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Hyperpolarization (biology)
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<h2 id="voltage-gated-ion-channels-and-hyperpolarization">Voltage-gated ion channels and hyperpolarization</h2> <p> Voltage gated <a href="/facts/Ion_channel/A46LARFH">ion channels</a> respond to changes in the membrane potential. Voltage gated potassium, chloride and sodium channels are key components in the generation of the action potential as well as hyper-polarization. These channels work by selecting an ion based on electrostatic attraction or repulsion allowing the ion to bind to the channel.<a class="footnote-ref" id="fnref:2" href="#fn:2"><sup>2</sup></a> This releases the water molecule attached to the channel and the ion is passed through the pore. Voltage gated sodium channels open in response to a stimulus and close again. This means the channel either is open or not, there is no part way open. Sometimes the channel closes but is able to be reopened right away, known as channel gating, or it can be closed without being able to be reopened right away, known as channel inactivation. </p><p>At <a href="/facts/Resting_potential/F5IHsRLA">resting potential</a>, both the <a href="/facts/Gating_(electrophysiology)/SSoIPT3m">voltage gated</a> sodium and potassium channels are closed but as the cell membrane becomes depolarized the voltage gated sodium channels begin to open up and the neuron begins to depolarize, creating a <a href="/facts/Minor_loop_feedback/KGlfekpv">current feedback loop</a> known as the <a href="/facts/Hodgkin_cycle/kgUxLA3v">Hodgkin cycle</a>.<a class="footnote-ref" id="fnref:3" href="#fn:3"><sup>3</sup></a> However, potassium ions naturally move out of the cell and if the original depolarization event was not significant enough then the neuron does not generate an action potential. If all the sodium channels are open, however, then the neuron becomes ten times more permeable to sodium than potassium, quickly depolarizing the cell to a peak of +40 mV.<a class="footnote-ref" id="fnref:4" href="#fn:4"><sup>4</sup></a> At this level the sodium channels begin to inactivate and voltage gated potassium channels begin to open. This combination of closed sodium channels and open potassium channels leads to the neuron re-polarizing and becoming negative again. The neuron continues to re-polarize until the cell reaches ~ –75 mV,<a class="footnote-ref" id="fnref:5" href="#fn:5"><sup>5</sup></a> which is the equilibrium potential of potassium ions. This is the point at which the neuron is hyperpolarized, between –70 mV and –75 mV. After hyperpolarization the potassium channels close and the natural permeability of the neuron to sodium and potassium allows the neuron to return to its resting potential of –70 mV. During the <a href="/facts/Refractory_period_(physiology)/mu1rMsNe">refractory period</a>, which is after hyper-polarization but before the neuron has returned to its resting potential the neuron is capable of triggering an action potential due to the sodium channels ability to be opened, however, because the neuron is more negative it becomes more difficult to reach the action potential threshold. </p><p><a href="/facts/HCN_channel/dy7S3JQw">HCN channels</a> are activated by hyperpolarization. </p><p>Recent research has shown that neuronal refractory periods can exceed 20 milliseconds where the relation between hyperpolarization and the neuronal refractory was questioned.