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Encyclopedia results for Depolarization

Depolarization





Encyclopedia results for Depolarization

  1. Ionotropic effect

    Orphan date April 2012 An ionotropic effect is a special kind of effect of a hormone on its target. The hormone activates or deactivates ionotropic receptor s ligand gated ion channels . The effect can be either positive or negative, whether the effect is a depolarization or a hyperpolarization respectively. Examples Noradrenaline aka. Norepinephrine has a positive ionotropic effect on heart muscle , when binding to beta 1 adrenergic receptor s on this tissue. ref name purves Neuroscience Purves , Third Edition, table 20 2 ref The result is an increased cardiac output . References references DEFAULTSORT Ionotropic Effect Category Membrane biology Category Electrophysiology Category Neurochemistry Category Molecular neuroscience ar ...   more details



  1. Potassium spatial buffering

    Multiple issues notability November 2008 context November 2008 orphan December 2008 unreferenced December 2008 Potassium Spatial Buffering is a mechanism for the regulation of extracellular potassium concentration by astrocyte s. The depolarization of neuron s tends to raise potassium concentration in the extracellular fluid. If a significant rise occurs, it will interfere with neuronal signaling by depolarizing neurons. Astrocytes have large numbers of potassium ion channels facilitating removal of potassium ions from the extracellular fluid. They are taken up at one region of the astrocyte and then distributed throughout the cytoplasm of the cell, and further to its neighbors via gap junction s. This keeps extracellular potassium at levels that prevent interference with normal propagation of an action potential . DEFAULTSORT Potassium Spatial Buffering Category Biology Biology stub ...   more details



  1. Surfactant-albumin ratio

    orphan date March 2010 The surfactant albumin ratio is a test for assessing Fetus fetal lung maturity. ref name pmid10920328 cite journal author Liu KZ, Shaw RA, Dembinski TC, Reid GJ, Ying SL, Mantsch HH title Comparison of infrared spectroscopic and fluorescence depolarization assays for fetal lung maturity journal Am. J. Obstet. Gynecol. volume 183 issue 1 pages 181 7 year 2000 month July pmid 10920328 doi 10.1067 mob.2000.105345 url http linkinghub.elsevier.com retrieve pii S0002 9378 00 77338 8 ref References reflist Obstetrical procedures Category Embryology medicine stub ...   more details



  1. Bathmotropic

    channels and its effect on closing rate Bot generated title ref causes a partial depolarization ... pii S016752730500269X ref causes a partial depolarization of the resting membrane potential Norepinephrine ... Mild hypoxia causes a partial depolarization of the muscle membrane Ischaemia causes a partial depolarization ... Marked hyperkalemia causes a marked depolarization of the resting membrane potential Hypokalemia ... Acetyl choline same as parasympathetic stimulation Marked hypoxia causes a marked depolarization ...   more details



  1. Ventricular action potential

    Unreferenced date December 2009 In electrocardiography , the ventricular myocyte cell potential membrane potential is about 90 mV at rest, which is close to the potassium reversal potential . When an action potential is generated, the membrane potential rises above this level in four distinct phases. The beginning of the action potential, phase 0, specialized integral membrane protein membrane proteins ion channel voltage gated sodium channels in the cell membrane selectively allow sodium ion s to enter the cell. This causes the membrane potential to rise at a rate of about 300 V s. As the membrane voltage rises to about 40 mV sodium channels close due to a process called inactivation. The Na channel opening is followed by inactivation. Na inactivation comes with slowly activating Ca2 channels at the same time as a few fast K channels open. There is a balance between the outward flow of K and the inward flow of Ca2 causing a plateau of length in variables. The delayed opening of more Ca2 activated K channels, which are activated by build up of Ca2 in the sarcoplasm, while the Ca2 channels close, ends the plateau. This leads to repolarisation. The depolarization of the membrane allows calcium channels to open as well. As sodium channels close calcium provides current to maintain the potential around 20 mV. The plateau lasts on the order of 100 ms. At the time that calcium channels are getting activated, channels that mediate the transient outward potassium current open as well. This outward potassium current causes a small dip in membrane potential shortly after action potential depolarization . This current is observed in human and dog action potentials, but not in guinea pig action potentials. action potential Repolarization is accomplished by channels that open slowly and are mostly activated at the end of the action potential slow delayed rectifier channels , and channels that open quickly but are inactivated until the end of the action potential rapid delayed re ...   more details



