Related Experiment Video
Updated: Jul 28, 2026

Pluripotent Stem Cell Derived Cardiac Cells for Myocardial Repair
Published on: February 3, 2017
Effects of selenium, selenium-enriched spirulina and phycocyanin on myocarditis stress parameters on LPS-induced
Thomas Castel1, Karine Pichavant-Rafini1, Michaël Théron1
1Univ Brest, Laboratory ORPHY, IBSAM, Brest, France.
Abstract:
Myocarditis is strongly represented in septic patients and is associated with a higher mortality rate. Spirulina platensis (Spi), a blue-green algae, has anti-inflammatory properties and can be enriched with selenium, an antioxidant essential oligoelement. In addition, phycocyanin (PC), a biliprotein extract from spirulina, displays interesting anti-inflammatory and antiapoptotic effects. In this study, the objective was to determine the cardioprotective effects of Sodium selenite (Se), Spi, Spi + Se (SeSP) and PC on LPS-induced inflammation, apoptosis, and oxidative stress parameters. H9c2 cells were co-treated with or without LPS (5 μg/mL) and Se (0.5 μM), Spi (2.5 μg/mL), SeSP (0.5 μM Se + 2.5 μg/mL Spi) and PC (0.1 μg/mL) for 24 h. Inflammation was investigated by measurement of NFκB activation, IL-6, and caspase 1 expression, while apoptosis was measured by Bax, Bcl-2, and caspase-3 expression. Furthermore, GPx and SOD activities were analyzed, as well as isoprostanes and nrf-2 expression. Activation of MAPK Junk and p38 was also determined. Our results demonstrated that Se could only reduce p65 S536 phosphorylation. SeSP could limit Bax expression, while an increase in IL-6 was detected without LPS. Moreover, PC could reduce IL-6 and Caspase-1 expression and could have promising properties to decrease LPS-induced myocarditis outcomes.
Related Concept Videos
Inflammatory Response
Inflammation can be triggered by various stimuli, such as impact, abrasion, chemical irritation, infections, and extreme hot or cold temperatures. These can damage cells and connective tissue fibers,...
Myocarditis I: Introduction
Inflammation: Introduction
Acute Inflammation I: Inflammatory Response
Acute Inflammation III: Local and Systemic Effects
Chronic Inflammation: Introduction

