Three semi-analytical solutions for one-dimensional, reactive tracer migration through a porous medium are derived and used to evaluate TCE time concentration profiles.
These findings suggest that reactive astrocyte migration may constitute a new therapeutic target for the early phase of SCI (Renault-Mihara et al, 2008).
These findings reveal a novel effect of GSK-3 inhibition that could improve recovery from SCI and suggest that the pharmacological stimulation of reactive astrocyte migration holds promise as a new therapeutic strategy for the treatment of SCI.
However, further studies in relevant models are needed to examine whether the stimulation of reactive astrocyte migration through GSK-3 inhibition does indeed limit the development of these cystic cavities.
In conclusion, our findings reveal a novel beneficial effect of GSK-3 inhibition for SCI and suggest that the pharmacological stimulation of reactive astrocyte migration holds promise as a new therapeutic strategy for the treatment of SCI.
In linear acenes, the benzenoid character of the π-sextet is diluted when increasing the length of the hydrocarbon [82]; higher acenes are much more reactive due to migration of the π-sextet and loss of the aromatic nature.
