Feasibility study of incident dark-field video microscope for measuring microcirculatory variables in the mouse dorsal skinfold chamber model

Despite the importance of microcirculation in organ function, monitoring microcirculation is not a routine practice. With developments in microscopic technology, incident dark field (IDF) microscopy (Cytocam) has allowed visualization of the microcirculation. Dorsal skinfold chamber (DSC) mouse mode...

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Published inAcute and critical care Vol. 36; no. 1; pp. 29 - 36
Main Authors Kang, Christine, Cho, Ah-Reum, Lee, Hyeon Jeong, Kim, Hyae Jin, Kim, Eun-Jung, Jeo, Soeun, Hong, Jeong-Min, Moon, Daehoan
Format Journal Article
LanguageEnglish
Published Korea (South) Korean Society of Critical Care Medicine 01.02.2021
대한중환자의학회
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ISSN2586-6052
2586-6060
2586-6060
DOI10.4266/acc.2020.00969

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Abstract Despite the importance of microcirculation in organ function, monitoring microcirculation is not a routine practice. With developments in microscopic technology, incident dark field (IDF) microscopy (Cytocam) has allowed visualization of the microcirculation. Dorsal skinfold chamber (DSC) mouse model has been used to investigate microcirculation physiology. By employing Cytocam-IDF imaging with DSC model to assess microcirculatory alteration in lipopolysaccharide (LPS)-induced endotoxemia, we attempted to validate availability of Cytocam-IDF imaging of microcirculation. DSC was implanted in eight BALB/c mice for each group; control and sepsis. Both groups were given 72 hours to recover from surgery. The sepsis group had an additional 24-hour period of recovery post-LPS injection (4 mg/kg). Subsequently, a video of the microcirculation was recorded using Cytocam. Data on microcirculatory variables were obtained. Electron microscopy was implemented using lanthanum fixation to detect endothelial glycocalyx degradation. The microcirculatory flow index was significantly lower (control, 2.8±0.3; sepsis, 2.1±0.8; P=0.033) and heterogeneity index was considerably higher (control, 0.10±0.15; sepsis, 0.53±0.48; P=0.044) in the sepsis group than in the control group. Electron microscopy revealed glycocalyx demolishment in the sepsis group. Cytocam showed reliable ability for observing changes in the microcirculation under septic conditions in the DSC model. The convenience and good imaging quality and the automatic analysis software available for Cytocam-IDF imaging, along with the ability to perform real-time in vivo experiments in the DSC model, are expected to be helpful in future microcirculation investigations.
AbstractList Background Despite the importance of microcirculation in organ function, monitoring microcirculation is not a routine practice. With developments in microscopic technology, incident dark field (IDF) microscopy (Cytocam) has allowed visualization of the microcirculation. Dorsal skinfold chamber (DSC) mouse model has been used to investigate microcirculation physiology. By employing Cytocam-IDF imaging with DSC model to assess microcirculatory alteration in lipopolysaccharide (LPS)-induced endotoxemia, we attempted to validate availability of Cytocam-IDF imaging of microcirculation. Methods DSC was implanted in eight BALB/c mice for each group; control and sepsis. Both groups were given 72 hours to recover from surgery. The sepsis group had an additional 24-hour period of recovery post-LPS injection (4 mg/kg). Subsequently, a video of the microcirculation was recorded using Cytocam. Data on microcirculatory variables were obtained. Electron microscopy was implemented using lanthanum fixation to detect endothelial glycocalyx degradation. Results The microcirculatory flow index was significantly lower (control, 2.8±0.3; sepsis, 2.1±0.8; P=0.033) and heterogeneity index was considerably higher (control, 0.10±0.15; sepsis, 0.53±0.48; P=0.044) in the sepsis group than in the control group. Electron microscopy revealed glycocalyx demolishment in the sepsis group. Conclusions Cytocam showed reliable ability for observing changes in the microcirculation under septic conditions in the DSC model. The convenience and good imaging quality and the automatic analysis software available for Cytocam-IDF imaging, along with the ability to perform real-time in vivo experiments in the DSC model, are expected to be helpful in future microcirculation investigations.
