The Early Diagnostic Efficacy of Serum Histone H3 in Rabbit Urosepsis Model

Objective. We want to explore the changing law of circulating histones in the acute stage of urosepsis and to find more sensitive and specific biomarkers for diagnosing urosepsis as early as possible. Methods. Twenty healthy male New Zealand rabbits were randomly divided into 4 groups (N=5): the con...

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Veröffentlicht in:BioMed research international 2021, Vol.2021 (1), p.9969344-9969344
Hauptverfasser: Zhang, Xiaolu, Zhan, Xiangcheng, Huang, Bisheng, Li, Saiyang, Xu, Yunfei
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Zhan, Xiangcheng
Huang, Bisheng
Li, Saiyang
Xu, Yunfei
description Objective. We want to explore the changing law of circulating histones in the acute stage of urosepsis and to find more sensitive and specific biomarkers for diagnosing urosepsis as early as possible. Methods. Twenty healthy male New Zealand rabbits were randomly divided into 4 groups (N=5): the control group, sham group, model group of LPS 600 μg/kg, and model group of LPS 1000 μg/kg. Heart rate (HR), respiration rate (RR), rectal temperature (T), and mean arterial pressure (MAP) were examined at 1, 3, 6, 12, and 24 hours after operation. Besides, peripheral blood cell counts (RBC, WBC, PLT, and Hb) and C reaction protein (CRP) were tested at 1, 3, and 6 hours after operation, while the levels of histone H3, MMP-9, TIMP-1, and procalcitonin (PCT) in the serum were tested at 1, 3, and 6 hours after operation by ELISA. The heart, left lung, liver, and left kidney were harvested for HE stain and observed to research the pathological change of these tissues. Results. (1) The general status of rabbits: rabbits in the control and sham groups came out in 2 h after operation and regain to drink and eat in 12-24 h after operation. State of the rabbits in the control group was better than that in the sham group. Rabbits in the model groups were languid after operation and stopped to drink and eat. (2) Vital signs of rabbits: there was no statistic difference in HR (P=0.238) and RR (P=0.813) among all groups. MAP of the model groups decreased at 3 h postoperative, but transient (P
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We want to explore the changing law of circulating histones in the acute stage of urosepsis and to find more sensitive and specific biomarkers for diagnosing urosepsis as early as possible. Methods. Twenty healthy male New Zealand rabbits were randomly divided into 4 groups (N=5): the control group, sham group, model group of LPS 600 μg/kg, and model group of LPS 1000 μg/kg. Heart rate (HR), respiration rate (RR), rectal temperature (T), and mean arterial pressure (MAP) were examined at 1, 3, 6, 12, and 24 hours after operation. Besides, peripheral blood cell counts (RBC, WBC, PLT, and Hb) and C reaction protein (CRP) were tested at 1, 3, and 6 hours after operation, while the levels of histone H3, MMP-9, TIMP-1, and procalcitonin (PCT) in the serum were tested at 1, 3, and 6 hours after operation by ELISA. The heart, left lung, liver, and left kidney were harvested for HE stain and observed to research the pathological change of these tissues. Results. (1) The general status of rabbits: rabbits in the control and sham groups came out in 2 h after operation and regain to drink and eat in 12-24 h after operation. State of the rabbits in the control group was better than that in the sham group. Rabbits in the model groups were languid after operation and stopped to drink and eat. (2) Vital signs of rabbits: there was no statistic difference in HR (P=0.238) and RR (P=0.813) among all groups. MAP of the model groups decreased at 3 h postoperative, but transient (P&lt;0.001). The T of the LPS 1000 group decreased at 6 h postoperative (P=0.003). (3) The change of biomarkers: H3 level of the LPS groups in the serum increased at 1 h postoperative (P&lt;0.01); MMP-9 of the LPS 1000 group increased at 1 h postoperative (P&lt;0.01); WBC of the model groups decreased at 3 h postoperative (P&lt;0.05); PLT of the LPS 1000 group is significantly increased at 1 h postoperative (P&lt;0.05); no statistic difference was found in CRP, PCT, and TIMP-1 among all groups. (4) Pathological sections: no abnormal performance was found in the control and sham groups. Glomerulus of the model groups was out of shape and necrosis with obvious renal tubule expansion. Pulmonary pathology showed alveolar septum diffuse increased and inflammatory infiltrate. Change of the LPS 1000 group was more serious than that of the LPS 600 group. Conclusions. Ligating the ureter after an injection of 1000 μg/kg LPS into the ureter of the rabbit can establish the animal model of urosepsis. Histone H3 increase immediately at 1 h postoperative and are promised to be biomarkers of urosepsis, which are more effective than WBC, CRP, and PCT.