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. Author manuscript; available in PMC: 2017 May 1.
Published in final edited form as: Mol Cell Biochem. 2016 Mar 29;416(1-2):11–22. doi: 10.1007/s11010-016-2688-z

Table 1. Mitochondrial respiration of β-alanine treated and untreated permeabilized cardiomyocytes.

Condition Substrate State 3 rate State 4 rate RCR P/O ratio
Control Glu-Mal 1.0 (43.61) 1.0 (11.03) 1.0 (3.7) 2.65 ± 0.2
β-alanine Glu-Mal 0.78 ± 0.08* 0.9 ± 0.09 0.8 ± 0.1* 2.24 ± 0.17*
Control Succinate 1.0 (65.4) 1.0 (15.8) 1.0 (3.3) 1.47 ± 0.12
β-alanine Succinate 0.98 ± 0.09 1.2 ± 0.1 0.95 ± 0.07 1.31 ± 0.08

All of the control groups were normalized to 1.0, with the actual values shown in parentheses. The control and β-alanine-treated cardiomyocytes were incubated in medium containing either 4 mM glutamate + 2 mM malate or 5 mM succinate. After a steady-state rate of state 2 respiration was observed, 1 μmol of ADP was added and the rate of state 3 respiration was determined. When ADP levels were depleted, state 4 respiration was determined

RCR respiratory control ratio. Values shown represent means ± S.E.M. of 3–4 different experiments. Asterisks denote a significant difference between the control and β-alanine-treated groups (p < 0.05). Because the experiments were performed with different preparations, all data were normalized relative to the control cells