Cell and Molecular Neuroscience Syllabus Fall 2016 Lecture Time

Total Page:16

File Type:pdf, Size:1020Kb

Cell and Molecular Neuroscience Syllabus Fall 2016 Lecture Time BIOL 3409: ST: Cell and Molecular Neuroscience Syllabus Fall 2016 Lecture Time: T, F 1:35 – 3:15 PM Lecture Location: Richards Hall 231 Instructor Information: Dr. Jennifer Ingemi Email: [email protected] Office Location: 380 Nightingale Hall, dial ext. 6510 to be let in Office Hours: M, F 10 AM- 12 PM or by appointment Course Description: At its core the principles that govern the communication between cells of the nervous system are determined by their molecular components. The molecular landscape defines the individual properties of a neuron and the function of neuronal networks as a whole. This new course will take an interdisciplinary approach, combining molecular biology, cell biology, pharmacology and genetics to address the fundamental molecular properties of neurons and neuronal networks. The course will focus on neuronal signaling through the function of ion channels and receptors, supramolecular mechanisms like synaptic transmission and axonal transport and the molecular mechanisms that underlie biological networks and neural coding of information. Throughout the semester we will use the fundamental understanding of molecular networks as a framework to explore the mechanisms that underlie neurological diseases and disorders. Additionally, we will discuss current treatments and therapies that rely on modulating neuronal signaling through molecular interactions. Prerequisites: BIOL 2301 Course Objectives: 1. Strengthen your knowledge of the molecular basis of neuron function 2. Gain an appreciation for the complexity of molecular interactions that comprises neural network function. 3. Refine your ability to think and write critically, using your knowledge of molecular processes to interpret primary literature, explain disease etiology and the drug treatment processes. Learning Outcomes: By the end of the course students will be able to: 1. Describe, in detail, the molecular mechanisms of neuronal communication 2. Identify molecules involved in each step of intercellular communication, information processing, and neuronal cell metabolism. 3. Explain how information is integrated and stored in the nervous system at the network and cellular level. 4. Describe how changes in molecular processes influence cellular function and lead to aberrant neuronal communication found disease sates. 5. Evaluate, in writing and orally, current theories and relevant scientific research on how pharmacological agents are used to affect molecular processes in the treatment of neuropsychiatric disorders. Course Materials: Text (Recommended): Byrne, JH., et al. (2014). From Molecules to Networks: An Introduction to Cellular and Molecular Neuroscience. (3rd. ed). London, UK: Academic Press., ISBN-13: 978- 0-12-397179-1. Additional readings from primary literature, supplemental handouts, videos, lecture slides and detailed assignment information can be found on the Blackboard site associated with this course. It will be your responsibility to check Blackboard often. Course Format: Although this course is based on a traditional lecture and discussion, it will challenge you to think beyond the “memorize and regurgitate” learning style. You will be asked to integrate basic concepts in cellular biology and genetics to discuss how molecular networks influence neuron function. Together, we will explore the literature to how changes in the molecular landscape of neurons influence disease and how current treatments aim to correct these changes. The ability to analyze literature and communicate your ideas effectively is critical for a scientist no matter what career path you choose. I hope that by challenging you to read, write and think critically that you will gain a solid base for developing these skills so that you can succeed as a scientist for the rest of your career at the level college and beyond. To that end, portions of the course will rely on your participation in class, so please come prepared to participate by keeping up with the assigned readings for each lecture. I encourage everyone to participate in the discussion while being respectful to your peers ideas and questions. If, at any time, we are covering a topic that is relevant or related to your co-op experience (or one you are planning to do), please share your experience and/or insight with the class. Lecture slides and corresponding textbook page references will be posted on Blackboard by 11 AM before class to help you with note taking. I will record my lectures via Tegrity (see “Tegrity Classes” on Blackboard) and make them available to you for your reference when studying or in the case that you miss class. This is NOT and online course, so watching recorded lectures in lieu of attending class on a regular basis is not advised. Unexpected computer issues might arise, and I cannot guarantee that each lecture will be recorded. If you miss class, Blackboard is your greatest resource to finding out what you missed and how you should