</description><identifier>ISSN: 2314-6133</identifier><identifier>EISSN: 2314-6141</identifier><identifier>DOI: 10.1155/2021/9969344</identifier><identifier>PMID: 34327242</identifier><language>eng</language><publisher>United States: Hindawi</publisher><subject>Alveoli ; Analysis ; Animal models ; Animals ; Antibiotics ; Arterial Pressure ; Biomarkers ; Blood cells ; Blood pressure ; Body Temperature ; C-Reactive Protein - metabolism ; Calculi, Urinary ; Care and treatment ; Causes of ; Complications and side effects ; Diagnosis ; Disease Models, Animal ; DNA binding proteins ; Early Diagnosis ; Enzyme-linked immunosorbent assay ; Enzymes ; Gelatinase B ; Glomerulus ; Health aspects ; Heart rate ; Histone H3 ; Histones ; Histones - blood ; Infections ; Inflammation ; Kidneys ; Laboratories ; Leukocyte Count ; Lipopolysaccharides ; Male ; Matrix Metalloproteinase 9 - metabolism ; Measurement ; Medical prognosis ; Methods ; Necrosis ; Organ Specificity ; Peripheral blood ; Platelet Count ; Procalcitonin ; Procalcitonin - blood ; Rabbits ; Risk factors ; ROC Curve ; Sensitivity and Specificity ; Sepsis ; Sepsis - blood ; Sepsis - diagnosis ; Sepsis - pathology ; Sepsis - physiopathology ; Septum ; Surgery ; Tissue inhibitor of metalloproteinase 1 ; Tissue Inhibitor of Metalloproteinase-1 - blood ; Tumor necrosis factor-TNF ; Ureter ; Urinary tract infections ; Urogenital system ; Urology ; Vital Signs</subject><ispartof>BioMed research international, 2021, Vol.2021 (1), p.9969344-9969344</ispartof><rights>Copyright © 2021 Xiaolu Zhang et al.</rights><rights>COPYRIGHT 2021 John Wiley &amp; Sons, Inc.</rights><rights>Copyright © 2021 Xiaolu Zhang et al. This is an open access article distributed under the Creative Commons Attribution License (the “License”), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License. https://creativecommons.org/licenses/by/4.0</rights><rights>Copyright © 2021 Xiaolu Zhang et al. 2021</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c570t-bacb90e70ef2eb966ef3ca0ff030f1ea4156a52605c3e130d4ec3758e95de4983</citedby><cites>FETCH-LOGICAL-c570t-bacb90e70ef2eb966ef3ca0ff030f1ea4156a52605c3e130d4ec3758e95de4983</cites><orcidid>0000-0003-1288-8361</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC8310443/pdf/$$EPDF$$P50$$Gpubmedcentral$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC8310443/$$EHTML$$P50$$Gpubmedcentral$$Hfree_for_read</linktohtml><link.rule.ids>230,314,727,780,784,885,4022,27922,27923,27924,53790,53792</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/34327242$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><contributor>Huang, Tao</contributor><contributor>Tao Huang</contributor><creatorcontrib>Zhang, Xiaolu</creatorcontrib><creatorcontrib>Zhan, Xiangcheng</creatorcontrib><creatorcontrib>Huang, Bisheng</creatorcontrib><creatorcontrib>Li, Saiyang</creatorcontrib><creatorcontrib>Xu, Yunfei</creatorcontrib><title>The Early Diagnostic Efficacy of Serum Histone H3 in Rabbit Urosepsis Model</title><title>BioMed research international</title><addtitle>Biomed Res Int</addtitle><description>Objective. We want to explore the changing law of circulating histones in the acute stage of urosepsis and to find more sensitive and specific biomarkers for diagnosing urosepsis as early as possible. Methods. Twenty healthy male New Zealand rabbits were randomly divided into 4 groups (N=5): the control group, sham group, model group of LPS 600 μg/kg, and model group of LPS 1000 μg/kg. Heart rate (HR), respiration rate (RR), rectal temperature (T), and mean arterial pressure (MAP) were examined at 1, 3, 6, 12, and 24 hours after operation. Besides, peripheral blood cell counts (RBC, WBC, PLT, and