Reversal of Propofol-induced Depression of the Hypoxic Ventilatory Response by BK-channel Blocker ENA-001: A Randomized Controlled Trial

Author:

Jansen Simone C.1,van Lemmen Maarten2,Olofsen Erik3,Moss Laurence4,Pergolizzi Joseph V.5,Miller Thomas6,Colucci Robert D.7,van Velzen Monique8,Kremer Philip9,Dahan Albert10ORCID,van der Schrier Rutger11,Niesters Marieke12

Affiliation:

1. 1Department of Anesthesiology, Leiden University Medical Center, Leiden, The Netherlands.

2. 2Department of Anesthesiology, Leiden University Medical Center, Leiden, The Netherlands.

3. 3Department of Anesthesiology, Leiden University Medical Center, Leiden, The Netherlands.

4. 4Centre for Human Drug Research, Leiden, The Netherlands.

5. 5Enalare Therapeutics Inc., Princeton, New Jersey; NEMA Research Inc., Naples, Florida.

6. 6Enalare Therapeutics Inc., Princeton, New Jersey; Department of Pediatrics, Sidney Kimmel Medical College, Thomas Jefferson University, Philadelphia, Pennsylvania.

7. 7NEMA Research Inc., Naples, Florida; Colucci & Associates, LLC, Newtown, Connecticut.

8. 8Department of Anesthesiology, Leiden University Medical Center, Leiden, The Netherlands.

9. 9Centre for Human Drug Research, Leiden, The Netherlands.

10. 10Department of Anesthesiology, Leiden University Medical Center, Leiden, The Netherlands; PainLess Foundation, Leiden, The Netherlands.

11. 11Department of Anesthesiology, Leiden University Medical Center, Leiden, The Netherlands.

12. 12Department of Anesthesiology, Leiden University Medical Center, Leiden, The Netherlands; PainLess Foundation, Leiden, The Netherlands.

Abstract

Background The use of anesthetics may result in depression of the hypoxic ventilatory response. Since there are no receptor-specific antagonists for most anesthetics, there is the need for agnostic respiratory stimulants that increase respiratory drive irrespective of its cause. The authors tested whether ENA-001, an agnostic respiratory stimulant that blocks carotid body BK-channels, could restore the hypoxic ventilatory response during propofol infusion. They hypothesize that ENA-001 is able to fully restore the hypoxic ventilatory response. Methods In this randomized, double-blind crossover trial, 14 male and female healthy volunteers were randomized to receive placebo and low- and high-dose ENA-001 on three separate occasions. On each occasion, isohypercapnic hypoxic ventilatory responses were measured during a fixed sequence of placebo, followed by low- and high-dose propofol infusion. The authors conducted a population pharmacokinetic/pharmacodynamic analysis that included oxygen and carbon dioxide kinetics. Results Twelve subjects completed the three sessions; no serious adverse events occurred. The propofol concentrations were 0.6 and 2.0 µg/ml at low and high dose, respectively. The ENA-001 concentrations were 0.6 and 1.0 µg/ml at low and high dose, respectively. The propofol concentration that reduced the hypoxic ventilatory response by 50% was 1.47 ± 0.20 µg/ml. The steady state ENA-001 concentration to increase the depressed ventilatory response by 50% was 0.51 ± 0.04 µg/ml. A concentration of 1 µg/ml ENA-001 was required for full reversal of the propofol effect at the propofol concentration that reduced the hypoxic ventilatory response by 50%. Conclusions In this pilot study, the authors demonstrated that ENA-001 restored the hypoxic ventilatory response impaired by propofol. This finding is not only of clinical importance but also provides mechanistic insights into the peripheral stimulation of breathing with ENA-001 overcoming central depression by propofol. Editor’s Perspective What We Already Know about This Topic What This Article Tells Us That Is New

Publisher

Ovid Technologies (Wolters Kluwer Health)

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