Muscle-tendon unit mechanobiological responses to consecutive high strain cyclic loading

In response to a mechanical stimulus, tendons have a slower tissue renewal rate compared to muscles. This could over time lead to a higher mechanical demand (experienced strain) for the tendon, especially when a high strain magnitude exercise is repeated without sufficient recovery. The current study investigated the adaptive responses of the triceps surae (TS) muscle-tendon unit (MTU) and extracellular matrix turnover-related biomarkers to repetitive high tendon strain cyclic loading. Eleven young male adults performed a progressive resistance exercise over 12 consecutive days, consisting of high Achilles tendon (AT) strain cyclic loading (90% MVC) with one leg once a day (LegT1) and the alternate leg three times a day (LegT3). Exercise-related changes in TS MTU mechanical properties and serum concentrations of extracellular matrix turnover-related biomarkers were analysed over the intervention period. Both legs demonstrated similar increases in maximal AT force (∼10%) over the 12-day period of exercise. A ∼20% increase in maximal AT strain was found for LegT3 (p<0.05) already after 8 consecutive exercise days, along with a corresponding decrease in AT stiffness. These effects were maintained even after a 48h rest period. The AT mechanical properties for LegT1 were unaltered. Biomarker analysis revealed no sign of inflammation, but altered collagen turnover and delayed increase in the collagen type I synthesis rate. Accordingly, we suggest that tendon is vulnerable to frequent high-magnitude and volume of cyclic mechanical loading, as accumulation of micro-damage can potentially exceed the rate of biological repair, leading to increased maximal tendon strai

Setting up and modelling of overflowing fed-batch cultures of Bacillus subtilis for the production and continuous removal of lipopeptides

This work is related to the setup of overflowing exponential fed-batch cultures (O-EFBC) derived from carbon limited EFBC dedicated to the production of mycosubtilin, an antifungal lipopeptide belonging to the iturin family. O-EFBC permits the continuous removal of the product from the bioreactor achieving a complete extraction of mycosubtilin. This paper also provides a dynamical Monod-based growth model of this process that is accurate enough to simulate the evolution of the specific growth rate and to correlate it to the mycosubtilin specific productivity. Two particular and dependant phenomena related to the foam overflow are taken into account by the model: the outgoing flow rate of a broth volume and the loss of biomass. Interestingly, the biomass concentration in the foam was found to be lower than the biomass concentration in the bioreactor relating this process to a recycling one. Parameters of this model are the growth yield on substrate and the maximal specific growth rate estimated from experiments led at feed rates of 0.062, 0.071 and 0.086 h --1. The model was extrapolated to five additional experiments carried out at feed rates of 0.008, 0.022, 0.040, 0.042 and 0.062 h --1 enabling the correlation of the mean specific growth rates with productivity results. Finally, a feed rate of 0.086 h --1 corresponding to a mean specific growth rate of 0.070 h --1 allowed a specific productivity of 1.27 mg of mycosubtilin g --1 of dried biomass h --1

Cavitation-generated free radicals during shock wave exposure: investigations with cell-free solutions and suspended cells

Extracorporeally generated shock waves as used in lithotripsy of urinary and biliary stones exhibit side effects in vivo. Furthermore, these shock waves destroy eukaryotic cells during in vitro treatment in suspension. A possible cause of these damaging effects might be cavitation, the growth and collapse of bubbles in liquids exposed to tensile stresses. During the collapse, temperature inside these cavitation bubbles rises up to several thousand K, leading to the formation of free radicals. We demonstrated the occurrence of cavitation-generated free radicals by direct reaction with fluorescent dyes in solution after shock wave treatment and investigated the resulting cell killing by variation of the cellular antioxidative defense status. We present evidence for the generation of intracellular free radicals during shock wave treatment of suspended cells

