In the News February 5, 2018
Total Page:16
File Type:pdf, Size:1020Kb
Load more
Recommended publications
-
Missing Link Connects Diabetes and Alzheimer's Disease
Missing Link Connects Diabetes and Alzheimer’s Disease A gene called PGC-1! is associated with the onset of Type 2 diabetes, associated with dementia and but it has shown to decrease in Alzheimer’s disease dementia cases. an accumulation in the brain of The gene is a potential target for regulating glucose, according to an abnormal protein known as new research led by Giulio Maria Pasinetti, MD, PhD, the Aidekman "-amyloid. This abnormal protein Family Professor in Neurology, and Professor of Psychiatry and causes plaque buildup in the Geriatrics and Adult Development. The study was recently published brain, which is linked to cognitive in Archives of Neurology. deterioration in Alzheimer’s disease. The PGC-1! gene, which plays an important role in regulating We may be able to link a gene—whose glucose metabolism, is considered a potential target for treating alteration may lead to diabetes—to a Type 2 diabetes. Giulio Maria Pasinetti, MD, PhD mechanism that would promote conditions Using a mouse model of associated with Alzheimer’s disease. Alzheimer’s disease, Dr. Pasinetti and his team also found that promoting PGC-1! content in brain cells reduces the hyperglycemic- — GIULIO MARIA PASINETTI, MD, PHD mediated production of "-amyloid. The findings could help researchers identify potential pharmacological treatments that might promote PGC-1! expression Previous studies suggest that Type 2 diabetes is a risk factor for in the brain cells of Alzheimer’s patients. “We need to discover Alzheimer’s disease. The relationship between the two conditions is new therapeutic approaches for Alzheimer’s disease by looking at “a fascinating new area of research,” says Dr. -
Cytokine Gene Expression As a Function of the Clinical Progression of Alzheimer Disease Dementia
ORIGINAL CONTRIBUTION Cytokine Gene Expression as a Function of the Clinical Progression of Alzheimer Disease Dementia James D. Luterman, PhD; Vahram Haroutunian, PhD; Shrishailam Yemul, PhD; Lap Ho, PhD; Dushyant Purohit, MD; Paul S. Aisen, MD; Richard Mohs, MD; Giulio Maria Pasinetti, MD, PhD Background: Inflammatory cytokines have been linked gyrus (P,.01). When stratified by the Consortium to to Alzheimer disease (AD) neurodegeneration, but little Establish a Registry for Alzheimer’s Disease (CERAD) is known about the temporal control of their expression neuropathological criteria, IL-6 mRNA expression in in relationship to clinical measurements of AD demen- both the entorhinal cortex (P,.05) and superior tem- tia progression. poral gyrus (P,.01) correlated with the level of neuro- fibrillary tangles but not neuritic plaques. However, in Design and Main Outcome Measures: We mea- the entorhinal cortex, TGF-b1 mRNA did not correlate sured inflammatory cytokine messenger RNA (mRNA) with the level of either neurofibrillary tangles or neu- expression in postmortem brain specimens of elderly sub- ritic plaques. Interestingly, in the superior temporal jects at different clinical stages of dementia and neuro- gyrus, TGF-b1 mRNA expression negatively correlated pathological dysfunction. with neurofibrillary tangles (P,.01) and showed no relationship to the pathological features of neuritic Setting and Patients: Postmortem study of nursing plaques. home patients. Conclusions: The data are consistent with the hypoth- Results: In brains of cognitively normal control sub- esis that cytokine expression may differentially contrib- jects, higher interleukin 6 (IL-6) and transforming ute to the vulnerability of independent cortical regions growth factor b1 (TGF-b1) mRNA expression was during the clinical progression of AD and suggest that observed in the entorhinal cortex and superior temporal an inflammatory cytokine response to the pathological gyrus compared with the occipital cortex. -
