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<ArticleSet>
<Article>
<Journal>
				<PublisherName>Payame Noor University</PublisherName>
				<JournalTitle>Experimental animal Biology</JournalTitle>
				<Issn>2322-2387</Issn>
				<Volume>1</Volume>
				<Issue>1</Issue>
				<PubDate PubStatus="epublish">
					<Year>2012</Year>
					<Month>09</Month>
					<Day>22</Day>
				</PubDate>
			</Journal>
<ArticleTitle>Trichoderma reesei endoglucanases increase by butanol concentration method</ArticleTitle>
<VernacularTitle>Trichoderma reesei endoglucanases increase by butanol concentration method</VernacularTitle>
			<FirstPage>1</FirstPage>
			<LastPage>11</LastPage>
			<ELocationID EIdType="pii">130</ELocationID>
			
			
			<Language>FA</Language>
<AuthorList>
<Author>
					<FirstName>Behzad</FirstName>
					<LastName>Laamerad*</LastName>
<Affiliation>Assistant Prof. of Biochemistry</Affiliation>

</Author>
</AuthorList>
				<PublicationType>Journal Article</PublicationType>
			<History>
				<PubDate PubStatus="received">
					<Year>2012</Year>
					<Month>03</Month>
					<Day>15</Day>
				</PubDate>
			</History>
		<Abstract>Cellulase products usage in industry is in demand considerably. This enzyme is used in paper, paint, oil and textile industries. Cellulase can convert cellulose to glucose and then glucose can be converted to ethanol which this process can be replaced with fossil fuels. Cellulose is a polysaccharide that can be renewable and may be in future providing fuel for transportation. Cellulase converts cellulose to soluble sugars. One of the most extensively studied organisms is the soft rot fungus &lt;em&gt;Trichoderma reesei.&lt;/em&gt; This fungus produces a complete set of cellulolytic enzymes that are able to cleave β- 1, 4- glycosidic bonds present in cellulose or cellulose derivatives. One of the key enzymes in the multi- enzyme complexes is endoglucanase which is purified from different method. By using the butanol to concentrate this enzyme, we obtained remarkable active enzyme. The amount of cellobiohydrolases are much more than the concentration of endoglucanases (mentioned by several articles) in &lt;em&gt;Trichoderma reesei&lt;/em&gt;. In this experiment, we could obtain the concentration of endoglucanases 20% more than cellobiohydrolases.</Abstract>
			<OtherAbstract Language="FA">Cellulase products usage in industry is in demand considerably. This enzyme is used in paper, paint, oil and textile industries. Cellulase can convert cellulose to glucose and then glucose can be converted to ethanol which this process can be replaced with fossil fuels. Cellulose is a polysaccharide that can be renewable and may be in future providing fuel for transportation. Cellulase converts cellulose to soluble sugars. One of the most extensively studied organisms is the soft rot fungus &lt;em&gt;Trichoderma reesei.&lt;/em&gt; This fungus produces a complete set of cellulolytic enzymes that are able to cleave β- 1, 4- glycosidic bonds present in cellulose or cellulose derivatives. One of the key enzymes in the multi- enzyme complexes is endoglucanase which is purified from different method. By using the butanol to concentrate this enzyme, we obtained remarkable active enzyme. The amount of cellobiohydrolases are much more than the concentration of endoglucanases (mentioned by several articles) in &lt;em&gt;Trichoderma reesei&lt;/em&gt;. In this experiment, we could obtain the concentration of endoglucanases 20% more than cellobiohydrolases.</OtherAbstract>
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			<Object Type="keyword">
			<Param Name="value">butanol</Param>
			</Object>
			<Object Type="keyword">
			<Param Name="value">Cellulase</Param>
			</Object>
			<Object Type="keyword">
			<Param Name="value">endoglucanase</Param>
			</Object>
			<Object Type="keyword">
			<Param Name="value">Trichoderma reesei</Param>
			</Object>
		</ObjectList>
<ArchiveCopySource DocType="pdf">https://eab.journals.pnu.ac.ir/article_130_dfded5723971d0c0c2c5679655a90553.pdf</ArchiveCopySource>
</Article>

