Guest guest Posted May 3, 2001 Report Share Posted May 3, 2001 Reelin, Virus and Schizophrenia/ Autism is Mom's Fault?/ Brain Art FEAT DAILY NEWSLETTER Sacramento, California http://www.feat.org " Healing Autism: No Finer a Cause on the Planet " ______________________________________________________ Search www.feat.org/search/news.asp Also: * Study Tries to Prove Autism is Mom’s Fault * Measles Virus In Inflammatory Bowel Disease & Autism Cases * Brain Chemical Plays Multiple Roles * Genes That May Predict Alcoholism, Depression * Looking Within: The Brain As Art Reelin, Virus and Schizophrenia Defective corticogenesis and reduction in Reelin immunoreactivity in cortex and hippocampus of prenatally infected neonatal mice. Mol Psychiatry 1999 Mar;4(2):145-54 Fatemi SH, Emamian ES, Kist D, Sidwell RW, Nakajima K, Akhter P, Shier A, Sheikh S, K Department of Psychiatry, University of Minnesota Medical School, Minneapolis 55455, USA. fatem002@... Recent reports indicate an association between second trimester human influenza viral infection and later development of schizophrenia. Postmortem human brain studies also provide evidence for reduction in Reelin mRNA (an important secretory protein responsible for normal lamination of the brain) in schizophrenic brains. We hypothesized that human influenza infection in day 9 pregnant mice would alter the expression of reelin in day 0 neonatal brains. Prenatally-infected murine brains from postnatal day 0 showed significant reductions in reelin-positive cell counts in layer I of neocortex and other cortical and hippocampal layers when compared to controls. Whereas layer I Cajal-Retzius cells produced significantly less Reelin in infected animals, the same cells showed normal production of calretinin and nNOS when compared to control brains. Moreover, prenatal viral infection caused decreases in neocortical and hippocampal thickness. These results implicate a potential role of prenatal viral infection in causation of neuronal migration abnormalities via reduction in Reelin production in neonatal brains. PMID: 10208446, UI: 99223145 * * * Study Tries to Prove Autism is Mom’s Fault [bruno Bettelheim refuses to die.] http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?cmd=Retrieve & db=PubMed & list_ui ds=11285082 & dopt=Abstract Early intervention for infants with autistic spectrum disorders in Japan. 1: Pediatr Int 2001 Apr;43(2):202-8 Kobayashi R, Takenoshita Y, Kobayashi H, Kamijo A, Funaba K, Takarabe M. Department of Social Work, Tokai University School of Health Sciences; Department of Psychiatry, Saint nna Medical School; Tokai University Graduate School of Health Sciences, Kanagawa and; Faculty of Education, Ryukyu University, Okinawa, Japan. Background: To date, many researchers in Japan have assumed that the cause of autistic spectrum disorders is attributable to some disorder in the ability of the child. However, we have been working on the premise that autistic spectrum disorders are brought about by relationship disturbances in early infancy and have been attempting to validate this hypothesis through early intervention. Methods: We have examined the developmental process of affective communication in infants with autistic spectrum disorders. We have postulated that approach-avoidance motivational conflict (Richer) is the primary factor impeding the development of affective communication and have focused therapeutic intervention on this perspective. Results: As a result, attachment behavior was markedly improved in children, but affective communication with their mothers was not. Examining the mothers' images of themselves in infancy in mother-infant psychotherapy, problems that the mothers had themselves in infancy with attachment behavior to t heir own mothers affected the mothers' internal representation of their children, leading to active evolution of mother-child interaction and development of affective communication between the mother and child. Conclusion: In this context, the basis and significance of the internal representation of both parties being determinants in the quality of mother-child communication are discussed. Our goal in early intervention is not the elevation of a child's linguistic-cognitive abilities, but the creation of a comforting relationship in which both parent and child can live securely, without strain. PMID: 11285082 [PubMed - in process] >> DO SOMETHING ABOUT AUTISM NOW << Subscribe, Read, then Forward the FEAT Daily Newsletter. To Subscribe go to www.feat.org/FEATnews No Cost! * * * Measles Virus In Inflammatory Bowel Disease And Autism Cases Measles virus persistence in specimens of Inflammatory bowel disease