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Biomedical subjects

B I Henry

Publications and source records attributed to B I Henry.

5 recordsLinked to original sources
PubMed2006

Anomalous diffusion with linear reaction dynamics: from continuous time random walks to fractional reaction-diffusion equations.

We have revisited the problem of anomalously diffusing species, modeled at the mesoscopic level using continuous time random walks, to include linear reaction dynamics. If a constant proportion of walkers are added or removed instantaneously at the start of each step then the long time asymptotic limit yields a fractional reaction-diffusion equation with a fractional order temporal derivative operating on both the standard diffusion term and a linear reaction kinetics term. If the walkers are added or removed at a constant per capita rate during the waiting time between steps then the long time asymptotic limit has a standard linear reaction kinetics term but a fractional order temporal derivative operating on a nonstandard diffusion term. Results from the above two models are compared with a phenomenological model with standard linear reaction kinetics and a fractional order temporal derivative operating on a standard diffusion term. We have also developed further extensions of the CTRW model to include more general reaction dynamics.

Journal Article↗
PubMed2005

Functionally relevant measures of spatial complexity in neuronal dendritic arbors.

We introduce a set of scaling exponents for characterizing global 3D morphologic properties of mass distribution, branching and taper in neuronal dendritic arbors, capable of distinguishing functionally relevant changes in dendritic complexity that standard Sholl analysis and fractal analysis cannot. We demonstrate that the scaling exponent for mass distribution, d(M), comprises a sum of independent scaling exponents for branching, d(N), and taper, d(T). The accuracy of experimental measurements of the scaling exponents was verified using computer generated self-similar binary trees of known fractal dimension, and with prescribed amounts of branching and taper. The theory was applied to measuring 3D spatial complexity in the apical and basal dendritic trees of two functionally distinct types of macaque monkey neocortical pyramidal neurons: long corticocortical projection neurons from superior temporal cortex to area 46 of the prefrontal cortex (PFC), and local projection neurons within area 46 of the PFC. Two distinct scaling subregions (proximal and medial) were identified in both apical and basal trees of the two neuron types, and scaling exponents were fitted. A small but significant difference in mass scaling in the proximal region distinguished long from local projection neurons. Interestingly, both classes of neuron exhibited a homeostatic pattern of mass distribution across the two regions: despite large differences between proximal and medial regions in branching and tapering exponents, these effects were compensatory, resulting in a uniform, slow reduction of mass with distance from the soma, over both scaling regions of the apical and basal trees. Given a uniformly excitable membrane, the electrotonic properties of dendritic arbors depend entirely upon mass distribution, and its relative contributions from dendritic branching and taper. By capturing each of these complex morphologic properties in a single, globally descriptive parameter, the new 3D scaling exponents introduced in this study permit efficient morphometric characterization of complex dendritic arbors in the fewest possible parameters, that can be directly related to their electrotonic properties, and hence to neuronal function.

Animals↗
PubMed2005

Turing pattern formation in fractional activator-inhibitor systems.

Activator-inhibitor systems of reaction-diffusion equations have been used to describe pattern formation in numerous applications in biology, chemistry, and physics. The rate of diffusion in these applications is manifest in the single parameter of the diffusion constant, and stationary Turing patterns occur above a critical value of d representing the ratio of the diffusion constants of the inhibitor to the activator. Here we consider activator-inhibitor systems in which the diffusion is anomalous subdiffusion; the diffusion rates are manifest in both a diffusion constant and a diffusion exponent. A consideration of this problem in terms of continuous-time random walks with sources and sinks leads to a reaction-diffusion system with fractional order temporal derivatives operating on the spatial Laplacian. We have carried out an algebraic stability analysis of the homogeneous steady-state solution in fractional activator-inhibitor systems, with Gierer-Meinhardt reaction kinetics and with Brusselator reaction kinetics. For each class of reaction kinetics we identify a Turing instability bifurcation curve in the two-dimensional diffusion parameter space. The critical value of d , for Turing instabilities, decreases monotonically with the anomalous diffusion exponent between unity (standard diffusion) and zero (extreme subdiffusion). We have also carried out numerical simulations of the governing fractional activator-inhibitor equations and we show that the Turing instability precipitates the formation of complex spatiotemporal patterns. If the diffusion of the activator and inhibitor have the same anomalous scaling properties, then the surface profiles of these patterns for values of d slightly above the critical value varies from smooth stationary patterns to increasingly rough and nonstationary patterns as the anomalous diffusion exponent varies from unity towards zero. If the diffusion of the activator is anomalous subdiffusion but the diffusion of the inhibitor is standard diffusion, we find stable stationary Turing patterns for values of d well below the threshold values for pattern formation in standard activator-inhibitor systems.

Journal Article↗
PubMed2003

Random walks on finite lattice tubes.

Exact results are obtained for random walks on finite lattice tubes with a single source and absorbing lattice sites at the ends. Explicit formulas are derived for the absorption probabilities at the ends and for the expectations that a random walk will visit a particular lattice site before being absorbed. Results are obtained for lattice tubes of arbitrary size and each of the regular lattice types: square, triangular, and honeycomb. The results include an adjustable parameter to model the effects of strain, such as surface curvature, on the surface diffusion. Results for the triangular lattice tubes and the honeycomb lattice tubes model diffusion of adatoms on single walled zig-zag carbon nanotubes with open ends.

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