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<Article>
<Journal>
				<PublisherName>Faculty of Veterinary Medicine, Shahrekord University</PublisherName>
				<JournalTitle>Iranian Journal of Veterinary Clinical Sciences</JournalTitle>
				<Issn>2423-3625</Issn>
				<Volume>19</Volume>
				<Issue>2</Issue>
				<PubDate PubStatus="epublish">
					<Year>2026</Year>
					<Month>02</Month>
					<Day>20</Day>
				</PubDate>
			</Journal>
<ArticleTitle>Effect of Zinc Hydroxychloride Supplementation on Pulmonary Hypertension Parameters, Zinc Retention, and Bone Strength in Broiler Chickens Under High-Altitude Rearing Conditions</ArticleTitle>
<VernacularTitle>Effect of Zinc Hydroxychloride Supplementation on Pulmonary Hypertension Parameters, Zinc Retention, and Bone Strength in Broiler Chickens Under High-Altitude Rearing Conditions</VernacularTitle>
			<FirstPage>3</FirstPage>
			<LastPage>14</LastPage>
			<ELocationID EIdType="pii">116673</ELocationID>
			
<ELocationID EIdType="doi">10.22034/ijvcs.2026.14832.1086</ELocationID>
			
			<Language>FA</Language>
<AuthorList>
<Author>
					<FirstName>Amir</FirstName>
					<LastName>Parvaresh</LastName>
<Affiliation>4 Department of Animal Science, Faculty of Agriculture, Shahrekord University, Shahrekord, Iran</Affiliation>
<Identifier Source="ORCID">0009-0005-8200-3858</Identifier>

</Author>
<Author>
					<FirstName>Behnam</FirstName>
					<LastName>Ahmadipour</LastName>
<Affiliation>Department of Animal Science, Faculty of Agriculture, Shahrekord University, Shahrekord, Iran.</Affiliation>
<Identifier Source="ORCID">0000-0002-4254-145X</Identifier>

</Author>
<Author>
					<FirstName>Samira</FirstName>
					<LastName>Abaszadeh</LastName>
<Affiliation>Department of Animal Science, Faculty of Agriculture, Shahrekord University, Shahrekord, Iran</Affiliation>
<Identifier Source="ORCID">0000-0002-7443-232X</Identifier>

</Author>
<Author>
					<FirstName>Amir</FirstName>
					<LastName>Afshar Bakeshlo</LastName>
<Affiliation>Department of Animal Sciences, Shahid Bahonar Agriculture School, Pakdasht, Tehran, Iran</Affiliation>
<Identifier Source="ORCID">0009-0004-5348-3103</Identifier>

</Author>
</AuthorList>
				<PublicationType>Journal Article</PublicationType>
			<History>
				<PubDate PubStatus="received">
					<Year>2025</Year>
					<Month>12</Month>
					<Day>28</Day>
				</PubDate>
			</History>
		<Abstract>This study aimed to evaluate the effect of different levels of zinc hydroxychloride (HCZ) on pulmonary hypertension-related parameters, zinc element storage, and tibia bone strength in broiler chickens under high-altitude environmental conditions (2100m). In this research, 200 Ross 308 male broiler chicks from 23 to 42 days of age were used for a completely randomized design in 4 treatments and 5 replicates. The experimental treatments included a basal diet and 25, 50, and 75 mg of HCZ per kg of basal feed, which were added to the control diet. HCZ consumption led to a decrease in the RV to TV ratio, an increase in nitric oxide concentration, a decrease in hematocrit, and a decrease in the heterophil to lymphocyte ratio (P&lt;0.05). As the retention of zinc in breast muscle, liver, and tibia bone increased (P&lt;0.05), the increased bone fracture force indicated an increase in tibia bone strength (P&lt;0.05). Overall, the results showed that consuming 75 mg of HCZ improved physiological and immune responses, increased zinc storage in bone tissue, breast, and liver, improved growth parameters and tibia bone strength, and cardiopulmonary performance of broiler chickens under hypoxic conditions. Therefore, a level of 75 mg HCZ is recommended for use in poultry farms.</Abstract>
			<OtherAbstract Language="FA">This study aimed to evaluate the effect of different levels of zinc hydroxychloride (HCZ) on pulmonary hypertension-related parameters, zinc element storage, and tibia bone strength in broiler chickens under high-altitude environmental conditions (2100m). In this research, 200 Ross 308 male broiler chicks from 23 to 42 days of age were used for a completely randomized design in 4 treatments and 5 replicates. The experimental treatments included a basal diet and 25, 50, and 75 mg of HCZ per kg of basal feed, which were added to the control diet. HCZ consumption led to a decrease in the RV to TV ratio, an increase in nitric oxide concentration, a decrease in hematocrit, and a decrease in the heterophil to lymphocyte ratio (P&lt;0.05). As the retention of zinc in breast muscle, liver, and tibia bone increased (P&lt;0.05), the increased bone fracture force indicated an increase in tibia bone strength (P&lt;0.05). Overall, the results showed that consuming 75 mg of HCZ improved physiological and immune responses, increased zinc storage in bone tissue, breast, and liver, improved growth parameters and tibia bone strength, and cardiopulmonary performance of broiler chickens under hypoxic conditions. Therefore, a level of 75 mg HCZ is recommended for use in poultry farms.</OtherAbstract>
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			<Param Name="value">High altitude</Param>
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			<Object Type="keyword">
			<Param Name="value">Bone strength</Param>
			</Object>
			<Object Type="keyword">
			<Param Name="value">Pulmonary hypertension</Param>
			</Object>
			<Object Type="keyword">
			<Param Name="value">Zinc hydroxychloride</Param>
			</Object>
		</ObjectList>
<ArchiveCopySource DocType="pdf">https://ijvcs.sku.ac.ir/article_116673_bc8c119f1afbe85bc6037297cdf0fb08.pdf</ArchiveCopySource>
</Article>

