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Introduction:Type 2 diabetes (T2D) is a widely distributed disease that affects largepopulation worldwide. This study aimed to verify the role ofGinkgo biloba(GB) extractand magnetized water (MW) on the survival rate and functional capabilities of pancreaticβ-cells in type 2 diabetic rats.Materials and methods:T2D was induced by feeding the rats on a high-fat diet (20% fat,45% carbohydrate, 22% protein) for eight weeks followed by intra-peritoneal injection of asingle low dose of streptozotocin (25mg/Kg). Forty rats were randomly assigned to fourgroups (n=10 rats) as follows: non treated control and three diabetic groups. One diabeticgroup served as a positive control (diabetic), while the other two groups were orallyadministered with water extract of GB leaves (0.11 g/kg/day) and MW (600 gauss) forfour weeks, respectively.Results:Theβ-cell mass and insulin expression in these cells increased markedly after bothtreatments, particularly in GB treated group. In addition, the immune-expression of the twoantioxidant enzymes; glutathione and superoxide dismutase 2 (SOD2) in the pancreatic tissuedemonstrated a down-regulation in GB and MW treated groups as compared with thediabetic group.Conclusion:A four-week treatment of GB and MW protected pancreaticβ-cell cells andimproved their insulin expression and antioxidant status in type 2 diabetic rats.

Introduction:Type 2 diabetes (T2D) is a widely distributed disease that affects largepopulation worldwide. This study aimed to verify the role ofGinkgo biloba(GB) extractand magnetized water (MW) on the survival rate and functional capabilities of pancreaticβ-cells in type 2 diabetic rats.Materials and methods:T2D was induced by feeding the rats on a high-fat diet (20% fat,45% carbohydrate, 22% protein) for eight weeks followed by intra-peritoneal injection of asingle low dose of streptozotocin (25mg/Kg). Forty rats were randomly assigned to fourgroups (n=10 rats) as follows: non treated control and three diabetic groups. One diabeticgroup served as a positive control (diabetic), while the other two groups were orallyadministered with water extract of GB leaves (0.11 g/kg/day) and MW (600 gauss) forfour weeks, respectively.Results:Theβ-cell mass and insulin expression in these cells increased markedly after bothtreatments, particularly in GB treated group. In addition, the immune-expression of the twoantioxidant enzymes; glutathione and superoxide dismutase 2 (SOD2) in the pancreatic tissuedemonstrated a down-regulation in GB and MW treated groups as compared with thediabetic group.Conclusion:A four-week treatment of GB and MW protected pancreaticβ-cell cells andimproved their insulin expression and antioxidant status in type 2 diabetic rats.

Introduction:Type 2 diabetes (T2D) is a widely distributed disease that affects largepopulation worldwide. This study aimed to verify the role ofGinkgo biloba(GB) extractand magnetized water (MW) on the survival rate and functional capabilities of pancreaticβ-cells in type 2 diabetic rats.Materials and methods:T2D was induced by feeding the rats on a high-fat diet (20% fat,45% carbohydrate, 22% protein) for eight weeks followed by intra-peritoneal injection of asingle low dose of streptozotocin (25mg/Kg). Forty rats were randomly assigned to fourgroups (n=10 rats) as follows: non treated control and three diabetic groups. One diabeticgroup served as a positive control (diabetic), while the other two groups were orallyadministered with water extract of GB leaves (0.11 g/kg/day) and MW (600 gauss) forfour weeks, respectively.Results:Theβ-cell mass and insulin expression in these cells increased markedly after bothtreatments, particularly in GB treated group. In addition, the immune-expression of the twoantioxidant enzymes; glutathione and superoxide dismutase 2 (SOD2) in the pancreatic tissuedemonstrated a down-regulation in GB and MW treated groups as compared with thediabetic group.Conclusion:A four-week treatment of GB and MW protected pancreaticβ-cell cells andimproved their insulin expression and antioxidant status in type 2 diabetic rats.

