 |
Previous Article | Next Article 
The Journal of Neuroscience, January 1, 2003, 23(1):287-296
Provision of Brain-Derived Neurotrophic Factor via Anterograde
Transport from the Eye Preserves the Physiological Responses of
Axotomized Geniculate Neurons
Matteo
Caleo1, 2,
Paolo
Medini2,
Christopher S.
von
Bartheld3, and
Lamberto
Maffei1, 2
1 Istituto di Neuroscienze del Consiglio Nazionale
delle Ricerche and 2 Scuola Normale Superiore, 56100 Pisa,
Italy, and 3 Department of Physiology and Cell Biology,
University of Nevada School of Medicine, Reno, Nevada 89557
The neurotrophic factors of the nerve growth factor family
(neurotrophins) have been shown to promote neuronal survival after brain injury and in various models of neurodegenerative conditions. However, it has not been determined whether neurotrophin treatment results in the maintenance of function of the rescued cells. Here we
have used the retrograde degeneration of geniculate neurons as a model
system to evaluate neuronal rescue and sparing of function after
administration of brain-derived neurotrophic factor (BDNF). Death of
geniculate neurons was induced by a visual cortex lesion in adult rats,
and exogenous BDNF was delivered to the axotomized geniculate cells via
anterograde transport after injection into the eye. By microelectrode
recordings from the geniculate in vivo we have
measured several physiological parameters such as contrast threshold, spatial resolution (visual acuity), signal-to-noise ratio,
temporal resolution, and response latency. In control lesioned animals
we found that geniculate cell dysfunction precedes the onset of
neuronal death, indicating that an assessment of neuronal number per se
is not predictive of functional performance. The administration of BDNF
resulted in a highly significant cell-saving effect up to 2 weeks
after the cortical damage and maintained nearly normal physiological
responses in the geniculate. This preservation of function in adult
axotomized neurons suggests possible therapeutic applications of BDNF.
Key words:
BDNF; anterograde transport; neuronal death; retrograde degeneration; lateral geniculate nucleus; functional
sparing
Copyright © 2003 Society for Neuroscience 0270-6474/03/231287-10$05.00/0
This article has been cited by other articles:

|
 |

|
 |
 
M.-L. Baudet, D. Rattray, B. T. Martin, and S. Harvey
Growth Hormone Promotes Axon Growth in the Developing Nervous System
Endocrinology,
June 1, 2009;
150(6):
2758 - 2766.
[Abstract]
[Full Text]
[PDF]
|
 |
|

|
 |

|
 |
 
J. Gardiner, D. Barton, R. Overall, and J. Marc
Neurotrophic Support and Oxidative Stress: Converging Effects in the Normal and Diseased Nervous System
Neuroscientist,
February 1, 2009;
15(1):
47 - 61.
[Abstract]
[PDF]
|
 |
|

|
 |

|
 |
 
M. A. D.-L. de Carrizosa, C. J. Morado-Diaz, J. J. Tena, B. Benitez-Temino, M. L. Pecero, S. R. Morcuende, R. R. de la Cruz, and A. M. Pastor
Complementary Actions of BDNF and Neurotrophin-3 on the Firing Patterns and Synaptic Composition of Motoneurons
J. Neurosci.,
January 14, 2009;
29(2):
575 - 587.
[Abstract]
[Full Text]
[PDF]
|
 |
|

|
 |

|
 |
 
L. Costantin, Y. Bozzi, C. Richichi, A. Viegi, F. Antonucci, M. Funicello, M. Gobbi, T. Mennini, O. Rossetto, C. Montecucco, et al.
Antiepileptic Effects of Botulinum Neurotoxin E
J. Neurosci.,
February 23, 2005;
25(8):
1943 - 1951.
[Abstract]
[Full Text]
[PDF]
|
 |
|

|
 |

|
 |
 
D. J. Seecharan, A. L. Kulkarni, L. Lu, G. D. Rosen, and R. W. Williams
Genetic Control of Interconnected Neuronal Populations in the Mouse Primary Visual System
J. Neurosci.,
December 3, 2003;
23(35):
11178 - 11188.
[Abstract]
[Full Text]
[PDF]
|
 |
|
|

|