Time-resolved fluorescence intensity issued from a heterogeneous slab: Sensitivity characterization

Optical imaging using fluorescent contrast agents has become an interesting tool to differentiate diseased lesions from normal tissue. However, several sensitivity characterizations may strongly influence the time-dependent fluorescence measurements. Herein, we present a numerical model based on the finite element method that allows the simulation of time-resolved reflectance and transmittance signals from heterogeneous media mimicking breast tissues with an embedded fluorescent object (tumor). The influence, on the computed signals, of several tumor depths, as well as various fluorophore concentrations and several fluorescent markers targeting are analyzed. The results show the possibility of uncoupling location depth from the shape of the target. Therefore, the analysis of the time to reach half the maximum intensity is validated as a good localization scheme. Then, the transmitted data show that the maximal detected intensity at the bottom of the medium is very sensitive to the dye concentration but not to the tumor shape. Moreover, the strong competition between concentration determination and fluorophore distribution is presented. These results will lead to a better detection and localization of tumors

Optimisation of movement detection and artifact removal during laser speckle contrast imaging

Introduction Laser speckle contrast imaging (LSCI) allows an easy non-contact monitoring of the cutaneous blood flow (CBF), but is highly sensitive to movement artifacts (ARTm). Subtraction of a signal recorded on an adhesive opaque surface (AOS) close to the area of interest was reported as a mean of reducing noise from the raw skin LSCI (LSCIsk) signal, provided an individual calibration was performed. Assuming that AOS = a · CBF + b · ARTm, an ideal patch should completely block the light reflection due to CBF and thus be insensitive to skin blood flow changes (“a” ~ 0), while keeping a reflection signal amplitude similar to the one from the skin in case of artifact (“b” ~ 1). This ideal AOS has not been determined and may discriminate flow from movements during LSCI recordings. Materials and methods We tested different AOSs to determine their “a” and “b” parameters in 35 and 34 healthy volunteers, respectively. The AOS surface providing results as close as possible to an ideal AOS, was used for a point-by-point de-noising of post occlusive reactive hyperemia (PORH) on two different days in 15 new subjects. Correlation of raw, smoothed (average smoothing over 1 s intervals) and denoised signals was tested through a cross-correlation analysis of the two POHR tests. Results The optimal “a” and “b” values were obtained with a homemade bilayer adhesive patch (a = 0.06 ± 0.05 and b = 1.03 ± 0.17) whereas other tested AOS had “a” values ranging from 0.05 to 0.23 and “b” values ranging from 2.69 to 3.82. Using the bilayer adhesive patch the cross-correlation between the two tests of POHR increased from 0.330 ± 0.128 for raw, to 0.461 ± 0.168 for smoothed and 0.649 ± 0.128 for denoised signals respectively (p < 0.05 from raw coefficients). Conclusion The home-made bilayer adhesive seems the optimal AOS for the removal of ARTm from the LSCIsk signal while respecting CBF signal. This specific AOS allows for an efficient de-noising of LSCI measurements without the need for individual calibration

Forebrain Deletion of αGDI in Adult Mice Worsens the Pre-Synaptic Deficit at Cortico-Lateral Amygdala Synaptic Connections

The GDI1 gene encodes αGDI, which retrieves inactive GDP-bound RAB from membranes to form a cytosolic pool awaiting vesicular release. Mutations in GDI1 are responsible for X-linked Intellectual Disability. Characterization of the Gdi1-null mice has revealed alterations in the total number and distribution of hippocampal and cortical synaptic vesicles, hippocampal short-term synaptic plasticity and specific short-term memory deficits in adult mice, which are possibly caused by alterations of different synaptic vesicle recycling pathways controlled by several RAB GTPases. However, interpretation of these studies is complicated by the complete ablation of Gdi1 in all cells in the brain throughout development. In this study, we generated conditionally gene-targeted mice in which the knockout of Gdi1 is restricted to the forebrain, hippocampus, cortex and amygdala and occurs only during postnatal development. Adult mutant mice reproduce the short-term memory deficit previously reported in Gdi1-null mice. Surprisingly, the delayed ablation of Gdi1 worsens the pre-synaptic phenotype at cortico-amygdala synaptic connections compared to Gdi1-null mice. These results suggest a pivotal role of αGDI via specific RAB GTPases acting specifically in forebrain regions at the pre-synaptic sites involved in memory formation

A new method to determine arterial distensibility in small arteries

Several methods allow to measure arterial distensibilty. One of them consists in estimating the direct distensibility (D) from diameter and distending blood pressure. Herein, we propose a new method to assess the distensibility in small arteries which is based on spectral analysis of time motion mode ultrasound images of radial arteries. A Fourier transform was performed on intensity of upper and lower walls. Spectral amplitude at heart frequency from both wall spectra was estimated and summed (SumAmp). SumAmp was then compared with direct distensibility. A significant correlation was found between SumAmp and D (r = 0.7, p = 0.02)

Effets de la fluorescence résiduelle dans les tissus biologiques sur les signaux de fluorescence résolus temporellement par la méthode des éléments finis

RésuméUn modèle numérique basé sur la méthode des éléments finis est proposé afin d’analyser l’influence, sur les signaux de fluorescence résolus dans le temps, de la fluorescence résiduelle présente dans les milieux environnant une lésion tumorale. Nous appliquons une méthode de soustraction des données dans le cas d’une concentration imparfaite des agents de fluorescence au sein de la tumeur. Nous montrons ainsi les limites de la méthode de soustraction pour un faible contraste de fluorescence tumeur/milieu ambiant. En particulier, nous analysons l’extraction du temps de demi-montée et du maximum de l’intensité de fluorescence en fonction de la profondeur de la cible fluorescente. A computational model based on finite element method is derived to examine how the simulated time-dependent signals are related to the presence of residual fluorescence in biological media surrounding a fluorescent object. We apply a subtraction technique on recorded data when imperfect uptake of fluorescing agent into the tumor is considered. We show the limits of the subtracting method for low target: background fluorescent absorption contrast by extracting the time to reach the half maximum and analyzing the maximum of the time-resolved signals versus target depth