Zarzio Ameliorates Non-alcoholic Fatty Liver Induced By a High Fat Diet in a Rat Experimental Model: A Histological and Immunohistochemical Study/Zarzio Mejora el Higado Graso no Alcoholico Inducido por una Dieta Rica en Grasas en un Modelo Experimental en Ratas: Un Estudio Histologico e Inmunohistoquimico

The therapeutic effect of a granulocyte-colony stimulating factor (G-CSF) biosimilar drug, zarzio, on non-alcoholic fatty liver disease (NAFLD) in a rat model was investigated in this study. Thirty-two rats were randomly divided into four groups. Groups I and II were fed a standard laboratory diet,...

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Veröffentlicht in:International journal of morphology 2023-11, Vol.41 (6), p.1887
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description The therapeutic effect of a granulocyte-colony stimulating factor (G-CSF) biosimilar drug, zarzio, on non-alcoholic fatty liver disease (NAFLD) in a rat model was investigated in this study. Thirty-two rats were randomly divided into four groups. Groups I and II were fed a standard laboratory diet, whereas groups III and IV were fed a high fat diet (HFD) for 14 weeks. After 12 weeks of feeding, groups I and III were administered normal saline, and groups II and IV were intraperitoneally administered zarzio (200 mg/kg/day) for two consecutive weeks. Hematoxylin-eosin (H&E) staining was used to assess hepatic and pancreatic morphology in all groups, oil red O (ORO) staining for lipid accumulation, Masson's staining for fibrosis, and immunohistochemistry assay for hepatic protein expression of insulin receptor substrate 1 (IRS1), nuclear factor erythroid 2-related factor 2 (Nrf2), tumour necrosis factor alpha (TNF-[alpha]) and pancreatic caspase-3. The NAFLD rats (group III) developed hepatic steatosis with increased lipid accumulation, perisinusoidal fibrosis, upregulated IRS1, TNF-[alpha] (all P
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Thirty-two rats were randomly divided into four groups. Groups I and II were fed a standard laboratory diet, whereas groups III and IV were fed a high fat diet (HFD) for 14 weeks. After 12 weeks of feeding, groups I and III were administered normal saline, and groups II and IV were intraperitoneally administered zarzio (200 mg/kg/day) for two consecutive weeks. Hematoxylin-eosin (H&amp;E) staining was used to assess hepatic and pancreatic morphology in all groups, oil red O (ORO) staining for lipid accumulation, Masson's staining for fibrosis, and immunohistochemistry assay for hepatic protein expression of insulin receptor substrate 1 (IRS1), nuclear factor erythroid 2-related factor 2 (Nrf2), tumour necrosis factor alpha (TNF-[alpha]) and pancreatic caspase-3. The NAFLD rats (group III) developed hepatic steatosis with increased lipid accumulation, perisinusoidal fibrosis, upregulated IRS1, TNF-[alpha] (all P&lt;0.05) without a significant increase in Nrf2 protein expression compared with normal control. In comparison, model rats treated with zarzio (group IV) showed significant rejuvenation of the hepatic architecture, reduction of fat accumulation, and fibrosis. This was accompanied by the upregulation of Nrf2, downregulation of IRS1 and TNF-[alpha] protein expression (all P&lt;0.05). No correlation was detected between NAFLD and non-alcoholic fatty pancreas disease (NAFPD). However, the pancreatic [beta]-cells in group III showed increased caspase-3 expression, which was decreased (P&lt;0.05) in group I V. In conclusion, zarzio ameliorates NAFLD by improving the antioxidant capacity of liver cells, reducing hepatic IRS1, TNF-[alpha] protein expression and pancreatic [beta]-cells apoptosis, suggesting that zarzio could be used as a potential therapy for NAFLD. KEY WORDS: Non-alcoholic fatty liver disease; Zarzio; Granulocyte colony stimulating factor; Nuclear factor erythroid 2-related factor 2; Tumour necrosis factor alpha; Insulin receptor substrates.</description><identifier>ISSN: 0717-9367</identifier><language>spa</language><publisher>Universidad de La Frontera, Facultad de Medicina</publisher><subject>Antioxidants ; Diet ; Fatty liver ; Health aspects ; Immunohistochemistry ; Pancreatic beta cells</subject><ispartof>International journal of morphology, 2023-11, Vol.41 (6), p.1887</ispartof><rights>COPYRIGHT 2023 Universidad de La Frontera, Facultad de Medicina</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784</link.rule.ids></links><search><creatorcontrib>Baokbah, Tourki A.S</creatorcontrib><title>Zarzio Ameliorates Non-alcoholic Fatty Liver Induced By a High Fat Diet in a Rat Experimental Model: A Histological and Immunohistochemical Study/Zarzio Mejora el Higado Graso no Alcoholico Inducido por una Dieta Rica en Grasas en un