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. 2019 Aug 23;9:12306. doi: 10.1038/s41598-019-48744-7

Table 6.

Hyperoxia mdx Hemodynamic Data.

Baseline Dobutamine Esmolol Significance
Heart Rate (bpm) 490 ± 17.2 (8) 562 ± 6.9 (8) 399 ± 10.2 (8) b,c
End-Systolic Pressure (mmHg) 93.1 ± 2.19 (8) 104 ± 2.59 (8) 69.7 ± 6.11 (8) c,d
End-Diastolic Pressure (mmHg) 8.84 ± 1.22 (8) 8.61 ± 1.02 (8) 10.3 ± 0.771 (8)
Maximum dP/dt (mmHg/s) 8478 ± 464 (8) 13460 ± 303 (8) 3974 ± 479 (8) a,b,d
Minimum dP/dt (mmHg/s) 8402 ± 389 (8) 9418 ± 292 (8) 4464 ± 688 (8) b,c,d
Tau (msec) 7.23 ± 0.61 (8) 6.5 ± 0.691 (8) 15.3 ± 3.9 (8)
End-Diastolic Volume (μl) 38.6 ± 3.19 (8) 37.7 ± 4.93 (8) 50.1 ± 5.1 (8)
End-Systolic Volume (μl) 25.4 ± 2.29 (8) 17.5 ± 1.52 (8) 41.2 ± 5.2 (8)
Cardiac Output (μl/min) 9738 ± 749 (8) 14288 ± 3075 (8) 7382 ± 2017 (8)
PRSW (mmHg⋅μl/μl) 66.1 ± 3.38 (8) 85.4 ± 3.63 (8) 40.3 ± 7.45 (8)

Significant testing by three-way ANOVA with genotype, oxygen therapy protocol, and hemodynamic protocol treatment as factors with Tukey post-hoc test. a; signifies difference between baseline and dobutamine with hyperoxic protocol in mdx mice; b: signifies difference between baseline and esmolol with hyperoxic treatment in mdx mice; c: signifies an overall genotype effect; d: represents an overall difference between hyperoxia and normoxic treatment; e: represents an overall difference between HBOT and hyperoxic treatment.

HHS Vulnerability Disclosure