<?xml version="1.0" encoding="utf-8"?>
<journal>
<title>The Neuroscience Journal of Shefaye Khatam</title>
<title_fa>مجله علوم اعصاب شفای خاتم</title_fa>
<short_title>Shefaye Khatam</short_title>
<subject>Medical Sciences</subject>
<web_url>http://shefayekhatam.ir</web_url>
<journal_hbi_system_id>1</journal_hbi_system_id>
<journal_hbi_system_user>admin</journal_hbi_system_user>
<journal_id_issn>2322-1887</journal_id_issn>
<journal_id_issn_online>2345-4814</journal_id_issn_online>
<journal_id_pii></journal_id_pii>
<journal_id_doi>10.61882/shefa</journal_id_doi>
<journal_id_iranmedex></journal_id_iranmedex>
<journal_id_magiran></journal_id_magiran>
<journal_id_sid></journal_id_sid>
<journal_id_nlai></journal_id_nlai>
<journal_id_science></journal_id_science>
<language>fa</language>
<pubdate>
	<type>jalali</type>
	<year>1396</year>
	<month>1</month>
	<day>1</day>
</pubdate>
<pubdate>
	<type>gregorian</type>
	<year>2017</year>
	<month>4</month>
	<day>1</day>
</pubdate>
<volume>5</volume>
<number>2</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>P 106: Effects of Dimethyl Sulfoxide on NLRP3 Inflammasome and Alzheimer's Disease</title_fa>
	<title>P 106: Effects of Dimethyl Sulfoxide on NLRP3 Inflammasome and Alzheimer's Disease</title>
	<subject_fa>تحقیقات پایه در علوم اعصاب</subject_fa>
	<subject>Basic research in Neuroscience</subject>
	<content_type_fa>مروری</content_type_fa>
	<content_type>Review --- Open Access, CC-BY-NC</content_type>
	<abstract_fa>&lt;table border=&quot;0&quot; cellpadding=&quot;5px&quot; cellspacing=&quot;2&quot; dir=&quot;rtl&quot; id=&quot;table_article&quot; style=&quot;font-family: Tahoma; background-color: rgb(251, 250, 249); break-inside: avoid !important;&quot; width=&quot;100%&quot;&gt;
	&lt;tbody style=&quot;break-inside: avoid !important; font-size: 12px; margin-top: 0px; line-height: 2.2; margin-bottom: 0px; text-align: justify;&quot;&gt;
		&lt;tr style=&quot;break-inside: avoid !important;&quot;&gt;
			&lt;td class=&quot;abstractmed&quot; colspan=&quot;2&quot; style=&quot;break-inside: avoid !important;&quot;&gt;
			&lt;p style=&quot;font-size: 12px; margin-top: 0px; margin-bottom: 0px; text-align: center;&quot;&gt;&lt;span style=&quot;color: rgb(0, 0, 0); font-size: 12px; line-height: 20.8px;&quot;&gt;لطفاً به چکیده انگلیسی مراجعه شود.&lt;/span&gt;&lt;/p&gt;
			&lt;/td&gt;
		&lt;/tr&gt;
		&lt;tr style=&quot;break-inside: avoid !important;&quot;&gt;
		&lt;/tr&gt;
	&lt;/tbody&gt;
&lt;/table&gt;

&lt;p&gt;&lt;/p&gt;
</abstract_fa>
	<abstract>&lt;p&gt;Alzheimer&amp;#39;s disease (AD), the most ordinary form of dementia and extracellular accumulation of Amyloid-&amp;beta; (A&amp;beta;) in senile plaques, is an important and a main event in the pathogenesis of AD. Deposition of A&amp;beta; Peptide initiates a spectrum of cellular responses that are interposed by the resident neuroimmune cells of the brain, the microglia. Recently, a novel inflammasome signaling&amp;nbsp; pathway has been uncovered and A&amp;beta; can activate the NLRP3 inflammasome in microglia, which is fundamental for the secretion&amp;nbsp; of pro-inflammatory cytokines&amp;nbsp; and subsequent inflammatory events .More importantly , the activation of&amp;nbsp; NLRP3 inflammasome has demonstrated&amp;nbsp; a serious role in AD pathogenesis by interposing a harmful chronic inflammatory response, while inhibition of&amp;nbsp; NLRP3 mainly protected from loss of spatial memory and decreased A&amp;beta; deposition in an AD mouse model. Dimethyl Sulfoxide (DMSO) is an amphipathic molecule that is widely used as a solvent for biological compounds .In addition, DMSO has been studied as a medicine for the treatment of inflammation, cystitis, and arthritis. Based on the anti-inflammatory characteristics of DMSO,&amp;nbsp; the effects of DMSO on activation of inflammasomes has elucidated, which are cytoplasmic multi-protein complexes&amp;nbsp; that interpose the maturation of interleukin (IL)-1&amp;beta; by activating caspase-1 (casp1). The aim is discussing about effects of DMSO on NLRP3 inflammasome and AD. It has proved that DMSO attenuates IL-1&amp;beta; maturation, casp1 activity, and ASC pyroptosome formation by NLRP3 inflammasome activators. DMSO is a selective inhibitor of the NLRP3 inflammasomes. The anti-inflammatory effect of DMSO was further proved in animal studies, LPS-endotoxin sepsis, and inflammatory bowel disease models. DMSO shows anti-inflammatory characteristics, attenuates NLRP3 inflammasome activation. According to studies, it is hypothesized that DMSO inhibits activation of inflammasomes, NLRP3, CASP1 in Alzheimer&amp;#39;s disease that are pathogenesis by mediating a harmful chronic inflammatory response.&lt;/p&gt;
</abstract>
	<keyword_fa></keyword_fa>
	<keyword>Alzheimer's disease, NLRP3, Casp1, Inflammasome, DMSO</keyword>
	<start_page>137</start_page>
	<end_page>137</end_page>
	<web_url>http://shefayekhatam.ir/browse.php?a_code=A-10-24-956&amp;slc_lang=en&amp;sid=1</web_url>


<author_list>
	<author>
	<first_name>Reyhane </first_name>
	<middle_name></middle_name>
	<last_name>Shahraki</last_name>
	<suffix></suffix>
	<first_name_fa>Reyhane </first_name_fa>
	<middle_name_fa></middle_name_fa>
	<last_name_fa>Shahraki</last_name_fa>
	<suffix_fa></suffix_fa>
	<email>reyshah75@gmail.com</email>
	<code>100319475328460012116</code>
	<orcid>100319475328460012116</orcid>
	<coreauthor>Yes
</coreauthor>
	<affiliation>Student Research Committee, Faculty of Medicine, Mashhad University of Medical Sciences, Mashhad, Iran</affiliation>
	<affiliation_fa>Student Research Committee, Faculty of Medicine, Mashhad University of Medical Sciences, Mashhad, Iran</affiliation_fa>
	 </author>


</author_list>


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