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

Author:

Algera Hyke1,van der Schrier Rutger2,Cavalla David3,van Velzen Monique4,Roozekrans Margot5,McMorn Alison6,Snape Michael7,Horrigan Joseph P.8,Evans Stuart9,Kiernan Bernard10,Sarton Elise11,Olofsen Erik12,Niesters Marieke13,Dahan Albert14

Affiliation:

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

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

3. 3 Numedicus Ltd., Cambridge, United Kingdom

4. 4 Department of Anesthesiology, Leiden University Medical Center, Leiden, The Netherlands

5. 5 Department of Anesthesiology, Leiden University Medical Center, Leiden, The Netherlands; and Department of Anesthesiology, Noordwest Ziekenhuisgroep, Alkmaar, The Netherlands

6. 6 AMO Pharma Ltd., Leeds, United Kingdom

7. 7 AMO Pharma Ltd., Leeds, United Kingdom

8. 8 AMO Pharma Ltd., Leeds, United Kingdom

9. 9 AMO Pharma Ltd., Leeds, United Kingdom

10. 10 AMO Pharma Ltd., Leeds, United Kingdom

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

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

13. 13 Department of Anesthesiology, Leiden University Medical Center, Leiden, The Netherlands

14. 14 Department of Anesthesiology, Leiden University Medical Center, Leiden, The Netherlands; and PainLess Foundation, Leiden, The Netherlands

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. Editor’s Perspective What We Already Know about This Topic What This Article Tells Us That Is New

Publisher

Ovid Technologies (Wolters Kluwer Health)

Subject

Anesthesiology and Pain Medicine

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