Synergistic Effects of Commonly Used Intensive Care Unit Drugs and High Temperature on Skeletal Muscle at the Cellular and Tissue Levels.

BACKGROUND

Several drugs are commonly administered to patients with high body temperature in intensive care units. However, previous in vitro studies have investigated only the independent effects of high temperatures or drugs on various cultured cells. This study explored the hypothesis that pharmacologic treatment with representative intensive care unit drugs induces lethal effects on cultured skeletal muscle and engineered muscle tissue at high temperatures.

METHODS

Human skeletal muscle cultures were treated with the representative drugs propofol, dexmedetomidine, and acetaminophen at 37°, 39°, and 41°C for various exposure times. To investigate the effects of the drug treatments, cell viability, lactate dehydrogenase activity, caspase activity, and endoplasmic reticulum (ER) stress were analyzed. Conformational changes in myotubes and functional changes in contractile muscle tissue were also assessed. All experiments were repeated at least three times.

RESULTS

Dexmedetomidine and acetaminophen had no observable adverse effects at high temperatures, whereas propofol treatment at greater than 200 μM resulted in increased lactate dehydrogenase activity and myotube detachment. Furthermore, this cellular injury was associated with intracellular calcium overload and upregulation of the ER stress-related genes CHOP, GRP78/Bip, and GRP94. Propofol treatment also decreased the contractile ability of muscle tissues at 39°C ( vs . 37°C propofol; 95% CI, 30.72 to 114.87%; P < 0.001). Additionally, although tauroursodeoxycholic acid, an ER stress inhibitor, alleviated the increase in caspase-3/7 activity at 39°C (95% CI, 38.10 to 145.22%; P < 0.001) and mitigated myotube detachment, it did not result in notable functional improvement in muscle contraction.

CONCLUSIONS

These results demonstrate that propofol had harmful effects on skeletal muscle cells and tissues at high temperatures in vitro . As these synergistic effects were closely associated with ER stress, tauroursodeoxycholic acid could mitigate propofol-induced apoptosis at high temperatures. These findings could help improve drug treatment for patients, including their functional prognosis in the clinical setting.