<Article>
<Journal>
				<PublisherName>Payame Noor University</PublisherName>
				<JournalTitle>Experimental animal Biology</JournalTitle>
				<Issn>2322-2387</Issn>
				<Volume>1</Volume>
				<Issue>1</Issue>
				<PubDate PubStatus="epublish">
					<Year>2012</Year>
					<Month>09</Month>
					<Day>22</Day>
				</PubDate>
			</Journal>
<ArticleTitle>The Effect of Ldopa on Creating Dependency of Morphine in Male Mature Mice Using Conditioned Place Preference (CPP) Method</ArticleTitle>
<VernacularTitle>The Effect of Ldopa on Creating Dependency of Morphine in Male Mature Mice Using Conditioned Place Preference (CPP) Method</VernacularTitle>
			<FirstPage>12</FirstPage>
			<LastPage>23</LastPage>
			<ELocationID EIdType="pii">416</ELocationID>
			
			
			<Language>FA</Language>
<AuthorList>
<Author>
					<FirstName>Seyed Ebrahim</FirstName>
					<LastName>Hosseini</LastName>
<Affiliation>MSc. of Animal Biology, Fars Science and Research Branch, Islamic Azad University.</Affiliation>

</Author>
<Author>
					<FirstName>F.</FirstName>
					<LastName>Firozirad</LastName>
<Affiliation>Assistant Prof. of Animal Biology, Fars Science and Research Branch, Islamic Azad University</Affiliation>

</Author>
<Author>
					<FirstName>H.</FirstName>
					<LastName>Aqababa</LastName>
<Affiliation>Assistant Prof. of Animal Biology, Fars Science and Research Branch, Islamic Azad University</Affiliation>

</Author>
</AuthorList>
				<PublicationType>Journal Article</PublicationType>
			<History>
				<PubDate PubStatus="received">
					<Year>2012</Year>
					<Month>02</Month>
					<Day>23</Day>
				</PubDate>
			</History>
		<Abstract>Introduction:&lt;br /&gt;Morphine and other opioid drugs through by increasing brain dopaminergic systems are used to induce dependence and craving. This study investigated the effects of Ldopa as dopamine precursor on creating dependency of morphine.&lt;br /&gt;Materials and Methods:&lt;br /&gt;In this study, 56 male mature mice (about 80 days old) with a weight of 30-35 grams were enrolled as the experimental, sham and the control groups. The experimental groups included 5 subgroups treated with either morphine, Ldopa with dose of minimum, Ldopa with dose of maximum, morphine+ Ldopa with dose of minimum and morphine+ Ldopa with dose of maximum. Morphine was used for dependency and Ldopa was used as dopamine precursor and CCP method was used to estimate dependency. The data were statistically analyzed by independent Student’s t-test using SPSS version 18.&lt;br /&gt;Results:&lt;br /&gt;Results showed no meaningful difference between the control and the witness groups. However, there was a meaningful difference between the control group with morphine, Ldopa and Ldopa+morphine groups in preferring a location to receive morphine. And also no meaningful difference between the Ldopa+morphine group in preferring the location for receiving the drug compared with the group receiving morphine alone.&lt;br /&gt;Conclusion:&lt;br /&gt;Morphine through stimulating mesolimbic dopaminergic nerve pathways and Ldopa through increased production of dopamine in the brain are causes increasing dependence.</Abstract>
			<OtherAbstract Language="FA">Introduction:&lt;br /&gt;Morphine and other opioid drugs through by increasing brain dopaminergic systems are used to induce dependence and craving. This study investigated the effects of Ldopa as dopamine precursor on creating dependency of morphine.&lt;br /&gt;Materials and Methods:&lt;br /&gt;In this study, 56 male mature mice (about 80 days old) with a weight of 30-35 grams were enrolled as the experimental, sham and the control groups. The experimental groups included 5 subgroups treated with either morphine, Ldopa with dose of minimum, Ldopa with dose of maximum, morphine+ Ldopa with dose of minimum and morphine+ Ldopa with dose of maximum. Morphine was used for dependency and Ldopa was used as dopamine precursor and CCP method was used to estimate dependency. The data were statistically analyzed by independent Student’s t-test using SPSS version 18.&lt;br /&gt;Results:&lt;br /&gt;Results showed no meaningful difference between the control and the witness groups. However, there was a meaningful difference between the control group with morphine, Ldopa and Ldopa+morphine groups in preferring a location to receive morphine. And also no meaningful difference between the Ldopa+morphine group in preferring the location for receiving the drug compared with the group receiving morphine alone.&lt;br /&gt;Conclusion:&lt;br /&gt;Morphine through stimulating mesolimbic dopaminergic nerve pathways and Ldopa through increased production of dopamine in the brain are causes increasing dependence.</OtherAbstract>
		<ObjectList>
			<Object Type="keyword">
			<Param Name="value">Morphine dependency</Param>
			</Object>
			<Object Type="keyword">
			<Param Name="value">Ldopa</Param>
			</Object>
			<Object Type="keyword">
			<Param Name="value">Conditioned Place Preference (CPP) method</Param>
			</Object>
		</ObjectList>
<ArchiveCopySource DocType="pdf">https://eab.journals.pnu.ac.ir/article_416_5dbb196a14d97b50215066921e8de641.pdf</ArchiveCopySource>
</Article>

