Research Article - (2012) Volume 0, Issue 0

Atypical Kinetics of Valproic Acid Glucuronidation In vitro and In vivo in Humans

Harvey Wong1*, Binfeng Xia1, Vincent Tong2, Sanjeev Kumar2 and Jane R Kenny1
1Drug Metabolism and Pharmacokinetics, Genentech Inc., South San Francisco, CA, USA
2Merck and Co, Rahway, NJ, USA
*Corresponding Author: Dr. Harvey Wong, Drug Metabolism and Pharmacokinetics, Genentech Inc., 1 DNA Way, MS 412a, South San Francisco, CA, 94080, USA Email:

Abstract

Atypical kinetics has been observed in vitro for both cytochrome P450 and UDP-glucuronosyltransferase catalyzed enzymatic reactions. The in vitro and in vivo kinetics of valproic acid- glucuronide (VPA-glucuronide) formation was investigated in humans.
VPA-glucuronide formation kinetics was investigated in vitro using human cryoperserved hepatocytes (pool of 10). Estimates of Vmax app (39.5 ± 3.3 pmol/min/106 cells), S50 app (224 ± 34 µM) and n (2.34 ± 0.28) was obtained by fitting VPA-glucuronide formation rate vs VPA incubation concentration data to the Hill equation. In vitro EadieHofstee plots were “hooked” and characteristic of atypical sigmoidal/autoactivation kinetics.
In vivo Eadie-Hofstee plots of VPA-glucuronide formation rate (calculated from urinary excretion rate data for VPA-glucuronide) were constructed using data from four human subjects given a 1000 mg VPA oral dose [1]. The positive slope of linear regression lines for these plots was consistent with in vivo atypical sigmoidal/autoactivation kinetics.
In summary, these data build upon our previous observations in sheep and provide the first demonstration that VPA-glucuronide formation exhibits atypical kinetics in vitro in human hepatocytes. Available in vivo data is consistent with in vitro results suggesting that VPA-glucuronidation exhibits atypical sigmoidal/autoactivation kinetics in vivo in humans.

Introduction

Valproic acid (2-propylpentanoic acid, VPA) is a broad spectrum anticonvulsant with a unique branched-chain fatty acid structure [2]. Previously, we observed evidence of both in vitro and in vivo autoactivation kinetics of VPA-glucuronide formation in sheep [3]. Approximately, 70-80% of the administered VPA dose is metabolized to VPA-glucuronide such that manifestation of in vivo autoactivation kinetics was evident in both the appearance of VPA-glucuronide in urine and the decline of unbound VPA in plasma. In humans, VPAglucuronide is a major metabolite of VPA accounting for 10-70% of the administered dose [4]. The UDP-glucuronosyltransferases (UGT) capable of metabolizing VPA in humans include UGT1A4, UGT1A6, UGT1A8, UGT1A9, UGT 1A10 and UGT2B7 [5,6]. Interestingly, glucuronidation reactions involving UGT1A6 and UGT2B7 have shown evidence of autoactivation kinetics with substrates other than VPA [7,8]. Reports of enhanced rates of glucuronidation in humans at high doses of VPA (1000 mg) have been previously described in literature [9]. These enhanced rates could not be accounted for entirely by increases in unbound VPA concentrations that occurred with increasing dose and are consistent with autoactivation kinetic behavior. Thus, well-designed in vitro enzyme kinetics studies of VPA glucuronidation spanning a clinically relevant VPA concentration range may show evidence of in vitro autoactivation kinetics of VPA glucuronidation. In addition, careful examination of the clinical literature on VPA in humans may reveal evidence of in vivo atypical sigmoidal/autoactivation kinetics consistent with our observations in sheep. The objective of the current study is to characterize the kinetics of VPA-glucuronide formation in vitro using human hepatocytes. In addition, in vivo data on VPA-glucuronidation in humans will examined for evidence of atypical sigmoidal/autoactivation kinetics.

Materials and Methods

In vitro valproic acid glucuronidation kinetics

The formation kinetics of VPA-glucuronide were examined in cryopreserved human hepatocytes (pool of 10) (CellzDirect Inc., Durham, NC) under the following incubation conditions: VPA (6.4 to 800 μM) and 0.5 × 106 cells/ml human liver hepatocytes in Dulbecco’s Modified Eagle Medium fortified with glucose. The incubations were performed in triplicate on three separate occasions at each VPA concentration in an incubator at 37°C, 95% humidity and 5% CO2. The total incubation volume was 100 μL. Incubations were terminated at 60 minutes by the addition of 200 μL of ice-cold acetonitrile containing the internal standard (diclofenac at 0.1 μM final concentration; Sigma- Aldrich Co., St. Louis, MO) and 3% formic acid. The resulting samples were centrifuged at 3000 g for 10 minutes at 4°C and 10 μL of the supernatant was injected into a liquid chromatography coupled with a tandem mass spectrometer (LC-MS/MS) for quantitation of VPAglucuronide.

