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April 27, 2026The Proceedings of the Thermal Engineering Conference0 citationsOpen Access

Investigation of storage time dependence on cytoprotective effect by pressurized dissolution of argon gas in cold storage

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KMKenshi MimuraKitasato University Medical CenterKYKazuhiro YoshidaNagasaki UniversityRSRina SakaiKobe University Hospital

Key Points

  • The aim is to assess how storage time affects the cytoprotective effect of pressurized argon gas on heart cell monolayers.
  • Monolayers of rat heart striated myocytes were cultured for 24 hours and then exposed to 0 and 0.8 MPa of argon gas before cold storage at 6°C.
  • Storage duration varied from 0 to 72 hours, after which cell viability was assessed using a water-soluble tetrazolium salts assay.
  • Cell viability was low after 24 hours without pressurization, but significantly improved with pressure.
  • At 48 and 72 hours, cell viability was still low even with argon pressurization, though slightly better compared to non-pressurized conditions.

Abstract

The storage time dependence on protective effect by pressurized dissolution of argon gas in cold storage on a rat heart striated myocytes monolayer were investigated. The cell monolayers incubated in a culture dish for 24 h were prepared as test samples. The samples were pressurized in 0 and 0.8 MPa in argon gas, and then preserved at 6°C for 0 to 72 h. The pressure-dependent cell viability was evaluated using water-soluble tetrazolium salts assay. The results showed that protective effect in after 24 h was low without pressure, but it was high with pressure. The protective effects in storage time of 48 h and 72 h were low even with pressurized dissolution of argon gas, but they were slightly higher than that without it.

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Cite This Study

Mimura et al. (2025) studied this question.

synapsesocial.com/papers/69eefcf4fede9185760d3b0chttps://doi.org/10.1299/jsmeted.2025.b13
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