  1. Cardiac pacemaker

    , but contract relatively weakly. Cells in the SA node spontaneously depolarization depolarize ... decreases as time goes on, partly causing the slow depolarization. As well as this, there is a slow ... serves to make the cell more positive. This relatively slow depolarization continues until ... enter phase 0. Phase 0 Upstroke Though much faster than the depolarization caused by the funny ... to that in an axon . The SA and AV node do not have fast sodium channels like neurons, and the depolarization ...   more details



  1. Ophanin

    proteins inhibit depolarization induced smooth muscle contraction to different extents. Compared ... , while also having Phe189, does not affect depolarization induced contraction. ref name Biophysics Mode of action There is no direct evidence of a particular mode of action of ophanin blocking depolarization ... ref in regards to ablomin, another snake venom toxin from the CRISP family that also blocks depolarization ... for ophanin. Since ablomin only blocks contraction induced by depolarization, but not by caffeine ... artery. ref name biochem cite journal doi 10.1042 BJ20020191 title Membrane depolarization induced ...   more details



  1. Receptor potential

    Receptor potential , a type of graded potential, is the transmembrane potential difference of a sensory receptor . ref Cite book ref harv first Bertil last Hille authorlink Bertil Hille title Ion Channels of Excitable Membranes edition 3rd year 2001 publisher Sinauer location Sunderland, Massachusetts chapter Chapter 8. Sensory transduction and excitable cells. pages 237&ndash 268 isbn 0878933212 ref A receptor potential is often produced by sensory transduction . It is generally a depolarization depolarizing event resulting from inward current electricity current flow. The influx of current will often bring the membrane potential of the sensory receptor towards the threshold for triggering an action potential . A receptor potential is a form of graded potential. An example of this is in a taste bud , where taste is converted into an electrical signal sent to the brain. When stimulated, the taste bud triggers the release of neurotransmitter through exocytosis of synaptic vesicles from the presynaptic membrane. The neurotransmitter molecules diffuse across the synaptic cleft to the postsynaptic membrane. Graded potentials vary in size. They arise from the summation of the individual actions of ligand gated ion channel proteins, and decrease over time and space. They are distinct from Voltage gated ion channel voltage gated sodium and potassium channels . ref Harvnb Hille 2001 pp 169&ndash 200 . Chapter 6. Ligand gated channels of fast chemical synapses. ref References reflist DEFAULTSORT Receptor Potential Category Receptors Category Electrophysiology de Rezeptorpotential id Potensial reseptor ...   more details



  1. Epicardium

    Infobox Anatomy Name Epicardium Latin lamina visceralis pericardii serosi GraySubject GrayPage Image Gray968.png Caption A transverse section of the thorax, showing the contents of the middle and the posterior mediastinum. The pleural and pericardial cavities are exaggerated since normally there is no space between parietal and visceral pleura and between pericardium and heart. Image2 Caption2 Precursor System Artery Vein Nerve Lymph MeshName MeshNumber DorlandsPre l 02 DorlandsSuf 12476850 Epicardium describes the outer layer of heart tissue from Greek language Greek epi outer, cardium heart . When considered as a part of the pericardium , it is the inner layer, or visceral pericardium , continuous with the serous layer. Its largest constituent is connective tissue and functions as a protective layer. The visceral pericardium apparently produces the pericardial fluid , which lubricates motion between the inner and outer layers of the pericardium . During ventricular contraction, the wave of depolarization moves from endocardial to epicardial surface. See also Myocardium The middle muscle layer of the heart Endocardium The innermost layer of the heart External links http sprojects.mmi.mcgill.ca embryology cvs heart tube.html UMichAtlas ht pericard2 MRI of chest, lateral view Heart Category Cardiac anatomy circulatory stub az Epikard bs Epikard ca Epicardi de Epikard es Epicardio fr picarde it Epicardio hu Epicardium nl Epicard pl Nasierdzie ro Epicard sk Epikard ...   more details