View Final Program
142nd ANNUAL MEETING OF THE AMERICAN ANA2017 NEUROLOGICAL ASSOCIATION SAN DIEGO, CA • OCTOBER 15-17, 2017 SHERATON SAN DIEGO HOTEL & MARINA EXPLORE • EXAMINE • INVESTIGATE FINAL PROGRAM OCTOBER 14, 2017 | Pre-Meeting Symposium: Big Science and the BRAIN Initiative 2017.MYANA.org 142nd ANNUAL MEETING OF THE AMERICAN ANA2017 NEUROLOGICAL ASSOCIATION SAN DIEGO, CA • OCTOBER 15 -17, 2017 SHERATON SAN DIEGO HOTEL & MARINA ND Please note some session titles may have changed since this program was printed. Please refer THE 142 ANA to your Mobile app for the most current session updates. ANNUAL MEETING LETTER FROM THE CHAIR 3 Enjoy outstanding scientific SCHEDULE AT A GLANCE 4 symposia covering the latest HOTEL FLOOR PLANS 6 research in the fields of neurology and neuroscience GENERAL INFORMATION 7 while taking the opportunity WIRELESS CONNECTION 8 to network with leaders in the world of academic neurology CONTINUING MEDICAL EDUCATION 8 at the 142nd ANA Annual ANNUAL MEETING MOBILE APP 8 Meeting in San Diego, CA, October 15-17, 2017. PROGRAMS BY DAY 9 SATURDAY OCT 14 9 MEETING LOCATION SUNDAY OCT 15 9 Sheraton San Diego MONDAY OCT 16 17 Hotel & Marina 1380 Harbor Island Drive TUESDAY OCT 17 25 San Diego, California 92101 IN MEMORIAM 28 ONSITE MEETING CONTACTS SPEAKER ABSTRACTS 29 Registration and meeting questions: THANK YOU TO OUR SUPPORTERS & EXHIBITORS 42 [email protected] FUTURE MEETING DATES 42 OR visit the registration desk Bay View Foyer 2017 AWARDEES 43 (located in Marina Tower Lobby Level) ACADEMIC NEUROLOGY REPRESENTATIVES FROM JAPAN 47 Saturday, October 14 2017 ABSTRACT REVIEWERS 48 3:00 PM–7:00 PM BOARD OF DIRECTORS 49 Sunday, October 15 6:00 AM–5:45 PM ANA 2017 COMMITTEES, SUBCOMMITTEES & TASK FORCES 50 Monday, October 16 6:30 AM–5:45 PM Tuesday, October 17 6:30 AM–2:15 PM #ANAMTG2017 ANA 2017 FROM THE CHAIR Dear Colleagues, It is a pleasure to welcome you to the 142nd Annual Meeting of the American Neurological Association (ANA). -
Cannabis and the Developing Brain: Insights Into Its Long-Lasting Effects
8250 • The Journal of Neuroscience, October 16, 2019 • 39(42):8250–8258 Mini-Symposium Cannabis and the Developing Brain: Insights into Its Long-Lasting Effects Yasmin L. Hurd,1 XOlivier J. Manzoni,2 Mikhail V. Pletnikov,3 Francis S. Lee,4 Sagnik Bhattacharyya,5 and X Miriam Melis6 1Department of Psychiatry and Department of Neuroscience, Icahn School of Medicine at Mount Sinai, New York, New York 10029, 2Aix Marseille University, Institut National de la Sante´ et de la Recherche Me´dicale, Institut de neurobiologie de la méditerranée, 13273 Marseille, France, and Cannalab, Cannabinoids Neuroscience Research International Associated Laboratory, Institut National de la Sante´ et de la Recherche Me´dicale, 13273 Marseille, France, 3Department of Psychiatry and Behavioral Sciences, Solomon H. Snyder Department of Neuroscience, Johns Hopkins University School of Medicine, Baltimore, Maryland 21205, 4Department of Psychiatry, Sackler Institute for Developmental Psychobiology, Weill Cornell Medical College, New York, New York 10065, 5Department of Psychosis Studies, Institute of Psychiatry, Psychology and Neuroscience, King’s College London, London SE5 8AF, United Kingdom, and 6Department of Biomedical Sciences, Division of Neuroscience and Clinical Pharmacology, University of Cagliari, 09042 Cagliari, Italy The recent shift in sociopolitical debates and growing liberalization of cannabis use across the globe has raised concern regarding its impact on vulnerable populations, such as pregnant women and adolescents. Epidemiological studies have long demonstrated a rela- tionship between developmental cannabis exposure and later mental health symptoms. This relationship is especially strong in people with particular genetic polymorphisms, suggesting that cannabis use interacts with genotype to increase mental health risk. Seminal animalresearchdirectlylinkedprenatalandadolescentexposuretodelta-9-tetrahydrocannabinol,themajorpsychoactivecomponentof cannabis, with protracted effects on adult neural systems relevant to psychiatric and substance use disorders. -
