<?xml version="1.0" encoding="utf-8"?>
<journal>
<title>Iranian Biomedical Journal</title>
<title_fa>مجله بیومدیکال ایران</title_fa>
<short_title>IBJ</short_title>
<subject>Basic Sciences</subject>
<web_url>http://ibj.pasteur.ac.ir</web_url>
<journal_hbi_system_id>1</journal_hbi_system_id>
<journal_hbi_system_user>admin</journal_hbi_system_user>
<journal_id_issn>1028-852X</journal_id_issn>
<journal_id_issn_online>2008-823X</journal_id_issn_online>
<journal_id_pii>-</journal_id_pii>
<journal_id_doi>10.61882/ibj</journal_id_doi>
<journal_id_iranmedex></journal_id_iranmedex>
<journal_id_magiran></journal_id_magiran>
<journal_id_sid>-</journal_id_sid>
<journal_id_nlai>8888</journal_id_nlai>
<journal_id_science>-</journal_id_science>
<language>en</language>
<pubdate>
	<type>jalali</type>
	<year>1385</year>
	<month>7</month>
	<day>1</day>
</pubdate>
<pubdate>
	<type>gregorian</type>
	<year>2006</year>
	<month>10</month>
	<day>1</day>
</pubdate>
<volume>10</volume>
<number>4</number>
<publish_type>online</publish_type>
<publish_edition>1</publish_edition>
<article_type>fulltext</article_type>
<articleset>
	<article>


