{"id":65283,"date":"2015-04-11T07:44:02","date_gmt":"2015-04-11T11:44:02","guid":{"rendered":"http:\/\/www.euvolution.com\/prometheism-transhumanism-posthumanism\/gene-loss-creates-eating-disorder-related-behaviors-in-mice\/"},"modified":"2015-04-11T07:44:02","modified_gmt":"2015-04-11T11:44:02","slug":"gene-loss-creates-eating-disorder-related-behaviors-in-mice","status":"publish","type":"post","link":"https:\/\/www.euvolution.com\/prometheism-transhumanism-posthumanism\/transhuman-news-blog\/gene-medicine\/gene-loss-creates-eating-disorder-related-behaviors-in-mice\/","title":{"rendered":"Gene loss creates eating disorder-related behaviors in mice"},"content":{"rendered":"<p><p>  Study advances understanding of neurological circuits that might  be targeted to treat anorexia nervosa<\/p>\n<p>    Building on their discovery of a gene linked to eating    disorders in humans, a team of researchers at the University of    Iowa has now shown that loss of the gene in mice leads to    several behavioral abnormalities that resemble behaviors seen    in people with anorexia nervosa.  <\/p>\n<p>    The team, led by Michael Lutter, MD, PhD, assistant professor    of psychiatry in the UI Carver College of Medicine, found that    mice that lack the estrogen-related receptor alpha (ESRRA) gene    are less motivated to seek out high-fat food when they are    hungry and have abnormal social interactions. The effect was    stronger in female mice, which also showed increased    obsessive-compulsive-like behaviors.  <\/p>\n<p>    The study also shows that ESRRA levels are controlled by energy    status in the mice. Restricting calorie intake to 60 percent of    normal over several days significantly increased levels of    ESRRA in the brains of normal mice.  <\/p>\n<p>    \"Decreased calorie intake usually motivates animals, including    humans, to seek out high-calorie food. These findings suggest    that loss of ESRRA activity may disrupt that response,\" Lutter    says.  <\/p>\n<p>    Anorexia nervosa and bulimia nervosa are common and severe    mental illnesses. Lutter notes that although 50 to 70 percent    of the risk of getting an eating disorder is inherited,    identifying the genes that mediate this risk has proven    difficult.  <\/p>\n<p>    ESRRA is a transcription factor - a gene that turns on other    genes. Lutter and his colleagues previously found that a    mutation that reduces ESRRA activity is associated with an    increased risk for eating disorders in human patients. Although    ESRRA is expressed in many brain regions that are disrupted in    anorexia, almost nothing was known about its function in the    brain. In the new study, published online April 9 in the    journal Cell Reports, Lutter's team manipulated ESRRA    in mice to investigate the gene's role in behavior.  <\/p>\n<p>    \"This work identifies estrogen-related receptor alpha as one of    the genes that is likely to contribute to the risk of getting    anorexia nervosa or bulimia nervosa,\" Lutter says. \"Clearly    social factors, particularly the western ideal of thinness,    contribute the remaining 'non-genetic' risk, and the increasing    rate of eating disorders over the past several decades is    likely due to social factors, not genetics,\" he adds.  <\/p>\n<p>    Through a series of experiments with genetically engineered    mice, Lutter and his team showed that mice without the ESRRA    gene have behavioral abnormalities related to eating and social    behavior. In particular, mice without ESRRA show reduced effort    to work for high-fat food when they are hungry. The mice also    exhibited impaired social interaction and female mice without    the gene show increased compulsive grooming, which may mimic    obsessive-compulsive-type behavior in humans.  <\/p>\n<p>    In order to refine their understanding of the effects of ESRRA    in the brain, the researchers selectively removed the gene from    particular brain regions that have been associated with eating    disorders. They found that removing the gene from the    orbitofrontal cortex was associated with increased    obsessive-compulsive-type behaviors in female mice, while loss    of ESRRA from the prefrontal cortex produced mice that were    less willing to work to get high-fat food when they were    hungry.  <\/p>\n<p><!-- Auto Generated --><\/p>\n<p>Read the original:<br \/>\n<a target=\"_blank\" href=\"http:\/\/www.eurekalert.org\/pub_releases\/2015-04\/uoih-glc040815.php\/RK=0\/RS=GMoqd8oH5I93lFl.u5ykRzTWYg4-\" title=\"Gene loss creates eating disorder-related behaviors in mice\">Gene loss creates eating disorder-related behaviors in mice<\/a><\/p>\n","protected":false},"excerpt":{"rendered":"<p> Study advances understanding of neurological circuits that might be targeted to treat anorexia nervosa Building on their discovery of a gene linked to eating disorders in humans, a team of researchers at the University of Iowa has now shown that loss of the gene in mice leads to several behavioral abnormalities that resemble behaviors seen in people with anorexia nervosa. The team, led by Michael Lutter, MD, PhD, assistant professor of psychiatry in the UI Carver College of Medicine, found that mice that lack the estrogen-related receptor alpha (ESRRA) gene are less motivated to seek out high-fat food when they are hungry and have abnormal social interactions.  <a href=\"https:\/\/www.euvolution.com\/prometheism-transhumanism-posthumanism\/transhuman-news-blog\/gene-medicine\/gene-loss-creates-eating-disorder-related-behaviors-in-mice\/\">Continue reading <span class=\"meta-nav\">&rarr;<\/span><\/a><\/p>\n","protected":false},"author":1,"featured_media":0,"comment_status":"closed","ping_status":"closed","sticky":false,"template":"","format":"standard","meta":{"footnotes":""},"categories":[21],"tags":[],"class_list":["post-65283","post","type-post","status-publish","format-standard","hentry","category-gene-medicine"],"_links":{"self":[{"href":"https:\/\/www.euvolution.com\/prometheism-transhumanism-posthumanism\/wp-json\/wp\/v2\/posts\/65283"}],"collection":[{"href":"https:\/\/www.euvolution.com\/prometheism-transhumanism-posthumanism\/wp-json\/wp\/v2\/posts"}],"about":[{"href":"https:\/\/www.euvolution.com\/prometheism-transhumanism-posthumanism\/wp-json\/wp\/v2\/types\/post"}],"author":[{"embeddable":true,"href":"https:\/\/www.euvolution.com\/prometheism-transhumanism-posthumanism\/wp-json\/wp\/v2\/users\/1"}],"replies":[{"embeddable":true,"href":"https:\/\/www.euvolution.com\/prometheism-transhumanism-posthumanism\/wp-json\/wp\/v2\/comments?post=65283"}],"version-history":[{"count":0,"href":"https:\/\/www.euvolution.com\/prometheism-transhumanism-posthumanism\/wp-json\/wp\/v2\/posts\/65283\/revisions"}],"wp:attachment":[{"href":"https:\/\/www.euvolution.com\/prometheism-transhumanism-posthumanism\/wp-json\/wp\/v2\/media?parent=65283"}],"wp:term":[{"taxonomy":"category","embeddable":true,"href":"https:\/\/www.euvolution.com\/prometheism-transhumanism-posthumanism\/wp-json\/wp\/v2\/categories?post=65283"},{"taxonomy":"post_tag","embeddable":true,"href":"https:\/\/www.euvolution.com\/prometheism-transhumanism-posthumanism\/wp-json\/wp\/v2\/tags?post=65283"}],"curies":[{"name":"wp","href":"https:\/\/api.w.org\/{rel}","templated":true}]}}