Safety and Pharmacokinetics of Oral Cannabidiol When Administered Concomitantly with Intravenous Fentanyl Rajita Sinha, Phd, Didier Jutras-Aswad, MD, MS, Marilyn A
ORIGINAL RESEARCH Safety and Pharmacokinetics of Oral Cannabidiol When Administered Concomitantly With Intravenous Fentanyl 08/15/2018 on BhDMf5ePHKav1zEoum1tQfN4a+kJLhEZgbsIHo4XMi0hCywCX1AWnYQp/IlQrHD3XI41p+sDLxYskzzWJHpwFPA3MvB4/FX5gh6vcjyLLl1kCfZEXLPTKQ== by https://journals.lww.com/journaladdictionmedicine from Downloaded in Humans Downloaded Alex F.Manini, MD, MS, Georgia Yiannoulos, MS, Mateus M. Bergamaschi, PhD, from Stephanie Hernandez, MD, MS, Ruben Olmedo, MD, Allan J. Barnes, BSc, Gary Winkel, PhD, https://journals.lww.com/journaladdictionmedicine Rajita Sinha, PhD, Didier Jutras-Aswad, MD, MS, Marilyn A. Huestis, PhD, and Yasmin L. Hurd, PhD Results: SAFTEE data were similar between groups without res- Objectives: Cannabidiol (CBD) is hypothesized as a potential treat- piratory depression or cardiovascular complications during any test ment for opioid addiction, with safety studies an important first step session. After low-dose CBD, tmax occurred at 3 and 1.5 hours in for medication development. We determined CBD safety and phar- by sessions 1 and 2, respectively. After high-dose CBD, tmax occurred at BhDMf5ePHKav1zEoum1tQfN4a+kJLhEZgbsIHo4XMi0hCywCX1AWnYQp/IlQrHD3XI41p+sDLxYskzzWJHpwFPA3MvB4/FX5gh6vcjyLLl1kCfZEXLPTKQ== macokinetics when administered concomitantly with a high-potency 3 and 4 hours in sessions 1 and 2, respectively. There were no signif- opioid in healthy subjects. icant differences in plasma CBD or cortisol (AUC P = NS) between Methods: This double-blind, placebo-controlled cross-over study of sessions. CBD, coadministered with intravenous fentanyl, was conducted at Conclusions: Cannabidiol does not exacerbate adverse effects asso- the Clinical Research Center in Mount Sinai Hospital, a tertiary care ciated with intravenous fentanyl administration. Coadministration of medical center in New York City. Participants were healthy volunteers CBD and opioids was safe and well tolerated. -
FDA Office of Women's Health US Food and Drug Administration
FDA OFFICE OF WOMEN’S HEALTH SCIENTIFIC CONFERENCE CBD & Other Cannabinoids Sex and Gender Differences in Use and Responses Thursday, November 19, 2020 | 9:00 AM–4:00 PM EST Virtual Meeting CBD and Other Cannabinoids: Sex and Gender Differences in Use and Responses | 1 !/"'""'', 11 U.S. FOOD & DRUG •J ADMINISTRATION Dear Colleagues, On behalf of the U.S. Food and Drug Administration's (FDA) Office of Women's Health (OWH), I am pleased to welcome you to today's conference, "CBD and Other Cannabinoids: Sex and Gender Differences in Use and Responses." The mission of FDA is to protect and promote public health. A top priority for OWH is to identify and monitor emerging areas of interest and potential concern for the health of women. Cannabidiol (CBD) products are appearing everywhere - from medical cannabis dispensaries, to pharmacies, to gas stations. Many of these products are illegally marketed and purport to target a myriad of health concerns, including conditions more commonly experienced by women than men, such as chronic pain, sleep disturbances, anxiety and depression. Given that little is known about how and if many cannabis derived products work, how and why women are using them, and their potential associated risks, there is a mounting need to consolidate and communicate what we know about these products and to identify knowledge gaps. Further, the use of these products during pregnancy and lactation raises additional questions and concerns. The purpose of today's meeting is to highlight the needed and existing research to address the many "who", "what", and "why" questions surrounding products containing CBD and other cannabinoids. -