prepare for the next class. Getting Help: Students who need additional help with the course should see the instructor as soon as possible. I am available during office hours or by appointment to answer questions or provide extra help in person. I am also happy to answer questions via email and will respond within 24 hours of receipt of your message. Until you receive a response from me, assume I have not received your email. Do NOT wait until the end of the semester to seek additional help. Course Agenda: Below is a list of the topics we will hopefully cover and dates for exams, quizzes and assignments that will occur during the semester. Additional readings for in class discussion will be assigned to you during the semester. These assignments will be announced in class and the materials posted to Blackboard in advance. In the event there is a class cancellation, all due dates (exams, quizzes, homework, readings, etc.) will be shifted to the next class period. Week Topic Chapters/Readings Introduction to Molecular 1 Neuroscience/Review of Cellular Chapter 1 Sept. 9 Components of Nervous Tissues Regulation of Neuronal Gene Expression Chapter 5 2 Neurogenesis and Subcellular Organization Sept. 13 & 16 Chapter 2 of the Nervous System: Axons v. Dendrites Subcellular Organization of the Nervous System: Molecular Transport Chapter 2 3 Sept. 20 & 23 Sept. 23: Quiz 1 Chapter 3 Energy Metabolism in the Brain Molecular Properties of Ion Channels Chapter 11 4 Sept. 27 & 30 Membrane Biophysics: Membrane Chapter 12 & 13 Potential and Voltage-Gated Ion Channels I Oct. 4: EXAM I 5 Oct. 4 & 7 Oct. 7 – Class Cancelled Biophysics of Voltage-Gated Ion Channels Chapter 13 6 II Oct. 11 & 14 Membrane Biophysics: Action Potential Chapter 12 & 14 Neurotransmitters: Classical and Non- Chapter 8 Classical 7 Oct. 18 & 21 Release of Neurotransmitter: Stimulus/ Secretion Coupling I Chapter 15 Oct 21: Group Project Proposals Due Oct. 25: Quiz 2 Release of Neurotransmitter: Chapter 15 8 Stimulus/Secretion Coupling II Oct. 25 & 28 Neurotransmitter Receptors: Ionotropic v. Chapter 10 metabotropic Intracellular Signaling Pathways I Chapter 4 9 Nov. 1 & 4 Nov. 4: Exam 2 Intracellular Signaling Pathways II Chapter 4 & 6 10 Nov. 8 & 11 Nov. 11 – Veteran’s Day, No Class Nervous System Damage: Axon Degeneration and Repair 11 Nov. 15 & 18 Gap Junctions Chapter 9 Postsynaptic Potentials and Synaptic Chapter 16 12 Integration Nov. 22 & 25 Nov. 25 – No Class: Happy Thanksgiving! Nov. 29: Quiz 3 Chapter 17 13 Information Processing in Dendrites Nov. 29 & Information Processing In Neural Networks Chapter 19 Dec. 2 Dec. 2 - Group Presentations Synaptic Plasticity 14 Dec. 6 - Group Presentations Chapter 18 & 20 Dec. 6 Dec. 6 – Final Reports Due Dec. 9 - 16 EXAM III – TBD (FINALS WEEK) Grading and Evaluation: Performance in the course will be graded according to the breakdown listed below. Exams I-III: 60% Exam I: 20%, Tuesday, October 4th Exam II: 20%, Friday, November 4th Exam III: 20%, during finals week date TBD Group Project: 20% Quizzes: 20% Exams: Throughout the course there will be three, closed-book, closed note, unit exams (this includes your final exam). Each exam will cover primarily the material that is covered in that unit. However, knowledge of fundamental concepts covered earlier in the semester will be assumed as we progress through more advanced topics. In total, exams account for 60% of your final course grade Exams will consist of: o Multiple choice o Matching o Problem solving o Short answer Final Examination: The final exam schedule is announced by the University well in advance of finals. Do not purchase airplane tickets, etc. until you know the date of your final exams including this course. If you find that you have a scheduling conflict between the final for this course and another course, it is your responsibility to complete and submit the final exam conflict form available through the Registrar’s Office online at URL: http://www.northeastern.edu/registrar/form- finex-conflict.pdf Quizzes: There will be three quizzes throughout the semester. The purpose of the quizzes is to encourage you to review your lecture notes and study, as well as to monitor the effectiveness the lectures. They will be given at the beginning of the class period and should take no more than 30 minutes to complete and consist of multiple choice, short answer and/or fill in the blank. They will account for 20% of your final course grade. Quiz 1: Friday, September 23rd Quiz 2: Tuesday, October 25th Quiz 3: Tuesday, November 29th Exam and Quiz Make Up Policy: Make up exams and quizzes can be scheduled should you have an unavoidable health or personal emergency. Only ONE make up quiz or exam will be allowed per student for the semester. Please contact me as soon as possible if you have a conflict with a quiz or exam so we can make the appropriate considerations. Drug Advertisement Group Project: During the semester you will be given the opportunity to apply your understanding of the mechanisms and principles underlying molecular interactions and neuron function and present your ideas to the class.
