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. Author manuscript; available in PMC: 2009 Sep 1.
Published in final edited form as: J Pharm Pharmacol. 2008 Sep;60(9):1175–1182. doi: 10.1211/jpp.60.9.0009

Table 2.

Effect of 10 mM saccharolactone on the hydrolysis of estradiol 3-glucuronide (E-3-G, 100 μM) and estradiol 17-glucuronide (E-17-G, 200 μM). Estradiol glucuronide concentrations were measured by HPLC before and after 6 hour incubation with human liver, intestine, kidney, and lung microsomes, insect cell expressed UGTs, and control cells.

Glucuronide Saccharolactone pHLM Intestine Kidney Lung UGT2B7 UGT1A1 Insect control HEK293control Buffer
E-3-G 82±1a,b 104±3 104±1a,b 85±6 77±9 77±2 90±5 102±4 101±5
+ 84±2a 101±3 110±3 80.9±5a 91±5 87±7 89±7 98±10 95±4
E-17-G 86±2b 110±4b 104±3 92±6 75±5 71±4 88±3 104±3 102±13
+ 84±3 106±2 116±2 86±3 89±5 85±3 88±4 101±8 95±3

Data are presented as mean±s.d. of percent glucuronide remaining after 6 hours, n=3.

a

P<0.01 comparing 0 hr timepoint vs. 6 hr timepoint.

b

P<0.05 comparing 6 hour timepoint with and without saccharolactone by unpaired t-test.