Hb) and C reaction protein (CRP) were tested at 1, 3, and 6 hours after operation, while the levels of histone H3, MMP-9, TIMP-1, and procalcitonin (PCT) in the serum were tested at 1, 3, and 6 hours after operation by ELISA. The heart, left lung, liver, and left kidney were harvested for HE stain and observed to research the pathological change of these tissues. Results. (1) The general status of rabbits: rabbits in the control and sham groups came out in 2 h after operation and regain to drink and eat in 12-24 h after operation. State of the rabbits in the control group was better than that in the sham group. Rabbits in the model groups were languid after operation and stopped to drink and eat. (2) Vital signs of rabbits: there was no statistic difference in HR (P=0.238) and RR (P=0.813) among all groups. MAP of the model groups decreased at 3 h postoperative, but transient (P&lt;0.001). The T of the LPS 1000 group decreased at 6 h postoperative (P=0.003). (3) The change of biomarkers: H3 level of the LPS groups in the serum increased at 1 h postoperative (P&lt;0.01); MMP-9 of the LPS 1000 group increased at 1 h postoperative (P&lt;0.01); WBC of the model groups decreased at 3 h postoperative (P&lt;0.05); PLT of the LPS 1000 group is significantly increased at 1 h postoperative (P&lt;0.05); no statistic difference was found in CRP, PCT, and TIMP-1 among all groups. (4) Pathological sections: no abnormal performance was found in the control and sham groups. Glomerulus of the model groups was out of shape and necrosis with obvious renal tubule expansion. Pulmonary pathology showed alveolar septum diffuse increased and inflammatory infiltrate. Change of the LPS 1000 group was more serious than that of the LPS 600 group. Conclusions. Ligating the ureter after an injection of 1000 μg/kg LPS into the ureter of the rabbit can establish the animal model of urosepsis. Histone H3 increase immediately at 1 h postoperative and are promised to be biomarkers of urosepsis, which are more effective than WBC, CRP, and PCT.</description><subject>Alveoli</subject><subject>Analysis</subject><subject>Animal models</subject><subject>Animals</subject><subject>Antibiotics</subject><subject>Arterial Pressure</subject><subject>Biomarkers</subject><subject>Blood cells</subject><subject>Blood pressure</subject><subject>Body Temperature</subject><subject>C-Reactive Protein - metabolism</subject><subject>Calculi, Urinary</subject><subject>Care and treatment</subject><subject>Causes of</subject><subject>Complications and side effects</subject><subject>Diagnosis</subject><subject>Disease Models, Animal</subject><subject>DNA binding proteins</subject><subject>Early Diagnosis</subject><subject>Enzyme-linked immunosorbent assay</subject><subject>Enzymes</subject><subject>Gelatinase B</subject><subject>Glomerulus</subject><subject>Health aspects</subject><subject>Heart rate</subject><subject>Histone H3</subject><subject>Histones</subject><subject>Histones - blood</subject><subject>Infections</subject><subject>Inflammation</subject><subject>Kidneys</subject><subject>Laboratories</subject><subject>Leukocyte Count</subject><subject>Lipopolysaccharides</subject><subject>Male</subject><subject>Matrix Metalloproteinase 9 - metabolism</subject><subject>Measurement</subject><subject>Medical prognosis</subject><subject>Methods</subject><subject>Necrosis</subject><subject>Organ Specificity</subject><subject>Peripheral blood</subject><subject>Platelet Count</subject><subject>Procalcitonin</subject><subject>Procalcitonin - blood</subject><subject>Rabbits</subject><subject>Risk factors</subject><subject>ROC Curve</subject><subject>Sensitivity and Specificity</subject><subject>Sepsis</subject><subject>Sepsis - blood</subject><subject>Sepsis - diagnosis</subject><subject>Sepsis - pathology</subject><subject>Sepsis - physiopathology</subject><subject>Septum</subject><subject>Surgery</subject><subject>Tissue inhibitor of metalloproteinase 1</subject><subject>Tissue Inhibitor of Metalloproteinase-1 - blood</subject><subject>Tumor necrosis factor-TNF</subject><subject>Ureter</subject><subject>Urinary tract infections</subject><subject>Urogenital system</subject><subject>Urology</subject><subject>Vital