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. 2021 Feb 26;101(6):680–689. doi: 10.1038/s41374-021-00538-0

Fig. 5. L-carnitine suppressed hypertonic stress-induced increases of intracellular Ca2+ concentration.

Fig. 5

A Hypertonic challenge (450 mOsmol/l) induced an increase in Ca2+ influx (n = 55) whereas non-treated control cells maintained a constant Ca2+ baseline (n = 13). B Same experiment as shown in A, but in the presence of L-carnitine. L-carnitine (1 mmol/l) clearly suppressed the hypertonic-induced Ca2+ increase (n = 73). C Summary of the experiments with hypertonicity and L-carnitine. The asterisks (*) designate significant increases in [Ca2+]i with hypertonicity (t = 300 s; n = 55; p < 0.005; paired tested) compared to control (t = 100 s). The hashtags (#) indicate statistically significant differences in fluorescence ratios between hypertonic challenge with and without L-carnitine (t = 300 s; n = 55–73; p < 0.005; non-paired tested).