	<language>en</language>
	<article_id_doi></article_id_doi>
	<title_fa>اثر مهاری سموم مختلف بر کانال‌های پتاسیمی Kv3.4 در سلول‌های RLE</title_fa>
	<title>The Blocking Activity of Different Toxins against Potassium Channels Kv3.4 in RLE Cells</title>
	<subject_fa></subject_fa>
	<subject></subject>
	<content_type_fa>مقاله کامل</content_type_fa>
	<content_type>Full Length/Original Article</content_type>
	<abstract_fa></abstract_fa>
	<abstract>&lt;span style=&quot;FONT-FAMILY: &#039;Times New Roman&#039; FONT-SIZE: 11pt mso-bidi-font-family: &#039;Traditional Arabic&#039; mso-fareast-language: EN-US mso-ansi-language: EN-US&quot;&gt;&lt;strong&gt;&lt;font size=&quot;2&quot;&gt;Background: &lt;/font&gt;&lt;/strong&gt;&lt;/span&gt;&lt;span style=&quot;FONT-FAMILY: &#039;Times New Roman&#039; FONT-SIZE: 11pt mso-bidi-font-family: &#039;Traditional Arabic&#039; mso-fareast-language: EN-US mso-ansi-language: EN-US&quot;&gt;&lt;font size=&quot;2&quot;&gt;K&lt;sup&gt;+&lt;/sup&gt; channel toxins are essential tools for the first purifications, analysis of subunit structures and brain localization of voltage-gated K&lt;sup&gt;+&lt;/sup&gt; (Kv) channels. The effects of a lot of toxins on Kv are not fully known. &lt;b&gt;Methods: &lt;/b&gt;Using whole-cell patch clamping technique the action of a series of toxins on Kv3.4 current in rat liver cells with expressed Kv3.4 channels (RLE) cloned cells was investigated. The cells were grown in Williams E medium and after 6-8 days, they were suitable for patch clamping. A family of currents was recorded during voltage-clamp&lt;/font&gt; &lt;font size=&quot;2&quot;&gt;steps to various potentials applied from a holding potential of -60 mV to 60-80 mV in 10 mV increments.&lt;b&gt; Results: &lt;/b&gt;Upon depolarization, all channels were opened with a sigmoidal time course, reached to the peak within a few 10th&amp;nbsp;of &lt;/font&gt;&lt;font size=&quot;5&quot;&gt;&lt;font size=&quot;2&quot;&gt;milliseconds and then slowly inactivated.&amp;nbsp;Bath application of tetraethyl ammonium (TEA) or 3, 4-diaminopyridine (DAP) reduced the current dose dependently and inhibited it completely at 3 mM and 25 muM respectively.&amp;nbsp;The Bunodosoma granulifera (BgK) and&amp;nbsp;Heteractis magnifica (HmK)&amp;nbsp;toxins&amp;nbsp;at concentrations up to 30 and 10 muM&amp;nbsp;respectively could not&amp;nbsp;&lt;/font&gt;&lt;/font&gt;&lt;/span&gt;&lt;span style=&quot;FONT-FAMILY: &#039;Times New Roman&#039; FONT-SIZE: 11pt mso-bidi-font-family: &#039;Traditional Arabic&#039; mso-fareast-language: EN-US mso-ansi-language: EN-US&quot;&gt;&lt;font size=&quot;5&quot;&gt;&lt;font size=&quot;2&quot;&gt;completely inhibit&lt;/font&gt; &lt;/font&gt;&lt;font size=&quot;2&quot;&gt;the current. On the hand, toxins such as beta&lt;/font&gt;&lt;/span&gt;&lt;span style=&quot;FONT-FAMILY: &#039;Times New Roman&#039; FONT-SIZE: 11pt mso-bidi-font-family: &#039;Traditional Arabic&#039; mso-fareast-language: EN-US mso-ansi-language: EN-US&quot;&gt;&lt;font size=&quot;2&quot;&gt;-bungarotoxin, corotoxin, novel toxin and dendrotoxins I (DIP) and K (DPK) even in high concentrations (up to 100 mM) had not any significant effect on Kv3.4 current. Comparison of chemical structures of these effective&lt;/font&gt; &lt;font size=&quot;2&quot;&gt;agents with other reported effective toxins such as blood depressing substances (BDS I and II) show no homology between them, but specially the potency of 3, 4-DAP is comparable with these toxins. &lt;b&gt;Conclusion: &lt;/b&gt;These results showed that, the Kv3.4 is more sensitive than other Kv3.4 channels.&lt;/font&gt;&lt;/span&gt;</abstract>
	<keyword_fa></keyword_fa>
	<keyword>Patch clamping, Voltage-gated K+ (Kv)3.4 channel, Rat liver cells with expressed Kv3.4 channels (RLE) cells, Tetraethyl ammonium (TEA), 3, 4-Diaminopyridine (DAP)</keyword>
	<start_page>169</start_page>
	<end_page>174</end_page>
	<web_url>http://ibj.pasteur.ac.ir/browse.php?a_code=A-10-1-196&amp;slc_lang=en&amp;sid=1</web_url>


<author_list>
	<author>
	<first_name>Mehdi</first_name>
	<middle_name></middle_name>
	<last_name>Saberi</last_name>
	<suffix></suffix>
	<first_name_fa>مهدی</first_name_fa>
	<middle_name_fa></middle_name_fa>
	<last_name_fa>صابری</last_name_fa>
	<suffix_fa></suffix_fa>
	<email>m_s_saber@yahoo.com</email>
	<code></code>
	<orcid></orcid>
	<coreauthor>Yes
</coreauthor>
	<affiliation></affiliation>
	<affiliation_fa></affiliation_fa>
	 </author>


	<author>
	<first_name>Edward G.</first_name>
	<middle_name></middle_name>
	<last_name>Rowan</last_name>
	<suffix></suffix>
	<first_name_fa>Edward G.</first_name_fa>
	<middle_name_fa></middle_name_fa>
	<last_name_fa>Rowan</last_name_fa>
	<suffix_fa></suffix_fa>
	<email></email>
	<code></code>
	<orcid></orcid>
	<coreauthor>No</coreauthor>
	<affiliation></affiliation>
	<affiliation_fa></affiliation_fa>
	 </author>


</author_list>


	</article>
</articleset>
</journal>