<Article>
<Journal>
				<PublisherName>Faculty of Veterinary Medicine, Shahrekord University</PublisherName>
				<JournalTitle>Iranian Journal of Veterinary Clinical Sciences</JournalTitle>
				<Issn>2423-3625</Issn>
				<Volume>19</Volume>
				<Issue>2</Issue>
				<PubDate PubStatus="epublish">
					<Year>2026</Year>
					<Month>02</Month>
					<Day>20</Day>
				</PubDate>
			</Journal>
<ArticleTitle>The Effect of Simultaneous Administration of Weissella confusa Probiotic and Astaxanthin Pigment on Selected Immune Indices of Rainbow Trout (Oncorhynchus mykiss)</ArticleTitle>
<VernacularTitle>The Effect of Simultaneous Administration of Weissella confusa Probiotic and Astaxanthin Pigment on Selected Immune Indices of Rainbow Trout (Oncorhynchus mykiss)</VernacularTitle>
			<FirstPage>15</FirstPage>
			<LastPage>24</LastPage>
			<ELocationID EIdType="pii">116674</ELocationID>
			
<ELocationID EIdType="doi">10.22034/ijvcs.2026.14888.1090</ELocationID>
			
			<Language>FA</Language>
<AuthorList>
<Author>
					<FirstName>Syavash</FirstName>
					<LastName>Asadi</LastName>
<Affiliation>¹ Ph.D. Student in Aquatic Animal Health and Diseases, Faculty of Veterinary Medicine, Shahrekord University, Shahrekord, Iran</Affiliation>

</Author>
<Author>
					<FirstName>Shafigh</FirstName>
					<LastName>Shafiei</LastName>
<Affiliation>Department of Food Hygiene and Quality Control, Faculty of Veterinary Medicine, Shahrekord University, Shahrekord, Iran</Affiliation>

</Author>
<Author>
					<FirstName>Masoud</FirstName>
					<LastName>Ghorbanpoor</LastName>
<Affiliation>Department of Pathobiology, Faculty of Veterinary Medicine, Shahrekord University, Shahrekord, Iran</Affiliation>
<Identifier Source="ORCID">0000-0002-0301-4577</Identifier>

</Author>
<Author>
					<FirstName>Esamail</FirstName>
					<LastName>Pirali</LastName>
<Affiliation>Department of Fishery Science, Faculty of Natural Resources and Earth Sciences, Shahrekord University, Shahrekord, Iran</Affiliation>

</Author>
</AuthorList>
				<PublicationType>Journal Article</PublicationType>
			<History>
				<PubDate PubStatus="received">
					<Year>2026</Year>
					<Month>01</Month>
					<Day>19</Day>
				</PubDate>
			</History>
		<Abstract>Aquaculture, as a key component of global food production, requires strategies to reduce disease-related losses and improve the health of cultured fish. Nuritional supplements such as probiotics and antioxidants have been recognized as promising tools for enhancing fish immunity. &lt;br&gt;In this study, the simultaneous effect of the probiotic Weissella confusa and the antioxidant pigment astaxanthin on the expression of immune-related genes in rainbow trout (Oncorhynchus mykiss) was investigated. A total of 240 fish were divided into four treatments (control, probiotic, astaxanthin, and combined; each treatment in three replicates with 20 fish per replicate) and fed for 28 days. Expression levels of IFN-γ, IL-6, IL-10, IL-12, IL-17, and TNF-α were measured in the anterior kidney and spleen using qPCR. &lt;br&gt;The combined treatment showed the highest (P&lt;0.05) upregulation of IL-10, IL-12, IL-17, and TNF-α compared to other groups. IFN-γ expression increased on day 14 in the combined group but declined by day 28. Moreover, IL-6 expression was significantly higher (P&lt;0.05) in the probiotic and combined groups on day 28. The temporal expression patterns indicated dynamic regulation and synergistic effects of probiotic and astaxanthin supplementation. &lt;br&gt;It appears that concurrent administration of Weissella confusa and astaxanthin enhances molecular immune markers in rainbow trout and may serve as an effective nutritional strategy to improve health and disease resistance in aquaculture production.</Abstract>
			<OtherAbstract Language="FA">Aquaculture, as a key component of global food production, requires strategies to reduce disease-related losses and improve the health of cultured fish. Nuritional supplements such as probiotics and antioxidants have been recognized as promising tools for enhancing fish immunity. &lt;br&gt;In this study, the simultaneous effect of the probiotic Weissella confusa and the antioxidant pigment astaxanthin on the expression of immune-related genes in rainbow trout (Oncorhynchus mykiss) was investigated. A total of 240 fish were divided into four treatments (control, probiotic, astaxanthin, and combined; each treatment in three replicates with 20 fish per replicate) and fed for 28 days. Expression levels of IFN-γ, IL-6, IL-10, IL-12, IL-17, and TNF-α were measured in the anterior kidney and spleen using qPCR. &lt;br&gt;The combined treatment showed the highest (P&lt;0.05) upregulation of IL-10, IL-12, IL-17, and TNF-α compared to other groups. IFN-γ expression increased on day 14 in the combined group but declined by day 28. Moreover, IL-6 expression was significantly higher (P&lt;0.05) in the probiotic and combined groups on day 28. The temporal expression patterns indicated dynamic regulation and synergistic effects of probiotic and astaxanthin supplementation. &lt;br&gt;It appears that concurrent administration of Weissella confusa and astaxanthin enhances molecular immune markers in rainbow trout and may serve as an effective nutritional strategy to improve health and disease resistance in aquaculture production.</OtherAbstract>
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			<Object Type="keyword">
			<Param Name="value">Rainbow trout</Param>
			</Object>
			<Object Type="keyword">
			<Param Name="value">probiotic</Param>
			</Object>
			<Object Type="keyword">
			<Param Name="value">Astaxanthin</Param>
			</Object>
			<Object Type="keyword">
			<Param Name="value">cytokine</Param>
			</Object>
			<Object Type="keyword">
			<Param Name="value">Weissella confusa</Param>
			</Object>
		</ObjectList>
<ArchiveCopySource DocType="pdf">https://ijvcs.sku.ac.ir/article_116674_87188e3f6185e00360616932cdf22143.pdf</ArchiveCopySource>
</Article>

