The Good, the Bad, and the Deadly: Adenosinergic Mechanisms Underlying Sudden Unexpected Death in Epilepsy

被引:26
|
作者
Purnell, Benton [1 ]
Murugan, Madhuvika [1 ]
Jani, Raja [1 ]
Boison, Detlev [1 ,2 ,3 ]
机构
[1] Rutgers State Univ, Robert Wood Johnson Med Sch, Dept Neurosurg, Piscataway, NJ USA
[2] Rutgers State Univ, Dept Neurosurg, Rutgers Neurosurg HOPE Ctr, New Brunswick, NJ 08901 USA
[3] Rutgers State Univ, Brain Hlth Inst, Piscataway, NJ USA
关键词
adenosine; epilepsy; SUDEP; status epilepticus; seizure-induced respiratory arrest; adenosine kinase; adenosine receptors; epileptogenesis; ACTIVITY-DEPENDENT RELEASE; NOREPINEPHRINE REUPTAKE INHIBITOR; HYPERCAPNIC VENTILATORY RESPONSE; CORTICAL SPREADING DEPRESSION; GENERALIZED EEG SUPPRESSION; INDUCED RESPIRATORY ARREST; TRANSIENT FOCAL ISCHEMIA; CORTEX KINDLED SEIZURES; TEMPORAL-LOBE EPILEPSY; A(2A) RECEPTOR AGONIST;
D O I
10.3389/fnins.2021.708304
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
Adenosine is an inhibitory modulator of neuronal excitability. Neuronal activity results in increased adenosine release, thereby constraining excessive excitation. The exceptionally high neuronal activity of a seizure results in a surge in extracellular adenosine to concentrations many-fold higher than would be observed under normal conditions. In this review, we discuss the multifarious effects of adenosine signaling in the context of epilepsy, with emphasis on sudden unexpected death in epilepsy (SUDEP). We describe and categorize the beneficial, detrimental, and potentially deadly aspects of adenosine signaling. The good or beneficial characteristics of adenosine signaling in the context of seizures include: (1) its direct effect on seizure termination and the prevention of status epilepticus; (2) the vasodilatory effect of adenosine, potentially counteracting postictal vasoconstriction; (3) its neuroprotective effects under hypoxic conditions; and (4) its disease modifying antiepileptogenic effect. The bad or detrimental effects of adenosine signaling include: (1) its capacity to suppress breathing and contribute to peri-ictal respiratory dysfunction; (2) its contribution to postictal generalized EEG suppression (PGES); (3) the prolonged increase in extracellular adenosine following spreading depolarization waves may contribute to postictal neuronal dysfunction; (4) the excitatory effects of A(2A) receptor activation is thought to exacerbate seizures in some instances; and (5) its potential contributions to sleep alterations in epilepsy. Finally, the adverse effects of adenosine signaling may potentiate a deadly outcome in the form of SUDEP by suppressing breathing and arousal in the postictal period. Evidence from animal models suggests that excessive postictal adenosine signaling contributes to the pathophysiology of SUDEP. The goal of this review is to discuss the beneficial, harmful, and potentially deadly roles that adenosine plays in the context of epilepsy and to identify crucial gaps in knowledge where further investigation is necessary. By better understanding adenosine dynamics, we may gain insights into the treatment of epilepsy and the prevention of SUDEP.
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页数:15
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