  1. Euler?Liljestrand mechanism

    mergeto Hypoxic pulmonary vasoconstriction discuss Talk Hypoxic pulmonary vasoconstriction Merger proposal date May 2010 The Euler Liljestrand mechanism describes the connection between Ventilation physiology ventilation and blood circulation perfusion of the lung . If the ventilation in a part of the lung decreases, this leads to local Hypoxia medical hypoxia and to vasoconstriction in that part. This adaptive mechanism is beneficial, because it diminishes the amount of blood that passes the lung without being Oxygen saturation oxygenated . The mechanism was discovered by two Sweden Swedish pharmacologist s, Ulf von Euler and G ran Liljestrand at the Department of Pharmacology of Karolinska Institute in Stockholm . The molecular mechanism seems to be mediated by oxygen sensitive potassium ion channel s in the cell membrane of pulmonary smooth muscle . With a low partial pressure of oxygen, these channels are blocked, leading to the depolarization of the cell membrane. Calcium channels are activated and cause the influx of Ca sup 2 sup ions over the membrane and to the release of calcium from the endoplasmic reticulum . The rise of calcium concentration causes contraction of the blood vessels smooth muscle fibers and the resulting vasoconstriction . Histamine has also been implicated in this mechanism. References Von Euler, US Liljestrand, G 1946 . Observations on the pulmonary arterial blood pressure in the cat . Acta Physiol. Scand. 12 301 320 cite pmid 171630 cite pmid 12924 anatomy stub Category Respiratory physiology Category Cardiovascular physiology de Euler Liljestrand Mechanismus es Mecanismo Euler Liljestrand ...   more details



  1. Rheobase

    File rheobase chronaxie.png thumb alt Alt text Fig. 1 Rheobase and chronaxie are points defined on the strength duration curve for stimulus of an excitable tissue. In neuroscience , rheobase is the minimal current amplitude of indefinite duration practically, a few hundred milliseconds that results in the depolarization threshold of the cell membranes being reached i.e. an action potential or the contraction of a muscle . In the case of a nerve or single muscle cell, rheobase is half the current that needs to be applied for the duration of chronaxie to result in an action potential or muscle twitch. ref name ashley Ashley, et al. Determination of the Chronaxie and Rheobase of Denervated Limb Muscles in Conscious Rabbits. Artificial Organs , Volume 29 Issue 3 Page 212 March 2005 ref This can be understood better by looking at a strength duration relationship Fig. 1 . ref name flashman Fleshman et al. Rheobase, input resistance, and motor unit type in medial gastrocnemius motoneurons in the cat. Journal of Neurophysiology, 1981. ref See also Chronaxie References reflist Category Nervous system Category Neurophysiology neuroscience stub de Rheobase es Reobase fr Rh obase ro Reobaz ru ...   more details



  1. Myogenic mechanism

    The myogenic mechanism is how artery arteries and arteriole s react to an increase or decrease of blood pressure to keep the blood flow within the blood vessel constant. The smooth muscle of the blood vessels reacts to the stretching of the muscle by opening ion channels, which cause the muscle to depolarization depolarize , leading to muscle contraction. This significantly reduces the volume of blood able to pass through the lumen anatomy lumen , which reduces blood flow through the blood vessel. Alternatively when the smooth muscle in the blood vessel relaxes, the ion channels close, resulting in vasodilation of the blood vessel this increases the rate of flow through the lumen. This system is especially significant in the kidneys , where the glomerular filtration rate the rate of blood filtration by the nephron is particularly sensitive to changes in blood pressure. However, with the aid of the myogenic mechanism, the glomerular filtration rate remains very insensitive to changes in human blood pressure. External links http www.ncbi.nlm.nih.gov entrez query.fcgi?db pubmed&cmd Retrieve&dopt AbstractPlus&list uids 8087076&query hl 5&itool pubmed DocSum Moore L.C., A. Rich, and D. Casellas. Ascending myogenic autoregulation interactions between tubuloglomerular feedback and myogenic mechanisms.. Bull. Math. Biol. 56 391 410, 1994. med stub Cardiovascular physiology Category Cardiovascular physiology es Mecanismo miog nico ...   more details