Recommended publications
  • The Creation of Neuroscience
    The Creation of Neuroscience The Society for Neuroscience and the Quest for Disciplinary Unity 1969-1995 Introduction rom the molecular biology of a single neuron to the breathtakingly complex circuitry of the entire human nervous system, our understanding of the brain and how it works has undergone radical F changes over the past century. These advances have brought us tantalizingly closer to genu- inely mechanistic and scientifically rigorous explanations of how the brain’s roughly 100 billion neurons, interacting through trillions of synaptic connections, function both as single units and as larger ensem- bles. The professional field of neuroscience, in keeping pace with these important scientific develop- ments, has dramatically reshaped the organization of biological sciences across the globe over the last 50 years. Much like physics during its dominant era in the 1950s and 1960s, neuroscience has become the leading scientific discipline with regard to funding, numbers of scientists, and numbers of trainees. Furthermore, neuroscience as fact, explanation, and myth has just as dramatically redrawn our cultural landscape and redefined how Western popular culture understands who we are as individuals. In the 1950s, especially in the United States, Freud and his successors stood at the center of all cultural expla- nations for psychological suffering. In the new millennium, we perceive such suffering as erupting no longer from a repressed unconscious but, instead, from a pathophysiology rooted in and caused by brain abnormalities and dysfunctions. Indeed, the normal as well as the pathological have become thoroughly neurobiological in the last several decades. In the process, entirely new vistas have opened up in fields ranging from neuroeconomics and neurophilosophy to consumer products, as exemplified by an entire line of soft drinks advertised as offering “neuro” benefits.
    [Show full text]
  • Epigenetic Pathways Through Which Experiences Become Linked with Biology
    Development and Psychopathology 27 (2015), 637–648 # Cambridge University Press 2015 doi:10.1017/S0954579415000206 Epigenetic pathways through which experiences become linked with biology a b PATRICK O. MCGowan AND TANIA L. ROTH aUniversity of Toronto; and bUniversity of Delaware Abstract This article highlights the defining principles, progress, and future directions in epigenetics research in relation to this Special Issue. Exciting studies in the fields of neuroscience, psychology, and psychiatry have provided new insights into the epigenetic factors (e.g., DNA methylation) that are responsive to environmental input and serve as biological pathways in behavioral development. Here we highlight the experimental evidence, mainly from animal models, that factors such as psychosocial stress and environmental adversity can become encoded within epigenetic factors with functional consequences for brain plasticity and behavior. We also highlight evidence that epigenetic marking of genes in one generation can have consequences for future generations (i.e., inherited), and work with humans linking epigenetics, cognitive dysfunction, and psychiatric disorder. Though epigenetics has offered more of a beginning than an answer to the centuries-old nature–nurture debate, continued research is certain to yield substantial information regarding biological determinants of central nervous system changes and behavior with relevance for the study of developmental psychopathology. Experiences, particularly those occurring during sensitive peri- To better understand the consequences of early and later- ods of development, are well recognized for their ability to ca- life stress on epigenetic mechanisms in this capacity, this nalize neurobiological trajectories and yield significant conse- has required the utilization of experimental rodent models quences for lifelong health and mental well-being.
