PT  - JOURNAL ARTICLE
AU  - Michael Z. Liao
AU  - Chunying Gao
AU  - Brian R. Phillips
AU  - Naveen K. Neradugomma
AU  - Lyrialle W. Han
AU  - Deepak Kumar Bhatt
AU  - Bhagwat Prasad
AU  - Danny D. Shen
AU  - Qingcheng Mao
TI  - Pregnancy Increases Norbuprenorphine Clearance in Mice by Induction of Hepatic Glucuronidation
AID  - 10.1124/dmd.117.076745
DP  - 2018 Feb 01
TA  - Drug Metabolism and Disposition
PG  - 100--108
VI  - 46
IP  - 2
4099  - http://dmd.aspetjournals.org/content/46/2/100.short
4100  - http://dmd.aspetjournals.org/content/46/2/100.full
SO  - Drug Metab Dispos2018 Feb 01; 46
AB  - Norbuprenorphine (NBUP) is the major active metabolite of buprenorphine (BUP) that is commonly used to treat opiate addiction during pregnancy; it possesses 25% of BUP’s analgesic activity and 10 times BUP’s respiratory depression effect. To optimize BUP’s dosing regimen during pregnancy with better efficacy and safety, it is important to understand how pregnancy affects NBUP disposition. In this study, we examined the pharmacokinetics of NBUP in pregnant and nonpregnant mice by administering the same amount of NBUP through retro-orbital injection. We demonstrated that the systemic clearance (CL) of NBUP in pregnant mice increased ∼2.5-fold compared with nonpregnant mice. Intrinsic CL of NBUP by glucuronidation in mouse liver microsomes from pregnant mice was ∼2 times greater than that from nonpregnant mice. Targeted liquid chromatography tandem-mass spectrometry proteomics quantification revealed that hepatic Ugt1a1 and Ugt2b1 protein levels in the same amount of total liver membrane proteins were significantly increased by ∼50% in pregnant mice versus nonpregnant mice. After scaling to the whole liver with consideration of the increase in liver protein content and liver weight, we found that the amounts of Ugt1a1, Ugt1a10, Ugt2b1, and Ugt2b35 protein in the whole liver of pregnant mice were significantly increased ∼2-fold compared with nonpregnant mice. These data suggest that the increased systemic CL of NBUP in pregnant mice is likely caused by an induction of hepatic Ugt expression and activity. The data provide a basis for further mechanistic analysis of pregnancy-induced changes in the disposition of NBUP and drugs that are predominately and extensively metabolized by Ugts.