Obesity & Weight Management
Giulio Maria Pasinetti, J Obes Wt Loss Ther 2012, 2:9 http://dx.doi.org/10.4172/2165-7904.S1.003 International Conference and Exhibition on Obesity & Weight Management December 3-5, 2012 DoubleTree by Hilton Philadelphia, USA HDAC IIa-specific inhibitors as a potential novel therapy for type 2 diabetes-mediated cognitive deterioration in alzheimer’s disease Giulio Maria Pasinetti Mount Sinai School of Medicine, USA ur laboratory recently demonstrated that epigenetic chromatin modifications associated with type-2 diabetes (T2DM) may Oplay a role in brain pathophysiology in neurodegenerative disorders. We previously discovered that there are significant changes in the expression of select chromatin modification enzymes, such as histone deacetylases (HDACs), in the brains of T2DM subjects compared to control subjects, and that these changes coincide with altered expression of proteins involved in synaptic function, such as PSD95 and synaptophysin. We hypothesized that T2DM may induce epigenetic modifications associated with increased susceptibility to Alzheimer’s disease (AD)-type neurodegeneration. Using a mouse model of diet- induced T2DM, we found that, similar to humans, T2DM mice showed differential expression of epigenetic-modifying enzymes in the brain compared to controls. In particular, we found significant up-regulation of HDAC class IIa, including HDACs 4, 5, and 9, in the brains of diabetic mice. These alterations coincided with increased susceptibility to oligomeric Aβ (oAβ) induced synaptic toxicity and oAβ-induced synaptic dysfunction, as assessed by long term potentiation (LTP). Most interestingly, we found that inhibition of class IIa HDACs using an HDAC IIa-specific inhibitor, MC1568, increased transcription levels of PSD95 and synaptophysin in primary neuron cultures from C57Bl6/J mice and prevented LTP deficits found in old-T2DM mouse ex vivo hippocampal slices. -
Internships in Behavioral Neuroscience 2010-2019(Opens In
Marymount Manhattan College Student Research/Internships/Independent Studies 2010-2019 Last updated 10/24/2019 All offsite research experiences listed, were actively pursued and coordinated by Deirtra-Hunter-Romagnoli to provide multiple opportunities for MMC students to work in renown academic research laboratories or professional clinical institutions across New York City. Research internship opportunities for students included working with stem cells, utilizing human and animal experimental protocols to learn more about neurological diseases like multiple sclerosis, alzheimers, addiction and how social hierarchies can influence psychological conditions. Emphasis was placed on neuroscience laboratories however when alternate laboratory opportunities presented themselves I was easily able to place MMC students from different disciplines. More recently, a growing number of students outside of the Natural Sciences Division have taken part in these research internship opportunities. Specifically, there has been an increase in the number of Theatre, Dance and Business students declaring a neuroscience minor and taking advantage of new research opportunities including options recently available at the MMC Music, Mind and Brain Behavioral Neuroscience Laboratory. Most research experiences culminated with students presenting final results at a professional research forum and some students also have published abstracts. All onsite research experiences and Independent study projects were supervised or co-supervised by Deirtra Hunter-Romagnoli. The following descriptions of coordinated research experiences are listed by academic year and a brief summary of the laboratory focus is included. When available current updates of student’s current professional trajectory/status are included. Academic Year 2018-2019 Icahn School of Medicine at Mount Sinai Hospital: Neuroscience Department 1.Martine Faustin (Class of 2019) Worked in the Lab of Molecular Psychiatry with Dr. -
