USC (US) — Learned fear keeps us from repeating risky mistakes, but it can also backfire. A brain protein linked to autism spectrum disorders could be the culprit.
New research from neuroscientists and molecular biologists looks into severe over-worry, in which the fear perseveres even when there’s nothing to be afraid of.
In a study appearing this week in the Proceedings of the National Academy of Sciences, the researchers examined mice without the enzymes monoamine oxidase A and B (MAO A/B), which sit next to each other in our genetic code as well as on that of mice.
Prior research has found an association between deficiencies of these enzymes in humans and developmental disabilities along the autism spectrum such as clinical perseverance—the inability to change or modulate actions along with social context.
“These mice may serve as an interesting model to develop interventions to these neuropsychiatric disorders,” says senior author Jean C. Shih, professor of pharmacology and pharmaceutical sciences at the School of Pharmacy and the Keck School of Medicine at University of Southern California (USC).
“The severity of the changes in the MAO A/B knockout mice compared to MAO A knockout mice supports the idea that the severity of autistic-like features may be correlated to the amounts of monoamine levels, particularly at early developmental stages.”
Shih’s work looks at the neurobiological and biochemical mechanisms behind such behaviors as aggression and anxiety. In this latest study, Shih and her co-investigators expand their past research on MAO A/B, which regulates neurotransmitters known as monoamines, including serotonin, norepinephrine, and dopamine.
New context, same fear
Comparing mice without MAO A/B with their wild-type littermates, the researchers found significant differences in how the mice without MAO A/B processed fear and other types of learning. Mice without MAO A/B and wild mice were put in a new, neutral environment and given a mild electric shock.
All mice showed learned fear the next time they were tested in the same environment, with the MAO A/B knockout mice displaying a greater degree of fear.
But while wild mice continued to explore other new environments freely after the trauma, mice without the MAO A/B enzymes generalized their phobia to other contexts—their fear spilled over onto places where they should have no reason to be afraid.
“The neural substrates processing fear in the brain is very different in these mice,” says lead author Chanpreet Singh, a former USC doctoral student who is now at California Institute of Technology (Caltech).
“Enhanced learning in the wrong context is a disorder and is exemplified by these mice. Their brain is not letting them forget. In a survival issue, you need to be able to forget things.”
The mice without MAO A and MAO B also learned eye-blink conditioning much more quickly than wild mice, which has also been noted in autistic patients but not in mice missing only one of these enzymes.
Types of learning
Importantly, the mice without MAO A/B did not display any differences in learning for spatial skills and object recognition, the researchers found, “but in their ability to learn an emotional event, the [MAO A/B knockout mice] are very different than wild types,” Singh says.
He continues: “When both enzymes are missing, it significantly increases the levels of neurotransmitters, which causes developmental changes, which leads to differential expression of receptors that are very important for synaptic plasticity—a measure of learning—and to behavior that is quite similar to what we see along the autism spectrum.”
The National Institute of Mental Health of the National Institutes of Health and the Eunice Kennedy Shriver National Institute of Child Health and Human Development of the National Institutes of Health supported the research. Additional co-authors contributed from the University of Kansas, Caltech, and USC.