scholarly journals Investigation of Changes in Anomalous Diffusion Parameters in a Mouse Model of Brain Tumour

Author(s):  
Qianqian Yang ◽  
Simon Puttick ◽  
Zara C. Bruce ◽  
Bryan W. Day ◽  
Viktor Vegh
2019 ◽  
Author(s):  
Naor Granik ◽  
Elias Nehme ◽  
Lucien E. Weiss ◽  
Maayan Levin ◽  
Michael Chein ◽  
...  

AbstractDiffusion plays a crucial role in many biological processes including signaling, cellular organization, transport mechanisms, and more. Direct observation of molecular movement by single-particle tracking experiments has contributed to a growing body of evidence that many cellular systems do not exhibit classical Brownian motion, but rather anomalous diffusion. Despite this evidence, characterization of the physical process underlying anomalous diffusion remains a challenging problem for several reasons. First, different physical processes can exist simultaneously in a system. Second, commonly used tools to distinguish between these processes are based on asymptotic behavior, which is inaccessible experimentally in most cases. Finally, an accurate analysis of the diffusion model requires the calculation of many observables, since different transport modes can result in the same diffusion power-law α, that is obtained from the commonly used mean-squared-displacement (MSD) in its various forms. The outstanding challenge in the field is to develop a method to extract an accurate assessment of the diffusion process using many short trajectories with a simple scheme that is applicable at the non-expert level.Here, we use deep learning to infer the underlying process resulting in anomalous diffusion. We implement a neural network to classify single particle trajectories according to diffusion type – Brownian motion, fractional Brownian motion (FBM) and Continuous Time Random Walk (CTRW). We further use the net to estimate the Hurst exponent for FBM, and the diffusion coefficient for Brownian motion, demonstrating its applicability on simulated and experimental data. The networks outperform time averaged MSD analysis on simulated trajectories while requiring as few as 25 time-steps. Furthermore, when tested on experimental data, both network and ensemble MSD analysis converge to similar values, with the network requiring half the trajectories required for ensemble MSD. Finally, we use the nets to extract diffusion parameters from multiple extremely short trajectories (10 steps).


2014 ◽  
Vol 207 (9) ◽  
pp. 451 ◽  
Author(s):  
Zhi-Yan Han ◽  
Wilfrid Richer ◽  
Carlo Lucchesi ◽  
Paul Fréneaux ◽  
André Nicolas ◽  
...  
Keyword(s):  

2020 ◽  
Vol 7 (4) ◽  
pp. 667-676
Author(s):  
Yahia Z. Rawash

In this paper the stretch function resulting from solving the fractional-order Bloch equations using fractional calculus was discussed. This function has promising results to represent diffusion signal decay from MRI images. Conventional analyses of (DWI) measurements resolve the normalized magnetization decay profiles in terms of discrete and mono-exponential components with distinct lifetimes. In complex, heterogeneous biological and biophysical samples such as tissue, multi-exponential decay functions can appear to provide truer representation to normalized magnetization decay profile than the assumption of a mono-exponential decay, but the assumption of multiple discrete components is arbitrary and is often erroneous. Moreover, interactions, between both normalized magnetization and with their environment, can result in complex normalized magnetization decay profiles that represent a continuous distribution of lifetimes. The purpose in this paper is to study different factors that influence the stretch function strength, clarity, and contrast of MRI magnetization signal relaxation by manipulating the anomalous diffusion parameters Δ,δ,Gz,β and μ. of Bloch equations. Through this study, it was found that complex normalized magnetization decay profiles behave like stretch exponential function inside power law. Further developments of this study may be useful in optimizing anomalous diffusion in tissues with neurodegenerative, and ischemic diseases.


Author(s):  
H. D. Geissinge ◽  
L.D. Rhodes

A recently discovered mouse model (‘mdx’) for muscular dystrophy in man may be of considerable interest, since the disease in ‘mdx’ mice is inherited by the same mode of inheritance (X-linked) as the human Duchenne (DMD) muscular dystrophy. Unlike DMD, which results in a situation in which the continual muscle destruction cannot keep up with abortive regenerative attempts of the musculature, and the sufferers of the disease die early, the disease in ‘mdx’ mice appears to be transient, and the mice do not die as a result of it. In fact, it has been reported that the severely damaged Tibialis anterior (TA) muscles of ‘mdx’ mice seem to display exceptionally good regenerative powers at 4-6 weeks, so much so, that these muscles are able to regenerate spontaneously up to their previous levels of physiological activity.


1998 ◽  
Vol 13 (11-s4) ◽  
pp. S178-S184 ◽  
Author(s):  
PETER KONTUREK ◽  
TOMASZ BRZOZOWSKI ◽  
STANISLAW KONTUREK ◽  
ELZBIETA KARCZEWSKA ◽  
ROBERT PAJDO ◽  
...  

Sign in / Sign up

Export Citation Format

Share Document