Abstract
Sidestream dark field imaging represents a novel, noninvasive method to study the microcirculation in humans and animals. To-date, it has been used extensively in various peripheral tissues (e.g. sublingual area, intestinal mucosa), however no data for the ocular vasculature, including the iridial microcirculation, are currently available. Therefore, the aim of this study was to examine the reliability and reproducibility of sidestream dark field imaging within the iridial microcirculation in experimental animals. Male Lewis rats were anaesthetized and the iris microvasculature was observed using an sidestream dark field probe gently placed against a cover slip covering the right eye. All video sequences recorded were analysed off-line by using AVA 3.0 software (MicroVision Medical, Amsterdam, The Netherlands). Results are expressed as mean (+/-SE) or median (interquartile range). Clear images were recorded from each animal and the total number of analysable video sequences was 50. All raw data for selected vessel density parameters passed normality test. The total all and small vessel density (in mm mm-2) were 22,6 (+/-0,58) and 19,6 (+/-0,68), respectively. The perfused all and small vessel density were 20,9 (+/-0,61) and 19,1 (+/-0,65), respectively. The mean values of all iris vessel density parameters are shown in Figure 4. The DeBacker Score (n/mm) was 15,2 (+/-0,45), the proportion of perfused vessel was 94,5% (89,899,1%), and the MFI was 3 points (33). Taken together, these results indicate that SDF imaging provides a reliable and noninvasive method to examine the iridial microvascular bed in vivo and, thus, may provide unique opportunities for the study of the iridial vascular network in various experimental and clinical settings and disease models. 4 Vessel Density. TAVD = Total all vessel density; PAVD = Perfused all vessel density; TSVD = Total small vessel density; PSVD = Perfused small vessel density. Data are shown as a mean (+/-SE), small vessels are referred to diameter = 25 um.