The impact and mechanism of ampakine CX1739 on protection against respiratory depression in rats

Future Med Chem. 2020 Dec;12(23):2093-2104. doi: 10.4155/fmc-2020-0256. Epub 2020 Oct 8.

Abstract

Background: Abuse of analgesic and sedative drugs often leads to severe respiratory depression and sometimes death. Approximately 69,000 people worldwide die annually from opioid overdoses. Purpose: This work aimed to investigate whether CX1739 can be used for emergency treatment of acute respiratory depression due to drug abuse. Results: First, the results clarify that CX1739 is a low-impact ampakine that can safely activate α-amino-3-hydroxy-5-methyl-4-isoxazolepropionic acid (AMPA) receptors without causing excito-neurotoxicity. Second, CX1739 rapidly crossed the blood-brain barrier (Tmax = 2 min), which meets the requirement of rapid onset of action in vivo. Our work provides preliminarily confirmation that high-dose intravenous administration of CX1739 can immediately reverse respiratory depression in animal models of respiratory depression caused by opioid agonist 030418, pentobarbital sodium and ethanol.

Keywords: CX1739; ampakine; drug abuse; respiratory depression.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Analgesics, Opioid / chemical synthesis
  • Analgesics, Opioid / chemistry
  • Analgesics, Opioid / pharmacology*
  • Animals
  • Blood-Brain Barrier / drug effects
  • Male
  • Molecular Structure
  • Protective Agents / chemical synthesis
  • Protective Agents / chemistry
  • Protective Agents / pharmacology*
  • Rats
  • Rats, Sprague-Dawley
  • Respiratory Insufficiency / drug therapy*

Substances

  • Analgesics, Opioid
  • Protective Agents