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Current methods slow metabolism or sustain physiological support, but neither eliminates ischemia-reperfusion injury, which shortens storage and drives organ discard. Embryonic diapause and hibernation show that mammalian cells retain a latent capacity for reversible metabolic arrest. Screening the PI3K-mTOR axis, we identified a dual inhibitor that reversibly pauses embryonic stem cells at ambient oxygen and holds mouse embryos in arrest for 8.5 days. Combined with a mitochondria-targeted hydrogen sulfide donor, this yields TorPause, a two-component flush compatible with existing preservation protocols. 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