Author/Authors :
Kang, Christine Department of Anesthesia and Pain Medicine - Pusan National University School of Medicine - Yangsan, Korea , Cho, Ah-Reum Department of Anesthesia and Pain Medicine - Pusan National University School of Medicine - Yangsan, Korea , Lee, Hyeon Jeong Department of Anesthesia and Pain Medicine - Pusan National University School of Medicine - Yangsan, Korea , Kim, Hyae Jin Department of Anesthesia and Pain Medicine - Pusan National University School of Medicine - Yangsan, Korea , Kim, Eun-Jung Department of Dental Anesthesia and Pain Medicine - School of Dentistry - Pusan National University - Dental Research Institute - Yangsan, Korea , Jeon, Soeun Department of Anesthesia and Pain Medicine - Pusan National University School of Medicine - Yangsan, Korea , Hong, Jeong-Min Department of Anesthesia and Pain Medicine - Pusan National University School of Medicine - Yangsan, Korea , Moon, Daehoan Department of Anesthesia and Pain Medicine - Pusan National University School of Medicine - Yangsan, Korea
Abstract :
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.
Keywords :
dorsal skinfold chamber model , glycocalyx , incident dark field , microcirculation , sepsis