2020
DOI: 10.3390/neurolint12030017
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Istradefylline to Treat Patients with Parkinson’s Disease Experiencing “Off” Episodes: A Comprehensive Review

Abstract: Parkinson’s disease (PD) is a common neurodegenerative disorder that leads to significant morbidity and disability. PD is caused by a loss of dopaminergic, cholinergic, serotonergic, and noradrenergic neurons in the central nervous system (CNS), and peripherally; the syndromic parkinsonism symptoms of movement disorder, gait disorder, rigidity and tremor are mostly driven by the loss of these neurons in the basal ganglia. Unfortunately, a significant proportion of patients taking levodopa, the standard of care… Show more

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Cited by 28 publications
(12 citation statements)
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“…Adora2a, encoding for Adenosine A 2A receptor (A 2A R) is a G-protein coupled receptor that regulates the balance of adenosine/dopamine signalling through its interactions with D 2 R [ 95 97 ]. Adenosine decreases dopamine signalling through D 2 R, while A 2A R antagonists, such as caffeine are believed to enhance dopamine signalling through D 2 R [ 96 , 98 , 99 ]. Our RNAseq analysis revealed a downregulation of striatal and PFC Adora2a expression in Gdnf cHyper ;Nestin-Cre mice (Figs.…”
Section: Resultsmentioning
confidence: 99%
“…Adora2a, encoding for Adenosine A 2A receptor (A 2A R) is a G-protein coupled receptor that regulates the balance of adenosine/dopamine signalling through its interactions with D 2 R [ 95 97 ]. Adenosine decreases dopamine signalling through D 2 R, while A 2A R antagonists, such as caffeine are believed to enhance dopamine signalling through D 2 R [ 96 , 98 , 99 ]. Our RNAseq analysis revealed a downregulation of striatal and PFC Adora2a expression in Gdnf cHyper ;Nestin-Cre mice (Figs.…”
Section: Resultsmentioning
confidence: 99%
“…A 1 receptor knockout mice are more vulnerable to hypoxic/ischemic damage (Johansson et al, 2001), whereas the converse is true in A 2A receptor knockout mice (Chen et al, 1999). A 2A receptor antagonists alleviate hypoxic/ischemic damage in vivo (Gao and Phillis, 1994;Phillis, 1995;Von Lubitz et al, 1995) and the A 2A receptor antagonist KW-6002 is now FDA approved as an adjunct treatment for Parkinson's disease (Berger et al, 2020;Chen and Cunha, 2020). The Good: Adenosine increases seizure threshold, is critical for seizure termination, and may alleviate some of the adverse effects of seizures.…”
Section: Adenosine Is Neuroprotective Under Hypoxic Conditionsmentioning
confidence: 99%
“…These trials were evaluated by the FDA in 2008, which did not approve its use due to concern that the motor improvement shown in the trials was too small and not clinically significant. Further trials were then conducted, 22 and based on the newer data, the FDA did approve its use in 2019. [27][28][29] New formulations of levodopa designed to be used as needed…”
Section: Medications For Treatment Of Motor Fluctuationsmentioning
confidence: 99%