Introduction:Type 2 diabetes (T2D) is a widely distributed disease that affects largepopulation worldwide. This study aimed to verify the role ofGinkgo biloba(GB) extractand magnetized water (MW) on the survival rate and functional capabilities of pancreaticβ-cells in type 2 diabetic rats.Materials and methods:T2D was induced by feeding the rats on a high-fat diet (20% fat,45% carbohydrate, 22% protein) for eight weeks followed by intra-peritoneal injection of asingle low dose of streptozotocin (25mg/Kg). Forty rats were randomly assigned to fourgroups (n=10 rats) as follows: non treated control and three diabetic groups. One diabeticgroup served as a positive control (diabetic), while the other two groups were orallyadministered with water extract of GB leaves (0.11 g/kg/day) and MW (600 gauss) forfour weeks, respectively.Results:Theβ-cell mass and insulin expression in these cells increased markedly after bothtreatments, particularly in GB treated group. In addition, the immune-expression of the twoantioxidant enzymes; glutathione and superoxide dismutase 2 (SOD2) in the pancreatic tissuedemonstrated a down-regulation in GB and MW treated groups as compared with thediabetic group.Conclusion:A four-week treatment of GB and MW protected pancreaticβ-cell cells andimproved their insulin expression and antioxidant status in type 2 diabetic rats.

Introduction:Type 2 diabetes (T2D) is a widely distributed disease that affects largepopulation worldwide. This study aimed to verify the role ofGinkgo biloba(GB) extractand magnetized water (MW) on the survival rate and functional capabilities of pancreaticβ-cells in type 2 diabetic rats.Materials and methods:T2D was induced by feeding the rats on a high-fat diet (20% fat,45% carbohydrate, 22% protein) for eight weeks followed by intra-peritoneal injection of asingle low dose of streptozotocin (25mg/Kg). Forty rats were randomly assigned to fourgroups (n=10 rats) as follows: non treated control and three diabetic groups. One diabeticgroup served as a positive control (diabetic), while the other two groups were orallyadministered with water extract of GB leaves (0.11 g/kg/day) and MW (600 gauss) forfour weeks, respectively.Results:Theβ-cell mass and insulin expression in these cells increased markedly after bothtreatments, particularly in GB treated group. In addition, the immune-expression of the twoantioxidant enzymes; glutathione and superoxide dismutase 2 (SOD2) in the pancreatic tissuedemonstrated a down-regulation in GB and MW treated groups as compared with thediabetic group.Conclusion:A four-week treatment of GB and MW protected pancreaticβ-cell cells andimproved their insulin expression and antioxidant status in type 2 diabetic rats.

Introduction:Type 2 diabetes (T2D) is a widely distributed disease that affects largepopulation worldwide. This study aimed to verify the role ofGinkgo biloba(GB) extractand magnetized water (MW) on the survival rate and functional capabilities of pancreaticβ-cells in type 2 diabetic rats.Materials and methods:T2D was induced by feeding the rats on a high-fat diet (20% fat,45% carbohydrate, 22% protein) for eight weeks followed by intra-peritoneal injection of asingle low dose of streptozotocin (25mg/Kg). Forty rats were randomly assigned to fourgroups (n=10 rats) as follows: non treated control and three diabetic groups. One diabeticgroup served as a positive control (diabetic), while the other two groups were orallyadministered with water extract of GB leaves (0.11 g/kg/day) and MW (600 gauss) forfour weeks, respectively.Results:Theβ-cell mass and insulin expression in these cells increased markedly after bothtreatments, particularly in GB treated group. In addition, the immune-expression of the twoantioxidant enzymes; glutathione and superoxide dismutase 2 (SOD2) in the pancreatic tissuedemonstrated a down-regulation in GB and MW treated groups as compared with thediabetic group.Conclusion:A four-week treatment of GB and MW protected pancreaticβ-cell cells andimproved their insulin expression and antioxidant status in type 2 diabetic rats.

