Pretty much over my head but your doctor will understand. Have them put this into understandable terms and add it to your stroke protocol.
You do have a stroke protocol?
http://www.plosone.org/article/info%3Adoi%2F10.1371%2Fjournal.pone.0054519
Abstract
Axotomy
of central neurons leads to functional and structural alterations which
largely revert when neural progenitor cells (NPCs) are implanted in the
lesion site. The new microenvironment created by NPCs in the host
tissue might modulate in the damaged neurons the expression of a high
variety of molecules with relevant roles in the repair mechanisms,
including neurotrophic factors. In the present work, we aimed to analyze
changes in neurotrophic factor expression in axotomized neurons induced
by NPC implants. For this purpose, we performed immunofluorescence
followed by confocal microscopy analysis for the detection of vascular
endothelial growth factor (VEGF), brain-derived neurotrophic factor
(BDNF), neurotrophin-3 (NT-3) and nerve growth factor (NGF) on brainstem
sections from rats with axotomy of abducens internuclear neurons that
received NPC implants (implanted group) or vehicle injections
(axotomized group) in the lesion site. Control abducens internuclear
neurons were strongly immunoreactive to VEGF and BDNF but showed a weak
staining for NT-3 and NGF. Comparisons between groups revealed that
lesioned neurons from animals that received NPC implants showed a
significant increase in VEGF content with respect to animals receiving
vehicle injections. However, the immunoreactivity for BDNF, which was
increased in the axotomized group as compared to control, was not
modified in the implanted group. The modifications induced by NPC
implants on VEGF and BDNF content were specific for the population of
axotomized abducens internuclear neurons since the neighboring abducens
motoneurons were not affected. Similar levels of NT-3 and NGF
immunolabeling were obtained in injured neurons from axotomized and
implanted animals. Among all the analyzed neurotrophic factors, only
VEGF was expressed by the implanted cells in the lesion site.
Our
results point to a role of NPC implants in the modulation of
neurotrophic factor expression by lesioned central neurons, which might
contribute to the restorative effects of these implants.
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