Microbial Cell (May 2017)

The neuroprotective steroid progesterone promotes mitochondrial uncoupling, reduces cytosolic calcium and augments stress resistance in yeast cells

  • Slaven Stekovic,
  • Christoph Ruckenstuhl,
  • Phillip Royer,
  • Christof Winkler-Hermaden,
  • Didac Carmona-Gutierrez,
  • Kai-Uwe Fröhlich,
  • Guido Kroemer,
  • Frank Madeo

DOI
https://doi.org/10.15698/mic2017.06.577
Journal volume & issue
Vol. 4, no. 6
pp. 191 – 199

Abstract

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The steroid hormone progesterone is not only a crucial sex hormone, but also serves as a neurosteroid, thus playing an important role in brain function. Epidemiological data suggest that progesterone improves the recovery of patients after traumatic brain injury. Brain injuries are often connected to elevated calcium spikes, reactive oxygen species (ROS) and programmed cell death affecting neurons. Here, we establish a yeast model to study progesterone-mediated cytoprotection. External supply of progesterone protected yeast cells from apoptosis-inducing stress stimuli and resulted in elevated mitochondrial oxygen uptake accompanied by a drop in ROS generation and ATP levels during chronological aging. In addition, cellular Ca2+ concentrations were reduced upon progesterone treatment, and this effect occurred independently of known Ca2+ transporters and mitochondrial respiration. All effects were also independent of Dap1, the yeast orthologue of the progesterone receptor. Altogether, our observations provide new insights into the cytoprotective effects of progesterone.

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