VPA-glucuronide was quantitated using a modification of a LC-MS/MS method previously described by Wong et al. [3]. The instrument consisted of an Agilent 1200 liquid chromatography system (Agilent Technologies Inc. Santa Clara, CA) coupled with an Applied Biosystems ABI-4000 triple quadrapole mass spectrometer (Applied Biosystems Foster City, CA). Samples were injected by a CTC Analytics HTS PAL autosampler (Leap Technology Inc., Carrboro NC) onto Thermo Scientific Hypersil gold C18 column (50 mm × 1.9 mm i.d.; Thermo Electron Corporation, San Jose, CA). The mobile phase, consisting of (A) water with 0.1% formic acid and (B) acetonitrile with 0.1% formic acid, was delivered at a flow rate of 0.4 mL/min, using the following gradient program: 5% B for 0.4 min, linear gradient to 90% B between 0.4 and 3 min, held at 90 % B until 3.5 min, then reequilibrated to initial conditions after 3.5 min with the total run time was 5.5 min. The mass spectrometer was operated in the negative ion mode with multiple reaction monitoring (VPA-glucuronide: 319.0 > 143.0, internal standard: 293.9 > 250.0) at a collision energy of 28 ev and 17 ev. The dwell time for both channels was set at 100 ms. The calibration curve was prepared by spiking authentic standards to blank hepatocyte samples after the incubations were quenched. The peakarea ratio of VPA-glucuronide to internal standard was linear (r6 > 0.99) over a concentration range of VPA-glucuronide from 0.5 nM to 2500 nM. The coefficient of variation was less than 15% at all of the concentrations.

The rate of VPA-glucuronide formation vs. VPA concentration data from the human hepatocyte experiments were fitted to the Hill (Equation 1) and the Michaelis-Menten equation (Equation 2) using GraphPad Prism V4.02 (GraphPad Software Inc., San Diego, CA).

image (1)

image (2)

Where V is the rate of VPA glucuronidation, Vmax app is the apparent maximum rate of VPA glucuronidation, C is the VPA incubation concentration, and S50 app or Km app is the apparent substrate concentration where the rate of VPA-glucuronide formation is 50% of Vmax app, and n is the Hill coefficient.

Since clearance for compounds exhibiting sigmoidal/autoactivation kinetics are concentration dependent, calculation of maximal clearance due to autoactivation (CLmax) was performed using Equation 3 [10].

image (3)

In vivo Eadie-Hofstee Plots for VPA glucuronidation in humans

In vivo Eadie Hofstee Plots were generated using data extracted from Bialer et al. [1]. Figures of unbound VPA serum concentrationtime profiles and plots of amount of VPA-glucuronide remaining to be excreted in urine vs. time profiles were digitized using UN-SCAN-IT v6 (Silk Scientific Corporation, Orem, Utah). Urinary excretion rate of VPA-glucuronide (V) and unbound VPA serum concentrations at the midpoint of the urine collection interval (Cmid u) were calculated and used to generate in vivo Eadie-Hofstee plots (V versus V/Cmid u). Data is presented for four human subjects where ≥ 3 or more data points were available for plotting. For the remaining two subjects, only one or two data points were available for plotting in vivo Eadie-Hofstee plots due to less frequent urine collection during the post-dose period where VPA unbound concentrations could be measured; and therefore were excluded from the analysis. Linear regression of in vivo Eadie- Hofstee plots was performed using Microsoft Excel 2003 (Microsoft Corporation, Redmond, WA).

Results

In vitro valproic acid glucuronidation kinetics

Figure 1 shows plots of VPA-glucuronide formation rate vs. VPA incubation concentration and the corresponding Eadie-Hofstee plots from a representative human hepatocyte experiment fitted to the Hill (Figure 1A and 1B) or Michaelis-Menten equation (Figure 1C and 1D). A summary of the associated kinetic parameter estimates are presented in Table 1. The Eadie-Hofstee plot exhibits the “curved” shape that is characteristic of sigmoidal/autoactivation kinetics. It is better described by the fitted line generated using the Hill equation (Figure 1B) rather than the classical Michaelis-Menten equation (Figure 1D).

pharmaceutica-analytica-acta-human-hepatocyte

Figure 1: Plot of VPA-glucuronide formation rate vs VPA incubation concentration and a Eadie-Hofstee plot from a representative human hepatocyte (pool of 10) experiment fitted to the Hill (A and B) or Michaelis-Menten equation (C and D). V is defined as the rate of valproic acid-glucuronide formation and S is defined as substrate (VPA) concentration in the figure.

