HS in Critical Illness-A New Horizon for Sodium Thiosulfate?

Tamara Merz, Oscar McCook, Cosima Brucker, Christiane Waller, Enrico Calzia, Peter Radermacher, Thomas Datzmann

Journal: Biomolecules 2022;12(4):543

PMID: 35454132

Abstract

Ever since the discovery of endogenous HS and the identification of its cytoprotective properties, efforts have been made to develop strategies to use HS as a therapeutic agent. The ability of HS to regulate vascular tone, inflammation, oxidative stress, and apoptosis might be particularly useful in the therapeutic management of critical illness. However, neither the inhalation of gaseous HS, nor the administration of inorganic HS-releasing salts or slow-releasing HS-donors are feasible for clinical use. NaSO is a clinically approved compound with a good safety profile and is able to release HS, in particular under hypoxic conditions. Pre-clinical studies show promise for NaSO in the acute management of critical illness. A current clinical trial is investigating the therapeutic potential for NaSO in myocardial infarct. Pre-eclampsia and COVID-19 pneumonia might be relevant targets for future clinical trials.

Address: Institute for Anesthesiological Pathophysiology and Process Engineering, Ulm University Medical Center, 89081 Ulm, Germany.; Clinic for Anesthesiology and Intensive Care, Ulm University Medical Center, 89081 Ulm, Germany.; Department of Gynecology and Obstetrics, Nuremberg General Hospital, Paracelsus Medical University, 90419 Nuremberg, Germany.; Department of Psychosomatic Medicine and Psychotherapy, Nuremberg General Hospital, Paracelsus Medical University, 90419 Nuremberg, Germany.
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