High-frequency stimulation of the hippocampus protects against seizure activity and hippocampal neuronal apoptosis induced by kainic acid administration in macaques

Kainic acid (KA) administration is known to cause seizures and neuronal death in the hippocampus. High-frequency stimulation (HFS) of the hippocampus can be a promising method in the treatment of epilepsy while the mechanism of action is unknown yet. It remains unknown whether HFS is neuroprotective for hippocampal neurons following KA-induced seizures in macaques, although HFS has neuroprotective effects in animal models of Parkinson's disease. We therefore examined the effects of HFS on KA-induced seizures and neuronal survival in macaque's hippocampus. Seizure frequency following KA that led to seizures in macaques was strongly reduced by HFS of the hippocampus. In addition, administration of KA led to marked neuronal apoptosis in the hippocampus, accompanied by increased levels of Bax, activated caspase-3 and decreased levels of Bcl-2. HFS was found to attenuate changes in apoptosis-related proteins and robustly decreased neuronal loss following KA administration. These data indicate that hippocampal HFS can protect hippocampal neurons against KA neurotoxicity, and that HFS neuroprotection is likely to operate with inhibition of apoptosis.

[1]  D. Pei,et al.  Coactivation of GABA receptors inhibits the JNK3 apoptotic pathway via disassembly of GluR6‐PSD‐95‐MLK3 signaling module in KA‐induced seizure , 2010, Epilepsia.

[2]  R. Racine,et al.  Modification of seizure activity by electrical stimulation. 3. Mechanisms. , 1972, Electroencephalography and clinical neurophysiology.

[3]  A. Cole,et al.  Anatomical studies of DNA fragmentation in rat brain after systemic kainate administration , 1996, Neuroscience.

[4]  Effect of deep brain stimulation on substantia nigra neurons in a rat model of Parkinson's disease. , 2012, Chinese medical journal.

[5]  M. Grütter,et al.  Caspases: key players in programmed cell death. , 2000, Current opinion in structural biology.

[6]  M. Behbehani,et al.  Subthalamic nucleus stimulation increases brain derived neurotrophic factor in the nigrostriatal system and primary motor cortex. , 2011, Journal of Parkinson's disease.

[7]  S. Capaccioli,et al.  Bcl-2 phosphorylation and apoptosis activated by damaged microtubules require mTOR and are regulated by Akt , 2004, Oncogene.

[8]  S. Cory,et al.  The Bcl2 family: regulators of the cellular life-or-death switch , 2002, Nature Reviews Cancer.

[9]  Á. Simonyi,et al.  Kainic acid-mediated excitotoxicity as a model for neurodegeneration , 2007, Molecular Neurobiology.

[10]  Y. Ben-Ari,et al.  Limbic seizure and brain damage produced by kainic acid: Mechanisms and relevance to human temporal lobe epilepsy , 1985, Neuroscience.

[11]  M. Behbehani,et al.  Stimulation of the rat subthalamic nucleus is neuroprotective following significant nigral dopamine neuron loss , 2010, Neurobiology of Disease.

[12]  C. Wasterlain,et al.  Status epilepticus: pathophysiology and management in adults , 2006, The Lancet Neurology.

[13]  C. Thompson,et al.  bcl-x, a bcl-2-related gene that functions as a dominant regulator of apoptotic cell death , 1993, Cell.

[14]  M Velasco,et al.  Subacute Electrical Stimulation of the Hippocampus Blocks Intractable Temporal Lobe Seizures and Paroxysmal EEG Activities , 2000, Epilepsia.

[15]  Shigeomi Shimizu,et al.  Bcl‐2 family: Life‐or‐death switch , 2000, FEBS letters.

[16]  John S Duncan,et al.  Adult epilepsy , 2006, The Lancet.

[17]  M. Zimmermann,et al.  Up-regulation of bax and down-regulation of bc1–2 is associated with kainate-induced apoptosis in mouse brain , 1995, Neuroscience Letters.

[18]  Dirk Van Roost,et al.  Deep Brain Stimulation in Patients with Refractory Temporal Lobe Epilepsy , 2007, Epilepsia.

[19]  S. Orozco-Suárez,et al.  Effects of high frequency electrical stimulation and R-verapamil on seizure susceptibility and glutamate and GABA release in a model of phenytoin-resistant seizures , 2011, Neuropharmacology.

[20]  R. Racine,et al.  Modification of seizure activity by electrical stimulation. II. Motor seizure. , 1972, Electroencephalography and clinical neurophysiology.

[21]  D. Green,et al.  Suicidal Tendencies: Apoptotic Cell Death by Caspase Family Proteinases* , 1999, The Journal of Biological Chemistry.

[22]  J C Reed,et al.  Mechanisms of apoptosis. , 2000, The American journal of pathology.

[23]  Claudio Pollo,et al.  Electrode location and clinical outcome in hippocampal electrical stimulation for mesial temporal lobe epilepsy , 2013, Seizure.

[24]  Kristl Vonck,et al.  Long‐term amygdalohippocampal stimulation for refractory temporal lobe epilepsy , 2002, Annals of neurology.

[25]  L. Covolan,et al.  Behavioral characterization of pentylenetetrazol-induced seizures in the marmoset , 2008, Epilepsy & Behavior.

[26]  D. Fujikawa,et al.  Prolonged seizures and cellular injury: Understanding the connection , 2005, Epilepsy & Behavior.

[27]  D. Choi Excitotoxic cell death. , 1992, Journal of neurobiology.

[28]  A. Toga,et al.  The Rhesus Monkey Brain in Stereotaxic Coordinates , 1999 .

[29]  Richard J Smeyne,et al.  Caspase-3-dependent neuronal death in the hippocampus following kainic acid treatment. , 1999, Brain research. Molecular brain research.

[30]  G. Collingridge,et al.  Synaptic Kainate Receptors in CA1 Interneurons Gate the Threshold of Theta-Frequency-Induced Long-Term Potentiation , 2012, The Journal of Neuroscience.

[31]  E. Pralong,et al.  Chronic deep brain stimulation in mesial temporal lobe epilepsy , 2011, Seizure.