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<Article>
<Journal>
				<PublisherName>Payame Noor University</PublisherName>
				<JournalTitle>Experimental animal Biology</JournalTitle>
				<Issn>2322-2387</Issn>
				<Volume>9</Volume>
				<Issue>4</Issue>
				<PubDate PubStatus="epublish">
					<Year>2021</Year>
					<Month>04</Month>
					<Day>21</Day>
				</PubDate>
			</Journal>
<ArticleTitle>Investigation of anti–microbial ‎and anti-Alzheimer effects of ‎aqueous and hydro-alcoholic ‎extracts of Nigella sativa by ‎inhibiting the production of ‎amyloid fibrils</ArticleTitle>
<VernacularTitle>Investigation of anti–microbial ‎and anti-Alzheimer effects of ‎aqueous and hydro-alcoholic ‎extracts of Nigella sativa by ‎inhibiting the production of ‎amyloid fibrils</VernacularTitle>
			<FirstPage>89</FirstPage>
			<LastPage>101</LastPage>
			<ELocationID EIdType="pii">7685</ELocationID>
			
<ELocationID EIdType="doi">10.30473/eab.2021.49888.1759</ELocationID>
			
			<Language>FA</Language>
<AuthorList>
<Author>
					<FirstName>Sara</FirstName>
					<LastName>Ttajdoust</LastName>
<Affiliation>Assistant Professor, Department of biology, Astaneye ‎Ashrafiyeh Branch, Islamic Azad University, ‎Astaneye Ashrafiyeh, Iran.‎</Affiliation>

</Author>
<Author>
					<FirstName>Amir</FirstName>
					<LastName>Arasteh</LastName>
<Affiliation>Assistant Professor, Department of biology, Rasht ‎Branch, Islamic Azad University, Rasht, Iran</Affiliation>

</Author>
<Author>
					<FirstName>Seyedeh Mohadeseh</FirstName>
					<LastName>Mousavi Eshkiky</LastName>
<Affiliation>M.A., Department of biology, Rasht Branch, Islamic ‎Azad University, Rasht, Iran</Affiliation>

</Author>
</AuthorList>
				<PublicationType>Journal Article</PublicationType>
			<History>
				<PubDate PubStatus="received">
					<Year>2019</Year>
					<Month>11</Month>
					<Day>29</Day>
				</PubDate>
			</History>
		<Abstract>&lt;em&gt;Nigella sativa &lt;/em&gt;is an annual herbaceous plantthat has various pharmacological effects. In this research study, anti–microbial and anti–Alzheimer effects of aqueous and hydro–alcoholic extracts of &lt;em&gt;N. sativa&lt;/em&gt; were evaluated. After identification of hydro–alcoholic extract compounds by GC–MS, anti–microbial activity indices including well diffusion, MIC and MBC for &lt;em&gt;E. coli&lt;/em&gt; and&lt;em&gt; S.&lt;/em&gt; &lt;em&gt;aureus&lt;/em&gt;, were carried out by tube and agar dilution methods. In Anti–Alzheimer&#039;s effects of hydro–alcoholic extract of &lt;em&gt;N. sativa &lt;/em&gt;on bovine serum albumin were examined using Congo–red spectrophotometry and transmission electron microscopy. Oleic acid (52.18%) followed by palmitic (19.77%) and linoleic acid (14.96%) were the major fatty acids in the extract. The amounts of MIC and MBC for both &lt;em&gt;E. coli&lt;/em&gt; &lt;em&gt;and S. aureus&lt;/em&gt; were 30.6 and 61 mg.ml&lt;sup&gt;-1&lt;/sup&gt; respectively in hydro–alcoholic extract. Well diffusion method showed highest antimicrobial activity against &lt;em&gt;S. aureus&lt;/em&gt; with inhibition zone diameter of 22.67±0.29 mm, but aqueous extract did not any effects on bacteria. Congo–red spectrophotometry results showed that the absorbance of the protein sample (as a measure of amyloid fibril presence) was reduced by increasing the concentration of &lt;em&gt;N. sativa&lt;/em&gt; extract and the lowest percentage of adsorption, compared to the control (extract less), was observed at the highest concentration of extract (20 μL). These results were confirmed by transmission electron microscope. The present study shows that the &lt;em&gt;N. sativa&lt;/em&gt; seed, as a natural and valuable source, can be used for controlling the microbial infections and reducing symptoms in patients with Alzheimer&#039;s disease.</Abstract>
			<OtherAbstract Language="FA">&lt;em&gt;Nigella sativa &lt;/em&gt;is an annual herbaceous plantthat has various pharmacological effects. In this research study, anti–microbial and anti–Alzheimer effects of aqueous and hydro–alcoholic extracts of &lt;em&gt;N. sativa&lt;/em&gt; were evaluated. After identification of hydro–alcoholic extract compounds by GC–MS, anti–microbial activity indices including well diffusion, MIC and MBC for &lt;em&gt;E. coli&lt;/em&gt; and&lt;em&gt; S.&lt;/em&gt; &lt;em&gt;aureus&lt;/em&gt;, were carried out by tube and agar dilution methods. In Anti–Alzheimer&#039;s effects of hydro–alcoholic extract of &lt;em&gt;N. sativa &lt;/em&gt;on bovine serum albumin were examined using Congo–red spectrophotometry and transmission electron microscopy. Oleic acid (52.18%) followed by palmitic (19.77%) and linoleic acid (14.96%) were the major fatty acids in the extract. The amounts of MIC and MBC for both &lt;em&gt;E. coli&lt;/em&gt; &lt;em&gt;and S. aureus&lt;/em&gt; were 30.6 and 61 mg.ml&lt;sup&gt;-1&lt;/sup&gt; respectively in hydro–alcoholic extract. Well diffusion method showed highest antimicrobial activity against &lt;em&gt;S. aureus&lt;/em&gt; with inhibition zone diameter of 22.67±0.29 mm, but aqueous extract did not any effects on bacteria. Congo–red spectrophotometry results showed that the absorbance of the protein sample (as a measure of amyloid fibril presence) was reduced by increasing the concentration of &lt;em&gt;N. sativa&lt;/em&gt; extract and the lowest percentage of adsorption, compared to the control (extract less), was observed at the highest concentration of extract (20 μL). These results were confirmed by transmission electron microscope. The present study shows that the &lt;em&gt;N. sativa&lt;/em&gt; seed, as a natural and valuable source, can be used for controlling the microbial infections and reducing symptoms in patients with Alzheimer&#039;s disease.</OtherAbstract>
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			<Param Name="value">Anti-microbial effects</Param>
			</Object>
			<Object Type="keyword">
			<Param Name="value">Alzheimer’s disease</Param>
			</Object>
			<Object Type="keyword">
			<Param Name="value">‎Beta amyloid</Param>
			</Object>
			<Object Type="keyword">
			<Param Name="value">Nigella sativa</Param>
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<ArchiveCopySource DocType="pdf">https://eab.journals.pnu.ac.ir/article_7685_2eba195cfcd2ad7a879971c69d334e1c.pdf</ArchiveCopySource>
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