Hypokalemic Periodic Paralysis II BME 301 Spring 2008 Dr. Entcheva Group 6.

Slides:



Advertisements
Similar presentations
Modeling the Action Potential in a Squid Giant Axon And how this relates to the beating of your heart.
Advertisements

Na + and Ca 2+ CHANNELOPATHIES Na + channel (NaV1.4) Potassium aggravated myotonia Paramyotonia congenita Hyperkalemia periodic paralysis Hypokalemic periodic.
Understanding PP and treatment of HypoPP Biannual Meeting of the PPA Orlando, FL, 2011 Frank Lehmann-Horn, Senior Research Professor.
Medical Physiology PBL -1
Na + and Ca 2+ CHANNELOPATHIES Na + channel (NaV1.4) Potassium aggravated myotonia Paramyotonia congenita Hyperkalemia periodic paralysis Hypokalemic periodic.
Dr. Emmanuel Fournier La Salpêtrière Hospital, Paris, France
Migraine Management Lifestyle and Alternative Treatments
Epilepsy P. Ockuly, Champlin Park H.S. & B. Tapper, Agape H.S.
Hypokalemic Periodic Paralysis Type II: Mutations of the SCN4A Sodium Gene Presenting : Angela Galotti Jim Gettings Hala Mostafa The Rest :Matt Mancuso.
By Robert Johnson SPINAL MUSCULAR ATROPHY. SYMPTOMS INFANT Can have a breathing difficulty Difficulty feeding, food may go down windpipe instead of stomach.
Long QT Syndrome Type 3 (LQT 3) Mutations in SCN5A (Na+ Channel, I Na ) BME 301 Qaiyim Cheeseborough, Victoria Reyes, Kin Siu.
Long QT Syndrome Type 3 (LQT 3) Mutations in SCN5A (Na+ Channel, I Na ) BME 301 Silvia Castillo, Qaiyim Cheeseborough, Victoria Reyes, Kin Siu.
Cardiac Arrest Mirna Gonzalez Ninth Grade- 14 years of age.
Are you at Risk for Heart Disease?. The heart –Pumps ~5 liters of blood every minute –Beats about 10,000 times a day –Pumps blood and oxygen throughout.
Narcolepsy: There’s a Nap for That
Investigation of Possible Periodic Paralysis (P3)
By Nathan Campbell. A mineral is a naturally occurring inorganic solid with a definite chemical composition and an ordered atomic arrangement.
Grow Your Brain at Any Age Majid Fotuhi, MD PhD Howard County Office on Aging Columbia, MD March 28, 2014.
Six Steps to a Better Brain Majid Fotuhi, MD PhD March 6, 2014.
Kearns-Sayre Syndrome By Tommy Antony. Mitochondrial DNA Circular DNA Encodes for several RNA’s and Proteins Mitochondria produces energy for the body.
PHM142 Fall 2015 Instructor: Dr. Jeffrey Henderson.
Nerve Impulse. A nerve impulse is an impulse from another nerve or a stimulus from a nerve receptor. A nerve impulse causes:  The permeability of the.
Nerve Impulse. A nerve impulse is an impulse from another nerve or a stimulus from a nerve receptor. A nerve impulse causes:  The permeability of the.
Resting Membrane Potential. Membrane Potentials  Electrical signals are the basis for processing information and neuronal response  The impulses are.
Design of a Simulation Toolbox for Gastrointestinal Electrical Activity n BME 273: Senior Design Projects n John F Gouda n Advisor: Dr. Alan Bradshaw,
Voltage-Gated Ion Channels in Health and Disease jdk3 Principles of Neural Science, chapter 9.
 Indicate how frequently you engage in each of the following behaviors (1 = never; 2 = occasionally; 3 = most of the time; 4 = all of the time) 1.I eat.
The Heart has 3 Main Electrical channels that “fire” with every heart beat: –Sodium (Na + ), Potassium (K + ), Calcium (Ca ++ ) These 3 channels are in.
Design of a Simulation Toolbox for Gastrointestinal Electrical Activity n BME 273: Senior Design Projects n John F Gouda n Advisor: Dr. Alan Bradshaw,
HYPP Hyperkalemic Periodic Paralaysis M. BRANTLEY, LVT.
Genetic Diseases Cystic Fibrosis Albinism Phenylketonuria Macy VanArnam.
Objectives  To recognize existence of muscle diseases  To differentiate them from other disorders.  To know about various causes of myopathy.  To.
ResourcesChapter menu Copyright © by Holt, Rinehart and Winston. All rights reserved. Lifestyle Diseases Chapter 14.
A.K.A :acute cerebrovascular attack
Dr. Emmanuel Fournier La Salpêtrière Hospital, Paris, France
Effect of the antimalarial drug halofantrine in the long QT syndrome due to a mutation of the cardiac sodium channel gene SCN5A  Kirsi Piippo, MSc, Sam.
Nanette Safonts Period 3
Christian S. Meyhoff, MD, PhD
Dr. Emmanuel Fournier La Salpêtrière Hospital, Paris, France
Canavan Disease The causes of, detection of, symptoms of, and treatment of Canavan disease.
Glycogen Storage Diseases
A conceptual model of cardiac membrane fast sodium and slow calcium ion channels: at rest (A), during the initial phases of the fast-response (B and C),
Cardiac action potential
Molecular Determinants of Na+ and K+ Channel Regulation in Heart: Ion Channels as Targets of Neurohormones and Drugs.
414. A Novel Clinical Severity Scoring Measure in Canine X-Linked Myotubular Myopathy: Results Following Systemic AAV Gene Replacement    Molecular Therapy 
A Cardiac Sodium Channel Mutation Cosegregates With a Rare Connexin40 Genotype in Familial Atrial Standstill by W. Antoinette Groenewegen, Mehran Firouzi,
Biannual Meeting of the PPA
Hypertrophic Cardiomyopathy
Paul M. George, Gary K. Steinberg  Neuron 
Hyperkalemic Periodic Paralysis
The Sodium Channel: One Gene, Many Diseases!
The Sodium Channel: One Gene, Many Diseases!
12/30/2018 OSTEOPOROSIS.
Painful Channels Neuron
Ventricular Tachycardia in Structural Heart Disease
Cardiac Muscle Physiology
Volume 155, Issue 4, Pages (October 2018)
Cardiac Muscle Physiology
René van Gent, MD, Cornelis K. van der Ent, MD, PhD, Maroeska M
Volume 50, Issue 1, Pages (January 2014)
Calcium channelopathies
Is variant pathogenicity in the eye of the beholder
International Journal of Cardiology
Episodic Neurological Channelopathies
Aya Miyazaki et al. JACEP 2016;2:
Nat. Rev. Neurol. doi: /nrneurol
Volume 57, Issue 3, Pages (March 2000)
Gerald V Naccarelli, MD, Charles Antzelevitch, PhD 
Presentation transcript:

