Scientists at the Weizmann Institute prevented the onset of eating disorders through dietary intervention

Stressed Out from Birth

Humans are exposed to stress at different intensities throughout life but many researchers maintain that the critical effect of stress occurs prenatally, inside the womb.

Stress affects the body and can trigger illness – from psychiatric disorders to heart disease. Humans are exposed to stress at different intensities throughout life: as children, in adolescence, and in old age. But when is the impact of stress on our systems most powerful? Many researchers maintain that the critical effect occurs prenatally, inside the womb. This hypothesis was, until recently, based mainly on statistical data indicating a correlation between stress during pregnancy and susceptibility to disease. Now, Weizmann Institute of Science research, published in the journal Cell Metabolism, establishes, for the first time, a clear causal link between prenatal stress and the onset of eating disorders. Furthermore, in a study in mice, researchers successfully prevented the onset of a compulsive eating disorder by the sole means of a unique diet.

Moderate exposure to stress during pregnancy is not necessarily negative. The effect of stress on the fetus makes evolutionary sense with regard to survival – by providing mothers with a way to communicate with her unborn offspring about the world into which they are about to emerge. For example, when the mother inhabits an area of poor food availability, she would want to prompt the embryo to develop its body in an efficient and frugal manner and slow down its metabolic rate. Such maternal messages transmitted to the embryo are also termed fetal programming. Problems arise when the programming does not match actual conditions and demands; for example, a child who is programmed to slow their metabolism down, but is actually born into a culture with an abundance of high-calorie foods, may develop obesity and metabolic syndrome.

Eating disorders are currently more prevalent in the West than ever before, and are significantly higher among women than men. Binge eating disorder (BED), characterized by the compulsive overeating of high-calorie foods in short periods of time, is a common eating disorder, affecting about three percent of the population. BED usually erupts in late adolescence and greatly increases the risk of high blood pressure, diabetes, and heart disease – and also involves depression, low self-esteem, and anxiety disorders.

While a common tendency is to link eating disorders among girls and women to body images presented in Western pop culture, the new study shows that the high incidence of eating disorders among females is also seen in a model that simulates eating disorders in mice. In other words, eating disorders are more common in females in mice, too.

But why do some girls face an increased risk of developing an eating disorder while others do not, and how is this sensitivity influenced by processes that took place prenatally?

To investigate these and other questions, Prof. Alon Chen and his team in the Department of Neurobiology used a genetic system they developed to simulate the biological stress mechanisms in mice. The researchers injected antibiotic-susceptible viruses into the brains of pregnant mice, and, in the third and final week of pregnancy, added antibiotics to their drinking water in order to activate the system and cause the release of the stress hormone CRF [corticotrophin-releasing factor]. The pregnancies ended a week afterward, with the pups born into a favorable environment. Only some 10 weeks later, after they matured, were they nutritionally challenged in order to put their sensitivity to developing compulsive eating to the test: the mice were fed a “Western” diet, high in caloric value, over very short periods, which could trigger an impulse to binge eat.

The findings were clear: females born to mothers exposed to stress during pregnancy tended to develop a compulsive eating disorder following exposure to the environmental challenge.

The study was led by postdoctoral fellow Dr. Mariana Schroeder, with the participation of Drs. Maya Sharon Lebow, Yonat Drori, and Mira Jakovcevski; research students Tamar Polacheck and Mareen Engel; and Dr. Shifra Ben-Dor from the Department of Life Sciences Core Facilities.

Beyond identifying the link between stress during pregnancy and compulsive eating disorder, the research team sought to understand and uncover the mechanisms that programmed the brains of females who tended to develop an eating disorder. They repeated the experiment, but instead of waiting for the offspring to reach adulthood, they examined the embryonic brain prenatally. Says Prof. Chen: “We discovered a very interesting thing: looking at embryos’ brains, we saw large molecular differences between offspring whose mothers’ stress mechanism was activated and those in whose mothers it was not activated. However, in adulthood, the differences disappear. The differences will be expressed only when the mice are exposed to some form of challenge. This signifies that an epigenetic, rather than a genetic, marker was introduced at the embryonic stage as there was no change in the genes.”

Epigenetics (literally: on top of genetics) research addresses the molecular mechanisms that mediate environmental messages, and how these messages influence and shape the expression of our genome – without changing the DNA sequence or the genes themselves. In this case, messages that originated in the mother caused changes in the brains of the female embryos.

One of the most important epigenetic mechanisms is DNA methylation, a simple biochemical process in which a methyl group binds to a genetic segment, thereby determining the transcription level of a particular gene. In this research, the Weizmann scientists have shown, for the first time, that exposure to stress is expressed in sub-methylation in the hypothalamus, a brain region that regulates metabolic processes, hormone production, and stress reactions.

A methyl-balanced diet

But the most surprising part of the study lay ahead. The researchers found that by administering a diet of foods that affect the body’s methylation processes, such as folic acid, choline, methionine, and vitamins B12 and B6, they could prevent the ”predisposed” mice from developing a compulsive eating disorder.

“Perhaps the most unexpected finding in the study,” says Prof. Chen, “is that we succeeded in preventing the disorder from emerging simply by providing a balanced diet of methyl sources. Does this mean that a balanced diet would also help cure eating disorders in humans? It is important to note that the research was conducted on a mouse model at this stage, but all the biological genes and pathways it described are shared by mice and humans.”

Prof. Alon Chen’s research is supported by the Carl and Micaela Einhorn-Dominic Center for Brain Research, which he heads; the Nella and Leon Benoziyo Center for Neurosciences, which he heads; the Norman and Helen Asher Center for Brain Imaging, which he heads; the Perlman Family Foundation, Founded by Louis L. and Anita M. Perlman; the Irving Bieber, M.D. and Toby Bieber, M.D. Memorial Research Fund; the Adelis Foundation; the Appleton Family Trust; Mr. and Mrs. Bruno Licht, Brazil; the European Research Council; and the Ruhman Family Laboratory for Research in the Neurobiology of Stress.