<Article>
<Journal>
				<PublisherName>Payame Noor University</PublisherName>
				<JournalTitle>Experimental animal Biology</JournalTitle>
				<Issn>2322-2387</Issn>
				<Volume>1</Volume>
				<Issue>1</Issue>
				<PubDate PubStatus="epublish">
					<Year>2012</Year>
					<Month>10</Month>
					<Day>17</Day>
				</PubDate>
			</Journal>
<ArticleTitle>Structural study on pepsin stability in the presence of urea</ArticleTitle>
<VernacularTitle>Structural study on pepsin stability in the presence of urea</VernacularTitle>
			<FirstPage>24</FirstPage>
			<LastPage>30</LastPage>
			<ELocationID EIdType="pii">131</ELocationID>
			
			
			<Language>FA</Language>
<AuthorList>
<Author>
					<FirstName>M.</FirstName>
					<LastName>Kouhiyan</LastName>
<Affiliation>MSc of Biochemistry, payam Noor University</Affiliation>

</Author>
<Author>
					<FirstName>B.</FirstName>
					<LastName>Shareghi</LastName>
<Affiliation>Associated Professor, Shahrekord University</Affiliation>

</Author>
<Author>
					<FirstName>F.</FirstName>
					<LastName>Kouhiyan</LastName>
<Affiliation>MSc of Medical Physic, Isfahan University of Medical Sciences</Affiliation>