<Article>
<Journal>
				<PublisherName>Faculty of Veterinary Medicine, Shahrekord University</PublisherName>
				<JournalTitle>Iranian Journal of Veterinary Clinical Sciences</JournalTitle>
				<Issn>2423-3625</Issn>
				<Volume>19</Volume>
				<Issue>2</Issue>
				<PubDate PubStatus="epublish">
					<Year>2026</Year>
					<Month>02</Month>
					<Day>20</Day>
				</PubDate>
			</Journal>
<ArticleTitle>Detection of Streptococcus dysgalactiae, Candida albicans and Cryptococcus neoformans using PCR in milk of cows with mastitis</ArticleTitle>
<VernacularTitle>Detection of Streptococcus dysgalactiae, Candida albicans and Cryptococcus neoformans using PCR in milk of cows with mastitis</VernacularTitle>
			<FirstPage>25</FirstPage>
			<LastPage>35</LastPage>
			<ELocationID EIdType="pii">116666</ELocationID>
			
<ELocationID EIdType="doi">10.22034/ijvcs.2026.14940.1095</ELocationID>
			
			<Language>FA</Language>
<AuthorList>
<Author>
					<FirstName>Mahdiyeh</FirstName>
					<LastName>Sianati</LastName>
<Affiliation>MSc graduate, Department of Pathobiology, Faculty of Veterinary Medicine, Shahrekord University, Shahrekord- Iran</Affiliation>

</Author>
<Author>
					<FirstName>Ali</FirstName>
					<LastName>Kadivar</LastName>
<Affiliation>Department of Clinical Sciences, Faculty of Veterinary Medicine, Shahrekord University, Shahrekord- Iran</Affiliation>

</Author>
<Author>
					<FirstName>Somaye</FirstName>
					<LastName>Shahrokh Shahraki</LastName>
<Affiliation>Department of Pathobiology, Faculty of Veterinary Medicine, Shahrekord University, Shahrekord- Iran</Affiliation>

</Author>
<Author>
					<FirstName>Azam</FirstName>
					<LastName>Mokhtari</LastName>
<Affiliation>Department of Pathobiology, Faculty of Veterinary Medicine, Shahrekord University, Shahrekord- Iran</Affiliation>

</Author>
<Author>
					<FirstName>Zahra</FirstName>
					<LastName>Hemati</LastName>
<Affiliation>Department of Pathobiology, Faculty of Veterinary Medicine, Shahrekord University, Shahrekord- Iran</Affiliation>

</Author>
</AuthorList>
				<PublicationType>Journal Article</PublicationType>
			<History>
				<PubDate PubStatus="received">
					<Year>2026</Year>
					<Month>02</Month>
					<Day>19</Day>
				</PubDate>
			</History>
		<Abstract>Mastitis is a frequent and costly disease in dairy cattle. Streptococcus species, especially Streptococcus dysgalactiae (S. dysgalactiae), are major bacterial causes of this condition. Fungal mastitis can also occur, particularly in unsanitary environments or milking systems. Candida species are the most commonly isolated fungi in cases of bovine mastitis. Furthermore, Cryptococcus species have also been recognized as causative agents of mastitis in cattle. In this study, PCR was employed to assess the frequency of three mastitis-causing pathogens in cattle including S. dysgalactiae, Candida albicans (C. albicans), and Cryptococcus neoformans (C. neoformans) across both clinical and subclinical cases of bovine mastitis. A total of 100 milk samples were obtained from cows diagnosed with both clinical or subclinical mastitis. The samples were centrifuged, and the resulting precipitate was utilized for DNA extraction. Polymerase chain reaction (PCR) was then conducted using specific primers. Out of a total of 100 milk samples, 3 samples (3%), 4 samples (4%) and 1 sample (1%) were found to be positive for the presence of S. dysgalactiae, C. albicans and C. neoformans nucleic acid using the PCR method, respectively. Streptococcus dysgalactiae positive cases were all related to subclinical mastitis, and C. albicans and C. neoformans positive cases were all related to clinical mastitis. Given fungal mastitis&#039;s resistance to conventional therapies and its significant risks to the dairy sector, the results of this study will help determine the frequency of the infection and, consequently, the application of targeted management protocols.</Abstract>
			<OtherAbstract Language="FA">Mastitis is a frequent and costly disease in dairy cattle. Streptococcus species, especially Streptococcus dysgalactiae (S. dysgalactiae), are major bacterial causes of this condition. Fungal mastitis can also occur, particularly in unsanitary environments or milking systems. Candida species are the most commonly isolated fungi in cases of bovine mastitis. Furthermore, Cryptococcus species have also been recognized as causative agents of mastitis in cattle. In this study, PCR was employed to assess the frequency of three mastitis-causing pathogens in cattle including S. dysgalactiae, Candida albicans (C. albicans), and Cryptococcus neoformans (C. neoformans) across both clinical and subclinical cases of bovine mastitis. A total of 100 milk samples were obtained from cows diagnosed with both clinical or subclinical mastitis. The samples were centrifuged, and the resulting precipitate was utilized for DNA extraction. Polymerase chain reaction (PCR) was then conducted using specific primers. Out of a total of 100 milk samples, 3 samples (3%), 4 samples (4%) and 1 sample (1%) were found to be positive for the presence of S. dysgalactiae, C. albicans and C. neoformans nucleic acid using the PCR method, respectively. Streptococcus dysgalactiae positive cases were all related to subclinical mastitis, and C. albicans and C. neoformans positive cases were all related to clinical mastitis. Given fungal mastitis&#039;s resistance to conventional therapies and its significant risks to the dairy sector, the results of this study will help determine the frequency of the infection and, consequently, the application of targeted management protocols.</OtherAbstract>
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			<Object Type="keyword">
			<Param Name="value">mastitis</Param>
			</Object>
			<Object Type="keyword">
			<Param Name="value">Cattle</Param>
			</Object>
			<Object Type="keyword">
			<Param Name="value">Bacteria</Param>
			</Object>
			<Object Type="keyword">
			<Param Name="value">Fungus</Param>
			</Object>
			<Object Type="keyword">
			<Param Name="value">Molecular detection</Param>
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		</ObjectList>
<ArchiveCopySource DocType="pdf">https://ijvcs.sku.ac.ir/article_116666_07935ea47181e0a1c618afed85ab49a8.pdf</ArchiveCopySource>
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<Article>
<Journal>
				<PublisherName>Faculty of Veterinary Medicine, Shahrekord University</PublisherName>
				<JournalTitle>Iranian Journal of Veterinary Clinical Sciences</JournalTitle>
				<Issn>2423-3625</Issn>
				<Volume>19</Volume>
				<Issue>2</Issue>
				<PubDate PubStatus="epublish">
					<Year>2026</Year>
					<Month>02</Month>
					<Day>20</Day>
				</PubDate>
			</Journal>
<ArticleTitle>Effect of pomegranate peel extract on cadmium-induced brain toxicity in common carp (Cyprinus carpio); Histopathological evaluation</ArticleTitle>
<VernacularTitle>Effect of pomegranate peel extract on cadmium-induced brain toxicity in common carp (Cyprinus carpio); Histopathological evaluation</VernacularTitle>
			<FirstPage>37</FirstPage>
			<LastPage>46</LastPage>
			<ELocationID EIdType="pii">116671</ELocationID>
			
