Stroke is characterized by massive inflammation in areas surrounding the injury that magnifies damage to the brain. The liver X receptors (LXRs) are nuclear receptors that regulate cholesterol, lipid, and glucose metabolism. Synthetic LXR agonists have potent anti-inflammatory properties in a variety of settings, including neuroinflammation. However, the ability of LXR agonists to suppress stroke-associated inflammation has not been evaluated. Here, we have used time-lapse magnetic resonance imaging (MRI) to show that a single dose of an LXR ligand administered post-injury dramatically reduces brain damage in a model of acute brain ischemia. Neuroprotection was associated with suppression of neuroinflammation

Treatment with LXR agonists after focal cerebral ischemia prevents brain damage / L. Sironi, N. Mitro, M. Cimino, P. Gelosa, U. Guerrini, E. Tremoli, E. Saez. - In: FEBS LETTERS. - ISSN 0014-5793. - 582:23-24(2008), pp. 3396-3400. [10.1016/j.febslet.2008.08.035]

Treatment with LXR agonists after focal cerebral ischemia prevents brain damage

L. Sironi
Primo
;
N. Mitro
Secondo
;
P. Gelosa;U. Guerrini;E. Tremoli
Penultimo
;
2008

Abstract

Stroke is characterized by massive inflammation in areas surrounding the injury that magnifies damage to the brain. The liver X receptors (LXRs) are nuclear receptors that regulate cholesterol, lipid, and glucose metabolism. Synthetic LXR agonists have potent anti-inflammatory properties in a variety of settings, including neuroinflammation. However, the ability of LXR agonists to suppress stroke-associated inflammation has not been evaluated. Here, we have used time-lapse magnetic resonance imaging (MRI) to show that a single dose of an LXR ligand administered post-injury dramatically reduces brain damage in a model of acute brain ischemia. Neuroprotection was associated with suppression of neuroinflammation
Acute cerebral ischemia ; Experimental therapy ; Neuroprotection ; Nuclear receptor ; Transcriptional activator
Settore BIO/14 - Farmacologia
2008
Article (author)
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/2434/61753
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