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. 2007 Apr 16;151(3):367–376. doi: 10.1038/sj.bjp.0707235

Table 1.

Effect of CA feeding with or without co-treatment with PXR activators on liver function and total body weight

  ALT (U/l) AST (U/l) ALP (U/l) Total bilirubin (μM) Direct bilirubin (μM) Change in total body weight (%)
PXR+/+
 Control (4) 23±4 45±6 42±6 10.4±1.28 4.27±0.44 +2
 PCN (4) 28±6 64±14 38±2 15.5±3.08 8.60±2.05 NC
 CA (6) 1618±485a 1350±356a 202±32a 39.3±7.52a 33.8±10.4a −23
 CA+PCN (5) 358±77b 380±108b 62±12b 12.0±1.20b 7.52±0.68b −12
             
PXR−/−
 Control (4) 19±3 42±4 19±7 12.3±1.74 6.50±2.74 +2
 PCN (4) 13±5 38±12 11±6 15.8±4.10 11.2±4.27 −10
 CA (4) 95±8a 91±3a 31±7 10.7±1.54 6.87±1.03 −15
 CA+PCN (4) 85±6a 80±13a 23±5 15.3±1.37 7.58±0.68 −18

Abbreviations: ALP, alkaline phosphatase; ALT, alanine amino transferase; AST, aspartate aminotransferase; CA, cholic acid; PXR, pregnane X receptor; PCN, 5-pregnen-3β-ol-20-one-16α-carbonitrile; NC, no change.

PXR+/+ and PXR−/− mice were fed standard chow or a 1% CA-supplemented diet for 5 days with or without injection of the PXR activator PCN. Numbers in brackets indicate the number of mice in each treatment group. Blood samples were analysed for ALT, AST, ALP and bilirubin levels as indicators of liver function. Mice were weighed throughout the treatment period; the change in weight represents the difference in weight between the start and end of treatment. Results are presented as mean enzyme or bilirubin concentrations±s.e.m.

a

Significant from control P<0.05.

b

Significant from CA P<0.05.