and autism cases [This is all the information provided at the website address below. If any reader has this article, please contact me: Schafer@...] http://www.wkap.nl/oasis.htm/301652 Digestive Diseases and Sciences 46 (3):658-660, March 2001. © Plenum Publishing Corporation M. A. Afzal Division of Virology National Institute for Biological Standards and Control South Mimms, Potters Bar, Hertfordshire, EN6 3QG, UK P. D. Minor Division of Virology National Institute for Biological Standards and Control South Mimms, Potters Bar, Hertfordshire, EN6 3QG, UK S. Ghosh Gastrointestinal Unit, Department of Medicine University of Edinburgh, Western General Hospital Edinburgh, UK Li Jin Enteric and Respiratory Laboratory Central Public Health Laboratory Colindale, London NW9 5HT, UK\ ISSN 0163-2116 * * * Brain Chemical Plays Multiple Roles Substance may shed light on Parkinson’s, drug addiction http://www.newshub.com/cgibin/rd.cgi?10801949 A substance produced by the brain to help cells grow also helps a key chemical messenger do its job, a finding that could shed new light on Parkinson’s disease, schizophrenia and drug addiction, researchers say. ‘We don’t understand enough yet. But the important thing here is that the link has been established between BDNF and dopamine, and that’s an honest day’s work.’ — IRA B. BLACK Wood Medical School The Substance, brain-derived neurotrophic factor, has long been known to help brain cells mature and survive. The researchers found that BDNF also helps the messenger dopamine by providing a pathway used to deliver the message. The findings are reported in Thursday’s issue of the journal Nature by Pierre Sokoloff of INSERM, the French equivalent of the National Institutes of Health, and colleagues in Paris and Marseille, France. Working in mice, the scientists found that BDNF prompts brain cells to produce so-called D3 receptors, one type of the tiny structures to which dopamine binds to deliver its message. So, BDNF may play some role in several conditions involving the dopamine signaling system, such as Parkinson’s disease and drug addiction, researchers said. Brain autopsies of schizophrenia patients have also found higher than normal levels of BDNF, Sokoloff said. The researchers found that mice lacking BDNF had unusually few D3 receptors. They also found that when they reduced the population of D3 receptors in one part of the brain by chemical injection, they could largely restore the population by injecting BDNF. Role In Addiction In a commentary accompanying the paper, Francis J. White of the Chicago Medical School said substances that bind D3 receptors are effective at treating Parkinson’s and reducing cocaine-seeking behavior in animal versions of cocaine addiction. As a result, BDNF may be involved in the effects of the Parkinson’s medicine levodopa and in drug addiction, he said. Ira B. Black, chairman of the department of neuroscience and cell biology at Wood Medical School in Piscataway, N.J., said new treatments based on the research may be a way off. “We don’t understand enough yet,” Black said. “But the important thing here is that the link has been established between BDNF and dopamine, and that’s an honest day’s work.” © 2001 Associated Press. All rights reserved. This material may not be published, broadcast, rewritten or redistributed. * * * Genes That May Predict Alcoholism, Depression http://www.eurekalert.org/releases/apa-nsl043001.html Washington, D.C. - It has long been known that a direct link exists between alcohol and depression. Now data shows that a gene or genes on chromosome 1 may predispose some individuals to alcoholism and others to depression, according to a groundbreaking study in the May 2001 American Journal of Psychiatry, a monthly journal of the American Psychiatric Association. Researchers identified an area on chromosome 1 that is linked with vulnerability to alcoholism as well as affective disorders, primarily depression. Depending on circumstances, the gene or genes may manifest differently, in either of these forms. The study also showed that in many cases, the incidence of depression in individuals was secondary to alcoholism. The research was conducted as part of the Collaborative Study of the Genetics of Alcoholism, an ongoing study at nine research centers across the United States in which investigators have used a common protocol to gather clinical and biological data from several hundred families with more than one case of alcoholism. " With this new data we can now take a better look at patterns of diagnoses such as alcoholism and depression that run in families, " said I. Nurnberger, M.D., Ph.D., Director of the Institute