Respiratory Effects of the Atypical Tricyclic Antidepressant Tianeptine in Human Models of Opioid-induced Respiratory Depression

Anesthesiology. 2022 Oct 1;137(4):446-458. doi: 10.1097/ALN.0000000000004324.

Abstract

Background: Animal data suggest that the antidepressant and α-amino-3-hydroxy-5-methyl-4-isoxazolepropionic acid receptor modulator tianeptine is able to prevent opioid-induced respiratory depression. The hypothesis was that oral or intravenous tianeptine can effectively prevent or counteract opioid-induced respiratory depression in humans.

Methods: Healthy male and female volunteers participated in two studies that had a randomized, double blind, placebo-controlled, crossover design. First, oral tianeptine (37.5-, 50-, and 100-mg doses with 8 subjects) pretreatment followed by induction of alfentanil-induced respiratory depression (alfentanil target concentration, 100 ng/ml) was tested. Primary endpoint was ventilation at an extrapolated end-tidal carbon dioxide concentration of 55 mmHg (V̇E55). Next, the ability of four subsequent and increasing infusions of intravenous tianeptine (target tianeptine plasma concentrations 400, 1,000, 1,500, and 2,000 ng/ml, each given over 15 min) to counteract remifentanil-induced respiratory depression was determined in 15 volunteers. Ventilation was measured at isohypercpania (baseline ventilation 20 ± 2 l/min). The primary endpoint was minute ventilation during the 60 min of tianeptine versus placebo infusion.

Results: Alfentanil reduced V̇E55 to 13.7 (95% CI, 8.6 to 18.8) l/min after placebo pretreatment and to 17.9 (10.2 to 25.7) l/min after 50-mg tianeptine pretreatment (mean difference between treatments 4.2 (-11.5 to 3.0) l/min, P = 0.070). Intravenous tianeptine in the measured concentration range of 500 to 2,000 ng/ml did not stimulate ventilation but instead worsened remifentanil-induced respiratory depression: tianeptine, 9.6 ± 0.8 l/min versus placebo 15.0 ± 0.9 l/min; mean difference, 5.3 l/min; 95% CI, 2.5 to 8.2 l/min; P = 0.001, after 1 h of treatment.

Conclusions: Neither oral nor intravenous tianeptine were respiratory stimulants. Intravenous tianeptine over the concentration range of 500 to 2000 ng/ml worsened respiratory depression induced by remifentanil.

Publication types

  • Randomized Controlled Trial
  • Research Support, Non-U.S. Gov't
  • Research Support, U.S. Gov't, P.H.S.

MeSH terms

  • Alfentanil / pharmacology
  • Alfentanil / therapeutic use
  • Analgesics, Opioid / therapeutic use
  • Antidepressive Agents, Tricyclic / adverse effects
  • Carbon Dioxide / adverse effects
  • Double-Blind Method
  • Female
  • Humans
  • Male
  • Remifentanil / adverse effects
  • Respiratory Insufficiency* / chemically induced
  • Respiratory Insufficiency* / drug therapy
  • Respiratory System Agents*
  • Thiazepines
  • alpha-Amino-3-hydroxy-5-methyl-4-isoxazolepropionic Acid / adverse effects

Substances

  • Analgesics, Opioid
  • Antidepressive Agents, Tricyclic
  • Respiratory System Agents
  • Thiazepines
  • tianeptine
  • Carbon Dioxide
  • Alfentanil
  • alpha-Amino-3-hydroxy-5-methyl-4-isoxazolepropionic Acid
  • Remifentanil