    [Show full text]
  • Neurobiology and Behavior (NEURBIO) 1
    Neurobiology and Behavior (NEURBIO) 1 Neurobiology and Behavior (NEURBIO) Courses NEURBIO 200A. Research in Neurobiology and Behavior. 2-12 Units. Individual research with Neurobiology and Behavior faculty. Repeatability: Unlimited as topics vary. Restriction: Graduate students only. Neurobiology and Behavior Majors only. NEURBIO 200B. Research in Neurobiology and Behavior. 2-12 Units. Individual research with Neurobiology and Behavior faculty. Prerequisite: NEURBIO 200A Repeatability: Unlimited as topics vary. Restriction: Graduate students only. Neurobiology and Behavior Majors only. NEURBIO 200C. Research in Neurobiology and Behavior. 2-12 Units. Individual research with Neurobiology and Behavior faculty. Prerequisite: NEURBIO 200B Repeatability: Unlimited as topics vary. Restriction: Graduate students only. Neurobiology and Behavior Majors only. NEURBIO 201A. Research in Neurobiology and Behavior. 2-12 Units. Individual research with Neurobiology and Behavior faculty. Grading Option: Satisfactory/unsatisfactory only. Repeatability: Unlimited as topics vary. Restriction: Graduate students only. Neurobiology and Behavior Majors only. NEURBIO 201B. Research in Neurobiology and Behavior. 2-12 Units. Individual research with Neurobiology and Behavior faculty. Prerequisite: NEURBIO 201A Grading Option: Satisfactory/unsatisfactory only. Repeatability: Unlimited as topics vary. Restriction: Graduate students only. Neurobiology and Behavior Majors only. NEURBIO 201C. Research in Neurobiology and Behavior. 2-12 Units. Individual research with Neurobiology and Behavior faculty. Prerequisite: NEURBIO 201B Grading Option: Satisfactory/unsatisfactory only. Repeatability: Unlimited as topics vary. Restriction: Graduate students only. Neurobiology and Behavior Majors only. NEURBIO 202A. Foundations of Neuroscience. 2 Units. Intended to expose students to critical reading and analysis of the primary neuroscience literature. Instructors from departments associated with the Interdepartmental Neuroscience Program participate and discuss topics of current interest.
    [Show full text]
  • Neuroscience Major Requirements (Fall 2017 Or Later)
    Neuroscience Major Requirements (Fall 2017 or later) Undergraduate Program in Neuroscience : 1140 Undergrad. Science Bldg. (USB) : http://www.lsa.umich.edu/neurosci : [email protected] : 734-763-7984 (front desk) Why study Neuroscience? Neuroscience is the study of the nervous system. Neuroscientists aim to understand how the nervous system develops and functions on a cellular level as well as the mechanisms that underlie behavior, mental disorders and disease. The faculty teaching courses in the major include cellular and molecular neuroscientists appointed in the Department of Molecular, Cellular and Developmental Biology (MCDB) and behavioral and cognitive neuroscientists appointed in the Department of Psychology. This interdisciplinary program gives students the best of both of these worlds. Who should major in Neuroscience? Any student who wishes to pursue a career studying the nervous system or behavior. This is an excellent major for anyone interested in pre-health careers, graduate studies, or careers in the biotech industry. Exclusions: Students who elect a major in Neuroscience may not elect the following majors: Biochemistry Biology Biology, Health & Society (BHS) Biomolecular Science (BMS) Biopsychology, Cognition and Neuroscience (BCN) Cellular & Molecular Biology (CMB) CMBS (formerly CMB:BME) Molecular, Cellular, and Developmental Biology (MCDB) Microbiology Plant Biology Students who elect a major in Neuroscience may not elect a minor in Biology, Plant Biology, Chemistry, or Biochemistry. Students can double major in Psychology and Neuroscience or Cognitive Science and Neuroscience, but may only share a maximum of 3 courses between their two programs. How do I declare? Students interested in neuroscience are encouraged to meet with an advisor to discuss their academic plans as soon as possible! Students need not have completed all of the prerequisites of the major to declare, but should usually have completed the biology introductory sequence with a 2.0 or better and be in good academic standing.
