In piglets we tested the applicability of digital video microscopy and diffuse reflectance spectroscopy for non-invasive assessments of limbal and bulbar conjunctival microcirculation. A priori we postulated that the metabolic rate is higher in limbal as compared to bulbar conjunctiva, and that this difference is reflected in microvascular structure or function between the two locations. Two study sites, Oslo University Hospital (OUH), Norway and Cleveland Clinic (CC), USA, used the same video microscopy and spectroscopy techniques to record limbal and bulbar microcirculation in sleeping piglets. All recordings were analyzed with custom-made software to quantify functional capillary density, capillary flow velocity and microvascular oxygen saturation in measuring volumes of approximately 0.1 mm 3 . The functional capillary density was higher in limbus than in bulbar conjunctiva at both study sites (OUH: 18.1 ± 2.9 versus 12.2 ± 2.9 crossings per mm line, p < 0.01; CC: 11.3 ± 3.0 versus 7.1 ± 2.8 crossings per mm line, p < 0.01). Median categorial capillary blood flow velocity was higher in bulbar as compared with limbal recordings (CC: 3 (1–3) versus 1 (0–3), p < 0.01). Conjunctival microvascular oxygen saturation was 88 ± 5.9% in OUH versus 94 ± 7.5% in CC piglets. Non-invasive digital video microscopy and diffuse reflectance spectroscopy can be used to obtain data from conjunctival microcirculation in piglets. Limbal conjunctival microcirculation has a larger capacity for oxygen delivery as compared with bulbar conjunctiva.

Objective Clinical assessments and laser Doppler perfusion measurements (LDPM) of skin microcirculation have limited value, as they fail to capture events regulated by local metabolic needs at a papillary capillary level. This study aimed to examine the ability of computer‐assisted video microscopy (CAVM) and diffuse reflectance spectroscopy (DRS) to assess skin nutritive perfusion—compared to LDPM. Methods Healthy volunteers (n = 10) were examined after (≈1 and ≈24 h) an incision (5 × 1 mm) on the forearm, at 0.1 mm (only with CAVM), 2−3 mm, and 30 mm from the trauma. Results No changes were detected by CAVM after ≈1 h. After ≈24 h, 0−1 mm from the trauma, both CAVM parameters were increased: functional capillary density (capillary crossings/mm, 11.8 ± 1.4 vs. 7.3 ± 1.2, p < .01) and capillary flow velocities (CFV, %capillaries with brisk flow, 10 ± 6.8 vs. 1 ± 1, p < .01). At a distance of 2−3 mm, only CFV was increased (6.2 ± 6.1 vs. 1 ± 1, p < .05). DRS and LDPM measurements increased 2−3 mm from the trauma line in relation to baseline after both ≈1 and ≈24 h, that is, with DRS (%microvascular oxygen saturation): 45.8 ± 7.4% (baseline), 70.0 ± 12.5% (≈1 h), and 73.1 ± 10.4% (≈24 h), p < .01 and with LDPM (a.u.): 7.2 ± 2.5 (baseline), 28.3 ± 18.7 (≈1 h), and 45.9 ± 16.3 (≈24 h), p < .01. Conclusions ≈24 h after skin trauma, an increased function of the nutritive papillary capillaries can be detected by CAVM.

Remodeling of tissue is a way of maintaining homeostasis in response to physiological and pathological stimuli such as aging, disease, and injury. 1 Microscopy (electron and light) of skin biopsies has been used to visualize human microvascular anatomy, 2 and microvascular remodeling has been studied in animal models and computer simulation. 3 To capture dynamic processes, other methods are needed-for example, in vivo microscopy.Healing of a skin trauma leads to an increase in local metabolic rate for proliferation of cells and production of extracellular matrix. Because of poor diffusion capacity of O 2 in human tissues, the maximal O 2 diffusion distance from a perfused capillary