  1. Calcium sparks

    Context date October 2009 Ca2 sparks, which are small, brief, and highly localized releases of Ca2 , were first observed in cardiac myocytes 27 and then in skeletal muscle fibers 128, 266 . They occur spontaneously in frog skeletal muscle fibers in the resting state 128 and at higher frequencies during depolarization 128, 266 . The frequency of Ca2 sparks activated by depolarization steeply increases with voltage at 4 mV per e fold change 128 , which is similar to the voltage dependence of the activation of Ca2 release determined in whole fibers 6, 209 . Unlike the spark frequency, the spatiotemporal properties of sparks are almost identical at rest and during depolarizations to different potentials 128, 130, 141 . The pattern of occurrence of Ca2 sparks after the start of a large depolarization, i.e., the latency histogram of Ca2 sparks, is similar to the pattern of the rate of Ca2 release after depolarization showing Ca inactivation of Ca2 release 129, 130 . These results suggest that the Ca2 spark is the basic unit event of physiological Ca2 release. Calcium sparks are calcium release events that occur within muscle cells. They are important in a physiological process called excitation contraction coupling , which is crucial to muscle function. In essence, electrical stimulation of the outer surface of a muscle cell triggers via a mechanism dependent on the muscle type thousands of calcium sparks that spatio temporally summate to increase intracellular calcium levels. ref cite journal author Cannell MB, Cheng H, Lederer WJ title Spatial non uniformities in Ca2 i during excitation contraction coupling in cardiac myocytes journal Biophysical Journal volume 67 issue 5 pages 1942 56 year 1994 month November pmid 7858131 pmc 1225569 doi 10.1016 S0006 3495 94 80677 0 ref This increase in calcium subsequently activates calcium sensitive proteins that are responsible for cell shortening, or contraction. In muscle, action potentials lead to the opening of intracellular ca ...   more details



  1. HRS Computing

    Infobox software name HRS Computing logo File HRSComputingIcon.png HRS Computing s icon screenshot File HRSComputingExample.png 250px caption A screenshot of HRS Computing 2.0.0 collapsible author S. Carrazza, J. Duboisset released December 2008 latest release version 2.0.0 latest release date December 2010 latest preview version latest preview date frequently updated programming language C operating system 32 bit & 64 bit Windows br Linux br Mac OS br FreeBSD br platform Cross platform language English, French, Italian, Spanish, Portughese status Active 2008 genre Physics simulation license GNU General Public License website http hrscomputing.sf.net HRS Computing is an opensource scientific software which simulates the hyper Rayleigh scattering HRS in nonlinear optics . The software is designed for researchers, and it is used to verify the agreement between theoretical models and experimental data. Main features From the physics point of view the software provides coefficients that are useful for the determination of the microscopic structure of composites, molecules, etc. the dipolar and quadripolar coefficients the depolarization factor Using these coefficients, the software also provides the visualization of simulated polar graphics generated by HRS molecular position and dipolar momentum in 3D easy data and graphics export External links Commons category http hrscomputing.sourceforge.net HRS Computing official site See also Portal Free software Rayleigh scattering Category Physics software ...   more details



  1. Hyperpolarization (biology)

    Portal Neuroscience Hyperpolarization is a change in a cell biology cell s membrane potential that makes it more negative. It is the opposite of a depolarization . Hyperpolarization is often caused by efflux of potassium K sup sup a cation through potassium channel K sup sup channels , or influx of chloride Cl sup &ndash sup an anion through chloride channel Cl sup &ndash sup channels . On the other hand, influx of cation s, e.g. sodium Na sup sup through sodium channel Na sup sup channels or Calcium Ca sup 2 sup through Calcium channel Ca sup 2 sup channels , inhibits hyperpolarization. If a cell has Na sup sup or Ca sup 2 sup currents at rest, then inhibition of those currents will also result in a hyperpolarization. Because hyperpolarization is a change in membrane voltage , electrophysiology electrophysiologists measure it using electrophysiology Current clamp current clamp techniques. In voltage clamp , the membrane currents giving rise to hyperpolarization are either an increase in outward current, or a decrease in inward current. Examples Image Apshoot.jpg thumb right 300px Diagram of membrane potential changes during an action potential During the afterhyperpolarization period after an action potential , the membrane potential is more negative than when the cell is at the resting potential . In the figure to the right, this undershoot occurs at approximately 3 to 4 milliseconds ms on the time scale. The afterhyperpolarization is the time when the membrane potential is hyperpolarized relative to the resting potential. During the rising phase of an action potential, the membrane potential changes from negative to positive, a depolarization. In the figure, the rising phase is from approximately 1 to 2 ms on the graph. During the rising phase, once the membrane potential becomes positive, the membrane potential continues to depolarize overshoot until the peak of the action potential is reached at about 40 millivolts mV . After the peak of the action potential, a ...   more details



