PT  - JOURNAL ARTICLE
AU  - Abraham Martín
AU  - Boguslaw Szczupak
AU  - Vanessa Gómez-Vallejo
AU  - Maria Domercq
AU  - Ainhoa Cano
AU  - Daniel Padro
AU  - Clara Muñoz
AU  - Makoto Higuchi
AU  - Carlos Matute
AU  - Jordi Llop
TI  - <em>In Vivo</em> PET Imaging of the α4β2 Nicotinic Acetylcholine Receptor As a Marker for Brain Inflammation after Cerebral Ischemia
AID  - 10.1523/JNEUROSCI.3670-14.2015
DP  - 2015 Apr 15
TA  - The Journal of Neuroscience
PG  - 5998--6009
VI  - 35
IP  - 15
4099  - http://www.jneurosci.org/content/35/15/5998.short
4100  - http://www.jneurosci.org/content/35/15/5998.full
SO  - J. Neurosci.2015 Apr 15; 35
AB  - PET imaging of nicotinic acetylcholine receptors (nAChRs) could become an effective tool for the diagnosis and therapy evaluation of neurologic diseases. Despite this, the role of nAChRs α4β2 receptors after brain diseases such as cerebral ischemia and its involvement in inflammatory reaction is still largely unknown. To investigate this, we performed in parallel in vivo magnetic resonance imaging (MRI) and positron emission tomography (PET) with 2[18F]-fluoro-A85380 and [11C]PK11195 at 1, 3, 7, 14, 21, and 28 d after middle cerebral artery occlusion (MCAO) in rats. In the ischemic territory, PET with 2[18F]-fluoro-A85380 and [11C]PK11195 showed a progressive binding increase from days 3–7, followed by a progressive decrease from days 14–28 after cerebral ischemia onset. Ex vivo immunohistochemistry for the nicotinic α4β2 receptor and the mitochondrial translocator protein (18 kDa) (TSPO) confirmed the PET findings and demonstrated the overexpression of α4β2 receptors in both microglia/macrophages and astrocytes from days 7–28 after experimental ischemic stroke. Likewise, the role played by α4β2 receptors on neuroinflammation was supported by the increase of [11C]PK11195 binding in ischemic rats treated with the α4β2 antagonist dihydro-β-erythroidine hydrobromide (DHBE) at day 7 after MCAO. Finally, both functional and behavioral testing showed major impaired outcome at day 1 after ischemia onset, followed by a recovery of the sensorimotor function and dexterity from days 21–28 after experimental stroke. Together, these results suggest that the nicotinic α4β2 receptor could have a key role in the inflammatory reaction underlying cerebral ischemia in rats.