<ELocationID EIdType="doi">10.22034/ijvcs.2026.14894.1091</ELocationID>
			
			<Language>FA</Language>
<AuthorList>
<Author>
					<FirstName>Hossein</FirstName>
					<LastName>Jafarzadeh</LastName>
<Affiliation>Graduated of Veterinary Medicine, Faculty of Veterinary Medicine, Ferdowsi University of Mashhad, Mashhad, Iran</Affiliation>

</Author>
<Author>
					<FirstName>Soodeh</FirstName>
					<LastName>Alidadi</LastName>
<Affiliation>Department of Pathobiology, Faculty of Veterinary Medicine, Ferdowsi University of Mashhad</Affiliation>

</Author>
<Author>
					<FirstName>Davar</FirstName>
					<LastName>Shahsavani</LastName>
<Affiliation>Department of Food Hygiene and Aquaculture, Faculty of Veterinary Medicine, Ferdowsi University of Mashhad, Mashhad, Iran</Affiliation>

</Author>
</AuthorList>
				<PublicationType>Journal Article</PublicationType>
			<History>
				<PubDate PubStatus="received">
					<Year>2026</Year>
					<Month>01</Month>
					<Day>27</Day>
				</PubDate>
			</History>
		<Abstract>This research was conducted to investigate the protective effects of pomegranate peel extract on brain tissue in experimental cadmium poisoning in common carp. 150 common carp were randomly divided into 5 groups in triplicate and evaluated for four weeks. The control group did not receive cadmium, the cadmium group received 0.5 mg/L of cadmium chloride; the cadmium+1% extract group received 0.35 g of pomegranate peel extract (1% of food weight) in addition to 0.5 mg/L of cadmium chloride in water; the cadmium+2% extract group received 0.7 g of pomegranate peel extract (2% of food weight) in addition to cadmium; and the cadmium+4% extract group received 1.4 g of pomegranate peel extract (4% of food weight) in addition to cadmium equally in four meals. After the four-week treatment period, six fish from each group were randomly selected and tissue samples were taken from their brains, fixed in 10% neutral buffered formalin, and stained with hematoxylin and eosin. Histopathological changes observed in the brain tissue of the cadmium group included hyperemia, hemorrhage, degeneration and necrosis of neurons, edema and vacuolation, and gliosis. Different amounts of pomegranate peel extract, especially 2% and 4%, reduced changes, but only the cadmium+4% extract was significant compared to the cadmium group (p&lt;0.05). In general, it can be concluded that 4% pomegranate peel extract has significant protective effects on brain tissue in experimental cadmium poisoning in common carp.</Abstract>
			<OtherAbstract Language="FA">This research was conducted to investigate the protective effects of pomegranate peel extract on brain tissue in experimental cadmium poisoning in common carp. 150 common carp were randomly divided into 5 groups in triplicate and evaluated for four weeks. The control group did not receive cadmium, the cadmium group received 0.5 mg/L of cadmium chloride; the cadmium+1% extract group received 0.35 g of pomegranate peel extract (1% of food weight) in addition to 0.5 mg/L of cadmium chloride in water; the cadmium+2% extract group received 0.7 g of pomegranate peel extract (2% of food weight) in addition to cadmium; and the cadmium+4% extract group received 1.4 g of pomegranate peel extract (4% of food weight) in addition to cadmium equally in four meals. After the four-week treatment period, six fish from each group were randomly selected and tissue samples were taken from their brains, fixed in 10% neutral buffered formalin, and stained with hematoxylin and eosin. Histopathological changes observed in the brain tissue of the cadmium group included hyperemia, hemorrhage, degeneration and necrosis of neurons, edema and vacuolation, and gliosis. Different amounts of pomegranate peel extract, especially 2% and 4%, reduced changes, but only the cadmium+4% extract was significant compared to the cadmium group (p&lt;0.05). In general, it can be concluded that 4% pomegranate peel extract has significant protective effects on brain tissue in experimental cadmium poisoning in common carp.</OtherAbstract>
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			<Object Type="keyword">
			<Param Name="value">Cadmium chloride</Param>
			</Object>
			<Object Type="keyword">
			<Param Name="value">Pomegranate peel extract</Param>
			</Object>
			<Object Type="keyword">
			<Param Name="value">Histopathology</Param>
			</Object>
			<Object Type="keyword">
			<Param Name="value">Brain</Param>
			</Object>
			<Object Type="keyword">
			<Param Name="value">Common carp</Param>
			</Object>
		</ObjectList>
<ArchiveCopySource DocType="pdf">https://ijvcs.sku.ac.ir/article_116671_0df5aad16b899dbf494595a2197aacf7.pdf</ArchiveCopySource>
</Article>