</Author>
</AuthorList>
				<PublicationType>Journal Article</PublicationType>
			<History>
				<PubDate PubStatus="received">
					<Year>2012</Year>
					<Month>03</Month>
					<Day>13</Day>
				</PubDate>
			</History>
		<Abstract>Pepsin (E.C.3.4.23.1) is a juice gastric aspartic proteinase. It belongs to hydrolyses family. Its monomeris structure is consisting of two lobes that they are similar in size and folding. It consists of a single polypeptide chain of molecular weight 34644 Daltone and 327 aminoacid. Structural analysis shows that pepsin contains 1.2% basic residues, 13.1% acidic residues, 46.5% polar residues and 39.2% hydrophobic residues. Structural stability of pepsin was investigated by UV-VIS spectrophotometer and spectrophlorimetry. Spectral measurements were made by sodium phosphate buffer .02M at pH: 2 and temperatures between 30 and 100 º   C. It was observed that (1) high considerable enzyme stability, (2) enzyme stability decreases in the presence of urea at pH: 2. (3) thermodynamic parameters decline in the presence of urea. (4) Florescence intensity increase in the presence of urea.</Abstract>
			<OtherAbstract Language="FA">Pepsin (E.C.3.4.23.1) is a juice gastric aspartic proteinase. It belongs to hydrolyses family. Its monomeris structure is consisting of two lobes that they are similar in size and folding. It consists of a single polypeptide chain of molecular weight 34644 Daltone and 327 aminoacid. Structural analysis shows that pepsin contains 1.2% basic residues, 13.1% acidic residues, 46.5% polar residues and 39.2% hydrophobic residues. Structural stability of pepsin was investigated by UV-VIS spectrophotometer and spectrophlorimetry. Spectral measurements were made by sodium phosphate buffer .02M at pH: 2 and temperatures between 30 and 100 º   C. It was observed that (1) high considerable enzyme stability, (2) enzyme stability decreases in the presence of urea at pH: 2. (3) thermodynamic parameters decline in the presence of urea. (4) Florescence intensity increase in the presence of urea.</OtherAbstract>
		<ObjectList>
			<Object Type="keyword">
			<Param Name="value">Denaturation</Param>
			</Object>
			<Object Type="keyword">
			<Param Name="value">Pepsin</Param>
			</Object>
			<Object Type="keyword">
			<Param Name="value">Urea</Param>
			</Object>
			<Object Type="keyword">
			<Param Name="value">Structural stability</Param>
			</Object>
		</ObjectList>
<ArchiveCopySource DocType="pdf">https://eab.journals.pnu.ac.ir/article_131_624285dfec525655e2072a2dccc18c69.pdf</ArchiveCopySource>
</Article>

<Article>
<Journal>
				<PublisherName>Payame Noor University</PublisherName>
				<JournalTitle>Experimental animal Biology</JournalTitle>
				<Issn>2322-2387</Issn>
				<Volume>1</Volume>
				<Issue>1</Issue>
				<PubDate PubStatus="epublish">
					<Year>2012</Year>
					<Month>10</Month>
					<Day>17</Day>
				</PubDate>
			</Journal>
<ArticleTitle>In vitro assessment of final oocyte maturation index (GVBD) in Persian Sturgeon and broodstock selection</ArticleTitle>
<VernacularTitle>In vitro assessment of final oocyte maturation index (GVBD) in Persian Sturgeon and broodstock selection</VernacularTitle>
			<FirstPage>31</FirstPage>
			<LastPage>40</LastPage>
			<ELocationID EIdType="pii">132</ELocationID>
			
			
			<Language>FA</Language>
<AuthorList>
<Author>
					<FirstName>B.</FirstName>
					<LastName>Taneh</LastName>
<Affiliation>Lecturer of Biology, Payame Noor University</Affiliation>

</Author>
<Author>
					<FirstName>B.</FirstName>
					<LastName>Abtahi</LastName>
<Affiliation>Assistant Professor, Shahid Beheshti University</Affiliation>

</Author>
<Author>
					<FirstName>R.M.</FirstName>
					<LastName>Nazari</LastName>
<Affiliation>BSc., Shahid Rajaei Sturgeon fish farm – Sari</Affiliation>

