{"id":176631,"date":"2015-01-22T16:47:23","date_gmt":"2015-01-22T21:47:23","guid":{"rendered":"http:\/\/www.euvolution.com\/futurist-transhuman-news-blog\/uncategorized\/treatment-restores-sociability-in-autism-mouse-model.php"},"modified":"2015-01-22T16:47:23","modified_gmt":"2015-01-22T21:47:23","slug":"treatment-restores-sociability-in-autism-mouse-model","status":"publish","type":"post","link":"https:\/\/www.euvolution.com\/futurist-transhuman-news-blog\/human-genetics\/treatment-restores-sociability-in-autism-mouse-model.php","title":{"rendered":"Treatment restores sociability in autism mouse model"},"content":{"rendered":"<p><p>  Among the problems people with Autism spectrum disorders (ASD)  struggle with are difficulties with social behavior and  communication. That can translate to an inability to make  friends, engage in routine conversations, or pick up on the  social cues that are second nature to most people. Similarly, in  a mouse model of ASD, the animals, like humans, show little  interest in interacting or socializing with other mice.<\/p>\n<p>    One drug, risperidone, works in both humans and mice with ASD    to treat other symptoms of the disorder -- including repetitive    behaviors--but no medication has been found to help    socialization.  <\/p>\n<p>    Now researchers at UCLA have treated ASD mice with a    neuropeptide--molecules used by neurons to communicate with    each other--called oxytocin, and have found that it restores    normal social behavior. In addition, the findings suggest that    giving oxytocin as early as possible in the animal's life leads    to more lasting effects in adults and adolescents. This    suggests there may be critical times for treatment that are    better than others.  <\/p>\n<p>    The study appears in the January 21 online edition of the    journal Science Translational Medicine.  <\/p>\n<p>    Mouse models of neuropsychiatric diseases provide a platform    for understanding the mechanisms behind disorders and    development of new therapies, noted Daniel Geschwind, a UCLA    professor of psychiatry, neurology and human genetics, and    senior author of the study. In 2011, Geschwind and his    colleagues developed a mouse model for ASD by knocking out a    gene called CNTNAP2 (contactin-associated protein-like 2),    which scientists believe plays an important role in the brain    circuits responsible for language and speech. Previous research    has linked common CNTNAP2 variants to heightened autism risk in    the general population, while rare variants can lead to an    inherited form of autism called cortical dysplasia-focal    epilepsy syndrome (CDFE).  <\/p>\n<p>    It's known that the oxytocin is involved in regulating various    aspects of social behavior. Among its other roles, oxytocin    neurons in the brain's hypothalamus interact with several other    brain regions, including the amygdala, hippocampus, and frontal    cortex, where they influence such behaviors as fear, memory,    and social behavior.  <\/p>\n<p>    \"The oxytocin system is a key mediator of social behavior in    mammals, including humans, for maternal behavior, mother-infant    bonding, and social memory,\" said Geschwind, who holds UCLA's    Gordon and Virginia MacDonald Distinguished Chair in Human    Genetics and is the director of the Center for Autism Research    and Treatment at the Semel Institute for Neuroscience and Human    Behavior at UCLA. \"So it seemed like a natural target for us to    go after.\"  <\/p>\n<p>    In the ASD mice, the researchers found a decrease in the number    of oxytocin neurons in the hypothalamus and, overall, a    decrease in oxytocin levels throughout the brain. But when they    administered oxytocin to the ASD mice, sociability, defined as    time spent interacting normally with other mice, was restored.    Then, using a second strategy, the researchers also found that    by giving the mice melanocortin, an agonist (which binds to    specific receptors on a cell to activate it) caused a natural    release of oxytocin from brain cells, which also improved    social deficits.  <\/p>\n<p>    \"The study shows that a primary deficit in oxytocin may cause    the social problems in these mice, and that correcting this    deficit can correct social behavior,\" said Geschwind. \"We were    surprised as well to discover a relationship between the    cntnap2 protein and oxytocin--the absence of cntnap2 effected    oxytocin neurons in the hypothalamus.\"  <\/p>\n<p>    The biggest surprise, though, said Geschwind, was finding that    early postnatal administration of the oxytocin led to longer    positive effects upon social behavior when measured several    weeks later. \"This suggests that there may be critical windows    of time for treatment that are better than others.\"  <\/p>\n<p><!-- Auto Generated --><\/p>\n<p>Continued here: <\/p>\n<p><a target=\"_blank\" href=\"http:\/\/www.sciencedaily.com\/releases\/2015\/01\/150122154818.htm\/RK=0\/RS=fE5pa42x8sPAlvfOIgpHdddpYN4-\" title=\"Treatment restores sociability in autism mouse model\">Treatment restores sociability in autism mouse model<\/a><\/p>\n","protected":false},"excerpt":{"rendered":"<p> Among the problems people with Autism spectrum disorders (ASD) struggle with are difficulties with social behavior and communication. That can translate to an inability to make friends, engage in routine conversations, or pick up on the social cues that are second nature to most people. Similarly, in a mouse model of ASD, the animals, like humans, show little interest in interacting or socializing with other mice.  <a href=\"https:\/\/www.euvolution.com\/futurist-transhuman-news-blog\/human-genetics\/treatment-restores-sociability-in-autism-mouse-model.php\">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":{"limit_modified_date":"","last_modified_date":"","_lmt_disableupdate":"","_lmt_disable":"","footnotes":""},"categories":[4],"tags":[],"class_list":["post-176631","post","type-post","status-publish","format-standard","hentry","category-human-genetics"],"modified_by":null,"_links":{"self":[{"href":"https:\/\/www.euvolution.com\/futurist-transhuman-news-blog\/wp-json\/wp\/v2\/posts\/176631"}],"collection":[{"href":"https:\/\/www.euvolution.com\/futurist-transhuman-news-blog\/wp-json\/wp\/v2\/posts"}],"about":[{"href":"https:\/\/www.euvolution.com\/futurist-transhuman-news-blog\/wp-json\/wp\/v2\/types\/post"}],"author":[{"embeddable":true,"href":"https:\/\/www.euvolution.com\/futurist-transhuman-news-blog\/wp-json\/wp\/v2\/users\/1"}],"replies":[{"embeddable":true,"href":"https:\/\/www.euvolution.com\/futurist-transhuman-news-blog\/wp-json\/wp\/v2\/comments?post=176631"}],"version-history":[{"count":0,"href":"https:\/\/www.euvolution.com\/futurist-transhuman-news-blog\/wp-json\/wp\/v2\/posts\/176631\/revisions"}],"wp:attachment":[{"href":"https:\/\/www.euvolution.com\/futurist-transhuman-news-blog\/wp-json\/wp\/v2\/media?parent=176631"}],"wp:term":[{"taxonomy":"category","embeddable":true,"href":"https:\/\/www.euvolution.com\/futurist-transhuman-news-blog\/wp-json\/wp\/v2\/categories?post=176631"},{"taxonomy":"post_tag","embeddable":true,"href":"https:\/\/www.euvolution.com\/futurist-transhuman-news-blog\/wp-json\/wp\/v2\/tags?post=176631"}],"curies":[{"name":"wp","href":"https:\/\/api.w.org\/{rel}","templated":true}]}}