Precise Control of Target Temperature Using N(6)-Cyclohexyladenosine and Real-Time Control of Surface Temperature

利用N(6)-环己基腺苷精确控制目标温度并实时控制表面温度

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Abstract

Targeted temperature management is standard of care for cardiac arrest and is in clinical trials for stroke. N(6)-cyclohexyladenosine (CHA), an A(1) adenosine receptor (A(1)AR) agonist, inhibits thermogenesis and induces onset of hibernation in hibernating species. Despite promising thermolytic efficacy of CHA, prior work has failed to achieve and maintain a prescribed target core body temperature (T(b)) between 32°C and 34°C for 24 hours. We instrumented Sprague-Dawley rats (n = 19) with indwelling arterial and venous cannulae and a transmitter for monitoring T(b) and ECG, then administered CHA via continuous IV infusion or intraperitoneal (IP) injection. In the first experiment (n = 11), we modulated ambient temperature and increased the dose of CHA in an attempt to manage T(b). In the second experiment (n = 8), we administered CHA (0.25 mg/[kg·h]) via continuous IV infusion and modulated cage surface temperature to control T(b). We rewarmed animals by increasing surface temperature at 1°C h(-1) and discontinued CHA after T(b) reached 36.5°C. T(b), brain temperature (T(brain)), heart rate, blood gas, and electrolytes were also monitored. Results show that titrating dose to adjust for individual variation in response to CHA led to tolerance and failed to manage a prescribed T(b). Starting with a dose (0.25 mg/[kg·h]) and modulating surface temperature to prevent overcooling proved to be an effective means to achieve and maintain T(b) between 32°C and 34°C for 24 hours. Increasing surface temperature to 37°C during CHA administration brought T(b) back to normothermic levels. All animals treated in this way rewarmed without incident. During the initiation of cooling, we observed bradycardia within 30 minutes of the start of IV infusion, transient hyperglycemia, and a mild hypercapnia; the latter normalized via metabolic compensation. In conclusion, we describe an intravenous delivery protocol for CHA at 0.25 mg/(kg·h) that, when coupled with conductive cooling, achieves and maintains a prescribed and consistent target T(b) between 32°C and 34°C for 24 hours.

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