Hypokalemic Periodic Paralysis II BME 301 Spring 2008 Dr. Entcheva Group 6

Hypokalemic Periodic Paralysis II: Symptoms Weakness Paralysis Temporal duration: Up to 24 hours

Hypokalemic Periodic Paralysis II: Factors Mutation of SCN4A gene Situational: Excess of carbohydrates, salt, alcohol Immediate rest after strenuous activity Sudden temperature change

Hypokalemic Periodic Paralysis II: Action Potential * Jurkat-Rott, Karin, et al. Voltage-sensor sodium channel mutations cause hypokalemic periodic paralysis type 2 by enhanced inactivation and reduced current. PNAS Aug; 97(17): *

Hypokalemic Periodic Paralysis II: Treatment Preventative Diet low in Na and carbohydrates Avoidance of attack- inducing situations Acetazolamide (Diamox) During Attack Hospitalization Potassium Understanding through Modeling…

Hypokalemic Periodic Paralysis II: Modeling Model of diseased cell’s electrical activity using Matlab Creation of Graphical User Interface (GUI) Changes to code supplied by Dr. Entcheva

Hypokalemic Periodic Paralysis II: GUI

Hypokalemic Periodic Paralysis II: Code Changes

Two changes: K O & τ h

Change in [K]out

Changes to Tau h Tau_h in HypoPP is about 65% of the normal value Tauh =.65 No changes to Tau_m or Tau_j values  Tauj = Taum = 1

Hypokalemic Periodic Paralysis II: Sodium Gate *Taken from Dr. Entcheva’s BME 301 Spring 2008 in-class lecture.

Sensitivity analysis for [K]out

Sensitivity analysis [K]out cont.

Sensitivity Analysis for Tau h

Sensitivity Analysis for tau h

HypoPP2 affects Skeletal Muscle NOT CARDIAC MUSCLE!! * Jurkat-Rott, Karin, et al. Voltage-sensor sodium channel mutations cause hypokalemic periodic paralysis type 2 by enhanced inactivation and reduced current. PNAS Aug; 97(17):

Hypokalemic Periodic Paralysis II: Diseased Cardiac Ventricular Cell Simulation HypoPP2 Normal Cell

Hypokalemic Periodic Paralysis II: Skeletal Muscle Cell Simulation

Hypokalemic Periodic Paralysis II: Treatment of Cardiac Ventricular Cell Simulation

References 1. Mosenkis, Ari. Hypokalemic periodic paralysis. U.S. National Library of Medicine. 01 March Sternberg, Damien, Thierry Maisonobe, and Karin Jurkat-Rott. "Hypokalaemic Periodic Paralysis Type 2 Caused by Mutations At Codon 672 in the Muscle Sodium Channel Gene SCN4A." Brain: a Journal of Neurology 124 (2001): PubMed. 21 Mar Jurkat-Rott, Karin, et al. “Voltage-sensor sodium channel mutations cause hypokalemic periodic paralysis type 2 by enhanced inactivation and reduced current.” PNAS Aug; 97(17): Bulman DE, Scoggan KA, van Oene MD, Nicolle MW, Hahn AF, Tollar LL, et al. A novel sodium channel mutation in a family with hypokalemic periodic paralysis. Neurology 1999; 53: 1932–6. 5. Sansone, V et al. Treatment for periodic paralysis. Cochrane Database Syst Rev Jan 23;(1) 6. Hypokalemic Periodic Paralysis: A Model for a Clinical and Research Approach to a Rare Disorder. Neurotherapeutics, Volume 4, Issue 2, Pages B. Fontaine, E. Fournier, D. Sternberg, S. Vicart, N. Tabti