  1. Sinus rhythm

    fibers and allows the electrical impulse to end in the ventricles to initiate ventricular depolarization ...   more details



  1. Cardiac muscle cell

    , potassium and calcium to easily diffuse from cell to cell. This makes it easier for depolarization ... http cwx.prenhall.com bookbind pubbooks martinidemo chapter10 medialib CH10 html ch10 8.html ref Depolarization ... an impulse. The ions will then cross the cell memebrane causing depolarization . The movement ... muscle. The depolarization and contraction together cause a wave of movement to pass through the heart ... of time between depolarization and repolarization is long relatively speaking. This period ... as easily. Myocardial cells possess the property of automaticity or spontaneous depolarization ... is reached for depolarization. Calcium ions follow and extend the depolarization even further ...   more details



  1. Omega-grammotoxin SIA

    Omega grammotoxin SIA is a protein toxin that inhibits P, Q and N voltage gated calcium channels Ca sup 2 sup channels in neurons . Source The source of omega grammotoxin SIA is the venom of a tarantula spider Grammostola rosea . Chemistry Amino Acid Sequence Asp Cys Val Arg Phe Trp Gly Lys Cys Ser Gln Thr Ser Asp Cys Cys Pro His Leu Ala Cys Lys Ser Lys Trp Pro Arg Asn Ile Cys Val Trp Asp Gly Ser Val ref name sigmaaldrich http www.sigmaaldrich.com catalog search ProductDetail?ProdNo G2795&Brand SIGMA www.sigmaaldrich.com ref Molecular Formula C sub 177 sub H sub 268 sub N sub 52 sub O sub 50 sub S sub 6 sub ref name sigmaaldrich Omega grammotoxin SIA can be purified from Grammostola rosea venom by reverse phase high performance liquid chromatography . ref Lampe R.A. et al. Isolation and pharmacological characterization of omega grammotoxin SIA, a novel peptide inhibitor of neuronal voltage sensitive calcium channel responses. Mol Pharmacol. 1993 Aug 44 2 451 60 http www.ncbi.nlm.nih.gov entrez query.fcgi?CMD search&DB pubmed ref Target Omega Grammotoxin SIA is a 36 amino acid residue protein toxin from spider venom that inhibits P, Q and N type voltage gated calcium channels in neurons. It binds to the channels with high affinity if closed . It also binds to potassium channels but with lower affinity than to the calcium channels . ref Takeuchi K. et al. Solution Structure of v Grammotoxin SIA, A Gating Modifier of P Q and N type Ca21 Channel. J. Mol. Biol. 2002, 321 517 526 http www.pubmed.com ref The toxin binding site has high affinity when channels are in closed states and low affinity when channels are activated. 4 Mode of action It is believed that omega grammotoxin SIA inhibits channel function by binding with high affinity to closed, resting states of the channel and that bound toxin makes it more difficult for channels to be opened by depolarization , so much larger depolarization s are required for channel activation. ref Stefan I. McDonough et al. Voltage ...   more details



  1. Kurtoxin

    Orphan date November 2006 Citation style date September 2009 Kurtoxin is a toxin found in the venom of the scorpion Parabuthus transvaalicus . It affects the gating of voltage gated sodium channels and calcium channels . Source Kurtotoxin is found in the venom of the South African scorpion Parabuthus transvaalicus . Chemistry Kurtoxin is a protein containing 63 amino acid residues with a mass of 7386.1 Dalton unit daltons . It can be isolated from the venom of Parabuthus transvaalicus by reversed phase high performance liquid chromatography HPLC . Kurtoxin is closely related to scorpion toxins, a family of toxins that slow inactivation of voltage gated sodium channels . The complete primary amino acid sequence of kurtoxin is KIDGYPVDYW NCKRICWYNN KYCNDLCKGL KADSGYCWGW TLSCYCQGLP DNARIKRSGR CRA. Target In research on Xenopus oocyte s it was found that kurtoxin affects low threshold 1G and 1H calcium channels, but not the high threshold 1A, 1B, 1C, and 1E Ca channels. Like other scorpion toxins kurtoxin was also found to interact with voltage gated sodium channels . In rat neurons, less selectivity for kurtoxin on calcium channels is found. Here the toxin interacts with high affinity with T type, L type, N type, and P type channels. Mode of action Kurtoxin inhibits ion calcium channels by modifying channel gating. The effect of the toxin is voltage dependent. In a voltage clamp experiment it was found that calcium channels are more strongly inhibited by minor depolarization than by a strong depolarization of the cell. The peptide toxin binds close to the channel voltage sensor and thereby produces complex gating modifications specific for each channel type. In rats, kurtoxin inhibited T type, L type, and N type Ca channels and facilitated P type channels. Deactivation was accelerated in T type and L type channels, slowed down in P type channels and not affected in N type calcium channels. Kurtoxin also has an effect on sodium channels . It slows down both ac ...   more details



