Summary: ESP22, a substance found in a baby’s tears, makes female mice more likely to reject male sexual advances, researchers report.
Source: University of Tokyo.
A substance in young mice’s tears makes female mice more likely to reject male sexual advances. This research is part of ongoing efforts at the University of Tokyo to understand how animals communicate using chemicals called pheromones.
A new study in flies finds that alcohol hijacks this memory Direct connections between human and mouse behavior cannot be made because pheromones are highly species specific.
“If humans can detect anything in tears, we won’t use the same pheromone signal or receptor as mice. But we are investigating if species share the basic neurocircuitry of how the brain processes an olfactory signal to affect behavior,” said Professor Kazushige Touhara, leader of the research project.
Pheromone population control
Researchers hope to use the tear pheromone as a natural mouse birth control to reduce mouse populations in the future.
“It is unlikely that other animals would be affected because pheromones are so species specific. The sex-rejecting behavior is an innate instinct, so it’s also unlikely that the mice will learn to change their behavior or ignore the artificial pheromone,” said Touhara.
Only juvenile mice aged one to three weeks produce the pheromone, called exocrine gland-secreting peptide 22 (ESP22). ESP22 is not airborne and lacks a noticeable odor, but the pheromone spreads around the territory as mothers and young mice wipe tears while grooming.
Both mothers and virgin female mice reject male sexual advances after exposure to ESP22. Less female interest in sex would theoretically benefit juvenile mice by reducing the number of younger siblings competing for resources.
“ESP22 is difficult to artificially synthesize, so we want to find a smaller portion of the pheromone molecule that could be added to mouse drinking water. This could prevent mice breeding in areas where they are pests,” said Touhara.
ESP1 is an adult male pheromone that Touhara’s research group has previously studied for its role in enhancing female acceptance of sex. In this new study, researchers tracked how ESP22 and ESP1 are received and processed by the adult female mouse brain.
Pheromone signals from young mice overrode the signals from adult males. Virgin female mice rejected male advances when they were exposed to the sex-rejecting ESP22 even after being exposed to the sex-accepting ESP1.
Both sex-rejecting ESP22 and sex-accepting ESP1 pheromones are recognized by single, dedicated receptors in the nose. Specific neurons send the different pheromone signals to the brain. The presence of similar but specific ESP1 and ESP22 receptors helps reveal how animals evolved the ability to detect and interpret pheromone signals.
“The discovery of only one receptor for each pheromone shows us that single molecules can drastically affect animal behavior,” said Touhara.
Pheromones in the brain
Pheromone signals are routed to the medial amygdala, a small group of neurons in the brain.
“The medial amygdala is like a hub to receive and reroute pheromone signals,” said Kentaro Ishii, a co-first author of the research paper and fifth-year doctoral student working with Touhara.
ESP22 and ESP1 signals travel separately but in parallel until reaching the medial amygdala. After that point, the pheromones affect different neurocircuitry in the brain to create different behaviors. Ongoing research in the laboratory will explore pheromone-related neurocircuitry beyond the medial amygdala hub.
“The medial amygdala is still very mysterious, so we are excited to discover more details about how pheromone signals are sorted and routed after they are received there,” said Ishii.
“Additionally, we want to understand the complexity of how the brain computes and sorts olfactory signals in a natural environment, where animals are simultaneously exposed to many different pheromones and other chemical signals all the time,” said Ishii.
About this neuroscience research article
Funding: Japan Society for the Promotion of Science, ERATO Touhara Chemosensory Signal Project, National Institutes of Health funded the research.
Source: Kazushige Touhara – University of Tokyo Publisher: Organized by NeuroscienceNews.com. Image Source: NeuroscienceNews.com image is in the public domain. Original Research: Open access research for “Sexual rejection via a vomeronasal receptor-triggered limbic circuit” by Takuya Osakada, Kentaro K. Ishii, Hiromi Mori, Ryo Eguchi, David M. Ferrero, Yoshihiro Yoshihara, Stephen D. Liberles, Kazunari Miyamichi & Kazushige Touhara in Nature Communications. Published October 26 2018. doi:10.1038/s41467-018-07003-5
Cite This NeuroscienceNews.com Article
[cbtabs][cbtab title=”MLA”]University of Tokyo”Substance in Baby Tears Reduces Mom’s Interest in Sex: Mouse Study.” NeuroscienceNews. NeuroscienceNews, 26 October 2018. <https://neurosciencenews.com/baby-tears-mom-libido-10092/>.[/cbtab][cbtab title=”APA”]University of Tokyo(2018, October 26). Substance in Baby Tears Reduces Mom’s Interest in Sex: Mouse Study. NeuroscienceNews. Retrieved October 26, 2018 from https://neurosciencenews.com/baby-tears-mom-libido-10092/[/cbtab][cbtab title=”Chicago”]University of Tokyo”Substance in Baby Tears Reduces Mom’s Interest in Sex: Mouse Study.” https://neurosciencenews.com/baby-tears-mom-libido-10092/ (accessed October 26, 2018).[/cbtab][/cbtabs]
Sexual rejection via a vomeronasal receptor-triggered limbic circuit
Mating drive is balanced by a need to safeguard resources for offspring, yet the neural basis for negative regulation of mating remains poorly understood. In rodents, pheromones critically regulate sexual behavior. Here, we observe suppression of adult female sexual behavior in mice by exocrine gland-secreting peptide 22 (ESP22), a lacrimal protein from juvenile mice. ESP22 activates a dedicated vomeronasal receptor, V2Rp4, and V2Rp4 knockout eliminates ESP22 effects on sexual behavior. Genetic tracing of ESP22-responsive neural circuits reveals a critical limbic system connection that inhibits reproductive behavior. Furthermore, V2Rp4 counteracts a highly related vomeronasal receptor, V2Rp5, that detects the male sex pheromone ESP1. Interestingly, V2Rp4 and V2Rp5 are encoded by adjacent genes, yet couple to distinct circuits and mediate opposing effects on female sexual behavior. Collectively, our study reveals molecular and neural mechanisms underlying pheromone-mediated sexual rejection, and more generally, how inputs are routed through olfactory circuits to evoke specific behaviors.