Signs</subject><issn>2314-6133</issn><issn>2314-6141</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2021</creationdate><recordtype>article</recordtype><sourceid>RHX</sourceid><sourceid>EIF</sourceid><sourceid>ABUWG</sourceid><sourceid>AFKRA</sourceid><sourceid>AZQEC</sourceid><sourceid>BENPR</sourceid><sourceid>CCPQU</sourceid><sourceid>DWQXO</sourceid><sourceid>GNUQQ</sourceid><recordid>eNp9kc1rFDEYh4MottTePEvAi6Br8z2Ti1Dq6ooVQdtzyGTe7KbMJttkRtn_3iy7rh-H5pLA-_CE9_dD6DklbymV8oIRRi-0VpoL8QidMk7FTFFBHx_fnJ-g81LuSD0tVUSrp-iEC84aJtgp-nyzAjy3edji98EuYypjcHjufXDWbXHy-DvkaY0XoYwpAl5wHCL-ZrsujPg2pwKbEgr-knoYnqEn3g4Fzg_3Gbr9ML-5Wsyuv378dHV5PXOyIeOss67TBBoCnkGnlQLPnSXeE048BSuoVFYyRaTjQDnpBTjeyBa07EHolp-hd3vvZurW0DuIY7aD2eSwtnlrkg3m30kMK7NMP0zLKRGCV8GrgyCn-wnKaNahOBgGGyFNxTApG8a4IE1FX_6H3qUpx7rejhKtFpqqP9TSDmBC9Kn-63ZSc6m0amvwDX-YarlsiWayUm_2lKvplgz-uBglZle62ZVuDqVX_MXfYRzh3xVX4PUeWIXY25_hYd0vBeawWg</recordid><startdate>2021</startdate><enddate>2021</enddate><creator>Zhang, Xiaolu</creator><creator>Zhan, Xiangcheng</creator><creator>Huang, Bisheng</creator><creator>Li, Saiyang</creator><creator>Xu, Yunfei</creator><general>Hindawi</general><general>John Wiley &amp; 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Zhan, Xiangcheng ; Huang, Bisheng ; Li, Saiyang ; Xu, Yunfei</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c570t-bacb90e70ef2eb966ef3ca0ff030f1ea4156a52605c3e130d4ec3758e95de4983</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2021</creationdate><topic>Alveoli</topic><topic>Analysis</topic><topic>Animal models</topic><topic>Animals</topic><topic>Antibiotics</topic><topic>Arterial Pressure</topic><topic>Biomarkers</topic><topic>Blood cells</topic><topic>Blood pressure</topic><topic>Body Temperature</topic><topic>C-Reactive Protein - metabolism</topic><topic>Calculi, Urinary</topic><topic>Care and treatment</topic><topic>Causes of</topic><topic>Complications and side effects</topic><topic>Diagnosis</topic><topic>Disease Models, Animal</topic><topic>DNA binding proteins</topic><topic>Early Diagnosis</topic><topic>Enzyme-linked immunosorbent assay</topic><topic>Enzymes</topic><topic>Gelatinase B</topic><topic>Glomerulus</topic><topic>Health aspects</topic><topic>Heart rate</topic><topic>Histone H3</topic><topic>Histones</topic><topic>Histones - blood</topic><topic>Infections</topic><topic>Inflammation</topic><topic>Kidneys</topic><topic>Laboratories</topic><topic>Leukocyte Count</topic><topic>Lipopolysaccharides</topic><topic>Male</topic><topic>Matrix Metalloproteinase 9 - metabolism</topic><topic>Measurement</topic><topic>Medical prognosis</topic><topic>Methods</topic><topic>Necrosis</topic><topic>Organ Specificity</topic><topic>Peripheral blood</topic><topic>Platelet Count</topic><topic>Procalcitonin</topic><topic>Procalcitonin - blood</topic><topic>Rabbits</topic><topic>Risk factors</topic><topic>ROC Curve</topic><topic>Sensitivity and Specificity</topic><topic>Sepsis</topic><topic>Sepsis - blood</topic><topic>Sepsis - diagnosis</topic><topic>Sepsis - pathology</topic><topic>Sepsis - physiopathology</topic><topic>Septum</topic><topic>Surgery</topic><topic>Tissue inhibitor of metalloproteinase 1</topic><topic>Tissue Inhibitor of Metalloproteinase-1 - blood</topic><topic>Tumor necrosis factor-TNF</topic><topic>Ureter</topic><topic>Urinary tract infections</topic><topic>Urogenital system</topic><topic>Urology</topic><topic>Vital Signs</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Zhang, Xiaolu</creatorcontrib><creatorcontrib>Zhan, Xiangcheng</creatorcontrib><creatorcontrib>Huang, Bisheng</creatorcontrib><creatorcontrib>Li, Saiyang</creatorcontrib><creatorcontrib>Xu, Yunfei</creatorcontrib><collection>Hindawi Publishing Complete</collection><collection>Hindawi Publishing Subscription Journals</collection><collection>Hindawi Publishing Open Access Journals</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>ProQuest Central (Corporate)</collection><collection>Bacteriology Abstracts (Microbiology B)</collection><collection>Biotechnology Research Abstracts</collection><collection>Industrial and Applied Microbiology Abstracts (Microbiology A)</collection><collection>Neurosciences Abstracts</collection><collection>Toxicology Abstracts</collection><collection>Virology and AIDS Abstracts</collection><collection>Health &amp; 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We