  1. Grammotoxin

    File Grammostola Spatulata.jpg thumb right 200px G. spatulata , the source of the toxin Grammotoxin is a toxin in the venom of the tarantula Grammostola rosea Grammostola spatulata . It is a protein toxin that inhibits P , Q and N type voltage gated calcium channels Ca sup 2 sup channels in neurons . Grammotoxin is also known as omega grammotoxin SIA . Chemistry Grammotoxin is a 36 Amino Acid protein toxin, which has the following sequence Asp Cys Val Arg Phe Trp Gly Lys Cys Ser Gln Thr Ser Asp Cys Cys Pro His Leu Ala Cys Lys Ser Lys Trp Pro Arg Asn Ile Cys Val Trp Asp Gly Ser Val 1 Its chemical formula is C sub 177 sub H sub 268 sub N sub 52 sub O sub 50 sub S sub 6 sub ref http www.sigmaaldrich.com catalog search ProductDetail?ProdNo G2795&Brand SIGMA Grammotoxin SIA from Grammostola spatulata venom, 98 HPLC ref Grammotoxin can be purified from Grammostola spatulata venom by reverse phase high performance liquid chromatography . ref http www.ncbi.nlm.nih.gov entrez query.fcgi?CMD search&DB pubmed Lampe R.A. et al. Isolation and pharmacological characterization of omega grammotoxin SIA, a novel peptide inhibitor of neuronal voltage sensitive calcium channel responses. Mol Pharmacol. 1993 Aug 44 2 451 60 ref Mode of action The toxin binding site on the channels has high affinity for the toxins when they are closed and low affinity when channels are activated. ref name voltage http www.pubmed.com Stefan I. McDonough et al. Voltage Dependent Inhibition of N and P Type Calcium Channels by the Peptide Toxin v Grammotoxin SIA. Molucular pharmacology, 1997 52 1095 1104. ref As a result, the toxin preferentially binds to the closed channels. It binds at a region which contains the voltage sensing domains. When bound, the toxin makes it more difficult for channels to be opened by depolarization , so much larger depolarization s are required for channel activation. ref name voltage Grammotoxin also binds to potassium channels but with lower affinity than to the calcium cha ...   more details



  1. Afterdepolarization

    Afterdepolarizations are abnormal depolarization s of cardiac myocyte s that interrupt phase 2, phase 3, or phase 4 of the cardiac action potential in the electrical conduction system of the heart . Afterdepolarizations may lead to cardiac arrhythmia s. Early afterdepolarizations Early afterdepolarizations EADs occur with abnormal depolarization during phase 2 or phase 3, and are caused by an increase in the frequency of abortive action potential s before normal repolarization is completed. Phase 2 may be interrupted due to augmented opening of calcium channel s, while phase 3 interruptions are due to the opening of sodium channel s. Early afterdepolarizations can result in torsades de pointes , tachycardia , and other arrhythmia s. ref Cranefield, PF The Conduction of the Cardiac Impulse. New York, Future Publishing Co. 1975 ref Afterhyperpolarizations can also occur in cortical pyramidal neurons. There, they typically follow an action potential and are mediated by voltage gated sodium or chloride channels. This phenomenon requires potassium channels to close quickly to limit repolarization. It is responsible for the difference between regular spiking and intrinsically bursting pyramidal neurons. ref Nelson Spruston, Pyramidal Neurons dendritic structure and synaptic integration , 2008. Nature Reviews. Neuroscience. ref Delayed afterdepolarizations Delayed afterdepolarizations DADs , on the other hand, begin during phase 4 after repolarization is completed, but before another action potential would normally occur. They are due to elevated cytosolic calcium concentrations, as might be seen with digoxin toxicity. ref name Katzung Katzung, B Basic & Clinical Pharmacology , chapter 14 Agents Used in Cardiac Arrhythmias , The McGraw Hill Companies, 2007, ISBN 978 0 07 145154 6 ref ref name Lilly Lilly, L Pathophysiology of Heart Disease , chapter 11 Mechanisms of Cardiac Arrhthmias , Lippencott, Williams and Wilkens, 2007 ref The overload of the sarcoplasmic reticulum may ...   more details