Modelo Experimental en Ratas: Un Estudio Histologico e Inmunohistoquimico</title><title>International journal of morphology</title><description>The therapeutic effect of a granulocyte-colony stimulating factor (G-CSF) biosimilar drug, zarzio, on non-alcoholic fatty liver disease (NAFLD) in a rat model was investigated in this study. Thirty-two rats were randomly divided into four groups. Groups I and II were fed a standard laboratory diet, whereas groups III and IV were fed a high fat diet (HFD) for 14 weeks. After 12 weeks of feeding, groups I and III were administered normal saline, and groups II and IV were intraperitoneally administered zarzio (200 mg/kg/day) for two consecutive weeks. Hematoxylin-eosin (H&amp;E) staining was used to assess hepatic and pancreatic morphology in all groups, oil red O (ORO) staining for lipid accumulation, Masson's staining for fibrosis, and immunohistochemistry assay for hepatic protein expression of insulin receptor substrate 1 (IRS1), nuclear factor erythroid 2-related factor 2 (Nrf2), tumour necrosis factor alpha (TNF-[alpha]) and pancreatic caspase-3. The NAFLD rats (group III) developed hepatic steatosis with increased lipid accumulation, perisinusoidal fibrosis, upregulated IRS1, TNF-[alpha] (all P&lt;0.05) without a significant increase in Nrf2 protein expression compared with normal control. In comparison, model rats treated with zarzio (group IV) showed significant rejuvenation of the hepatic architecture, reduction of fat accumulation, and fibrosis. This was accompanied by the upregulation of Nrf2, downregulation of IRS1 and TNF-[alpha] protein expression (all P&lt;0.05). No correlation was detected between NAFLD and non-alcoholic fatty pancreas disease (NAFPD). However, the pancreatic [beta]-cells in group III showed increased caspase-3 expression, which was decreased (P&lt;0.05) in group I V. In conclusion, zarzio ameliorates NAFLD by improving the antioxidant capacity of liver cells, reducing hepatic IRS1, TNF-[alpha] protein expression and pancreatic [beta]-cells apoptosis, suggesting that zarzio could be used as a potential therapy for NAFLD. 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Thirty-two rats were randomly divided into four groups. Groups I and II were fed a standard laboratory diet, whereas groups III and IV were fed a high fat diet (HFD) for 14 weeks. After 12 weeks of feeding, groups I and III were administered normal saline, and groups II and IV were intraperitoneally administered zarzio (200 mg/kg/day) for two consecutive weeks. Hematoxylin-eosin (H&amp;E) staining was used to assess hepatic and pancreatic morphology in all groups, oil red O (ORO) staining for lipid accumulation, Masson's staining for fibrosis, and immunohistochemistry assay for hepatic protein expression of insulin receptor substrate 1 (IRS1), nuclear factor erythroid 2-related factor 2 (Nrf2), tumour necrosis factor alpha (TNF-[alpha]) and pancreatic caspase-3. The NAFLD rats (group III) developed hepatic steatosis with increased lipid accumulation, perisinusoidal fibrosis, upregulated IRS1, TNF-[alpha] (all P&lt;0.05) without a significant increase in Nrf2 protein expression compared with normal control. In comparison, model rats treated with zarzio (group IV) showed significant rejuvenation of the hepatic architecture, reduction of fat accumulation, and fibrosis. This was accompanied by the upregulation of Nrf2, downregulation of IRS1 and TNF-[alpha] protein expression (all P&lt;0.05). No correlation was detected between NAFLD and non-alcoholic fatty pancreas disease (NAFPD). However, the pancreatic [beta]-cells in group III showed increased caspase-3 expression, which was decreased (P&lt;0.05) in group I V. In conclusion, zarzio ameliorates NAFLD by improving the antioxidant capacity of liver cells, reducing hepatic IRS1, TNF-[alpha] protein expression and pancreatic [beta]-cells apoptosis, suggesting that zarzio could be used as a potential therapy for NAFLD. KEY WORDS: Non-alcoholic fatty liver disease; Zarzio; Granulocyte colony stimulating factor; Nuclear factor erythroid 2-related factor 2; Tumour necrosis factor alpha; Insulin receptor substrates.</abstract><pub>Universidad de La Frontera, Facultad de Medicina</pub></addata></record>
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subjects Antioxidants
Diet
Fatty liver
Health aspects
Immunohistochemistry
Pancreatic beta cells
title Zarzio Ameliorates Non-alcoholic Fatty Liver Induced By a High Fat Diet in a Rat Experimental Model: A Histological and Immunohistochemical Study/Zarzio Mejora el Higado Graso no Alcoholico Inducido por una Dieta Rica en Grasas en un Modelo Experimental en Ratas: Un Estudio Histologico e Inmunohistoquimico
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