<a class="footnote-ref" id="fnref:6" href="#fn:6"><sup>6</sup></a><a class="footnote-ref" id="fnref:7" href="#fn:7"><sup>7</sup></a> </p> <h2 id="experimental-technique">Experimental technique</h2> <p>Hyperpolarization is a change in membrane potential. <a href="/facts/Neuroscientist/DvcNRpyM">Neuroscientists</a> measure it using a technique known as <a href="/facts/Patch_clamping/N31m2GJI">patch clamping</a> that allows them to record ion currents passing through individual channels. This is done using a glass micropipette, also called a patch pipette, with a 1 micrometer diameter. There is a small patch that contains a few ion channels and the rest is sealed off, making this the point of entry for the current. Using an amplifier and a <a href="/facts/Voltage_clamp/pj0ms1H1">voltage clamp</a>, which is an electronic feedback circuit, allows the experimenter to maintain the membrane potential at a fixed point and the voltage clamp then measures tiny changes in current flow. The membrane currents giving rise to hyperpolarization are either an increase in outward current or a decrease in inward current.<a class="footnote-ref" id="fnref:8" href="#fn:8"><sup>8</sup></a> </p> <h2 id="examples">Examples</h2> <p><a href="/facts/GABA/vRTeQQUG">GABA receptors</a> are commonly known to downregulate neuronal activity by various means. </p> <ol><li><a href="/facts/GABAA_receptor/6G4rAGb3">GABAA</a> can induce hyperpolarization through an influx of Cl– ions. <a href="/facts/GABAA_receptor/6G4rAGb3">GABAA</a> itself is a <a href="/facts/Chloride_channel/Ervc5tBe">chloride ion channel</a>. <a class="footnote-ref" id="fnref:9" href="#fn:9"><sup>9</sup></a> This process of hyperpolarization is highly dependent on which direction Cl– flows. If Cl– travels into the cell, the flow of ions increases the voltage gradient. If Cl– flows out of the cell, the voltage gradient will decrease.</li> <li><a href="/facts/GABAB_receptor/dRomDjtq">GABAB</a> induces hyperpolarization through K+ ion influx into the neuron. Unlike GABAA, GABAB is a <a href="/facts/G_protein-coupled_receptor/0arUMkQc">G-Protein Coupled Receptor</a> that activates <a href="/facts/Potassium_channels/0QHmrHPn">potassium channels</a> via <a href="/facts/Protein_kinase_A/kaKoYfbp">Protein Kinase A</a> (PKA) activation. <a class="footnote-ref" id="fnref:10" href="#fn:10"><sup>10</sup></a> Potassium typically has a higher concentration inside the cell, while sodium typically has a higher concentration outside. When potassium channels open, K+ ions flow out of the cell and cause the cell's internal potential to become more negative. GABAB activation of PKA also leads to Ca channel inactivation in presynaptic neurons. This likely leads to inhibited synaptic transmission.</li></ol> <p>Hyperpolarization-activated cyclic nucleotide-gated (HCN) channels have been identified as channels that mediate hyperpolarization. They were initially discovered in pacemaker cells of the heart. <a class="footnote-ref" id="fnref:11" href="#fn:11"><sup>11</sup></a> These channels are controlled by cAMP, and activated by a hyperpolarized membrane. They allow the flow of Na+ and K+ ions, typically leading to a slight depolarization. </p> <h2 id="further-reading">Further reading</h2> <ul><li>Purves D, Augustine GJ, Fitzpatrick D, et al., eds. (2001). <a href="https://www.ncbi.nlm.nih.gov/books/NBK10799/"><i>Neuroscience</i></a> (2. ed.). Sunderland, Mass: Sinauer Assoc. <a href="/facts/ISBN_(identifier)/15AdSPa9">ISBN</a> 0-87893-742-0.</li> <li><a href="https://www.ncbi.nlm.nih.gov/books/bv.fcgi?call=bv.View..ShowTOC&rid=bnchm.TOC&depth=2">Basic Neurochemistry</a> Molecular, Cellular, and Medical Aspects by Siegel, et al.</li></ul> <h2 id="references">References</h2> <ol> <li id="fn:1"><p>Pack, Phillip E. "Cliffs AP Biology 3rd Edition" <a href="#fnref:1" class="footnote-back-ref">↩</a></p></li> <li id="fn:2"><p>Becker, W. M., Kleinsmith, L. J., Hardin, J., & Bertoni, G. P. (2009). Signal Transduction Mechanisms: I. Electrical and Synaptic Signaling in Neurons. The World of the Cell (7th ed., ). San Francisco: Pearson/Benjamin Cummings. <a href="#fnref:2" class="footnote-back-ref">↩</a></p></li> <li id="fn:3"><p>Becker, W. M., Kleinsmith, L. J., Hardin, J., & Bertoni, G. P. (2009). Signal Transduction Mechanisms: I. Electrical and Synaptic Signaling in