IBNS 2016 Program - Budapest, Hungary
IBNS 2016 Program - Budapest, Hungary Please note this is not the final program and is subject to change. Revised May 9, 2016 Tuesday, June 7 Council Meeting. 9:00-1:00 Tours. 1:00-6:00 Welcome Reception. 7:00-10:00 Student Social. 7:00-8:00 Wednesday, June 8 Sex differences in the brain: Implications for behavioral and biomedical research. Chair: Elena Choleris 8:00-8:30 Sex differences in rodent social behavior: Hormonal influences. Choleris, Elena; Clipperton- Allen, Amy; Ervin, Kelsy SJ; Lymer, Jennifer M; Gabor, Christopher S; Sheppard, Paul; Phan, Anna. 8:30-9:00 Sex matters: Hippocampal neurogenesis, Spatial Learning and Pattern Separation. Galea, Liisa A. M. 9:00-9:30 Estrogenic regulation of memory in males and females: Molecular mechanisms and implications for aging. Frick, Karyn M. 9:30-10:00 Sex differences in stroke and stroke therapies. Sohrabji, Farida. Epigenetic Regulation of Motivated Behaviors. Chair: Zuoxin Wang; Co-Chair: Mohamed Kabbaj 8:00-8:30 Role of DNA methyl-cytosine oxidation in cocaine action. Feng, Jian. 8:30-9:00 Methamphetamine-associated memory is regulated by histone methylation. Miller, Courtney A. 9:00-9:30 Influence of genomic imprinting on metabolism and behavior. Lu, Xin-Yun. 9:30-10:00 Epigenetics of Social Bonding in Prairie Voles. Kabbaj, Mohamed; Wang, Zuoxin; Liu, Yan; Elvir, Lindsay. Exhibits – Refreshment Break. 10:00-10:30 Keynote Speaker 10:30-11:30 High Times for Cannabis: Epigenetic Imprint and its Legacy on Brain and Behavior. Yasmin Hurd. Lunch. 11:30-1:30 Zebrafish and human brain disorders: A new tool in behavioral neuroscience. -
The Vulnerable Brain: Insights Into the Neurobiology of Addiction PPS
PPS Research Symposium 2015 The Vulnerable Brain: Insights into the Neurobiology of Addiction August 13, 2015 11:00 a.m. - 11:40 a.m. Rockwell Pavilion, MD Anderson Library Yasmin Hurd, Ph.D. Professor of Psychiatry, Neuroscience and Pharmacology & Systems Therapeutics, and Ward-Coleman Chair in Translational Neuroscience, Icahn School of Medicine at Mount Sinai Director of the Center for Addictive Disorders, Mount Sinai Behavioral Health System Dr. Yasmin Hurd is Professor of Psychiatry, Neuroscience and Pharmacology & Systems Therapeutics as well as the Ward-Coleman Chair in Translational Neuroscience at the Icahn School of Medicine in New York. She is also Director of the Center for Addictive Disorders in the Mount Sinai Behavioral Health System. She is an internationally renowned neuroscientist whose translational research examines the neurobiology of drug abuse and related psychiatric disorders. She is highly published in the field and leads a team of investigators in molecular biology, behavioral neuropharmacology, genetics and neuroimaging to study the human brain as well as translational animal models. Using multidisciplinary research approaches, her work has provided significant insights into the complex neurobiological mechanisms underlying addictive behavior as well as the molecular neuropathology associated with genetic vulnerability to addiction. Moreover, her novel research explores epigenetic mechanisms associated with developmental cannabis exposure that have long-term effects into adulthood and across generations. Additionally, her basic science research is complimented by clinical laboratory investigations for the development of new treatment interventions. Dr. Hurd has served as the Director of the MD/PhD program at the Icahn School of Medicine and was the founding Chair of the Diversity in Biomedical Research Committee. -