Despite the importance of microcirculation in organ function, monitoring microcirculation is not a routine practice. With developments in microscopic technology, incident dark field (IDF) microscopy (Cytocam) has allowed visualization of the microcirculation. Dorsal skinfold chamber (DSC) mouse model has been used to investigate microcirculation physiology. By employing Cytocam-IDF imaging with DSC model to assess microcirculatory alteration in lipopolysaccharide (LPS)-induced endotoxemia, we attempted to validate availability of Cytocam-IDF imaging of microcirculation.BACKGROUNDDespite the importance of microcirculation in organ function, monitoring microcirculation is not a routine practice. With developments in microscopic technology, incident dark field (IDF) microscopy (Cytocam) has allowed visualization of the microcirculation. Dorsal skinfold chamber (DSC) mouse model has been used to investigate microcirculation physiology. By employing Cytocam-IDF imaging with DSC model to assess microcirculatory alteration in lipopolysaccharide (LPS)-induced endotoxemia, we attempted to validate availability of Cytocam-IDF imaging of microcirculation.DSC was implanted in eight BALB/c mice for each group; control and sepsis. Both groups were given 72 hours to recover from surgery. The sepsis group had an additional 24-hour period of recovery post-LPS injection (4 mg/kg). Subsequently, a video of the microcirculation was recorded using Cytocam. Data on microcirculatory variables were obtained. Electron microscopy was implemented using lanthanum fixation to detect endothelial glycocalyx degradation.METHODSDSC was implanted in eight BALB/c mice for each group; control and sepsis. Both groups were given 72 hours to recover from surgery. The sepsis group had an additional 24-hour period of recovery post-LPS injection (4 mg/kg). Subsequently, a video of the microcirculation was recorded using Cytocam. Data on microcirculatory variables were obtained. Electron microscopy was implemented using lanthanum fixation to detect endothelial glycocalyx degradation.The microcirculatory flow index was significantly lower (control, 2.8±0.3; sepsis, 2.1±0.8; P=0.033) and heterogeneity index was considerably higher (control, 0.10±0.15; sepsis, 0.53±0.48; P=0.044) in the sepsis group than in the control group. Electron microscopy revealed glycocalyx demolishment in the sepsis group.RESULTSThe microcirculatory flow index was significantly lower (control, 2.8±0.3; sepsis, 2.1±0.8; P=0.033) and heterogeneity index was considerably higher (control, 0.10±0.15; sepsis, 0.53±0.48; P=0.044) in the sepsis group than in the control group. Electron microscopy revealed glycocalyx demolishment in the sepsis group.Cytocam showed reliable ability for observing changes in the microcirculation under septic conditions in the DSC model. The convenience and good imaging quality and the automatic analysis software available for Cytocam-IDF imaging, along with the ability to perform real-time in vivo experiments in the DSC model, are expected to be helpful in future microcirculation investigations.CONCLUSIONSCytocam showed reliable ability for observing changes in the microcirculation under septic conditions in the DSC model. The convenience and good imaging quality and the automatic analysis software available for Cytocam-IDF imaging, along with the ability to perform real-time in vivo experiments in the DSC model, are expected to be helpful in future microcirculation investigations.
Despite the importance of microcirculation in organ function, monitoring microcirculation is not a routine practice. With developments in microscopic technology, incident dark field (IDF) microscopy (Cytocam) has allowed visualization of the microcirculation. Dorsal skinfold chamber (DSC) mouse model has been used to investigate microcirculation physiology. By employing Cytocam-IDF imaging with DSC model to assess microcirculatory alteration in lipopolysaccharide (LPS)-induced endotoxemia, we attempted to validate availability of Cytocam-IDF imaging of microcirculation. DSC was implanted in eight BALB/c mice for each group; control and sepsis. Both groups were given 72 hours to recover from surgery. The sepsis group had an additional 24-hour period of recovery post-LPS injection (4 mg/kg). Subsequently, a video of the microcirculation was recorded using Cytocam. Data on microcirculatory variables were obtained. Electron microscopy was implemented using lanthanum fixation to detect endothelial glycocalyx degradation. The microcirculatory flow index was significantly lower (control, 2.8±0.3; sepsis, 2.1±0.8; P=0.033) and heterogeneity index was considerably higher (control, 0.10±0.15; sepsis, 0.53±0.48; P=0.044) in the sepsis group than in the control group. Electron microscopy revealed glycocalyx demolishment in the sepsis group. Cytocam showed reliable ability for observing changes in the microcirculation under septic conditions in the DSC model. The convenience and good imaging quality and the automatic analysis software available for Cytocam-IDF imaging, along with the ability to perform real-time in vivo experiments in the DSC model, are expected to be helpful in future microcirculation investigations.
