navneet Matharu, Andreas N. Rodriguez, Adriana M. Padilla-Roger, Kenichi Toma, Candice B. Herber, Stephanie M. Correa, Xin Duan, and Nadav Ahituv, all of UCSF; and Bruno Gegenhuber, of Cold Spring Harbor Laboratory School of Biological Sciences.
About this neuroscience and reproduction research news
Author: Laura Kurtzman Source: UCSF Contact: Laura Kurtzman – UCSF Image: The image is in the public domain
Oestrogen engages brain MC4R signalling to drive physical activity in female mice
Oestrogen depletion in rodents and humans leads to inactivity, fat accumulation and diabetes, underscoring the conserved metabolic benefits of oestrogen that inevitably decrease with age. In rodents, the preovulatory surge in 17β-oestradiol (E2) temporarily increases energy expenditure to coordinate increased physical activity with peak sexual receptivity.
Here we report that a subset of oestrogen-sensitive neurons in the ventrolateral ventromedial hypothalamic nucleus (VMHvl) projects to arousal centres in the hippocampus and hindbrain, and enables oestrogen to rebalance energy allocation in female mice. Surges in E2 increase melanocortin-4 receptor (MC4R) signalling in these VMHvl neurons by directly recruiting oestrogen receptor-α (ERα) to the Mc4r gene. Sedentary behaviour and obesity in oestrogen-depleted female mice were reversed after chemogenetic stimulation of VMHvl neurons expressing both MC4R and ERα. Similarly, a long-term increase in physical activity is observed after CRISPR-mediated activation of this node.
These data extend the effect of MC4R signalling — the most common cause of monogenic human obesity — beyond the regulation of food intake and rationalize reported sex differences in melanocortin signalling, including greater disease severity of MC4R insufficiency in women.
This hormone-dependent node illuminates the power of oestrogen during the reproductive cycle in motivating behaviour and maintaining an active lifestyle in women.