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. Author manuscript; available in PMC: 2009 Jun 1.
Published in final edited form as: Chem Res Toxicol. 2008 May 22;21(6):1295–1303. doi: 10.1021/tx800059j

Table 1.

Spectral constants and relative binding efficiencies for PCB 136 atropisomers with mouse hepatic microsomal P450 enzymesa

Spectral parameter (+)-PCB 136 (-)-PCB 136 (±)-PCB 136
Hepatic microsomes from NF-treated miceb
ΔAmax (absorbance unit/nmol P450) 0.011 0.005 0.008
Ksapp (μM) 9.2 2.9 4.2
ΔAmax/Ksapp (absorbance unit/nmol P450/M) 1200 1900 2000
Hepatic microsomes from PB-treated micec
ΔAmax (absorbance unit/nmol P450) 0.028 ± 0.002 0.020 ± 0.002 0.027 ± 0.001
Ksapp (μM) 8.2 ± 0.70 5.6 ± 1.0 7.0 ± 0.60
ΔAmax/Ksapp (absorbance unit/nmol P450/M) 3500 ± 450 3800 ± 480 3900 ± 430
Hepatic microsomes from DEX-treated micec
ΔAmax (absorbance unit/nmol P450) 0.026 ± 0.001 0.017 ± 0.001 0.020 ± 0.001
Ksapp (μM) 24 ± 5.4 7.6 ± 1.4 12 ± 2.8
ΔAmax/Ksapp (absorbance unit/nmol P450/M) 1200 ± 240 2400 ± 450 1800 ± 380
Hepatic microsomes from CO-treated miceb
ΔAmax (absorbance unit/nmol P450) 0.012 0.010 0.012
Ksapp (μM) 9.7 21 10
ΔAmax/Ksapp (absorbance unit/nmol P450/M) 1200 450 1200
a

Maximal absorbance change (ΔAmax), apparent spectral dissociation constant (Ksapp) and relative binding efficiency (ΔAmax/Ksapp) values were obtained for hepatic microsomes prepared from NF, PB, DEX and CO-treated female mice as described in Experimental Procedures.

b

Single measurement.

c

Mean ± SE of three determinations.