TABLE 2

P450-dependent specific activities measured in rat OM and liver microsomes (mean ± standard deviation) Metabolites were separated by HPLC. Dextrorphan was detected by fluorimetry, with an excitation wavelength of 200 nm and an emission wavelength of 305 nm, and quantified by reference to a standard concentration. All other metabolites were quantified after on-line radiochemical detection using reference products. Statistical significance of differences was tested with Student's t test. n = number of experiments.


Substrate

Measured Metabolite

Specific Activity

Student's t Test (P <)
OM (n = 4)
Liver (n = 4)
Phenacetin Acetaminophen 11,191 ± 1923 1431 ± 29 0.01
Chlorzoxazone 6-OH-Chlorzoxazone 10,070 ± 1722 3210 ± 415 0.01
Tolbutamide OH-Tolbutamide 8 ± 0 115 ± 17 0.01
Lauric acid ω-OH-Lauric acid 548 ± 73 473 ± 88 N.S.
Dextromethorphan Dextrorphan 2795 ± 173 2291 ± 203 0.01
Testosterone 2α-OH-Testosterone N.D. 4500 ± 837
2β-OH-Testosterone 2524 ± 291 N.D.
6α-OH-Testosterone N.D. N.D.
6β-OH-Testosterone 459 ± 67 1800 ± 231 0.01
7α-OH-Testosterone N.D. N.D.
15α-OH-Testosterone 3864 ± 482 N.D.
15β-OH-Testosterone 2454 ± 239 N.D.
16α-OH-Testosterone N.D. 5560 ± 1066
16β-OH-Testosterone N.D. N.D.
Androstenedione 608 ± 42 3600 ± 1208 0.01

x
1741 ± 226
N.D.

  • N.D., not detectable; x, unidentified metabolite.