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To determine the K M of NADH in the forward reaction, NADP + was held constant using glutathione reductase and oxidized glutathione (0.5 mM NADP + , 4 U/ml glutathione reductase, 1 mM oxidized glutathione and various concentrations of NADH) whereas determination of K M for NADP + was obtained using alcohol dehydrogenase to hold NADH concentrations constant (50 M NADH, 1.2 U/ml alcohol dehydrogenase, 130 mM ethanol, 6 mM hydrazine (pH 7.0) and various concentrations of NADP + )

A related study found that LND and BPTES were able to induce glycolysis and inhibit glutamine metabolism, which was accompanied by significant mitochondrial damage, ultimately blocking energy supply and posing a threat to tumour survival, to efficiently kill tumours