</Author>
</AuthorList>
				<PublicationType>Journal Article</PublicationType>
			<History>
				<PubDate PubStatus="received">
					<Year>2012</Year>
					<Month>04</Month>
					<Day>16</Day>
				</PubDate>
			</History>
		<Abstract>   One of the big problems on Sturgeon Fishes is select of the breeders that have high quality of gametes after hormone injection. So in this research Final oocyte maturation index (GVBD) in &lt;em&gt;in vitro&lt;/em&gt; for selection of Persian sturgeon Broodstock, &lt;em&gt;Acipenser&lt;/em&gt;&lt;em&gt; &lt;/em&gt;&lt;em&gt;persicus&lt;/em&gt;, was studied on 10 females captured from the Caspian Sea during reproduction season. About 150 oocytes from every broodstock, taken by hollow probe, were incubated in incubation media of RM&lt;sub&gt;2&lt;/sub&gt; containing 10 µg/l of progesterone for induction of the final oocyte maturation and assessment of GVBD index. Results indicated that significant differences in GVBD of the &lt;em&gt;in vitro &lt;/em&gt;and &lt;em&gt;in vivo &lt;/em&gt;were observed (&lt;sub&gt;٭٭&lt;/sub&gt;). However, Broodstockes with rate of GVBD in &lt;em&gt;in vitro&lt;/em&gt; higher than %50 had a significantly better ovulation, fertilization and incubation rates (&lt;sub&gt;٭&lt;/sub&gt;), from those with a GVBD lower than %50. It could be concluded that use from method of assessment of GVBD index under &lt;em&gt;in vitro&lt;/em&gt; circumstance was preferable to assessment of GVBD index under &lt;em&gt;in vivo&lt;/em&gt; and also nucleus polarization index for selection of suitable broodstock. &lt;br /&gt; </Abstract>
			<OtherAbstract Language="FA">   One of the big problems on Sturgeon Fishes is select of the breeders that have high quality of gametes after hormone injection. So in this research Final oocyte maturation index (GVBD) in &lt;em&gt;in vitro&lt;/em&gt; for selection of Persian sturgeon Broodstock, &lt;em&gt;Acipenser&lt;/em&gt;&lt;em&gt; &lt;/em&gt;&lt;em&gt;persicus&lt;/em&gt;, was studied on 10 females captured from the Caspian Sea during reproduction season. About 150 oocytes from every broodstock, taken by hollow probe, were incubated in incubation media of RM&lt;sub&gt;2&lt;/sub&gt; containing 10 µg/l of progesterone for induction of the final oocyte maturation and assessment of GVBD index. Results indicated that significant differences in GVBD of the &lt;em&gt;in vitro &lt;/em&gt;and &lt;em&gt;in vivo &lt;/em&gt;were observed (&lt;sub&gt;٭٭&lt;/sub&gt;). However, Broodstockes with rate of GVBD in &lt;em&gt;in vitro&lt;/em&gt; higher than %50 had a significantly better ovulation, fertilization and incubation rates (&lt;sub&gt;٭&lt;/sub&gt;), from those with a GVBD lower than %50. It could be concluded that use from method of assessment of GVBD index under &lt;em&gt;in vitro&lt;/em&gt; circumstance was preferable to assessment of GVBD index under &lt;em&gt;in vivo&lt;/em&gt; and also nucleus polarization index for selection of suitable broodstock. &lt;br /&gt; </OtherAbstract>
		<ObjectList>
			<Object Type="keyword">
			<Param Name="value">Acipenser persicus</Param>
			</Object>
			<Object Type="keyword">
			<Param Name="value">in vitro</Param>
			</Object>
			<Object Type="keyword">
			<Param Name="value">GVBD</Param>
			</Object>
			<Object Type="keyword">
			<Param Name="value">final oocyte maturation</Param>
			</Object>
			<Object Type="keyword">
			<Param Name="value">Broodstock Selection</Param>
			</Object>
		</ObjectList>
<ArchiveCopySource DocType="pdf">https://eab.journals.pnu.ac.ir/article_132_cb69f1a989328f1e2743fa65b7301dfa.pdf</ArchiveCopySource>
</Article>

<Article>
<Journal>
				<PublisherName>Payame Noor University</PublisherName>
				<JournalTitle>Experimental animal Biology</JournalTitle>
				<Issn>2322-2387</Issn>
				<Volume>1</Volume>
				<Issue>1</Issue>
				<PubDate PubStatus="epublish">
					<Year>2012</Year>
					<Month>10</Month>
					<Day>17</Day>
				</PubDate>
			</Journal>
<ArticleTitle>Infection rate of Linguatulaserrata nymphs in cattle slaughtered in 
Tabriz abattoir, Iran</ArticleTitle>
<VernacularTitle>Infection rate of Linguatulaserrata nymphs in cattle slaughtered in 
Tabriz abattoir, Iran</VernacularTitle>
			<FirstPage>41</FirstPage>
			<LastPage>49</LastPage>
			<ELocationID EIdType="pii">133</ELocationID>
			