Neurons. The World of the Cell (7th ed., ). San Francisco: Pearson/Benjamin Cummings. <a href="#fnref:3" class="footnote-back-ref">↩</a></p></li> <li id="fn:4"><p>Becker, W. M., Kleinsmith, L. J., Hardin, J., & Bertoni, G. P. (2009). Signal Transduction Mechanisms: I. Electrical and Synaptic Signaling in Neurons. The World of the Cell (7th ed., ). San Francisco: Pearson/Benjamin Cummings. <a href="#fnref:4" class="footnote-back-ref">↩</a></p></li> <li id="fn:5"><p>Becker, W. M., Kleinsmith, L. J., Hardin, J., & Bertoni, G. P. (2009). Signal Transduction Mechanisms: I. Electrical and Synaptic Signaling in Neurons. The World of the Cell (7th ed., ). San Francisco: Pearson/Benjamin Cummings. <a href="#fnref:5" class="footnote-back-ref">↩</a></p></li> <li id="fn:6"><p>Vardi, Roni; Tugendhaft, Yael; Sardi, Shira; Kanter, Ido (June 1, 2021). "Significant anisotropic neuronal refractory period plasticity". EPL (Europhysics Letters). 134 (6): 60007. arXiv:2109.02041. doi:10.1209/0295-5075/ac177a. ISSN 0295-5075. S2CID 237408101. <a href="https://doi.org/10.1209/0295-5075/ac177a" target="_blank">https://doi.org/10.1209/0295-5075/ac177a</a> <a href="#fnref:6" class="footnote-back-ref">↩</a></p></li> <li id="fn:7"><p>Sardi, Shira; Vardi, Roni; Tugendhaft, Yael; Sheinin, Anton; Goldental, Amir; Kanter, Ido (January 3, 2022). "Long anisotropic absolute refractory periods with rapid rise times to reliable responsiveness". Physical Review E. 105 (1): 014401. arXiv:2111.02689. Bibcode:2022PhRvE.105a4401S. doi:10.1103/PhysRevE.105.014401. PMID 35193251. S2CID 242757511. <a href="https://link.aps.org/doi/10.1103/PhysRevE.105.014401" target="_blank">https://link.aps.org/doi/10.1103/PhysRevE.105.014401</a> <a href="#fnref:7" class="footnote-back-ref">↩</a></p></li> <li id="fn:8"><p>Becker, W. M., Kleinsmith, L. J., Hardin, J., & Bertoni, G. P. (2009). Signal Transduction Mechanisms: I. Electrical and Synaptic Signaling in Neurons. The World of the Cell (7th ed., ). San Francisco: Pearson/Benjamin Cummings. <a href="#fnref:8" class="footnote-back-ref">↩</a></p></li> <li id="fn:9"><p>Luscher B, Fuchs T, Kilpatrick CL (2011). "GABAA receptor trafficking-mediated plasticity of inhibitory synapses". Neuron. 70 (3): 385–409. doi:10.1016/j.neuron.2011.03.024. PMC 3093971. PMID 21555068.{{cite journal}}: CS1 maint: multiple names: authors list (link) <a href="https://www.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&tool=sumsearch.org/cite&retmode=ref&cmd=prlinks&id=21555068" target="_blank">https://www.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&tool=sumsearch.org/cite&retmode=ref&cmd=prlinks&id=21555068</a> <a href="#fnref:9" class="footnote-back-ref">↩</a></p></li> <li id="fn:10"><p>Bowery NG, Bettler B, Froestl W, Gallagher JP, Marshall F, Raiteri M; et al. (2002). "International Union of Pharmacology. XXXIII. Mammalian gamma-aminobutyric acid(B) receptors: structure and function". Pharmacol Rev. 54 (2): 247–64. doi:10.1124/pr.54.2.247. PMID 12037141.{{cite journal}}: CS1 maint: multiple names: authors list (link) <a href="https://www.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&tool=sumsearch.org/cite&retmode=ref&cmd=prlinks&id=12037141" target="_blank">https://www.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&tool=sumsearch.org/cite&retmode=ref&cmd=prlinks&id=12037141</a> <a href="#fnref:10" class="footnote-back-ref">↩</a></p></li> <li id="fn:11"><p>DiFrancesco D (1993). "Pacemaker mechanisms in cardiac tissue". Annu Rev Physiol. 55: 455–72. doi:10.1146/annurev.ph.55.030193.002323. PMID 7682045. <a href="https://www.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&tool=sumsearch.org/cite&retmode=ref&cmd=prlinks&id=7682045" target="_blank">https://www.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&tool=sumsearch.org/cite&retmode=ref&cmd=prlinks&id=7682045</a> <a href="#fnref:11" class="footnote-back-ref">↩</a></p></li> </ol>