Quantitative Evaluation of Oxygenation and Metabolism in the Human Skeletal Muscle

The forearm muscles of five healthy males were monitored for changes in microvessel hemoglobin saturation (SO_2-TRS) by near infrared time-resolved spectroscopy (NIR_TRS) and changes in phosphorus metabolites by magnetic resonance spectroscopy (³¹P-MRS) during 12 min of resting arterial occlusion. Muscle oxygenation and phosphorus metabolites were also measured during grip exercises at varying intensities. Upon the initiation of occlusion, SO_2-TRS fell progressively until it reached a plateau in the latter half of the occlusion. Phosphocreatine (PCr) began to decrease around 6 min after the initiation of arterial occlusion. The resting O₂ store and O₂ consumption were 295 μM and 0.95 μM/sec, respectively-values which reasonably agree with the reported results. A significant correlation was observed between the changes in SO_2-TRS and PCr during exercise (r² = 0.80, p < 0.001). These results indicate that NIR_TRS is able to provide reliable information about resting metabolism and oxidative rate during exercise. NIR_TRS and MRS are useful to monitor oxygenation and energetics noninvasively in the human muscle.     

An invariance principle for non-symmetric Markov processes and reflecting diffusions in random domains

Summary We study an invariance principle for additive functionals of nonsymmetric Markov processes with singular mean forward velocities. We generalize results of Kipnis and Varadhan [KV] and De Masi et al. [De] in two directions: Markov processes are non-symmetric, and mean forward velocities are distributions. We study continuous time Markov processes. We use our result to homogenize non-symmetric reflecting diffusions in random domains.     

Dextran‐Based Self‐Healing Hydrogels Formed by Reversible Diels–Alder Reaction under Physiological Conditions

A dextran‐based self‐healing hydrogel is prepared by reversible Diels–Alder reaction under physiological conditions. Cytocompatible fulvene‐modified dextran as main polymer chains and dichloromaleic‐acid‐modified poly(ethylene glycol) as cross‐linkers are used. Both macro‐ and microscopic observation as well as the rheological recovery test confirm the self‐healing property of the dextran‐l‐poly(ethylene glycol) hydrogels (“l” means “linked‐by”). In addition, scanning electrochemical microscopy is used to qualitatively and quantitatively in situ track the self‐healing process of the hydrogel for the first time. It is found that the longitudinal depth of scratch on hydrogel surface almost completely healed at 37 °C after 7 h. This work represents a facile approach for fabrication of polysaccharide self‐healing hydrogel, which can be potentially used in several biomedical fields.

     

Dissipative or just nonextensive hydrodynamics? — Nonextensive/dissipative correspondence

We argue that there is correspondence between the perfect nonextensive hydrodynamics and the usual dissipative hydrodynamics, which we call nonextensive/dissipative correspondence (NexDC). It leads to simple expression for dissipative entropy current and allows for predictions for the ratio of bulk and shear viscosities to entropy density, ζ/s and η/F.     

The early history of convergence acceleration methods

The history of convergence acceleration methods in the 17th century is surveyed. Acceleration methods are classified into three categories.     

Metal-insulator transition of charge-transfer salts based on unsymmetrical donor DMET and metal halide anions (DMET)4(MCl4)(TCE)2 (M = Mn, Co, Cu, Zn; TCE = 1,1,2-trichloroethane)

New charge-transfer salts based on an unsymmetrical donor DMET [dimethyl(ethylenedithio)diselenadithiafulvalene] and metal halide anions (DMET)4MIICl4(TCE)2 (M = Mn, Co, Cu, Zn; TCE = 1,1,2-trichloroethane) have been synthesized and characterized by transport and magnetic measurements. The crystal structures of the DMET salts are isostructural, consisting of a quasi-one-dimensional stack of DMET and insulating layers containing metal halide anions and TCE. Semimetallic band structures are calculated by the tight-binding approximation. Metal-insulator transitions are observed at TMI = 25, 15, 5-20, and 13 K for M = Mn, Co, Cu, and Zn, respectively. The M = Cu salt exhibits anisotropic conduction at ambient pressure, being semiconducting in the intralayer current direction but metallic for the interplane current direction, down to T(MI). The metal-insulator transitions are suppressed under pressure. In the M = Co and Zn salts, large magnetoresistances with hysteresis are observed at low temperatures, on which Shubnikov-de Haas oscillations are superposed above 30 T. In the M = Cu salt, no hysteresis is observed but clear Shubnikov-de Haas oscillations are observed. The magnetoresistance is small and monotonic in the M = Mn salt. Paramagnetic susceptibilities of the spins of the magnetic ions are observed for the M = Mn, Co, and Cu salts with small negative Weiss temperatures of approximately 1 K. In the nonmagnetic M = Zn salt, Pauli-like pi-electron susceptibility that vanishes at TMI is observed. The ground state of the pi-electron system is understood as being a spin density wave state caused by imperfect nesting of the Fermi surfaces. In this pi-electron system, the magnetic ions of the M = Mn, Co, and Cu salts interact differently, exhibiting a variety of transport behaviors.     

Actin network formation by unidirectional polycation diffusion

We show that F-actins form three-dimensional giant network under uni-directional diffusion of polycations, at a dilute actin concentration (0.01 mg/mL) that only bundles are formed by homogeneous mixing with polycations. The mesh size of the actin network depends on polycation concentration and ionic strength, while bundle thickness of network depends only on ionic strength, which indicates that actin network is formed through nucleation-growth mechanism. The mesh size and the bundle thickness are determined by nucleus concentration and nucleus size, respectively. The atomic force microscopy measurement correlates the elasticity of the actin network, E, with the mesh size, xi, as E approximately xi-1, while the bundle thickness, D dependence of E cannot be described by a simple scaling relation. E approximately D6.5 when D is small and E approximately D0.1 when D is large. Our study on the self-assembly of actin network under asymmetric polycation condition would provide the crucial insight into the organization of biopolymers in polarized condition of cell.     

Intelligent gel – surface properties and functions of gels –

The sliding friction of various kinds of hydrogels has been studied and it was found that the frictional behaviors of the hydrogels do not conform to Amonton's law F = μW, which well describes the friction of solids. The frictional force and its dependencies of on the load are quite different depending on the chemical structures of the gels, surface properties of the opposing substrates, and the measurement condition. The gel friction is explained in terms of interfacial interaction, either attractive or repulsive, between the polymer chain and the solid surface. According to this model, the frictional is ascribed to the viscous flow of solvent at the interface in the repulsive case. In the attractive case, the force to detach the adsorbing chain from the substrate appears as friction. Surface adhesion between glass particles and gels measured by AFM showed a good correlation with the friction, which support the repulsion‐adsorption model proposed by authors.