Diabetes sepsis on Wistar rat strain (Rattus norvegicus) induced by streptozotocin and bacteria Staphylococcus aureus

Background and Aim: Sepsis is characterized by loss of control of the inflammatory response, which can be triggered by various microorganisms and toxic secretions. The mortality rate increases due to impaired endothelial function caused dysfunctional organ systems. Diabetes is closely related to sep...

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Main Authors: Dahliatul Qosimah, Dhita Evi Aryani, Ma. Asuncion Guiang Beltran, Aulanni'am Aulanni'am
Format: Article
Language:English
Published: Veterinary World 2019-06-01
Series:Veterinary World
Subjects:
Online Access:http://www.veterinaryworld.org/Vol.12/June-2019/19.pdf
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spelling doaj-394d093725034125bdf836ebee51663f2021-08-02T16:49:06ZengVeterinary WorldVeterinary World0972-89882231-09162019-06-0112684985410.14202/vetworld.2019.849-854Diabetes sepsis on Wistar rat strain (Rattus norvegicus) induced by streptozotocin and bacteria Staphylococcus aureusDahliatul Qosimah0Dhita Evi Aryani1Ma. Asuncion Guiang Beltran2Aulanni'am Aulanni'am3Laboratory of Microbiology and Immunology, Faculty of Veterinary Medicine, Brawijaya University, Indonesia.Laboratory of Pharmacology, Faculty of Veterinary Medicine, Brawijaya University, Indonesia.Department of Microbiology and Public Health , College of Veterinary Medicine, Tarlac Agricultural University, Camiling, Tarlac, Philippines.Laboratory of Biochemical, Faculty of Veterinary Medicine, Brawijaya University, Indonesia.Background and Aim: Sepsis is characterized by loss of control of the inflammatory response, which can be triggered by various microorganisms and toxic secretions. The mortality rate increases due to impaired endothelial function caused dysfunctional organ systems. Diabetes is closely related to sepsis. The study aimed to determine the method of using animal models of sepsis diabetes through a combination of streptozotocin (STZ) and Staphylococcus aureus infection based on biological marker parameters. Materials and Methods: A total of 30 male Wistar rats of 2.5-3 months old weighing approximately 150-250 g body weight (BW) divided into six treatment groups with five replications per group were used in the study. Treatment A was negative control (healthy rats) and Treatment B was the positive control (with diabetes) where rats were given STZ dose at 45 mg/kg BW on day 8 intraperitoneally (IP). The blood glucose was measured on day 10, Treatment C was a positive control (bacteria), rats inoculated with S. aureus with a concentration of 108 CFU/mL on day 8 given IP and observed sepsis conditions on day 10th. Treatment group (D, E, and F): Rats given STZ dose at 45 mg/kg BW on day 8th by IP and measured blood glucose on day 10th, then inoculated with S. aureus with different concentrations of 105 CFU/mL, 106 CFU/mL, and 107 CFU/mL on the 10th day, respectively, and were later observed the condition of sepsis on day 12th. Data on diabetes bacteremia were quantitative used blood glucose levels, the bacterial count, and C-reactive protein (CRP) and were analyzed using the one-way analysis of variance test with a confidence level of 95%. Physical examination (temperature and respiration) is qualitative. Results: Physical examination showed that all treatments had a normal temperature, an increased pulse in Groups D, E, and F and a decrease in respiratory rate in the treatment of E and F, the bacteria found in the vital organs in all groups, and CRP levels were not significantly different at all. Conclusion: Animal model of diabetes sepsis can be observed through a combination of pancreas damage, and respiration, the bacteria in the vital organs.http://www.veterinaryworld.org/Vol.12/June-2019/19.pdfanimal modeldiabetesinflammationsepsis
collection DOAJ
language English
format Article
sources DOAJ
author Dahliatul Qosimah
Dhita Evi Aryani
Ma. Asuncion Guiang Beltran
Aulanni'am Aulanni'am
spellingShingle Dahliatul Qosimah
Dhita Evi Aryani
Ma. Asuncion Guiang Beltran
Aulanni'am Aulanni'am
Diabetes sepsis on Wistar rat strain (Rattus norvegicus) induced by streptozotocin and bacteria Staphylococcus aureus
Veterinary World
animal model
diabetes
inflammation
sepsis
author_facet Dahliatul Qosimah
Dhita Evi Aryani
Ma. Asuncion Guiang Beltran
Aulanni'am Aulanni'am
author_sort Dahliatul Qosimah
title Diabetes sepsis on Wistar rat strain (Rattus norvegicus) induced by streptozotocin and bacteria Staphylococcus aureus
title_short Diabetes sepsis on Wistar rat strain (Rattus norvegicus) induced by streptozotocin and bacteria Staphylococcus aureus
title_full Diabetes sepsis on Wistar rat strain (Rattus norvegicus) induced by streptozotocin and bacteria Staphylococcus aureus
title_fullStr Diabetes sepsis on Wistar rat strain (Rattus norvegicus) induced by streptozotocin and bacteria Staphylococcus aureus
title_full_unstemmed Diabetes sepsis on Wistar rat strain (Rattus norvegicus) induced by streptozotocin and bacteria Staphylococcus aureus
title_sort diabetes sepsis on wistar rat strain (rattus norvegicus) induced by streptozotocin and bacteria staphylococcus aureus
publisher Veterinary World
series Veterinary World
issn 0972-8988
2231-0916
publishDate 2019-06-01
description Background and Aim: Sepsis is characterized by loss of control of the inflammatory response, which can be triggered by various microorganisms and toxic secretions. The mortality rate increases due to impaired endothelial function caused dysfunctional organ systems. Diabetes is closely related to sepsis. The study aimed to determine the method of using animal models of sepsis diabetes through a combination of streptozotocin (STZ) and Staphylococcus aureus infection based on biological marker parameters. Materials and Methods: A total of 30 male Wistar rats of 2.5-3 months old weighing approximately 150-250 g body weight (BW) divided into six treatment groups with five replications per group were used in the study. Treatment A was negative control (healthy rats) and Treatment B was the positive control (with diabetes) where rats were given STZ dose at 45 mg/kg BW on day 8 intraperitoneally (IP). The blood glucose was measured on day 10, Treatment C was a positive control (bacteria), rats inoculated with S. aureus with a concentration of 108 CFU/mL on day 8 given IP and observed sepsis conditions on day 10th. Treatment group (D, E, and F): Rats given STZ dose at 45 mg/kg BW on day 8th by IP and measured blood glucose on day 10th, then inoculated with S. aureus with different concentrations of 105 CFU/mL, 106 CFU/mL, and 107 CFU/mL on the 10th day, respectively, and were later observed the condition of sepsis on day 12th. Data on diabetes bacteremia were quantitative used blood glucose levels, the bacterial count, and C-reactive protein (CRP) and were analyzed using the one-way analysis of variance test with a confidence level of 95%. Physical examination (temperature and respiration) is qualitative. Results: Physical examination showed that all treatments had a normal temperature, an increased pulse in Groups D, E, and F and a decrease in respiratory rate in the treatment of E and F, the bacteria found in the vital organs in all groups, and CRP levels were not significantly different at all. Conclusion: Animal model of diabetes sepsis can be observed through a combination of pancreas damage, and respiration, the bacteria in the vital organs.
topic animal model
diabetes
inflammation
sepsis
url http://www.veterinaryworld.org/Vol.12/June-2019/19.pdf
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