๐”– Bobbio Scriptorium
โœฆ   LIBER   โœฆ

Plasticity and growth factors in injury response

โœ Scribed by Cotman, Carl W. ;Berchtold, Nicole C.


Publisher
John Wiley and Sons
Year
1998
Tongue
English
Weight
172 KB
Volume
4
Category
Article
ISSN
1080-4013

No coin nor oath required. For personal study only.

โœฆ Synopsis


The central nervous system (CNS) possesses a well-known capacity for circuitry rearrangement, or ''plasticity,'' which is maintained throughout life. Two well-studied categories of CNS plasticity are the circuitry rearrangement which occurs in response to injury and that which occurs in response to normal environmental stimuli. In an injury response, such as that which follows partial denervation of the hippocampus by unilateral removal of the entorhinal cortex, undamaged fibers in the denervated zone sprout and form new connections to replace lost synapses. In addition, rearrangement of circuitry also takes place in nondenervated zones which are functionally associated with the denervated circuitry. These observations indicate that the CNS is capable of major remodeling of neuronal circuitry, both in response to an injury as well as in the absence of a direct insult. Importantly, such plasticity reactions after injury appear to mediate recovery of lost function in hippocampal-dependent learning. Plasticity can also occur in response to relatively subtle stimuli, such as are found in an enriched environment or with exercise. Even tightly structured repetitive exercise, such as wheelrunning by rats, drives plasticity responses in brain regions such as the hippocampus, cortex, and cerebellum. Plasticity in response to injury and environmentally driven plasticity share similar molecular features, such as activation of growth factors, suggesting that some molecular events and mechanisms driving circuitry remodeling are common to all forms of plasticity. In this review, these two categories of CNS plasticity are discussed, using in vivo models to illustrate remodeling occurring after damage, as well as environmentally driven plasticity.


๐Ÿ“œ SIMILAR VOLUMES


Disulfide bond plasticity in epidermal g
โœ Benedetta A. Sampoli Benitez; Elizabeth A. Komives ๐Ÿ“‚ Article ๐Ÿ“… 2000 ๐Ÿ› John Wiley and Sons ๐ŸŒ English โš– 234 KB ๐Ÿ‘ 1 views

Epidermal growth factor (EGF) has a (1-3,2-4,5-6) disulfide-bonding pattern. This pattern is found in nearly all EGF-like domains, despite wide variation in sequences. Biological data from EGF and at least one EGF-like domain show that disulfide bond isomers have significant bioactivity and suggests

Plasticity of adolescent growth in boys
โœ Michael Hermanussen ๐Ÿ“‚ Article ๐Ÿ“… 1997 ๐Ÿ› John Wiley and Sons ๐ŸŒ English โš– 239 KB ๐Ÿ‘ 1 views

The present analysis examines the plasticity of adolescent growth in 21 selected historic and recent growth studies from 6 European countries, the U.S., and Japan, during the last 150 years. Mean stature at the age of 6 years has significantly increased by approximately 6 mm per decade (P < 0.05), w

Early growth response factor-1 mediates
โœ Natalia Gousseva; Kumudhini Kugathasan; Colin N. Chesterman; Levon M. Khachigian ๐Ÿ“‚ Article ๐Ÿ“… 2001 ๐Ÿ› John Wiley and Sons ๐ŸŒ English โš– 407 KB

Hyperinsulinemia in diabetes mellitus is a significant risk factor in the development of atherosclerosis and early restenosis after balloon angioplasty. These manifestations could be mediated by the ability of insulin to potentiate the cellular proliferative and reparative response of vascular cell

Basic fibroblast growth factor promotes
โœ Santa-Olalla, J. ;Covarrubias, L. ๐Ÿ“‚ Article ๐Ÿ“… 1999 ๐Ÿ› John Wiley and Sons ๐ŸŒ English โš– 306 KB ๐Ÿ‘ 1 views

Epidermal growth factor (EGF) and basic fibroblast growth factor (bFGF) induce proliferation of neural precursor cells from several central nervous system regions in vitro. We have previously described two neural precursor cell populations from 13.5 days postcoitium (dpc) mesencephalon, one forming

SPARC, an upstream regulator of connecti
โœ X. D. Zhou; M. M. Xiong; F. K. Tan; X. J. Guo; F. C. Arnett ๐Ÿ“‚ Article ๐Ÿ“… 2006 ๐Ÿ› John Wiley and Sons ๐ŸŒ English โš– 71 KB ๐Ÿ‘ 1 views

## Abstract ## Objective To differentiate the effects of inhibition of specific small interfering RNA (siRNA) of SPARC (secreted protein, acidic and rich in cysteine) and siRNA of connective tissue growth factor (CTGF) in cultured human fibroblasts, and to identify potential interrelationships bet