Standardisierte in-vitro-Modelle zur Charakterisierung von Stoßwellen

Zum jetzigen Zeitpunkt ist die physikalische Vermessung von Stoßwellen allerdings noch nicht problemlos möglich. Außerdem ist unbekannt, welche Stoßwellenparameter (wie Anstiegszeit und Dauer der Über- und Unterdruckamplitude) für die Steinzertrümmerung und die biologischen Nebenwirkungen bedeutsam sind. Wir haben deshalb vier in vitro-Modelle standardisiert, mit denen sich Wirkungen von Variationen der Behandlungsparameter schnell und zuverlässig aufzeigen lassen. Weiterhin kann die Stoßwellenwirkung auf Zellen, Gewebe und Steine in Lithotriptem mit unterschiedlichen Stoßwellenquellen getestet und verglichen werden

Sensivity of normal and malignant cells to shock waves

We examined the cytotoxic effect of shock waves for primary (embryonic chick kidney and thigh muscle) and permanently growing normal and malignant cells (human, rat, and mouse) in suspension. To avoid the influence of different media, the cells were suspended in phosphate buffered, saline and shock wave treated. In all cases the acute cytotoxic effect (measured by flow cytometry) was a function of the applied shock waves. The investigated cells differed in their LD 50 values which, however, do not reveal a general difference in sensitivity to shock waves for normal and malignant cells

Real-time 10Gbps polarization independent quasicoherent receiver for NG-PON2 access networks

© 2018 IEEE. Personal use of this material is permitted. Permission from IEEE must be obtained for all other uses, in any current or future media, including reprinting/republishing this material for advertising or promotional purposes,creating new collective works, for resale or redistribution to servers or lists, or reuse of any copyrighted component of this work in other worksIn this paper, we propose and test experimentally a real-time 10 Gbps polarization independent quasicoherent receiver for NG-PON2 access networks. The proposed 10 Gbps quasicoherent receiver exhibits a sensitivity of -35.2 dBm after 40 km SSMF transmission with a commercial generic EML as transmitter. This sensitivity means a 14.9 dB improvement over a direct detection scheme with a photodiode after 40 km SSMF transmission. Therefore, the use of the proposed 10 Gbps quasicoherent receiver with the tested EML will provide a power budget of 34.76 dB (class E1) and a splitting ratio of 128 after the 40 km SSMF transmission. Finally, the proposed 10 Gbps quasicoherent receiver allows a colorless and optical filterless operation because wavelength selection is done by tuning the local oscillator wavelength and using electrical intermediate frequency filtering.Peer ReviewedPostprint (author's final draft

Biophysical investigations of the in vitro effects of shock waves and ultrasound

To investigate the interactions of ultrasonic waves with biological tissues, we developed and standardized several in vitro models. Using these systems - artificial stones, human erythrocytes, L1210 mouse leukemia cells, multicellular spheroids, cavitation assay - we are able to elucidate the mechanisms of interaction as well as the cause of clinically observed side effects

Reduced cavitation-induced cellular damage by the antioxidative effect of vitamin E

Fragmentation of human urinary and biliary stones by shock waves in extracorporeal lithotripsy is accompanied by tissue damage. Both the fragmentation as well as the side effects are often attributed to cavitation. The hazardous potential of cavitation is not only of a physical nature but also of a chemical nature, because of the generation of free radicals, e.g. ·OH, ·H and ·O2. After the application of shock waves, we have demonstrated cavitation-generated free radicals in cell-free solutions and also in the surviving and intact suspended MGH-U1 cells by hydroethidine measurements. Under electron microscopical inspection, the same cells exhibited perinuclear cisternae, damaged mitochondria and numerous intracellular vacuoles. The contribution of free radicals to cell damage was investigated by reducing the vitamin E level in rats by a tocopherol free diet and by incubating L1210 cells in a tocopherol enriched medium. After 250 shock waves, ex vivo erythrocytes revealed a 75% increase in total cell disruption over cells from non-depleted rats. The in vitro experiments with L1210 cells exhibited a moderate protection by the addition of this scavenger of free radicals