<?xml version="1.0" encoding="UTF-8"?><?xml-stylesheet type="text/xsl" href="static/style.xsl"?><OAI-PMH xmlns="http://www.openarchives.org/OAI/2.0/" xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" xsi:schemaLocation="http://www.openarchives.org/OAI/2.0/ http://www.openarchives.org/OAI/2.0/OAI-PMH.xsd"><responseDate>2026-04-14T15:18:13Z</responseDate><request verb="GetRecord" identifier="oai:uvadoc.uva.es:10324/24724" metadataPrefix="mods">https://uvadoc.uva.es/oai/request</request><GetRecord><record><header><identifier>oai:uvadoc.uva.es:10324/24724</identifier><datestamp>2025-03-03T10:27:24Z</datestamp><setSpec>com_10324_32522</setSpec><setSpec>com_10324_952</setSpec><setSpec>com_10324_894</setSpec><setSpec>com_10324_43677</setSpec><setSpec>com_10324_954</setSpec><setSpec>com_10324_1134</setSpec><setSpec>com_10324_931</setSpec><setSpec>col_10324_32523</setSpec><setSpec>col_10324_43678</setSpec><setSpec>col_10324_1213</setSpec></header><metadata><mods:mods xmlns:mods="http://www.loc.gov/mods/v3" xmlns:doc="http://www.lyncode.com/xoai" xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" xsi:schemaLocation="http://www.loc.gov/mods/v3 http://www.loc.gov/standards/mods/v3/mods-3-1.xsd">
<mods:name>
<mods:namePart>Ureña, J.</mods:namePart>
</mods:name>
<mods:name>
<mods:namePart>López López, José Ramón</mods:namePart>
</mods:name>
<mods:name>
<mods:namePart>González Martínez, Constancio</mods:namePart>
</mods:name>
<mods:name>
<mods:namePart>López Barneo, José</mods:namePart>
</mods:name>
<mods:extension>
<mods:dateAvailable encoding="iso8601">2017-07-26T08:42:06Z</mods:dateAvailable>
</mods:extension>
<mods:extension>
<mods:dateAccessioned encoding="iso8601">2017-07-26T08:42:06Z</mods:dateAccessioned>
</mods:extension>
<mods:originInfo>
<mods:dateIssued encoding="iso8601">1989</mods:dateIssued>
</mods:originInfo>
<mods:identifier type="citation">Journal of General Physiology, 1989, vol. 93. p. 979-999</mods:identifier>
<mods:identifier type="issn">0022-1295</mods:identifier>
<mods:identifier type="uri">http://uvadoc.uva.es/handle/10324/24724</mods:identifier>
<mods:identifier type="doi">10.1085/jgp.93.5.979</mods:identifier>
<mods:identifier type="publicationfirstpage">979</mods:identifier>
<mods:identifier type="publicationlastpage">999</mods:identifier>
<mods:identifier type="publicationtitle">Journal of General Physiology</mods:identifier>
<mods:identifier type="publicationvolume">93</mods:identifier>
<mods:abstract>Ionic currents of enzymatically dispersed type 1 and type 11 cells of the carotid body have been studied using the whole cell variant of the patch-clamp technique. Type 11 cells only have a tiny, slowly activating outward potassium cur­ rent. By contrast, in every type 1 chemoreceptor cell studied we found (a) sodium,&#xd;
(b) calcium, and (e) potassium currents. (a) The sodium current has a fast activation time course and an activation threshold at --40 mV. At ali voltages inactivation follows a single exponential time course. The time constant of inactivation is 0.67 ms  at  O  mV.  Half  steady  state  inactivation  occurs  at  a membrane  potential  of&#xd;
--50 mV. (b) The calcium current is almost totally abolished when most of the extemal calcium is replaced by magnesium. The activation threshold of this cur­ rent is at --40 mV and at O mV it reaches a peak amplitude in 6-8 ms. The calcium current inactivates very slowly and only decreases to 27% of the maximal value at the end of 300-ms pulses to 40 mV. The calcium current was about two times larger when barium ions were used as charge carriers instead of calcium ions. Barium ions also shifted 15-20 mV toward negative voltages the conductance vs. voltage curve. Deactivation kinetics of the calcium current follows a biphasic time course well fitted by the sum of two exponentials. At -80 mV the slow com­ ponent has a time constant of 1.3 ± 0.4 ms whereas the fast component, with an amplitude about 20 times larger than the slow component, has a time constant of&#xd;
0.16 ± 0.03 ms. These results suggest that type 1 cells have predominantly fast deactivating calcium channels. The slow component of the tails may represent the activity of a small population of slowly deactivating calcium channels, although other possibilities are considered. (e) Potassium current seems to be mainly due to the activity of voltage-dependent potassium channels, but a small percentage of calcium-activated channels may also exist. This current activates slowly, reaches a peak amplitude in 5-1O ms, and thereafter slowly inactivates. Inactivation is almost complete in 250-300 ms. The potassium current is reversibly blocked by tetraeth­ ylammonium. Under current-clamp conditions type I cells can spontaneously fire large action potentials.</mods:abstract>
<mods:language>
<mods:languageTerm>eng</mods:languageTerm>
</mods:language>
<mods:accessCondition type="useAndReproduction">info:eu-repo/semantics/openAccess</mods:accessCondition>
<mods:accessCondition type="useAndReproduction">http://creativecommons.org/licenses/by-nc-nd/4.0/</mods:accessCondition>
<mods:accessCondition type="useAndReproduction">© 1989 The Rockefeller University Press</mods:accessCondition>
<mods:accessCondition type="useAndReproduction">Attribution-NonCommercial-NoDerivatives 4.0 International</mods:accessCondition>
<mods:titleInfo>
<mods:title>Ionic currents in dispersed chemoreceptor cells of the mammalian carotid body</mods:title>
</mods:titleInfo>
<mods:genre>info:eu-repo/semantics/article</mods:genre>
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