Summary: A new study reports reducing the strength of communication between the amygdala and prefrontal cortex helps reduce fear levels in mice.
Source: Weizmann Institute of Science.
Weakening communication between two parts of the brain in mice reduced their fear levels.
Erasing unwanted memories is still the stuff of science fiction, but Weizmann Institute scientists have now managed to erase one type of memory in mice. In a study reported in Nature Neuroscience, they succeeded in shutting down a neuronal mechanism by which memories of fear are formed in the mouse brain. After the procedure, the mice resumed their earlier fearless behavior, “forgetting” they had previously been frightened.
This research may one day help extinguish traumatic memories in humans – for example, in people with post-traumatic stress disorder, or PTSD. “The brain is good at creating new memories when these are associated with strong emotional experiences, such as intense pleasure or fear,” says team leader Dr. Ofer Yizhar. “That’s why it’s easier to remember things you care about, be they good or bad; but it’s also the reason that memories of traumatic experiences are often extremely long-lasting, predisposing people to PTSD.”
In the study, postdoctoral fellows Dr. Oded Klavir (now an investigator at the University of Haifa) and Dr. Matthias Prigge, both from Yizhar’s lab in the Neurobiology Department, together with departmental colleague Prof. Rony Paz and graduate student Ayelet Sarel, examined the communication between two brain regions: the amygdala and the prefrontal cortex. The amygdala plays a central role in controlling emotions, whereas the prefrontal cortex is mostly responsible for cognitive functions and storing long-term memories. Previous studies had suggested that the interactions between these two brain regions contribute to the formation and storage of aversive memories, and that these interactions are compromised in PTSD; but the exact mechanisms behind these processes were unknown.
In the new study, the researchers first used a genetically-engineered virus to mark those amygdala neurons that communicate with the prefrontal cortex. Next, using another virus, they inserted a gene encoding a light-sensitive protein into these neurons. When they shone a light on the brain, only the neurons containing the light-sensitive proteins became activated. These manipulations, belonging to optogenetics – a technique extensively studied in Yizhar’s lab – enabled the researchers to activate only those amygdala neurons that interact with the cortex, and then to map out the cortical neurons that receive input from these light-sensitive neurons.
Once they had achieved this precise control over the cellular interactions in the brain, they turned to exploring behavior: Mice that are less fearful are more likely to venture farther than others. They found that when the mice were exposed to fear-inducing stimuli, a powerful line of communication was activated between the amygdala and the cortex. The mice whose brains displayed such communication were more likely to retain a memory of the fear, acting frightened every time they heard the sound that had previously been accompanied by the fear-inducing stimuli. Finally, to clarify how this line of communication contributes to the formation and stability of memory, the scientists developed an innovative optogenetic technique for weakening the connection between the amygdala and the cortex, using a series of repeated light pulses. Indeed, once the connection was weakened, the mice no longer displayed fear upon hearing the sound. Evidently, “tuning down” the input from the amygdala to the cortex had destabilized or perhaps even destroyed their memory of fear.
Says Yizhar: “Our research has focused on a fundamental question in neuroscience: How does the brain integrate emotion into memory? But one day our findings may help develop better therapies targeting the connections between the amygdala and the prefrontal cortex, in order to alleviate the symptoms of fear and anxiety disorders.”
About this PTSD research article
Funding: Dr. Ofer Yizhar’s research is supported by Jean-Charles Schwartz and Marc – Antoine Schwartz; the Adelis Foundation; the Candice Appleton Family Trust; Paul and Lucie Schwartz, Georges; and the Vera Gersen Laboratory. Dr. Yizhar is the incumbent of the Gertrude and Philip Nollman Career Development Chair.
Source: Gizel Maimon – Weizmann Institute of Science Image Source: NeuroscienceNews.com image is credited to Weizmann Institute of Science. Original Research: Abstract for “Manipulating fear associations via optogenetic modulation of amygdala inputs to prefrontal cortex” by Oded Klavir, Matthias Prigge, Ayelet Sarel, Rony Paz & Ofer Yizhar in Nature Neuroscience. Published online March 13 2017 doi:10.1038/nn.4523
Cite This NeuroscienceNews.com Article
[cbtabs][cbtab title=”MLA”]Weizmann Institute of Science “Turning Down the Brain to Erase Fearful Memories: Mouse Study.” NeuroscienceNews. NeuroscienceNews, 10 April 2017. <https://neurosciencenews.com/otogenetics-fear-ptsd-6371/>.[/cbtab][cbtab title=”APA”]Weizmann Institute of Science (2017, April 10). Turning Down the Brain to Erase Fearful Memories: Mouse Study. NeuroscienceNew. Retrieved April 10, 2017 from https://neurosciencenews.com/otogenetics-fear-ptsd-6371/[/cbtab][cbtab title=”Chicago”]Weizmann Institute of Science “Turning Down the Brain to Erase Fearful Memories: Mouse Study.” https://neurosciencenews.com/otogenetics-fear-ptsd-6371/ (accessed April 10, 2017).[/cbtab][/cbtabs]
Manipulating fear associations via optogenetic modulation of amygdala inputs to prefrontal cortex
Fear-related disorders are thought to reflect strong and persistent fear memories. The basolateral amygdala (BLA) and the medial prefrontal cortex (mPFC) form strong reciprocal synaptic connections that play a key role in acquisition and extinction of fear memories. While synaptic contacts of BLA cells onto mPFC neurons are likely to play a crucial role in this process, the BLA connects with several additional nuclei within the fear circuit that could relay fear-associated information to the mPFC, and the contribution of direct monosynaptic BLA–mPFC inputs is not yet clear. Here we establish an optogenetic stimulation protocol that induces synaptic depression in BLA–mPFC synapses. In behaving mice, optogenetic high-frequency stimulation of BLA inputs to mPFC interfered with retention of cued associations, attenuated previously acquired cue-associated responses in mPFC neurons and facilitated extinction. Our findings demonstrate the contribution of BLA inputs to mPFC in forming and maintaining cued fear associations.
“Manipulating fear associations via optogenetic modulation of amygdala inputs to prefrontal cortex” by Oded Klavir, Matthias Prigge, Ayelet Sarel, Rony Paz & Ofer Yizhar in Nature Neuroscience. Published online March 13 2017 doi:10.1038/nn.4523