Introduction:Type 2 diabetes (T2D) is a widely distributed disease that affects largepopulation worldwide. This study aimed to verify the role ofGinkgo biloba(GB) extractand magnetized water (MW) on the survival rate and functional capabilities of pancreaticβ-cells in type 2 diabetic rats.Materials and methods:T2D was induced by feeding the rats on a high-fat diet (20% fat,45% carbohydrate, 22% protein) for eight weeks followed by intra-peritoneal injection of asingle low dose of streptozotocin (25mg/Kg). Forty rats were randomly assigned to fourgroups (n=10 rats) as follows: non treated control and three diabetic groups. One diabeticgroup served as a positive control (diabetic), while the other two groups were orallyadministered with water extract of GB leaves (0.11 g/kg/day) and MW (600 gauss) forfour weeks, respectively.Results:Theβ-cell mass and insulin expression in these cells increased markedly after bothtreatments, particularly in GB treated group. In addition, the immune-expression of the twoantioxidant enzymes; glutathione and superoxide dismutase 2 (SOD2) in the pancreatic tissuedemonstrated a down-regulation in GB and MW treated groups as compared with thediabetic group.Conclusion:A four-week treatment of GB and MW protected pancreaticβ-cell cells andimproved their insulin expression and antioxidant status in type 2 diabetic rats.

Introduction:Type 2 diabetes (T2D) is a widely distributed disease that affects largepopulation worldwide. This study aimed to verify the role ofGinkgo biloba(GB) extractand magnetized water (MW) on the survival rate and functional capabilities of pancreaticβ-cells in type 2 diabetic rats.Materials and methods:T2D was induced by feeding the rats on a high-fat diet (20% fat,45% carbohydrate, 22% protein) for eight weeks followed by intra-peritoneal injection of asingle low dose of streptozotocin (25mg/Kg). Forty rats were randomly assigned to fourgroups (n=10 rats) as follows: non treated control and three diabetic groups. One diabeticgroup served as a positive control (diabetic), while the other two groups were orallyadministered with water extract of GB leaves (0.11 g/kg/day) and MW (600 gauss) forfour weeks, respectively.Results:Theβ-cell mass and insulin expression in these cells increased markedly after bothtreatments, particularly in GB treated group. In addition, the immune-expression of the twoantioxidant enzymes; glutathione and superoxide dismutase 2 (SOD2) in the pancreatic tissuedemonstrated a down-regulation in GB and MW treated groups as compared with thediabetic group.Conclusion:A four-week treatment of GB and MW protected pancreaticβ-cell cells andimproved their insulin expression and antioxidant status in type 2 diabetic rats.

The present study aimed to investigate the clinical blood gas indices and histopathological consequences after intrathecal injection oftolfenamic acid and lidocaine Hcl and moreover, to elucidate the spinal safety of tolfenamic acid as a cyclooxygenase inhibitor indonkeys. Ten clinically healthy donkeys were divided into two groups, 5 animals each. The first group received lidocaine Hcl 2%and the second one received tolfenamic acid 4% intrathecally. The physical parameters and ataxia, analgesia, and motor blockadescores were recorded. Blood gases and acid base balance indices and histopathological examination were done. Blood pH level wassignificantlydecreased (P 0.05) and the blood pCO2level was significantly increased (P 0.05) 15 min after intrathecal injectionof tolfenamic acid. Additionally, there was a significant difference in the motor block scores between the two groups at 2 and 4 hpost-injection. Histopathological findings of the spinal cord of tolfenamic acid–injected group revealed neurodegeneration andnecrosis which were manifested clinically by paraplegia. In conclusion, the present study uncovered the analgesic and motor effectsof commercially prepared tolfenamic acid following intrathecalinjection in donkeys. Nevertheless, it is unsafe because of itsneurotoxic effect on the spinal cord which was manifested clinically by paraplegia of donkeys. On the other hand, intrathecaladministration of lidocaine Hcl was safe and causes nonserious cardiopulmonary changes.