<Article>
<Journal>
				<PublisherName>Faculty of Veterinary Medicine, Shahrekord University</PublisherName>
				<JournalTitle>Iranian Journal of Veterinary Clinical Sciences</JournalTitle>
				<Issn>2423-3625</Issn>
				<Volume>19</Volume>
				<Issue>2</Issue>
				<PubDate PubStatus="epublish">
					<Year>2026</Year>
					<Month>02</Month>
					<Day>20</Day>
				</PubDate>
			</Journal>
<ArticleTitle>The Protective Role of Alpha-Lipoic Acid on the Expression of Apoptosis-Related Genes in Mouse Spermatogonial Stem Cells During Freezing</ArticleTitle>
<VernacularTitle>The Protective Role of Alpha-Lipoic Acid on the Expression of Apoptosis-Related Genes in Mouse Spermatogonial Stem Cells During Freezing</VernacularTitle>
			<FirstPage>47</FirstPage>
			<LastPage>60</LastPage>
			<ELocationID EIdType="pii">116667</ELocationID>
			
<ELocationID EIdType="doi">10.22034/ijvcs.2026.15030.1100</ELocationID>
			
			<Language>FA</Language>
<AuthorList>
<Author>
					<FirstName>Kazam</FirstName>
					<LastName>Norouzi</LastName>
<Affiliation>Faculty of Veterinary Medicine, Shahrekord University</Affiliation>
<Identifier Source="ORCID">0000-0001-6428-4397</Identifier>

</Author>
<Author>
					<FirstName>Hassan</FirstName>
					<LastName>Nazari</LastName>
<Affiliation>Research Institute of Animal Embryo Technology</Affiliation>

</Author>
<Author>
					<FirstName>Ebrahim</FirstName>
					<LastName>Ahmadi</LastName>
<Affiliation>Research Institute of Animal Embryo Technology, Shahrekord university</Affiliation>

</Author>
<Author>
					<FirstName>Naser</FirstName>
					<LastName>Shams Esfandabadi</LastName>
<Affiliation>Department of Clinical Sciences, Faculty of Veterinary Medicine, Shahrekord University, Shahrekord- Iran.</Affiliation>

</Author>
<Author>
					<FirstName>Azita</FirstName>
					<LastName>Afzali</LastName>
<Affiliation>Department of Anatomical Sciences, Faculty of Medicine, Semnan University of Medical Sciences,
Semnan- Iran.
Nervous System Stem Cells Research Center, Neuroscience Research Institute, Semnan University of
Medical Sciences, Semnan- Iran.</Affiliation>

</Author>
</AuthorList>
				<PublicationType>Journal Article</PublicationType>
			<History>
				<PubDate PubStatus="received">
					<Year>2026</Year>
					<Month>05</Month>
					<Day>12</Day>
				</PubDate>
			</History>
		<Abstract>This study aimed to examine the protective role of alpha-lipoic acid (ALA) against damage caused by freeze-thawing in immature mouse spermatogonial stem cells (SSCs) by analyzing the expression of genes related to apoptosis. SSCs were extracted from the testes of 4–8-day-old C57 mice and, after verification through immunocytochemistry using the PLZF marker and an alkaline phosphatase activity test, were cultured for three weeks. The cells were then frozen in four groups: a control group without antioxidants and three groups treated with different ALA concentrations (0.2, 1, and 5 µM). Following thawing, the expression levels of BAX, BCL2, Caspase-3, and Caspase-9 were measured using Real-time PCR. Findings revealed that 1 µM ALA significantly lowered the expression of the pro-apoptotic genes BAX, Caspase-3, and Caspase-9, while significantly increasing the anti-apoptotic gene BCL2 (P&lt;0.05). The 0.2 µM dose also notably reduced BAX and Caspase-3 expression. However, the highest concentration (5 µM) showed no significant impact. The study concludes that alpha-lipoic acid, especially at 1 µM, can safeguard mouse spermatogonial stem cells from freeze-thaw damage by regulating key apoptosis-related gene expression and may serve as a beneficial additive in the cryopreservation medium for these cells.</Abstract>
			<OtherAbstract Language="FA">This study aimed to examine the protective role of alpha-lipoic acid (ALA) against damage caused by freeze-thawing in immature mouse spermatogonial stem cells (SSCs) by analyzing the expression of genes related to apoptosis. SSCs were extracted from the testes of 4–8-day-old C57 mice and, after verification through immunocytochemistry using the PLZF marker and an alkaline phosphatase activity test, were cultured for three weeks. The cells were then frozen in four groups: a control group without antioxidants and three groups treated with different ALA concentrations (0.2, 1, and 5 µM). Following thawing, the expression levels of BAX, BCL2, Caspase-3, and Caspase-9 were measured using Real-time PCR. Findings revealed that 1 µM ALA significantly lowered the expression of the pro-apoptotic genes BAX, Caspase-3, and Caspase-9, while significantly increasing the anti-apoptotic gene BCL2 (P&lt;0.05). The 0.2 µM dose also notably reduced BAX and Caspase-3 expression. However, the highest concentration (5 µM) showed no significant impact. The study concludes that alpha-lipoic acid, especially at 1 µM, can safeguard mouse spermatogonial stem cells from freeze-thaw damage by regulating key apoptosis-related gene expression and may serve as a beneficial additive in the cryopreservation medium for these cells.</OtherAbstract>
		<ObjectList>
			<Object Type="keyword">
			<Param Name="value">Spermatogonial stem cells</Param>
			</Object>
			<Object Type="keyword">
			<Param Name="value">Alpha-lipoic acid</Param>
			</Object>
			<Object Type="keyword">
			<Param Name="value">Cryopreservation</Param>
			</Object>
			<Object Type="keyword">
			<Param Name="value">Apoptosis</Param>
			</Object>
			<Object Type="keyword">
			<Param Name="value">Gene expression</Param>
			</Object>
			<Object Type="keyword">
			<Param Name="value">Mouse</Param>
			</Object>
		</ObjectList>
<ArchiveCopySource DocType="pdf">https://ijvcs.sku.ac.ir/article_116667_82ed7c6b71033c32eb01b6e549d58a4f.pdf</ArchiveCopySource>
</Article>