    [Show full text]
  • Lori Knackstedt
    Lori A. Knackstedt, PhD Psychology Department 114 Psychology Building P.O. Box 112250 Gainesville, FL 32611 Email: [email protected] Education Ph.D. 2005: Psychology; University of California, Santa Barbara, Santa Barbara, CA Advisor: Aaron Ettenberg Dissertation: “Motivating Factors Underlying the Co-administration of Cocaine and Alcohol” B.S. 1999: Bucknell University, Lewisburg, PA Major: Biology Magna cum laude Positions Held ______ 2012-present Assistant Professor Psychology Department University of Florida, Gainesville, FL 2008-2012 Research Assistant Professor Neurosciences Department Medical University of South Carolina, Charleston, SC 2005-2008 Post-doctoral Fellow Neurosciences Department Medical University of South Carolina, Charleston, SC Mentor: Peter Kalivas Teaching Experience 2010-2012 Lecturer: MUSC College of Medicine Lectured in the Neuroscience course component for 1rst year medical students and taught the 2 week neuroscience component of Gross Anatomy Lab 2005-2012 Adjunct Faculty: Psychology Dept., College of Charleston, Charleston, SC “PSYCH 103: Introduction to Psychological Science” “PSYCH 388: Psychology of Substance Abuse” “PSYCH 214: Behavioral Neuroscience” 2003-2004 Adjunct Faculty: Psych. Dept., Santa Barbara City College, Santa Barbara, CA “PSY 110: Intro to Physiological Psychology” C.V. Knackstedt 2 2003-2004 Instructor: University of California, Santa Barbara, Santa Barbara, CA “PSYCH 111: Concepts in Biological Psychology” “PSYCH 106: Brain and Behavior” Research Support Ongoing: NIDA: R01 DA033436 (PI:
    [Show full text]
  • Neuroscience
    MD Anderson Cancer Center UTHealth Graduate School of Biomedical Sciences Graduate Program in GSBSNEUROSCIENCE neurograd.org doctoral The MD Anderson Cancer Center UTHealth Graduate requirements School of Biomedical Sciences (GSBS) is a joint venture of Students must complete The University of Texas Health Science Center at Houston the following requirements to obtain the degree of (UTHealth) and The University of Texas MD Anderson Cancer Doctor of Philosophy with Center that offers Ph.D. and M.S. degrees in Neuroscience. a specialization in Neuroscience: Areas of research concentration include molecular, cellular, systems, cognitive, and translational neuroscience. There Research Rotations: First-year students obtain are more than 50 GSBS faculty members and more than hands-on research 25 graduate students representing sixteen departments of experience by participating in three research tutorials. UTHealth and MD Anderson currently in the Neuroscience Graduate Program. Coursework: All students in Neuroscience are required to take two Program Core All Ph.D. students receive full financial support throughout Courses (Molecular and Cellular Neuroscience, their training, which includes tuition, Systems Neuroscience) fees, stipend, and benefits. Annual and two advanced elective courses. Also required are competitive awards are available for the Ethical Dimensions outstanding research projects and of Biomedical Science, PROGRAM OVERVIEW Scientific Writing, and posters, and to support student travel Biostatistics for Life to scientific meetings. Scientists. Core Courses must be taken for credit and a grade of “B” or better must be earned. Transsynaptic labelling of dorsal raphe neurons (green) from crfr2+ serotonin neurons (red) Annual Retreat RESEARCH AREAS Candidacy Exam: To advance to candidacy, all students need to defend an NRSA-style proposal as part Our students have the opportunity to receive training and to conduct of a candidacy exam.
    [Show full text]
  • Neurobiology and Therapeutic Applications of Neurotoxins Targeting Transmitter Release - Sciencedirect
    8/25/2018 Neurobiology and Therapeutic Applications of Neurotoxins Targeting Transmitter Release - ScienceDirect Outline Download Export Pharmacology & Therapeutics Available online 25 August 2018 In Press, Accepted Manuscript Neurobiology and Therapeutic Applications of Neurotoxins Targeting Transmitter Release Saak V. Ovsepian a, b, c , Valerie B. O’Leary c, Naira M. Ayvazyan d, Ahmed Al-Sabi e, Vasilis Ntziachristos a, b, J. Oliver Dolly c Show more https://doi.org/10.1016/j.pharmthera.2018.08.016 Get rights and content ABSTRACT Synaptic transmission is a fundamental neurobiological process enabling exchange of signals between neurons as well as neurons and their non-neuronal effectors. The complex molecular machinery of the synaptic vesicle cycle and transmitter release has emerged and developed in the course of the evolutionary race, to ensure adaptive gain and survival of the fittest. In parallel, a generous arsenal of biomolecules and neuroactive peptides have co-evolved, which selectively target the transmitter release machinery, with the aim of subduing natural rivals or neutralizing prey. With the advance of neuropharmacology and quantitative biology, neurotoxins targeting presynaptic mechanisms have attracted major interest, revealing considerable potential as carriers of molecular cargo and probes for meddling synaptic transmission mechanisms for research and medical benefit. In this review, we investigate and discuss key facets employed by the most prominent bacterial and animal toxins targeting the presynaptic secretory machinery. We explore the cellular basis and molecular grounds for their tremendous potency and selectivity, with effects on a wide range of neural functions. Finally, we consider the emerging preclinical and clinical data advocating the use of active ingredients of neurotoxins for the advancement of molecular medicine and development of restorative therapies.
