Neurotransmitter Mechanisms of Ketamine and Ketamine–Magnesium Sulfate-Induced Hypothermia: Evidence for Serotonergic and Adrenergic Involvement Without GABAA Contributions

<b>Background:</b> Ketamine and magnesium sulfate are commonly used perioperatively to prevent shivering, a frequent and clinically relevant complication of spinal and general anesthesia. Although their hypothermic effects are well documented, the neurotransmitter mechanisms underlying these effects remain insufficiently understood. This study examines whether serotonergic, adrenergic (α<sub>2</sub>), and GABAergic (GABA<sub>A</sub>) systems contribute to hypothermia induced by ketamine and a ketamine-magnesium sulfate combination. <b>Methods:</b> Body temperature was measured in Wistar rats after administration of ketamine (10 mg/kg) or the ketamine (5 mg/kg)-magnesium sulfate (5 mg/kg) combination. To assess neurotransmitter involvement, animals received yohimbine (α<sub>2</sub> antagonist), methysergide (non-selective 5-HT antagonist), or bicuculline (GABA<sub>A</sub> antagonist) prior to ketamine or the drug combination. Data were analyzed using two-way repeated measures ANOVA followed by Tukey's post hoc test. <b>Results:</b> Yohimbine at 0.5 and 1 mg/kg significantly potentiated ketamine-induced hypothermia, while only 3 mg/kg enhanced the effect of the ketamine-magnesium sulfate combination. Methysergide had a bidirectional influence: 1 mg/kg methysergide deepened ketamine-induced hypothermia, whereas 0.5 mg/kg methysergide attenuated the hypothermic effect of the ketamine-magnesium sulfate combination. Bicuculline (1-2 mg/kg) did not alter the hypothermic responses to ketamine or the combination. <b>Conclusions:</b> These findings indicate that ketamine- and ketamine-magnesium sulfate-induced hypothermia is primarily modulated by serotonergic and adrenergic mechanisms, whereas GABA<sub>A</sub> receptor-dependent pathways do not appear to play a major role under the experimental conditions used. These results provide new mechanistic insights into NMDA antagonist-related thermoregulation and may help inform anesthetic strategies for shivering prevention and maintenance of perioperative thermal stability.

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Publication Details

Journal
Brain Sciences
Published
2026-02-04
DOI
https://doi.org/10.3390/brainsci16020189
Primary Topic
Thermal Regulation in Medicine
Type
article
Field-Weighted Citation Impact
0.00

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article

Neurotransmitter Mechanisms of Ketamine and Ketamine–Magnesium Sulfate-Induced Hypothermia: Evidence for Serotonergic and Adrenergic Involvement Without GABAA Contributions

Dragana Srebro, Ivana Ćirković, Ana Jotić, Sonja Vučković et al.
Brain Sciences
Thermal Regulation in Medicine
article

Neurotransmitter Mechanisms of Ketamine and Ketamine–Magnesium Sulfate-Induced Hypothermia: Evidence for Serotonergic and Adrenergic Involvement Without GABAA Contributions

Dragana Srebro, Ivana Ćirković, Ana Jotić, Sonja Vučković, Lara Samardžić, Katarina Savić Vujović, Branislava Medić
article en

Abstract

<b>Background:</b> Ketamine and magnesium sulfate are commonly used perioperatively to prevent shivering, a frequent and clinically relevant complication of spinal and general anesthesia. Although their hypothermic effects are well documented, the neurotransmitter mechanisms underlying these effects remain insufficiently understood. This study examines whether serotonergic, adrenergic (α<sub>2</sub>), and GABAergic (GABA<sub>A</sub>) systems contribute to hypothermia induced by ketamine and a ketamine-magnesium sulfate combination. <b>Methods:</b> Body temperature was measured in Wistar rats after administration of ketamine (10 mg/kg) or the ketamine (5 mg/kg)-magnesium sulfate (5 mg/kg) combination. To assess neurotransmitter involvement, animals received yohimbine (α<sub>2</sub> antagonist), methysergide (non-selective 5-HT antagonist), or bicuculline (GABA<sub>A</sub> antagonist) prior to ketamine or the drug combination. Data were analyzed using two-way repeated measures ANOVA followed by Tukey's post hoc test. <b>Results:</b> Yohimbine at 0.5 and 1 mg/kg significantly potentiated ketamine-induced hypothermia, while only 3 mg/kg enhanced the effect of the ketamine-magnesium sulfate combination. Methysergide had a bidirectional influence: 1 mg/kg methysergide deepened ketamine-induced hypothermia, whereas 0.5 mg/kg methysergide attenuated the hypothermic effect of the ketamine-magnesium sulfate combination. Bicuculline (1-2 mg/kg) did not alter the hypothermic responses to ketamine or the combination. <b>Conclusions:</b> These findings indicate that ketamine- and ketamine-magnesium sulfate-induced hypothermia is primarily modulated by serotonergic and adrenergic mechanisms, whereas GABA<sub>A</sub> receptor-dependent pathways do not appear to play a major role under the experimental conditions used. These results provide new mechanistic insights into NMDA antagonist-related thermoregulation and may help inform anesthetic strategies for shivering prevention and maintenance of perioperative thermal stability.

Brain SciencesVol. 16(2)
University of Belgrade (RS)
National Institutes of Health
Good health and well-being
Openalex Percentile: Top 66%
Thermal Regulation in Medicine
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