<Article>
<Journal>
				<PublisherName>Faculty of Veterinary Medicine, Shahrekord University</PublisherName>
				<JournalTitle>Iranian Journal of Veterinary Clinical Sciences</JournalTitle>
				<Issn>2423-3625</Issn>
				<Volume>19</Volume>
				<Issue>2</Issue>
				<PubDate PubStatus="epublish">
					<Year>2026</Year>
					<Month>02</Month>
					<Day>20</Day>
				</PubDate>
			</Journal>
<ArticleTitle>Evaluation of the Interaction between Exposure Time and Cryoprotectants Concentration on the Vitrification of Bovine Immature Oocytes with Cryotop</ArticleTitle>
<VernacularTitle>Evaluation of the Interaction between Exposure Time and Cryoprotectants Concentration on the Vitrification of Bovine Immature Oocytes with Cryotop</VernacularTitle>
			<FirstPage>61</FirstPage>
			<LastPage>69</LastPage>
			<ELocationID EIdType="pii">116670</ELocationID>
			
<ELocationID EIdType="doi">10.22034/ijvcs.2026.14938.1094</ELocationID>
			
			<Language>FA</Language>
<AuthorList>
<Author>
					<FirstName>Kaveh</FirstName>
					<LastName>Alizadeh</LastName>
<Affiliation>PhD Student in Veterinary Reproductive Technologies, Department of Clinical Sciences, Faculty of Veterinary Medicine, Shahrekord University, Shahrekord, Iran</Affiliation>

</Author>
<Author>
					<FirstName>Najmeh</FirstName>
					<LastName>Davoodian</LastName>
<Affiliation></Affiliation>

</Author>
<Author>
					<FirstName>Ali</FirstName>
					<LastName>Kadivar</LastName>
<Affiliation>Department of Clinical Sciences, Faculty of Veterinary Medicine, Shahrekord University, Shahrekord, Iran.</Affiliation>

</Author>
<Author>
					<FirstName>Ebrahim</FirstName>
					<LastName>Ahmadi</LastName>
<Affiliation>Research Institute of Animal Embryo Technology, Shahrekord University, Shahrekord, Iran.</Affiliation>

</Author>
<Author>
					<FirstName>Naser</FirstName>
					<LastName>Shams Esfandabadi</LastName>
<Affiliation>Department of Clinical Sciences, Faculty of Veterinary Medicine, Shahrekord University, Shahrekord, Iran.</Affiliation>

</Author>
</AuthorList>
				<PublicationType>Journal Article</PublicationType>
			<History>
				<PubDate PubStatus="received">
					<Year>2026</Year>
					<Month>02</Month>
					<Day>18</Day>
				</PubDate>
			</History>
		<Abstract>This study aimed to evaluate the interaction between exposure time and concentration of cryoprotective agents (CPAs) in the vitrification of bovine immature oocytes. A total of 212 cumulus-oocyte complexes (COCs) with optimal quality were subjected to five different vitrification protocols using the Cryotop method. Independent variables included various concentrations of ethylene glycol (EG) and dimethyl sulfoxide (DMSO) in equilibration (EM) and vitrification (VM) media, along with different exposure times (30 seconds to 3 minutes). Morphological assessment revealed that Protocol 1 (1 min EM with 10% EG/DMSO and 30 sec VM with 20% EG/DMSO) yielded the highest percentage of morphologically intact oocytes (83.34±4.24), though none achieved Grade C quality (live oocyte and &lt;50%dead cumulus cells). In contrast, Protocol 4 (2 minutes EM with 10% EG/DMSO and 45 seconds VM with 20% EG/DMSO) demonstrated the highest Grade C (44.18±0.07). Logistic regression analysis confirmed that 30-second exposure in VM significantly increased the likelihood of Grade B (live oocyte and &gt;50%dead cumulus cells) classification (P&lt;0.001), whereas extending EM time to 2 minutes decreased the probability of Grade C status (P&lt;0.001). These findings indicated that successful vitrification of bovine immature oocytes depends on the optimal balance between CPA concentration and exposure time, with Protocol 4 recommended as the optimal method for simultaneous preservation of morphology and viability.</Abstract>
			<OtherAbstract Language="FA">This study aimed to evaluate the interaction between exposure time and concentration of cryoprotective agents (CPAs) in the vitrification of bovine immature oocytes. A total of 212 cumulus-oocyte complexes (COCs) with optimal quality were subjected to five different vitrification protocols using the Cryotop method. Independent variables included various concentrations of ethylene glycol (EG) and dimethyl sulfoxide (DMSO) in equilibration (EM) and vitrification (VM) media, along with different exposure times (30 seconds to 3 minutes). Morphological assessment revealed that Protocol 1 (1 min EM with 10% EG/DMSO and 30 sec VM with 20% EG/DMSO) yielded the highest percentage of morphologically intact oocytes (83.34±4.24), though none achieved Grade C quality (live oocyte and &lt;50%dead cumulus cells). In contrast, Protocol 4 (2 minutes EM with 10% EG/DMSO and 45 seconds VM with 20% EG/DMSO) demonstrated the highest Grade C (44.18±0.07). Logistic regression analysis confirmed that 30-second exposure in VM significantly increased the likelihood of Grade B (live oocyte and &gt;50%dead cumulus cells) classification (P&lt;0.001), whereas extending EM time to 2 minutes decreased the probability of Grade C status (P&lt;0.001). These findings indicated that successful vitrification of bovine immature oocytes depends on the optimal balance between CPA concentration and exposure time, with Protocol 4 recommended as the optimal method for simultaneous preservation of morphology and viability.</OtherAbstract>
		<ObjectList>
			<Object Type="keyword">
			<Param Name="value">Vitrification</Param>
			</Object>
			<Object Type="keyword">
			<Param Name="value">Bovine immature oocyte</Param>
			</Object>
			<Object Type="keyword">
			<Param Name="value">Cryoprotectant agents</Param>
			</Object>
			<Object Type="keyword">
			<Param Name="value">Viability</Param>
			</Object>
		</ObjectList>
<ArchiveCopySource DocType="pdf">https://ijvcs.sku.ac.ir/article_116670_9b18fa61dad7129ff0a090458bc182b0.pdf</ArchiveCopySource>
</Article>