    [Show full text]
  • Neurotoxin-Induced Degeneration of Dopamine Neurons in Caenorhabditis Elegans
    Neurotoxin-induced degeneration of dopamine neurons in Caenorhabditis elegans Richard Nass*†, David H. Hall‡, David M. Miller III†§, and Randy D. Blakely*†¶ Departments of *Pharmacology and §Cell Biology and †Center for Molecular Neuroscience, Vanderbilt University School of Medicine, Nashville, TN 37232-6420; and ‡Center for Caenorhabditis elegans Anatomy, Albert Einstein College of Medicine, New York, NY 10461 Edited by Solomon H. Snyder, Johns Hopkins University School of Medicine, Baltimore, MD, and approved December 27, 2001 (received for review September 21, 2001) Parkinson’s disease is a complex neurodegenerative disorder char- vesicular packaging, and inactivation (16–19). Moreover, the acterized by the death of brain dopamine neurons. In mammals, genetics and cellular features of necrotic and apoptotic cell death dopamine neuronal degeneration can be triggered through expo- have been well described in C. elegans (20, 21), affording an sure to neurotoxins accumulated by the presynaptic dopamine opportunity to relate toxin-induced dopamine neuronal injury to transporter (DAT), including 6-hydroxydopamine (6-OHDA) and these pathways. 1-methyl-4-phenylpyridinium. We have established a system for the pharmacological and genetic evaluation of neurotoxin-induced Materials and Methods dopamine neuronal death in Caenorhabditis elegans. Brief (1 h) Strains and Maintenance. C. elegans strains were cultured on exposure of green fluorescent protein-tagged, living worms to bacterial lawns of either OP-50 or NA-22 at 22°C according to 6-OHDA causes selective degeneration of dopamine neurons. We standard methods (22). N2 Bristol is the wild-type strain. ced- demonstrate that agents that interfere with DAT function protect 1(e1735), ced-3(n717), ced-4(n1162), dpy-20(e1282), dpy- against 6-OHDA toxicity.
    [Show full text]
  • MCB 160: Cellular & Molecular Neuroscience (MWF Lecture +
    MCB 160: Cellular & Molecular Neuroscience (MWF lecture + required discussion, 4 units) An introductory survey of designed to provide a general understanding of the nervous system including how it functions, how it develops, and how it changes with learning and memory. Analysis from the level of molecules to cells to simple circuits to complex networks to higher brain functions. First half of the introductory 160- 161 sequence. Required textbook: Kandel et al., Principles of Neural Science, 5th Ed. One chapter will be assigned for each lecture. Grading: 25% Midterm 1, 25% Midterm 2, 50% Final Exam. Fall. Staff. 1 Introduction. Gross anatomy. Golgi vs. Cajal in the neuron doctrine. Structure of a neuron. Cell types. Cellular neurophysiology 2 The plasma membrane 3 Passive electrical properties of neurons 4 Origin of the membrane potential 5 Selective permeability of ion channels 6 Gating of ion channels 7 The action potential 8 Propagation of action potentials The synapse 9 Physiology of synaptic transmission 10 Molecular mechanisms of exocytosis and endocytosis 11 Postsynaptic receptors (ionotropic) 12 Synaptic excitation, inhibition, and integration 13 Neurotransmitters MIDTERM 1 14 Metabotropic receptors, intracellular messengers and neuromodulation 15 Dendrites, spines, and dendritic excitability 16 Preview of neural circuits and systems. A simple, completely understood sensorimotor pathway: crayfish tail flip escape response. Basic architecture of mammalian sensory and motor pathways. Synaptic plasticity 17 Synaptic plasticity and
    [Show full text]
  • Neuroscience - CLA (NSCI) 1
    Neuroscience - CLA (NSCI) 1 Neuroscience - CLA (NSCI) Courses NSCI 0817. Brain Matters. 3 Credit Hours. One of the last frontiers in science is the brain. We know a great deal about the structure and function of the brain and nervous system, but it is challenging to comprehend fully the complexity of a system made up of 100 billion components that are interacting with one another using tens of trillions of connections that can change and rewire during development and aging. Neuroscience is the multidisciplinary field in which brain research falls. Neuroscience is one of the fastest growing domains in all of science - and good bet for a future career path. Neuroscientists investigate brain function from the level of molecular genetics, to cellular dynamics, to brain anatomy and physiology, to relations between brain, behavior, and cognition, to brain development and aging, to diseases of the brain. In this course, we will touch on knowledge about the brain at all these levels, and more. We will also discuss case studies of brain impairment. NOTE: This course fulfills a Science & Technology (GS) requirement for students under GenEd and Science & Technology Second Level (SB) for students under Core. Students cannot receive credit for this course if they have successfully completed Psychology 0817. Course Attributes: GS Repeatability: This course may not be repeated for additional credits. NSCI 1002. Careers in Neuroscience. 1 Credit Hour. This course will cover the wide range career options available in Neuroscience, focusing on what is possible with an undergraduate and graduate degree. Traditional career paths will be discussed, such as medicine and research, as well as "non-traditional" paths in clinical/science administration.
