Related Experiment Video
Updated: Aug 16, 2026

09:36
Halogenated Agent Delivery in Porcine Model of Acute Respiratory Distress Syndrome via an Intensive Care Unit Type Device
Published on: September 24, 2020
Xenon does not trigger malignant hyperthermia in susceptible swine
1Universitätsklinik für Anästhesiologie, Universität Ulm, Germany. gebhard.froeba@medizin.uni-ulm.de
Anesthesiology
|October 16, 1999
Summary
Xenon anesthesia did not trigger malignant hyperthermia in susceptible swine. In contrast, halothane and succinylcholine rapidly induced fatal malignant hyperthermia episodes in all animals tested.
Area of Science:
- Anesthesiology
- Pharmacology
- Veterinary Medicine
Background:
- Xenon, a noble gas, possesses anesthetic properties and is being explored for human use.
- Malignant hyperthermia (MH) is a severe, hypermetabolic complication of anesthesia.
- Investigating xenon's potential to trigger MH in susceptible individuals is crucial for patient safety.
Purpose of the Study:
- To determine if xenon anesthesia can induce malignant hyperthermia in MH-susceptible swine.
- To assess the safety of xenon as an anesthetic agent in a preclinical model of MH.
Main Methods:
- Nine MH-susceptible Pietrain swine were ventilated with 70% xenon/oxygen for 2 hours.
- Hemodynamic, metabolic, and plasma catecholamine levels were monitored throughout xenon exposure.
- Animals were subsequently challenged with halothane and succinylcholine to confirm MH susceptibility.
Main Results:
- Xenon administration did not elicit any signs or biochemical markers of malignant hyperthermia.
- All swine developed fulminant and fatal malignant hyperthermia within 20 minutes after halothane and succinylcholine administration.
- This confirms the animals' susceptibility to known MH triggers.
Conclusions:
- Xenon does not appear to trigger malignant hyperthermia in MH-susceptible swine.
- Xenon may represent a safer anesthetic alternative for patients with MH susceptibility.
- Further research is warranted to confirm xenon's safety profile in human MH-susceptible populations.