Background: Despite the importance of microcirculation in organ function, monitoring microcirculationis not a routine practice. With developments in microscopic technology, incidentdark field (IDF) microscopy (Cytocam) has allowed visualization of the microcirculation. Dorsal skinfold chamber (DSC) mouse model has been used to investigate microcirculationphysiology. By employing Cytocam-IDF imaging with DSC model to assess microcirculatoryalteration in lipopolysaccharide (LPS)-induced endotoxemia, we attempted to validate availabilityof Cytocam-IDF imaging of microcirculation. Methods: DSC was implanted in eight BALB/c mice for each group; control and sepsis. Bothgroups were given 72 hours to recover from surgery. The sepsis group had an additional 24-hour period of recovery post-LPS injection (4 mg/kg). Subsequently, a video of the microcirculationwas recorded using Cytocam. Data on microcirculatory variables were obtained. Electronmicroscopy was implemented using lanthanum fixation to detect endothelial glycocalyxdegradation. Results: The microcirculatory flow index was significantly lower (control, 2.8±0.3; sepsis,2.1±0.8; P=0.033) and heterogeneity index was considerably higher (control, 0.10±0.15;sepsis, 0.53±0.48; P=0.044) in the sepsis group than in the control group. Electron microscopyrevealed glycocalyx demolishment in the sepsis group. Conclusions: Cytocam showed reliable ability for observing changes in the microcirculationunder septic conditions in the DSC model. The convenience and good imaging quality andthe automatic analysis software available for Cytocam-IDF imaging, along with the ability toperform real-time in vivo experiments in the DSC model, are expected to be helpful in futuremicrocirculation investigations. KCI Citation Count: 0
Author Hong, Jeong-Min
Jeo, Soeun
Kang, Christine
Cho, Ah-Reum
Moon, Daehoan
Lee, Hyeon Jeong
Kim, Hyae Jin
Kim, Eun-Jung
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10.1097/01.ccm.0000138558.16257.3f
10.1097/aln.0000000000001135
10.1016/j.bpa.2016.10.008
10.1186/cc11666
10.1097/shk.0b013e318157e926
10.1152/ajpheart.00034.2016
10.1186/cc6118
10.1093/bja/aev163
10.1097/ccm.0000000000001582
10.3791/55115
10.1016/j.mvr.2013.02.001
10.22203/ecm.v032a13
10.1186/s12880-015-0078-8
10.1186/s13054-020-2728-7
10.1186/cc14726
10.1007/s00134-018-5070-7
10.1159/000477419
10.1186/s13054-018-2292-6
10.1016/j.bpa.2016.10.001
10.1186/s13054-015-1102-7
10.1164/rccm.200109-016oc
10.1016/j.jcrc.2013.06.015
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Keywords glycocalyx
incident dark field
dorsal skinfold chamber model
microcirculation
sepsis
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References ref12
Nelson (ref27) 2008
ref14
ref10
Hua (ref2) 2018
ref1
ref17
ref16
ref19
ref18
Ellis (ref13) 2002
Ince (ref11) 2005
Kataoka (ref15) 2017
ref24
ref23
ref26
ref25
ref20
ref22
ref21
ref28
ref8
ref7
ref9
ref4
ref3
ref6
ref5
References_xml – start-page: H156
  volume-title: Effect of a maldistribution of microvascular blood flow on capillary O(2) extraction in sepsis
  year: 2002
  ident: ref13
– ident: ref7
  doi: 10.1177/1751143716678638
– ident: ref25
  doi: 10.1097/01.ccm.0000138558.16257.3f
– ident: ref23
  doi: 10.1097/aln.0000000000001135
– ident: ref18
  doi: 10.1016/j.bpa.2016.10.008
– ident: ref22
  doi: 10.1186/cc11666
– start-page: S13
  volume-title: The microcirculation is the motor of sepsis
  year: 2005
  ident: ref11
– start-page: 591
  volume-title: Micro-and macrocirculatory changes during sepsis and septic shock in a rat model
  year: 2018
  ident: ref2
– ident: ref12
  doi: 10.1097/shk.0b013e318157e926
– ident: ref20
  doi: 10.1152/ajpheart.00034.2016
– ident: ref19
  doi: 10.1186/cc6118
– ident: ref1
  doi: 10.1093/bja/aev163
– start-page: 874
  volume-title: Structural behavior of the endothelial glycocalyx is associated with pathophysiologic status in septic mice: an integrated approach to analyzing the behavior and function of the glycocalyx using both electron and fluorescence intravital microscopy
  year: 2017
  ident: ref15
– ident: ref10
  doi: 10.1097/ccm.0000000000001582
– ident: ref14
  doi: 10.3791/55115
– ident: ref28
  doi: 10.1016/j.mvr.2013.02.001
– ident: ref8
  doi: 10.22203/ecm.v032a13
– ident: ref6
  doi: 10.1186/s12880-015-0078-8
– ident: ref3
  doi: 10.1186/s13054-020-2728-7
– ident: ref5
  doi: 10.1186/cc14726
– ident: ref16
  doi: 10.1007/s00134-018-5070-7
– ident: ref9
  doi: 10.1159/000477419
– ident: ref26
  doi: 10.1186/s13054-018-2292-6
– ident: ref4
  doi: 10.1016/j.bpa.2016.10.001
– start-page: 623
  volume-title: Increased levels of glycosaminoglycans during septic shock: relation to mortality and the antibacterial actions of plasma
  year: 2008
  ident: ref27
– ident: ref21
  doi: 10.1186/s13054-015-1102-7
– ident: ref24
  doi: 10.1164/rccm.200109-016oc
– ident: ref17
  doi: 10.1016/j.jcrc.2013.06.015
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Snippet Despite the importance of microcirculation in organ function, monitoring microcirculation is not a routine practice. With developments in microscopic...
Background Despite the importance of microcirculation in organ function, monitoring microcirculation is not a routine practice. With developments in...
Background: Despite the importance of microcirculation in organ function, monitoring microcirculationis not a routine practice. With developments in...
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SubjectTerms dorsal skinfold chamber model
glycocalyx
incident dark field
microcirculation
Original
sepsis
마취과학
Title Feasibility study of incident dark-field video microscope for measuring microcirculatory variables in the mouse dorsal skinfold chamber model
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