			
			<Language>FA</Language>
<AuthorList>
<Author>
					<FirstName>M.</FirstName>
					<LastName>Mirzai</LastName>
<Affiliation>Asistance Professor of Parasitology, Veterinary Medicine, Kerman University, Iran</Affiliation>

</Author>
<Author>
					<FirstName>E.</FirstName>
					<LastName>Azimi</LastName>
<Affiliation>Msc of Biochemistry, Faculty of Basic Science, Payam Noor University, Tehran, Iran</Affiliation>

</Author>
<Author>
					<FirstName>M.</FirstName>
					<LastName>Sami</LastName>
<Affiliation>Asistance Professor of Food Hygiene, Veterinary Medicine, Kerman University, Iran</Affiliation>

</Author>
<Author>
					<FirstName>B.</FirstName>
					<LastName>Yavari</LastName>
<Affiliation>Msc of Physiology, Faculty of Basic Science, Tarbiat Moalleme Azarbayjan, Iran</Affiliation>

</Author>
<Author>
					<FirstName>Kh.</FirstName>
					<LastName>Badihi</LastName>
<Affiliation>Msc of Microbiology, Faculty of Basic Science,   Tonekabon Azad University, Iran</Affiliation>

</Author>
</AuthorList>
				<PublicationType>Journal Article</PublicationType>
			<History>
				<PubDate PubStatus="received">
					<Year>2012</Year>
					<Month>02</Month>
					<Day>13</Day>
				</PubDate>
			</History>
		<Abstract>   In this survey, the infection rate of &lt;em&gt;Linguatulaserrata&lt;/em&gt; nymphs in mesenteric lymph nodes (MLNs), livers and lungs of 400 cattle was studied in different seasons considering their sex and age in Tabriz abattoir. The lymph nodes, livers and lungs were examined macroscopically. A digestion method was also applied for investigation of liver and lung samples. The infection rate of &lt;em&gt;L. serrata&lt;/em&gt; nymphs in MLNs and livers was 17.2% and0.25% respectively. But none of the lung samples were infected. The infection rate in slaughtered cattle significantly increased with age (P0.05).Moreover, there was not any significant difference in infection rate through the different seasons of the year(P&gt;0.05).</Abstract>
			<OtherAbstract Language="FA">   In this survey, the infection rate of &lt;em&gt;Linguatulaserrata&lt;/em&gt; nymphs in mesenteric lymph nodes (MLNs), livers and lungs of 400 cattle was studied in different seasons considering their sex and age in Tabriz abattoir. The lymph nodes, livers and lungs were examined macroscopically. A digestion method was also applied for investigation of liver and lung samples. The infection rate of &lt;em&gt;L. serrata&lt;/em&gt; nymphs in MLNs and livers was 17.2% and0.25% respectively. But none of the lung samples were infected. The infection rate in slaughtered cattle significantly increased with age (P0.05).Moreover, there was not any significant difference in infection rate through the different seasons of the year(P&gt;0.05).</OtherAbstract>
		<ObjectList>
			<Object Type="keyword">
			<Param Name="value">cattle</Param>
			</Object>
			<Object Type="keyword">
			<Param Name="value">Linguatulaserrata</Param>
			</Object>
			<Object Type="keyword">
			<Param Name="value">Tabriz</Param>
			</Object>
		</ObjectList>
<ArchiveCopySource DocType="pdf">https://eab.journals.pnu.ac.ir/article_133_a41e2b5bf64c39af77341862b0ba4b14.pdf</ArchiveCopySource>
</Article>