  1. M current

    M current is a type of noninactivating potassium current first discovered in bullfrog sympathetic ganglion cells ref BROWN, D. A. & ADAMS, P. R. 1980 . Muscarinic suppression of a novel voltage sensitive K current in a vertebrate neurone. Nature, Lond. 283, 673 676. ref The M channel is a voltage gated K channel that is named after the receptor it is influenced by. The M channel is important in raising the threshold for firing an action potential. It is unique because it is open at rest and even more likely to be open during depolarization. Furthermore, when the MAChR muscarinic acetylcholine receptor mAChR is activated, the channel CLOSES. The M channel is a PIP sub 2 sub regulated ion channel see section Inhibition of M current . ref name Nicholls cite book first1 John G. last1 Nicholls first2 A. Robert last2 Martin first3 Paul A. last3 Fuchs first4 David A. last4 Brown first5 Mathew E. last5 Diamond last6 Weisblat first6 David A. year 2012 title From Neuron to Brain edition Fifth pages 229, 342 ref Actions of M currents phasic firing M channels are the reason for slow depolarizations produced by Ach and LHRH in the autonomic ganglia and other specified areas. 1. Initial depolarization of a neuron increases likelihood that M channels will open. 2. M channels generate an outward potassium current iK . 3. Potassium efflux counteracts sodium influx in Action potential action potential AP . Overall result full action potential is prevented. ref name Nicholls rp 343 Inhibition of M current tonic firing 2 molecules of Acetylcholine Acetylcholine Ach bind to mAchR . Potassium K channels become more likely to be closed. Neuron becomes tonic firing . ref name Nicholls rp 343 This reduction in M current is coupled with the actions of the Gq alpha subunit G sub q sub G protein . Specifically, the hydrolysis of PIP sub 2 sub to IP sub 3 sub . This hydrolysis causes PIP sub 2 sub , which is bound to the membrane, to become IP sub 3 sub and dissociate from the membrane into the ...   more details



  1. Cardiac action potential

    adjacent cells, certain cells of the heart have the ability to undergo spontaneous depolarization ... muscle automaticity . Phase 0 Phase 0 is the rapid depolarization phase. The slope of phase 0 represents the maximum rate of depolarization of the cell and is known as dV dt sub max sub . This phase ... of m , h and j becomes too small upon depolarization. Phase 1 Phase 1 of the action potential ..., i.e. without external electrical stimulation from the nervous system. This spontaneous depolarization ... depolarization the fastest are the primary pacemaker cells of the heart, and set the heart rate ..., generating the normal heart rate. Abnormal automaticity involves the abnormal spontaneous depolarization ... depolarization and create an action potential. Regulation by the autonomic nervous system The rate of depolarization and duration of the action potential in pacemaker cells is regulated by the parasympathetic ... levels which facilitates the opening of calcium channels thereby increasing the rate of depolarization ...   more details



  1. End-plate potential

    axon and arrives at the axon terminal, it opens calcium channels and causes a depolarization of the axon ... vesicles, each small depolarization MEPP sums together. This summation of MEPPs leads to a greater depolarization of the postsynaptic membrane and become an end plate potential. When the membrane reaches a certain value of depolarization 65mV , the voltage gated ion channels in the postsynaptic membrane open causes in influx of sodium ions and a sharp spike in depolarization. This spike causes an action .... In a normal muscular contraction, approximately 35 acetylcholine vesicles are released causing a depolarization ... spike in membrane polarity. There are five phases of an action potential threshold, depolarization, peak ...   more details



  1. Cardioversion

    into 3 subclasses a, b and c. Class Ia slows phase 0 depolarization in the ventricles and increases ... . Class Ic greatly slow phase 0 depolarization in the ventricles however unlike 1a have no effect on the refractory ... are beta blockers which inhibit SA and AV node depolarization and slow heart rate. They also decrease ...   more details




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