5-HT 4(a) Receptors Avert Opioid-Induced Breathing Depression Without Loss of Analgesia

Author:

Manzke Till1,Guenther Ulf1,Ponimaskin Evgeni G.1,Haller Miriam1,Dutschmann Mathias1,Schwarzacher Stephan1,Richter Diethelm W.1

Affiliation:

1. Department of Neuro- and Sensory Physiology, University of Goettingen, Humboldtallee 23, 37073 Goettingen, Germany. Center of Anesthesiology, University of Goettingen, Robert-KochStreet 40, 37075 Goettingen, Germany. Department of Anatomy, Kreuzbergring 36, 37075 Goettingen, Germany.

Abstract

Opiates are widely used analgesics in anesthesiology, but they have serious adverse effects such as depression of breathing. This is caused by direct inhibition of rhythm-generating respiratory neurons in the Pre-Boetzinger complex (PBC) of the brainstem. We report that serotonin 4(a) [5-HT 4( a ) ] receptors are strongly expressed in respiratory PBCneurons and that their selective activation protects spontaneous respiratory activity. Treatment of rats with a 5-HT 4 receptor–specific agonist overcame fentanyl-induced respiratory depression and reestablished stable respiratory rhythm without loss of fentanyl's analgesic effect. These findings imply the prospect of a fine-tuned recovery from opioid-induced respiratory depression, through adjustment of intracellular adenosine 3′,5′-monophosphate levels through the convergent signaling pathways in neurons.

Publisher

American Association for the Advancement of Science (AAAS)

Subject

Multidisciplinary

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