<Article>
<Journal>
				<PublisherName>Payame Noor University</PublisherName>
				<JournalTitle>Experimental animal Biology</JournalTitle>
				<Issn>2322-2387</Issn>
				<Volume>1</Volume>
				<Issue>1</Issue>
				<PubDate PubStatus="epublish">
					<Year>2012</Year>
					<Month>10</Month>
					<Day>17</Day>
				</PubDate>
			</Journal>
<ArticleTitle>Taxonomic study of blister beetles (Coleoptera: Meloidae) in Arak county, Iran</ArticleTitle>
<VernacularTitle>Taxonomic study of blister beetles (Coleoptera: Meloidae) in Arak county, Iran</VernacularTitle>
			<FirstPage>50</FirstPage>
			<LastPage>62</LastPage>
			<ELocationID EIdType="pii">134</ELocationID>
			
			
			<Language>FA</Language>
<AuthorList>
<Author>
					<FirstName>Atena</FirstName>
					<LastName>Faraji</LastName>
<Affiliation>Msc of Biological Sciences, Islamic Azad University North Tehran</Affiliation>

</Author>
<Author>
					<FirstName>Shahrokh</FirstName>
					<LastName>PashaieRad</LastName>
<Affiliation>Associate Professor, Faculty of Biological Sciences, Shahid Beheshti University</Affiliation>

</Author>
<Author>
					<FirstName>Alireza</FirstName>
					<LastName>Shayesteh‌far</LastName>
<Affiliation>Assistant Professor, Faculty of Sciences, Arak University</Affiliation>

</Author>
</AuthorList>
				<PublicationType>Journal Article</PublicationType>
			<History>
				<PubDate PubStatus="received">
					<Year>2011</Year>
					<Month>11</Month>
					<Day>30</Day>
				</PubDate>
			</History>
		<Abstract>   During the taxonomical investigations of Coleoptera (family: Meloidae) of the Arak County, in spring and summer 2010, 15 species of blister beetles belonging to the two subfamily (Nemognathinae and Meloinae), three tribes (Mylabrini, Lyttini and Nemognathini) and six genus (&lt;em&gt;Hycleus, Mylabris, Alosimus, Calydus, Teratolytta &lt;/em&gt;and&lt;em&gt; Nemognatha&lt;/em&gt;) were collected and identified. In this study the geographical distribution and identification key of the collected species of blister beetles were considered. This is the first time that Calydus ornaticollis species from Arak and Teratolytta flavipes species from Iran was reported. Morphological characters such as mesosternum, antennae, pronotum, and male reproductive organ were the main identification character that was used.</Abstract>
			<OtherAbstract Language="FA">   During the taxonomical investigations of Coleoptera (family: Meloidae) of the Arak County, in spring and summer 2010, 15 species of blister beetles belonging to the two subfamily (Nemognathinae and Meloinae), three tribes (Mylabrini, Lyttini and Nemognathini) and six genus (&lt;em&gt;Hycleus, Mylabris, Alosimus, Calydus, Teratolytta &lt;/em&gt;and&lt;em&gt; Nemognatha&lt;/em&gt;) were collected and identified. In this study the geographical distribution and identification key of the collected species of blister beetles were considered. This is the first time that Calydus ornaticollis species from Arak and Teratolytta flavipes species from Iran was reported. Morphological characters such as mesosternum, antennae, pronotum, and male reproductive organ were the main identification character that was used.</OtherAbstract>
		<ObjectList>
			<Object Type="keyword">
			<Param Name="value">Identification key</Param>
			</Object>
			<Object Type="keyword">
			<Param Name="value">Meloidae</Param>
			</Object>
			<Object Type="keyword">
			<Param Name="value">Blister beetles</Param>
			</Object>
			<Object Type="keyword">
			<Param Name="value">Arak C‍ounty</Param>
			</Object>
		</ObjectList>
<ArchiveCopySource DocType="pdf">https://eab.journals.pnu.ac.ir/article_134_4fb4a5f3c04d7ccfa394d644130bb5bd.pdf</ArchiveCopySource>
</Article>

