raclopride and Infarction--Middle-Cerebral-Artery

raclopride has been researched along with Infarction--Middle-Cerebral-Artery* in 2 studies

Other Studies

2 other study(ies) available for raclopride and Infarction--Middle-Cerebral-Artery

ArticleYear
Longitudinal imaging of the availability of dopamine transporter and D2 receptor in rat striatum following mild ischemia.
    Journal of cerebral blood flow and metabolism : official journal of the International Society of Cerebral Blood Flow and Metabolism, 2017, Volume: 37, Issue:2

    The changes in the availability of striatal dopamine transporter and dopamine D2 receptor after mild focal ischemia in rats were measured using a small animal positron emission tomography system. Mild focal ischemia was induced by 20-minute middle cerebral artery occlusion. [

    Topics: Animals; Corpus Striatum; Dopamine Plasma Membrane Transport Proteins; Infarction, Middle Cerebral Artery; Male; Positron-Emission Tomography; Raclopride; Rats, Wistar; Receptors, Dopamine D2

2017
In vivo imaging of dopaminergic neurotransmission after transient focal ischemia in rats.
    Journal of cerebral blood flow and metabolism : official journal of the International Society of Cerebral Blood Flow and Metabolism, 2013, Volume: 33, Issue:2

    The precise biologic mechanisms involved in functional recovery processes in response to stroke such as dopaminergic neurotransmission are still largely unknown. For this purpose, we performed in parallel in vivo magnetic resonance imaging and positron emission tomography (PET) with [(18)F]fluorodeoxyglucose ([(18)F]FDG) and [(11)C]raclopride at 1, 3, 7, 14, 21, and 28 days after middle cerebral artery occlusion in rats. In the ischemic territory, PET [(18)F]FDG showed a initial decrease in cerebral metabolism followed by a time-dependent recovery to quasi-normal values at day 14 after ischemia. The PET with [(11)C]raclopride, a ligand for dopamine D(2) receptor, showed a sustained binding during the first week after ischemia that declined dramatically from day 14 to day 28. Interestingly, a slight increase in [(11)C]raclopride binding was observed at days 1 to 3 followed by the uppermost binding at day 7 in the contralateral territory. Likewise, in vitro autoradiography using [(3)H]raclopride confirmed these in vivo results. Finally, the neurologic test showed major neurologic impairment at day 1 followed by a recovery of the cerebral function at day 28 after cerebral ischemia. Taken together, these results might suggest that dopamine D(2) receptor changes in the contralateral hemisphere could have a key role in functional recovery after cerebral ischemia.

    Topics: Animals; Brain Ischemia; Dopamine Antagonists; Dopaminergic Neurons; Fluorodeoxyglucose F18; Infarction, Middle Cerebral Artery; Male; Positron-Emission Tomography; Raclopride; Radiography; Radiopharmaceuticals; Rats; Rats, Sprague-Dawley; Receptors, Dopamine D2; Stroke; Synaptic Transmission; Time Factors

2013