want to explore the changing law of circulating histones in the acute stage of urosepsis and to find more sensitive and specific biomarkers for diagnosing urosepsis as early as possible. Methods. Twenty healthy male New Zealand rabbits were randomly divided into 4 groups (N=5): the control group, sham group, model group of LPS 600 μg/kg, and model group of LPS 1000 μg/kg. Heart rate (HR), respiration rate (RR), rectal temperature (T), and mean arterial pressure (MAP) were examined at 1, 3, 6, 12, and 24 hours after operation. Besides, peripheral blood cell counts (RBC, WBC, PLT, and Hb) and C reaction protein (CRP) were tested at 1, 3, and 6 hours after operation, while the levels of histone H3, MMP-9, TIMP-1, and procalcitonin (PCT) in the serum were tested at 1, 3, and 6 hours after operation by ELISA. The heart, left lung, liver, and left kidney were harvested for HE stain and observed to research the pathological change of these tissues. Results. (1) The general status of rabbits: rabbits in the control and sham groups came out in 2 h after operation and regain to drink and eat in 12-24 h after operation. State of the rabbits in the control group was better than that in the sham group. Rabbits in the model groups were languid after operation and stopped to drink and eat. (2) Vital signs of rabbits: there was no statistic difference in HR (P=0.238) and RR (P=0.813) among all groups. MAP of the model groups decreased at 3 h postoperative, but transient (P&lt;0.001). The T of the LPS 1000 group decreased at 6 h postoperative (P=0.003). (3) The change of biomarkers: H3 level of the LPS groups in the serum increased at 1 h postoperative (P&lt;0.01); MMP-9 of the LPS 1000 group increased at 1 h postoperative (P&lt;0.01); WBC of the model groups decreased at 3 h postoperative (P&lt;0.05); PLT of the LPS 1000 group is significantly increased at 1 h postoperative (P&lt;0.05); no statistic difference was found in CRP, PCT, and TIMP-1 among all groups. (4) Pathological sections: no abnormal performance was found in the control and sham groups. Glomerulus of the model groups was out of shape and necrosis with obvious renal tubule expansion. Pulmonary pathology showed alveolar septum diffuse increased and inflammatory infiltrate. Change of the LPS 1000 group was more serious than that of the LPS 600 group. Conclusions. Ligating the ureter after an injection of 1000 μg/kg LPS into the ureter of the rabbit can establish the animal model of urosepsis. Histone H3 increase immediately at 1 h postoperative and are promised to be biomarkers of urosepsis, which are more effective than WBC, CRP, and PCT.</abstract><cop>United States</cop><pub>Hindawi</pub><pmid>34327242</pmid><doi>10.1155/2021/9969344</doi><tpages>1</tpages><orcidid>https://orcid.org/0000-0003-1288-8361</orcidid><oa>free_for_read</oa></addata></record>
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2314-6141
language eng
recordid cdi_pubmedcentral_primary_oai_pubmedcentral_nih_gov_8310443
source MEDLINE; PubMed Central Open Access; Wiley Online Library Open Access; PubMed Central; Alma/SFX Local Collection
subjects Alveoli
Analysis
Animal models
Animals
Antibiotics
Arterial Pressure
Biomarkers
Blood cells
Blood pressure
Body Temperature
C-Reactive Protein - metabolism
Calculi, Urinary
Care and treatment
Causes of
Complications and side effects
Diagnosis
Disease Models, Animal
DNA binding proteins
Early Diagnosis
Enzyme-linked immunosorbent assay
Enzymes
Gelatinase B
Glomerulus
Health aspects
Heart rate
Histone H3
Histones
Histones - blood
Infections
Inflammation
Kidneys
Laboratories
Leukocyte Count
Lipopolysaccharides
Male
Matrix Metalloproteinase 9 - metabolism
Measurement
Medical prognosis
Methods
Necrosis
Organ Specificity
Peripheral blood
Platelet Count
Procalcitonin
Procalcitonin - blood
Rabbits
Risk factors
ROC Curve
Sensitivity and Specificity
Sepsis
Sepsis - blood
Sepsis - diagnosis
Sepsis - pathology
Sepsis - physiopathology
Septum
Surgery
Tissue inhibitor of metalloproteinase 1
Tissue Inhibitor of Metalloproteinase-1 - blood
Tumor necrosis factor-TNF
Ureter
Urinary tract infections
Urogenital system
Urology
Vital Signs
title The Early Diagnostic Efficacy of Serum Histone H3 in Rabbit Urosepsis Model
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