NIH Public Access Author Manuscript J Neurochem
NIH Public Access Author Manuscript J Neurochem. Author manuscript; available in PMC 2009 August 1. NIH-PA Author ManuscriptPublished NIH-PA Author Manuscript in final edited NIH-PA Author Manuscript form as: J Neurochem. 2008 August ; 106(4): 1503±1514. doi:10.1111/j.1471-4159.2008.05454.x. METABOLIC SYNDROME AND THE ROLE OF DIETARY LIFESTYLES IN ALZHEIMER’S DISEASE Giulio Maria Pasinetti1 and Jacqueline A. Eberstein2 1Center of Excellence for Research in Complementary and Alternative Medicine in Alzheimer©s Disease, Department of Psychiatry, The Mount Sinai School of Medicine 2Controlled Carbohydrate Nutrition, LLC. Abstract Since Alzheimer’s disease (AD) has no cure or preventive treatment, an urgent need exists to find a means of preventing, delaying the onset, or reversing the course of the disease. Clinical and epidemiological evidence suggests that lifestyle factors, especially nutrition, may be crucial in controlling AD. Unhealthy lifestyle choices lead to an increasing incidence of obesity, dyslipidemia and hypertension — components of the metabolic syndrome. These disorders can also be linked to AD. Recent research supports the hypothesis that calorie intake, among other nongenetic factors, can influence the risk of clinical dementia. In animal studies, high calorie intake in the form of saturated fat promoted AD-type amyloidosis, while calorie restriction via reduced carbohydrate intake prevented it. Pending further study, it is prudent to recommend to those at risk for AD — e.g., with a family history or features of metabolic syndrome, such as obesity, insulin insensitivity, etc. — to avoid foods and beverages with added sugars; to eat whole, unrefined foods with natural fats, especially fish, nuts and seeds, olives and olive oil; and to minimize foods that disrupt insulin and blood sugar balance. -
Petition to Add Opioid Use Disorder to the List of Medical Conditions for the New Mexico Medical Cannabis Program Background
Petition to Add Opioid Use Disorder to the List of Medical Conditions for the New Mexico Medical Cannabis Program Background: This petition was submitted to the New Mexico Sec. of Health and presented to the Medical Advisory Board (MAB), a group of expert clinicians tasked with evaluating petitions. Board members overwhelmingly voted approval of the petition (5-1). The Secretary rejected the MAB’s recommendation and declined to add opioid use disorder to the list of qualifying conditions in June 2017. The petitioner plans to refile at the next opportunity. _____________________________________________________________________________________ Name of Person Filing Petition: Anita Briscoe Names of Witnesses Providing Technical Evidence: Steve Jenison, MD, Former Chair, Medical Cannabis Advisory Board Pam Conry, APRN BC, Psychiatric Nurse Practitioner Florian Birkmeyer, MD, Psychiatrist Ramon H, patient Michael V, patient Lisa Chavez, Case Manager, UNM Forensic Psychiatry Willie Ford, Director, R Greenleaf Dispensary Jeffery Holland, Director, Endorphin Power Company _____________________________________________________________________________________ PETITION TO THE NM MEDICAL ADVISORY BOARD TO THE NEW MEXICO MEDICAL CANNABIS PROGRAM TO ADD OPIATE DEPENDENCE AS A QUALIFYING CONDITION Anita Briscoe, MS, APRN-BC 718 Adams NE, Albuquerque, NM 87110 505-720-9495 My name is Anita Willard Briscoe and I am a native New Mexican from Espanola, living in Albuquerque. I have been a nurse for 40 years, a psych nurse practitioner for 12 years. I have been referring patients to the cannabis program for 7 years. Over this past year I have observed that about 25% of my patients have stated independently that they were able to kick opiates with cannabis. They state it calms down their cravings, relaxes their craving anxiety and is helping them to keep off of opiates.