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α2-Adrenergic Agonists Induce Basic Fibroblast Growth Factor Expression in Photoreceptors In Vivo and Ameliorate Light Damage

Overview of attention for article published in The Journal of Neuroscience, October 1996
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Article details
Title
α2-Adrenergic Agonists Induce Basic Fibroblast Growth Factor Expression in Photoreceptors In Vivo and Ameliorate Light Damage
Published in
The Journal of Neuroscience, October 1996
DOI 10.1523/jneurosci.16-19-05986.1996
Pubmed ID
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Abstract

We observed an induction of basic fibroblast growth factor (bFGF) mRNA in the rat retina after systemic administration of the alpha 2-adrenergic agonists xylazine and clonidine. A single injection of xylazine or clonidine transiently increased bFGF mRNA. Preinjection of yohimbine, an alpha 2-adrenergic antagonist, completely inhibited this increase. Higher dosage of yohimbine inhibited the baseline expression of bFGF. Of particular interest is the finding that the induced bFGF expression occurred almost exclusively in the inner segment region of photoreceptors. No increase in bFGF mRNA was found in the brain after either xylazine or clonidine injection. Xylazine or clonidine given systemically before and during constant light exposure also reduces photoreceptor degeneration in albino rats. These results indicate that regulation of bFGF expression in photoreceptors is unique in the CNS and suggest that endogenous bFGF promotes photoreceptor survival.

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The data shown below were compiled from readership statistics for 28 Mendeley readers of this research output. Click here to see the associated Mendeley record.
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Geographical breakdown

Geographical breakdown
Country Count As %
Unknown 28 100%

Demographic breakdown

Readers by professional status
Readers by professional status Count As %
Other 6 21%
Researcher 5 18%
Professor 4 14%
Student > Ph. D. Student 3 11%
Student > Master 3 11%
Other 4 14%
Unknown 3 11%
Readers by discipline
Readers by discipline Count As %
Agricultural and Biological Sciences 9 32%
Medicine and Dentistry 6 21%
Neuroscience 4 14%
Chemistry 3 11%
Pharmacology, Toxicology and Pharmaceutical Science 2 7%
Other 0 0%
Unknown 4 14%