    [Show full text]
  • Molecular Neuroscience and Neuropharmacology (3 Credit Hours) GMS6023 Spring 2021 Delivery Format: in Person
    UNIVERSITY OF FLORIDA COLLEGE OF MEDICINE SYLLABUS NEUROSCIENCE Neuropharmacology and its Clinical Application (3 credit hours) NEW TITLE: Molecular Neuroscience and Neuropharmacology (3 credit hours) GMS6023 Spring 2021 Delivery Format: In person. DeWeese Auditorium – MBI, LG-101A Mondays 9:00am-12:00pm. Instructors: Dr. Habibeh Khoshbouei and Dr. Eduardo Candelario-Jalil Room Number: DeWeese Auditorium – MBI, LG-101A Phone Number: 352-273-8115 (Dr. Khoshbouei) and 352-273-7116 (Dr. Candelario-Jalil) Email Addresses: [email protected] and [email protected] Office Hours: Mondays 1-3pm and Wednesdays 9-11am (Office: L1-100J) Graduate Assistant: None Preferred Course Communications: Email Prerequisites: Doctoral students. You are expected to be familiar with basic Neuroscience concepts before starting this course series. If you are uncertain about the sufficiency of your background, you are encouraged to read through chapters one through ten in Neuroscience Online – an electronic textbook (Open Access) http://nba.uth.tmc.edu/neuroscience/ Purpose and Outcome This is one of the required courses for the Neuroscience concentration. It is intended for all PhD students interested in learning about the neurochemical basis for drug action. Course Overview This course surveys the basic principles of neuropharmacology with an emphasis on the molecular pharmacology of drugs used to treat CNS disorders. The specific focus of this course will be to provide a description of the cellular and molecular actions of drugs on synaptic transmission with in-depth discussion of drug-induced changes in functioning of the nervous system. We will examine how the neurotransmitter systems influence nervous system function as well as therapeutic targets affecting these neurotransmitter systems.
    [Show full text]
  • Epigenetic Mechanisms Governing Behavioral Reprogramming in the Ant Camponotus Floridanus
    University of Pennsylvania ScholarlyCommons Publicly Accessible Penn Dissertations 2018 Epigenetic Mechanisms Governing Behavioral Reprogramming In The Ant Camponotus Floridanus Riley John Graham University of Pennsylvania, [email protected] Follow this and additional works at: https://repository.upenn.edu/edissertations Part of the Genetics Commons, Molecular Biology Commons, and the Neuroscience and Neurobiology Commons Recommended Citation Graham, Riley John, "Epigenetic Mechanisms Governing Behavioral Reprogramming In The Ant Camponotus Floridanus" (2018). Publicly Accessible Penn Dissertations. 2883. https://repository.upenn.edu/edissertations/2883 This paper is posted at ScholarlyCommons. https://repository.upenn.edu/edissertations/2883 For more information, please contact [email protected]. Epigenetic Mechanisms Governing Behavioral Reprogramming In The Ant Camponotus Floridanus Abstract Eusocial insect colonies divide behaviors among specialist groups called castes. In some species, caste identity is determined by the interaction of endogenous (e.g. genomic) and exogenous (e.g. juvenile hormone from nurses) signals during larval development, suggesting epigenetic mechanisms underlie plastic traits tied to caste identity. Previous work demonstrated a link between patterns of histone H3 lysine 27 acetylation (H3K27ac) and caste-specific gene expression in Major and Minor workers of the ant Camponotus floridanus, and we hypothesized caste-specific behaviors such as foraging may be similarly regulated by histone acetylation.
    [Show full text]