of Psychiatric Research, Indiana University Medical Center and lead author of the study. " In the future, we may be able to predict whether an individual is likely to have these disorders. " Preliminary results in a separate series of families indicate similar findings. Pinpointing the specific genes involved will be an integral part of subsequent studies, Nurnberger said. The likelihood of overlap in genetic factors between alcoholism and affective disorders points up the need for further study of both populations, and it reinforces the importance of studying the interaction between the two conditions, Nurnberger said. [Evidence for a Locus on Chromosome 1 that Influences Vulnerability to Alcoholism and Affective Disorder, " by I. Nurnberger, Jr., M.D., Ph.D., et al., p. 718, American Journal of Psychiatry, May 2001.] * * * Looking Within: The Brain As Art A retrospective exhibit explores the evolving visualization of the brain. [The material presented in the following article contains elements of art, medicine and history and may not be appropriate subject matter for the pedestrian reader as it may induce sleepiness; in which case, do not read before driving or operating heavy equipment. By Stapleton, AMNews.] In 1991, the Institute of Medicine report, " Mapping the Brain and Its Functions: Integrating Enabling Technologies into Neuroscience Research, " declared that " neuroscience is an inherently visual science.” This theme is demonstrated by a current National Academy of Sciences' exhibit tracking 500 years of work illustrating the evolution of knowledge about the brain's form and function. With more than 60 images, The Art of Neuroscience: Image and Understanding 1518-2000, explores how this discipline is marked by an intersection of advances in artistic technique and scientific technology -- from 16th century woodcuts to advanced PET scans. " The idea of the exhibition is that the visual form is at least as powerful a way to communicate scientific knowledge as are words, " said Janis Tomlinson, PhD, curator and director of the Arts in the Academy program at the NAS. " But going back in [time], each attempt to illustrate anatomy, the brain, creates a footprint forward, " said Dr. Tomlinson. " When you try to record something in an image, it forces you to look harder to define what isn't that definite. The act of imaging forces you to see more.” The juxtapositions are striking. One illustration, a 1627 woodcut from the anatomical text, On the Structure of the Human Body, is hung near a 1994 Annie Leibowitz photograph, " Portrait of Laurie , MRI.” Together, these examples are interesting for a couple of reasons, according to Dr. Tomlinson. The early images are depersonalized. In contrast, Leibowitz' 20th-century photo shows a series of MRI images of one person, so specialized that it creates an unusual portrait, " a unique identifier of an individual, " Dr. Tomlinson said. Tracing neuroscience's images over time is a fascinating path that conveys how medical knowledge was both advanced and hamstrung by limits in technology. " A woodcut -- even in the hands of the famous anatomist Vesalius -- could not show the detail that would be revealed subsequently in engravings and until the 18th century, illustrations were printed only in black and white, " notes the exhibit's catalog. Consider, for instance, Estienne's De Dissectione Partium Corporis Humani from 1545. In a woodcut from this work, a muscular figure presents a dissected head for examination. However, the image, in terms of technical detail, is not very useful as a medical illustration, according to exhibit papers. Meanwhile, Bartolomeo Eustachio's work, circa 1552, involved the use of copper engraving, thereby involving more precise linear shading of the vertebrae. The illustration from Tabulae Anatomicae was used until 1817 when it was published in the Encyclopaedia Britannica. Dr. Tomlinson pointed out another copper engraving from Anatomia Humani Corporis, a 1685 work by Govard Bidloo. It is interesting because it reveals the perspective of both the anatomist and the artist. There is incredible attention paid not only to the brain or spinal cord, but also to the dissection -- " the details of the human intervention, " she said. Article continues at: http://www.ama-assn.org/sci-pubs/amnews/pick_01/hlsa0507.htm _______________________________________________________ Lenny Schafer, Editor PhD Ron Sleith Kay Stammers Editor@... Unsubscribe: FEATNews-signoff-request@... CALENDAR OF EVENTS submissions to Guppy events@... Quote Link to comment Share on other sites More sharing options...
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