<Article>
<Journal>
				<PublisherName>Faculty of Veterinary Medicine, Shahrekord University</PublisherName>
				<JournalTitle>Iranian Journal of Veterinary Clinical Sciences</JournalTitle>
				<Issn>2423-3625</Issn>
				<Volume>19</Volume>
				<Issue>2</Issue>
				<PubDate PubStatus="epublish">
					<Year>2026</Year>
					<Month>02</Month>
					<Day>20</Day>
				</PubDate>
			</Journal>
<ArticleTitle>Effect of IPN virus antigen loaded in chitosan particles and in alginate matrix on IL-12, IL-17 gene expression and white blood cell composition in rainbow trout (Oncorhynchus mykiss)</ArticleTitle>
<VernacularTitle>Effect of IPN virus antigen loaded in chitosan particles and in alginate matrix on IL-12, IL-17 gene expression and white blood cell composition in rainbow trout (Oncorhynchus mykiss)</VernacularTitle>
			<FirstPage>71</FirstPage>
			<LastPage>84</LastPage>
			<ELocationID EIdType="pii">116675</ELocationID>
			
<ELocationID EIdType="doi">10.22034/ijvcs.2026.14960.1096</ELocationID>
			
			<Language>FA</Language>
<AuthorList>
<Author>
					<FirstName>Behnam</FirstName>
					<LastName>Bakhtiarimoghadam</LastName>
<Affiliation>shahre-kord university</Affiliation>

</Author>
<Author>
					<FirstName>Shafigh</FirstName>
					<LastName>Shafiei</LastName>
<Affiliation>Shahre kord university</Affiliation>

</Author>
<Author>
					<FirstName>Sadegh</FirstName>
					<LastName>Shirian</LastName>
<Affiliation>shahrekord university</Affiliation>

</Author>
<Author>
					<FirstName>Esmail</FirstName>
					<LastName>Mirzaei</LastName>
<Affiliation>Shiraz Medical Sciences</Affiliation>

</Author>
<Author>
					<FirstName>Azam</FirstName>
					<LastName>Mokhtari</LastName>
<Affiliation>shahrr kord university</Affiliation>

</Author>
<Author>
					<FirstName>Zohre</FirstName>
					<LastName>Khorshidvand</LastName>
<Affiliation>Hamedan Medical Sciences</Affiliation>

</Author>
</AuthorList>
				<PublicationType>Journal Article</PublicationType>
			<History>
				<PubDate PubStatus="received">
					<Year>2026</Year>
					<Month>02</Month>
					<Day>27</Day>
				</PubDate>
			</History>
		<Abstract>Infectious pancreatic necrosis (IPN) is one of the major challenges in the aquaculture industry, particularly in in rainbow trout farming. This study aimed to evaluate the effect of an inactivated oral vaccine containing IPNV antigen loaded into chitosan nanoparticles and alginate matrix on the gene expression of IL-12, IL-17, and white blood cell composition in rainbow trout (Oncorhynchus mykiss). A total of 540 fish with an average weight of 3 ± 0.5 g were divided into six groups: control, positive control (nanoparticles without antigen), and four groups receiving free antigen (0.06 or 0.12 cc per fish) or antigen-loaded nanoparticles (0.06 or 0.12 cc per fish). Oral vaccination was performed on days 0 and 15, and sampling was conducted on day 30. The results showed that antigen administration, particularly at the higher dose and when associated with nanoparticles, significantly increased the percentage of lymphocytes and significantly decreased the percentage of neutrophils (P &lt; 0.05). The expression of IL-12 significantly increased in antigen-receiving groups, especially at the dose of 0.12 cc and in the group receiving antigen-loaded nanoparticles at 0.12 cc (P &lt; 0.05), whereas IL-17 expression showed no significant change. It is concluded that encapsulation of IPNV antigen in chitosan-alginate nanoparticles, as a controlled-release system, can enhance Th1-type adaptive immune responses through upregulation of IL-12 and shift white blood cell composition toward more specific immunity. However, antibody titer measurement and challenge tests are necessary for definitive conclusions.</Abstract>
			<OtherAbstract Language="FA">Infectious pancreatic necrosis (IPN) is one of the major challenges in the aquaculture industry, particularly in in rainbow trout farming. This study aimed to evaluate the effect of an inactivated oral vaccine containing IPNV antigen loaded into chitosan nanoparticles and alginate matrix on the gene expression of IL-12, IL-17, and white blood cell composition in rainbow trout (Oncorhynchus mykiss). A total of 540 fish with an average weight of 3 ± 0.5 g were divided into six groups: control, positive control (nanoparticles without antigen), and four groups receiving free antigen (0.06 or 0.12 cc per fish) or antigen-loaded nanoparticles (0.06 or 0.12 cc per fish). Oral vaccination was performed on days 0 and 15, and sampling was conducted on day 30. The results showed that antigen administration, particularly at the higher dose and when associated with nanoparticles, significantly increased the percentage of lymphocytes and significantly decreased the percentage of neutrophils (P &lt; 0.05). The expression of IL-12 significantly increased in antigen-receiving groups, especially at the dose of 0.12 cc and in the group receiving antigen-loaded nanoparticles at 0.12 cc (P &lt; 0.05), whereas IL-17 expression showed no significant change. It is concluded that encapsulation of IPNV antigen in chitosan-alginate nanoparticles, as a controlled-release system, can enhance Th1-type adaptive immune responses through upregulation of IL-12 and shift white blood cell composition toward more specific immunity. However, antibody titer measurement and challenge tests are necessary for definitive conclusions.</OtherAbstract>
		<ObjectList>
			<Object Type="keyword">
			<Param Name="value">Infectious Pancreatic Necrosis virus</Param>
			</Object>
			<Object Type="keyword">
			<Param Name="value">Chitosan nanoparticles</Param>
			</Object>
			<Object Type="keyword">
			<Param Name="value">Alginate</Param>
			</Object>
			<Object Type="keyword">
			<Param Name="value">IL-12</Param>
			</Object>
			<Object Type="keyword">
			<Param Name="value">IL-17</Param>
			</Object>
			<Object Type="keyword">
			<Param Name="value">Rainbow trout</Param>
			</Object>
			<Object Type="keyword">
			<Param Name="value">IPN</Param>
			</Object>
		</ObjectList>
<ArchiveCopySource DocType="pdf">https://ijvcs.sku.ac.ir/article_116675_b4bd0050a889379bcec828d6f03ad227.pdf</ArchiveCopySource>
</Article>