<Article>
<Journal>
				<PublisherName>Payame Noor University</PublisherName>
				<JournalTitle>Experimental animal Biology</JournalTitle>
				<Issn>2322-2387</Issn>
				<Volume>1</Volume>
				<Issue>1</Issue>
				<PubDate PubStatus="epublish">
					<Year>2012</Year>
					<Month>10</Month>
					<Day>17</Day>
				</PubDate>
			</Journal>
<ArticleTitle>Antioxidant activity status and heart failure in broilers with pulmonary hypertension syndrome (PHS )</ArticleTitle>
<VernacularTitle>Antioxidant activity status and heart failure in broilers with pulmonary hypertension syndrome (PHS )</VernacularTitle>
			<FirstPage>69</FirstPage>
			<LastPage>80</LastPage>
			<ELocationID EIdType="pii">136</ELocationID>
			
			
			<Language>FA</Language>
<AuthorList>
<Author>
					<FirstName>Mokhtar</FirstName>
					<LastName>Fathi</LastName>
<Affiliation>Assistant Professor, Payam Noor University</Affiliation>

</Author>
<Author>
					<FirstName>T.</FirstName>
					<LastName>Tanha</LastName>
<Affiliation>Assistant Professor, Payam Noor University</Affiliation>

</Author>
</AuthorList>
				<PublicationType>Journal Article</PublicationType>
			<History>
				<PubDate PubStatus="received">
					<Year>2012</Year>
					<Month>03</Month>
					<Day>18</Day>
				</PubDate>
			</History>
		<Abstract>   160 one-day-old male broiler chicks (Ross308) in 2 groups of 4 replicates were studied in each group20 chicks for each replicate were used. One group of these birds was rose in normal temperature (NT treatment) and the other group was raised in cold temperature induce PHS and heart failure (CT treatment). Glutathione peroxidase (GPX), superoxide dismutase SOD (, total antioxidant status (TAS) and malondialdehyde (MDA) content of both plasma and liver were determined at days 21 and 42 At the end of the experiment (day42), 2 chicks from each replicate were randomly selected and slaughtered. The heart was removed and the right ventricle was dissected away. The ratio of right ventricle weight to total ventricle weight (RV/TV) was calculated. Results showed that MDA content in plasma and liver of CT birds was greater than that of NT birds at day 21 and 42. GPX activity in plasma and liver of CT birds at day 21&amp;42 and SOD activity in plasma at day 42 were lower than that of NT birds. Furthermore, birds of NT treatment had a higher plasma TAS (P&lt;0.05) at both ages. Moreover, RV/TV ratio at day 42 and mortality in total period were significantly higher in CT birds.</Abstract>
			<OtherAbstract Language="FA">   160 one-day-old male broiler chicks (Ross308) in 2 groups of 4 replicates were studied in each group20 chicks for each replicate were used. One group of these birds was rose in normal temperature (NT treatment) and the other group was raised in cold temperature induce PHS and heart failure (CT treatment). Glutathione peroxidase (GPX), superoxide dismutase SOD (, total antioxidant status (TAS) and malondialdehyde (MDA) content of both plasma and liver were determined at days 21 and 42 At the end of the experiment (day42), 2 chicks from each replicate were randomly selected and slaughtered. The heart was removed and the right ventricle was dissected away. The ratio of right ventricle weight to total ventricle weight (RV/TV) was calculated. Results showed that MDA content in plasma and liver of CT birds was greater than that of NT birds at day 21 and 42. GPX activity in plasma and liver of CT birds at day 21&amp;42 and SOD activity in plasma at day 42 were lower than that of NT birds. Furthermore, birds of NT treatment had a higher plasma TAS (P&lt;0.05) at both ages. Moreover, RV/TV ratio at day 42 and mortality in total period were significantly higher in CT birds.</OtherAbstract>
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<ArchiveCopySource DocType="pdf">https://eab.journals.pnu.ac.ir/article_136_d87042a98eec44232704e18cef00367a.pdf</ArchiveCopySource>
</Article>
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