The effect of ketamine on the immature granulocyte and C-reactive protein concentration in rat models of sepsis

Background: Sepsis directly affects the immune system, leads tissue damage, and forms system organ dysfunction. The immunological biomarker of sepsis has a possibility to become an immunotherapy target of sepsis. This study was conducted to determine the effect of ketamine on the number of immature...

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Main Authors: Aswoco Andyk Asmoro, Isngadi Isngadi, Ristiawan Muji Laksono, Ibnu Firdiansayah, Agus Supriyanto
Format: Article
Language:English
Published: Wolters Kluwer Medknow Publications 2019-01-01
Series:Bali Journal of Anesthesiology
Subjects:
Online Access:http://www.bjoaonline.com/article.asp?issn=2549-2276;year=2019;volume=3;issue=3;spage=174;epage=177;aulast=Asmoro
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author Aswoco Andyk Asmoro
Isngadi Isngadi
Ristiawan Muji Laksono
Ibnu Firdiansayah
Agus Supriyanto
author_facet Aswoco Andyk Asmoro
Isngadi Isngadi
Ristiawan Muji Laksono
Ibnu Firdiansayah
Agus Supriyanto
author_sort Aswoco Andyk Asmoro
collection DOAJ
description Background: Sepsis directly affects the immune system, leads tissue damage, and forms system organ dysfunction. The immunological biomarker of sepsis has a possibility to become an immunotherapy target of sepsis. This study was conducted to determine the effect of ketamine on the number of immature granulocyte and C-reactive protein (CRP) concentration in rat models of sepsis. Materials and Methods: This study used thirty white mice (Rattus norvegicus) divided into six treatment groups. The negative control group received nothing, and the positive control (sepsis) group was fecal-induced peritonitis (FIP) by fecal administration (i. p). The treatment groups (A, B, C, and D) treat with ketamine 5 mg/kg body weight (i. p.) right after FIP, 3 h after FIP, 5 h after FIP, and intermittent every 2 h. The peripheral mononuclear blood cell was isolated 6 h after FIP. The immature granulocytes counted using a hematology analyzer while CRP concentration analyzed using kit enzyme-linked immunosorbent assay. Data were analyzed statistically using the one-way ANOVA test using SPSS version 20 software (P < 0.05). Results: Sepsis induction with FIP increases the number of immature granulocytes in animal models from 0.48% to 9.12% (P < 0.05) but did not affect CRP concentration (P > 0.05). The ketamine administration significantly decreases the immature granulocytes in Groups C (1.04%) and D (1.58%). Ketamine administration did not have a significant effect on CRP concentration. Conclusion: The ketamine administration at 5 h after FIP and intermittently every 2 h can be an alternative to be sepsis immunotherapy with immature granulocyte as the potential target.
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spelling doaj.art-a8e271a4770d4d33b70b9e7bde42b2212022-12-21T18:21:02ZengWolters Kluwer Medknow PublicationsBali Journal of Anesthesiology2549-22762019-01-013317417710.4103/BJOA.BJOA_5_19The effect of ketamine on the immature granulocyte and C-reactive protein concentration in rat models of sepsisAswoco Andyk AsmoroIsngadi IsngadiRistiawan Muji LaksonoIbnu FirdiansayahAgus SupriyantoBackground: Sepsis directly affects the immune system, leads tissue damage, and forms system organ dysfunction. The immunological biomarker of sepsis has a possibility to become an immunotherapy target of sepsis. This study was conducted to determine the effect of ketamine on the number of immature granulocyte and C-reactive protein (CRP) concentration in rat models of sepsis. Materials and Methods: This study used thirty white mice (Rattus norvegicus) divided into six treatment groups. The negative control group received nothing, and the positive control (sepsis) group was fecal-induced peritonitis (FIP) by fecal administration (i. p). The treatment groups (A, B, C, and D) treat with ketamine 5 mg/kg body weight (i. p.) right after FIP, 3 h after FIP, 5 h after FIP, and intermittent every 2 h. The peripheral mononuclear blood cell was isolated 6 h after FIP. The immature granulocytes counted using a hematology analyzer while CRP concentration analyzed using kit enzyme-linked immunosorbent assay. Data were analyzed statistically using the one-way ANOVA test using SPSS version 20 software (P < 0.05). Results: Sepsis induction with FIP increases the number of immature granulocytes in animal models from 0.48% to 9.12% (P < 0.05) but did not affect CRP concentration (P > 0.05). The ketamine administration significantly decreases the immature granulocytes in Groups C (1.04%) and D (1.58%). Ketamine administration did not have a significant effect on CRP concentration. Conclusion: The ketamine administration at 5 h after FIP and intermittently every 2 h can be an alternative to be sepsis immunotherapy with immature granulocyte as the potential target.http://www.bjoaonline.com/article.asp?issn=2549-2276;year=2019;volume=3;issue=3;spage=174;epage=177;aulast=Asmoroc-reactive proteinimmature granulocyteketaminesepsis
spellingShingle Aswoco Andyk Asmoro
Isngadi Isngadi
Ristiawan Muji Laksono
Ibnu Firdiansayah
Agus Supriyanto
The effect of ketamine on the immature granulocyte and C-reactive protein concentration in rat models of sepsis
Bali Journal of Anesthesiology
c-reactive protein
immature granulocyte
ketamine
sepsis
title The effect of ketamine on the immature granulocyte and C-reactive protein concentration in rat models of sepsis
title_full The effect of ketamine on the immature granulocyte and C-reactive protein concentration in rat models of sepsis
title_fullStr The effect of ketamine on the immature granulocyte and C-reactive protein concentration in rat models of sepsis
title_full_unstemmed The effect of ketamine on the immature granulocyte and C-reactive protein concentration in rat models of sepsis
title_short The effect of ketamine on the immature granulocyte and C-reactive protein concentration in rat models of sepsis
title_sort effect of ketamine on the immature granulocyte and c reactive protein concentration in rat models of sepsis
topic c-reactive protein
immature granulocyte
ketamine
sepsis
url http://www.bjoaonline.com/article.asp?issn=2549-2276;year=2019;volume=3;issue=3;spage=174;epage=177;aulast=Asmoro
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