<Article>
<Journal>
				<PublisherName>Faculty of Veterinary Medicine, Shahrekord University</PublisherName>
				<JournalTitle>Iranian Journal of Veterinary Clinical Sciences</JournalTitle>
				<Issn>2423-3625</Issn>
				<Volume>19</Volume>
				<Issue>2</Issue>
				<PubDate PubStatus="epublish">
					<Year>2026</Year>
					<Month>02</Month>
					<Day>20</Day>
				</PubDate>
			</Journal>
<ArticleTitle>Perineal Bladder Prolapse in Dogs: A Review of Diagnostic and Treatment Methods</ArticleTitle>
<VernacularTitle>Perineal Bladder Prolapse in Dogs: A Review of Diagnostic and Treatment Methods</VernacularTitle>
			<FirstPage>85</FirstPage>
			<LastPage>93</LastPage>
			<ELocationID EIdType="pii">116672</ELocationID>
			
<ELocationID EIdType="doi">10.22034/ijvcs.2026.14886.1088</ELocationID>
			
			<Language>FA</Language>
<AuthorList>
<Author>
					<FirstName>Moosa</FirstName>
					<LastName>Javdani</LastName>
<Affiliation></Affiliation>
<Identifier Source="ORCID">0000-0003-0975-2295</Identifier>

</Author>
<Author>
					<FirstName>Amin</FirstName>
					<LastName>Mohamadi</LastName>
<Affiliation>Mehregan Veterinary Clinic, Shahrekord- Iran.</Affiliation>

</Author>
<Author>
					<FirstName>Mohammad</FirstName>
					<LastName>Salimi Beni</LastName>
<Affiliation>Faculty of Veterinary Medicine, Shahrekord University, Shahrekord- Iran.</Affiliation>

</Author>
</AuthorList>
				<PublicationType>Journal Article</PublicationType>
			<History>
				<PubDate PubStatus="received">
					<Year>2026</Year>
					<Month>01</Month>
					<Day>08</Day>
				</PubDate>
			</History>
		<Abstract>Perineal bladder prolapse is a life-threatening complication in dogs with perineal hernia, primarily affecting small-breed, and intact male dogs. Delayed diagnosis and treatment can lead to urinary obstruction and systemic complications. This report describes a 9-year-old, 6.20 kg intact male Terrier dog with bilateral painful perineal swelling and urinary retention. Diagnostic evaluations included plain and contrast radiography (cystography), hematological and biochemical analyses. Elevated creatinine (3.5 mg/dL), blood urea nitrogen (47 mg/dL), and leukocytosis (21,000 cells/μL) were observed, along with tachycardia, tachypnea, and hyperthermia. Radiography confirmed a large perineal hernia with bladder retroflexion. The patient underwent emergency surgical intervention, including bladder reduction and concurrent cystopexy to prevent recurrence. Key diagnostic considerations for this condition include recognition of clinical signs (e.g., perineal mass), thorough physical examination, and diagnostic imaging. Immediate bladder decompression under sedation or anesthesia achieved via urinary catheterization and fluid therapy to correct electrolyte imbalances is crucial. Anesthetic challenges in these patients include hemodynamic instability due to hyperkalemia, hypotension induced by anesthetic agents, hypothermia, pain management, and aspiration pneumonia risk. Surgical interventions involve cystopexy, hernia repair, and neutering to minimize recurrence risk. Postoperative considerations requires monitoring urinary function, appropriate antibiotic therapy, pain management (opioid administration), fluid therapy, and restricted activity during recovery.</Abstract>
			<OtherAbstract Language="FA">Perineal bladder prolapse is a life-threatening complication in dogs with perineal hernia, primarily affecting small-breed, and intact male dogs. Delayed diagnosis and treatment can lead to urinary obstruction and systemic complications. This report describes a 9-year-old, 6.20 kg intact male Terrier dog with bilateral painful perineal swelling and urinary retention. Diagnostic evaluations included plain and contrast radiography (cystography), hematological and biochemical analyses. Elevated creatinine (3.5 mg/dL), blood urea nitrogen (47 mg/dL), and leukocytosis (21,000 cells/μL) were observed, along with tachycardia, tachypnea, and hyperthermia. Radiography confirmed a large perineal hernia with bladder retroflexion. The patient underwent emergency surgical intervention, including bladder reduction and concurrent cystopexy to prevent recurrence. Key diagnostic considerations for this condition include recognition of clinical signs (e.g., perineal mass), thorough physical examination, and diagnostic imaging. Immediate bladder decompression under sedation or anesthesia achieved via urinary catheterization and fluid therapy to correct electrolyte imbalances is crucial. Anesthetic challenges in these patients include hemodynamic instability due to hyperkalemia, hypotension induced by anesthetic agents, hypothermia, pain management, and aspiration pneumonia risk. Surgical interventions involve cystopexy, hernia repair, and neutering to minimize recurrence risk. Postoperative considerations requires monitoring urinary function, appropriate antibiotic therapy, pain management (opioid administration), fluid therapy, and restricted activity during recovery.</OtherAbstract>
		<ObjectList>
			<Object Type="keyword">
			<Param Name="value">perineal hernia</Param>
			</Object>
			<Object Type="keyword">
			<Param Name="value">bladder prolapse</Param>
			</Object>
			<Object Type="keyword">
			<Param Name="value">cystopexy</Param>
			</Object>
			<Object Type="keyword">
			<Param Name="value">Dog</Param>
			</Object>
		</ObjectList>
<ArchiveCopySource DocType="pdf">https://ijvcs.sku.ac.ir/article_116672_d18c2d9db8e18dc470a465a45f8f7047.pdf</ArchiveCopySource>
</Article>
</ArticleSet>
