Journal article
MK-212 precipitates seizure-induced death in amygdala-kindled mice via a non-5-HT2C receptor-mediated mechanism
Epilepsy & behavior, Vol.167, 110385
06/2025
DOI: 10.1016/j.yebeh.2025.110385
PMCID: PMC12034472
PMID: 40132446
Abstract
[Display omitted]
•The 5-HT2C receptor agonist MK-212 facilitates seizure-induced death following amygdala kindled seizures in mice.•The effects of MK-212 persist in mice lacking the 5-HT2C receptor.•MK-212 may allow the amygdala kindling model, which does not traditionally feature seizure-induced death, to be used in examinations of SUDEP pathophysiology.
Epilepsy is a common neurological condition that affects over 65 million people worldwide. Despite an increasing number of anti-seizure medications being made available, many patients do not find seizure freedom with medication. The leading cause of death in this refractory population is sudden unexpected death in epilepsy (SUDEP). Both human and animal research has implicated serotonin (5-HT) in modulating seizure proclivity, severity, and mortality. More recently, evidence has pointed to the 5-HT2C receptor as a salient target for investigating the mechanisms of seizure facilitation and mortality. Various seizures models have been used previously to assess the role of the 5-HT2C receptor in seizure expression and morphology. However, limbic kindling models have been underutilized in this endeavor. We used the selective 5-HT2C receptor agonist MK-212 to examine the effect of 5-HT2C receptor activation in amygdala kindled mice. C57BL/6J mice were instrumented with an EEG/EMG headmount and a bipolar electrode in the basolateral amygdala (BLA). The animals then received vehicle or MK-212 (10, 30 mg/kg) prior to seizure induction. 12.5 % of WT animals that received 10 mg/kg MK-212 experienced seizure-induced respiratory arrest and died following seizure induction. When the dose was raised to 30 mg/kg, 100 % of the animals succumbed following a seizure. These fatal seizures persisted when the same doses of MK-212 were administered to mice lacking the 5-HT2C receptor. This suggests that a non-5-HT2C mediated effect of MK-212 facilitates seizure-induced death in a dose-dependent manner. While amygdala kindling is not a model that is traditionally associated with seizure-induced death, these results suggest that there are circuits that, when recruited, will cause death following kindled seizures. Uncovering these circuits will both deepen our understanding of the amygdala kindling model and provide a new technique for researchers to test novel therapeutic interventions to lessen SUDEP risk.
Details
- Title: Subtitle
- MK-212 precipitates seizure-induced death in amygdala-kindled mice via a non-5-HT2C receptor-mediated mechanism
- Creators
- Katelyn G. Joyal - University of IowaNicole A. Boodhoo - University of IowaGordon F. Buchanan - University of Iowa
- Resource Type
- Journal article
- Publication Details
- Epilepsy & behavior, Vol.167, 110385
- DOI
- 10.1016/j.yebeh.2025.110385
- PMID
- 40132446
- PMCID
- PMC12034472
- NLM abbreviation
- Epilepsy Behav
- ISSN
- 1525-5050
- eISSN
- 1525-5069
- Publisher
- Elsevier Inc
- Grant note
- NIH/NINDS: F31 NS125955, R01 NS095842, NS129722 Iowa Office for Undergraduate Research (OUR) Fellowship AwardBeth L. Tross Epilepsy Professorship from the Carver College of Medicine at the University of Iowa
This work was supported by NIH/NINDS F31 NS125955 to K.G.J., an Iowa Office for Undergraduate Research (OUR) Fellowship Award to N. A.B., and NIH/NINDS R01 NS095842 and NS129722, and the Beth L. Tross Epilepsy Professorship from the Carver College of Medicine at the University of Iowa to G.F.B. Funding sources did not influence study design, data collection, analysis, interpretation, preparation of the manuscript, or the decision to publish.
- Language
- English
- Electronic publication date
- 03/25/2025
- Date published
- 06/2025
- Academic Unit
- Neurology; Iowa Neuroscience Institute
- Record Identifier
- 9984802193502771
Metrics
2 Record Views