Vagus Nerve Stimulation has Antidepressant Effects in the Kainic Acid Model for Temporal Lobe Epilepsy

• Published in: Brain stimulation Vol. 8; no. 1; pp. 13 - 20
• Main Authors: Grimonprez, Annelies, Raedt, Robrecht, Dauwe, Ine, Mollet, Lies, Larsen, Lars Emil, Meurs, Alfred, De Herdt, Veerle, Wadman, Wytse, Delbeke, Jean, Vonck, Kristl, Boon, Paul
• Format: Journal Article
• Language: English
• Published: United States Elsevier Inc 2015
• Subjects: Anhedonia; Animals; Choice Behavior; Depression; Depressive Disorder, Major - complications; Depressive Disorder, Major - therapy; Disease Models, Animal; Epilepsy, Temporal Lobe - chemically induced; Epilepsy, Temporal Lobe - complications; Epilepsy, Temporal Lobe - therapy; Kainic Acid; Kainic acid model; Male; Neurology; Rats; Status Epilepticus - chemically induced; Status Epilepticus - complications; Status Epilepticus - therapy; Temporal lobe epilepsy; Vagus Nerve Stimulation; kainic acid; saline; QAT; EEG; milliampere; Depression; Anhedonia; Kainic acid model; electroencephalogram; quinine aversion test; mA; KA; SPT; Vagus nerve stimulation; Temporal lobe epilepsy; VNS; saccharin preference test; SAL
• ISSN: 1935-861X; 1876-4754
• DOI: 10.1016/j.brs.2014.09.013

Abstract Background Depression is the most common psychiatric comorbidity in epilepsy patients. The lack of success with current pharmacological interventions for this patient population, highlights the importance of optimizing non-pharmacological neuromodulatory treatments such as vagus nerve stimulation (VNS). Studies on the antidepressant effect of VNS in epilepsy patients may be confounded by concurrent anti-epileptic drug therapy. To date, studies in epilepsy models overcoming this problem are lacking. Objective We investigated whether VNS affects anhedonia, a key symptom of major depression, in the kainic acid rat model for temporal lobe epilepsy. Methods Anhedonia was assessed in kainic acid (KA) and saline (SAL) injected rats using the saccharin preference test (SPT). To exclude differences in taste perception, the quinine aversion test (QAT) was performed. Both groups were randomly subdivided in a VNS and a SHAM group, yielding 4 experimental arms: KA-VNS, KA-SHAM, SAL-VNS and SAL-SHAM. Both VNS groups received 2 weeks of VNS, while the SHAM groups were not stimulated. Thereafter, the SPT and QAT were repeated. Results Saccharin preference was significantly reduced in the KA compared to the SAL rats ( P  < 0.05), without differences in quinine aversion. Two weeks of VNS significantly increased the saccharin preference in the KA-VNS group ( P  < 0.05), while it had no effect on quinine aversion. No effects of VNS or SHAM were found in the other groups. Conclusion The KA rats displayed anhedonia which was significantly decreased by VNS, indicating that this neuromodulatory treatment could likewise diminish depressive symptoms in patients suffering from temporal lobe epilepsy and comorbid depression.