  Vmaxapp (pmol/min/106 cells) S50app or Kmapp (µM) N
Hill 39.5 ± 3.3 224 ± 34 2.34 ± 0.28
Michaelis-Menten 89.8 ± 28.0 915 ± 472 -

Table 1: Summary of kinetic parameters describing VPA-glucuronide formation kinetics in human hepatocytes.

Based upon plots shown in Figure 1, in vitro VPA glucuronidation in human hepatocytes exhibits atypical sigmoidal/autoactivation kinetics under the VPA concentration range tested. Since clearance for compounds exhibiting sigmoidal/autoactivation kinetics are concentration dependent, calculation of maximal clearance due to autoactivation was performed using Equation 3. The estimated CLmax describing VPA-Glucuronidation was 15 mL/hr/kg.

In vivo Eadie-Hofstee Plots for VPA glucuronidation in humans

In vivo Eadie-Hofstee Plots for VPA glucuronidation are presented in Figure 2. The X-axis for in vivo Eadie-Hofstee Plots (V/ Cmid u) represents the average unbound intrinsic clearance for VPAglucuronidation over specific urine collection intervals. Since VPA glucuronidation did not appear to be saturated based upon the in vivo Eadie-Hofstee Plots, data from human subjects were not fit to either the Michaelis-Menten or Hill equation. Instead, data from in vivo Eadie- Hofstee Plots were fitted to a linear regression line and the associated equations are presented in Figure 2. The slope of the regression line was used to discriminate whether VPA-glucuronide formation in vivo exhibited kinetics that were consistent with either classical Michaelis- Menten kinetics or atypical sigmoidal/autoactivation kinetics since the slope of the Eadie-Hofstee Plots are uniquely negative and positive, respectively, at lower non-saturating substrate concentrations (Figure 3). For all four human subjects presented, the slope of the linear regression line was positive (3.92 to 6.03), consistent with sigmoidal/ autoactivation kinetics.

pharmaceutica-analytica-acta-sodium-valproate

Figure 2: (A-D) In vivo Eadie-Hofstee plots for VPA glucuronidation for four individuals following administration of a single 1000 mg oral dose of sodium valproate (V = urinary excretion rate of VPA-glucuronide; Cmidu = unbound VPA plasma concentration at the midpoint of the urine collection interval). Regression lines and associated equations are presented.

pharmaceutica-analytica-acta-Michaelis-Menten

Figure 3: Eadie-Hofstee Plots Illustrating Differences for Michaelis-Menten and Sigmoidal/ Autoactivation Kinetics.

Discussion

Aside from one report of atypical sigmoidal/autoactivation kinetics of VPA glucuronidation in vitro in sheep [3], this phenomenon has yet to be reported for VPA glucuronidation in vitro in humans or other species. Previous investigations characterizing the enzyme kinetics of VPA glucuronidation were not designed with autoactivation kinetics in mind and therefore, this phenomenon may have been missed. In an earlier manuscript [3], we reported our investigation into the translation of in vitro sigmoidal/autoactivation kinetics to the in vivo situation. Our efforts focused on the in vitro and in vivo kinetics of VPA glucuronidation in sheep. The unique in vivo disposition of valproic acid in sheep made it an ideal animal model to conduct our investigation. VPA is a low clearance compound that is primarily eliminated by the liver such that the clearance of unbound VPA is essentially its intrinsic metabolic clearance. In sheep, glucuronidation is the main route of VPA elimination (70 to 80%), and the urinary excretion of VPA-glucuronide is formation rate limited. Finally, VPA is a very safe compound, thus enabling the administration of high doses that result in a broad range of in vivo concentrations. Based upon these characteristics, evidence of in vivo sigmoidal/autoactivation kinetics manifested itself in both the unbound VPA plasma concentration-time profile, and in the urinary excretion of VPA-glucuronide following administration of a 100 mg/kg intravenous dose. Our observations of in vivo sigmoidal/autoactivation kinetics were further substantiated by in vitro experiments demonstrating autoactivation kinetics of VPAglucuronide formation using sheep liver microsomes [3] and sheep hepatocytes (unpublished data).

Since VPA shows minimal microsomal binding [3], in vitro incubation concentrations correspond to unbound concentrations in vivo. Human subjects in a clinical study described by Bailer et al. [1] received a single 1000 mg oral dose of valproic acid which resulted in unbound levels ranging from approximately 2.5 to 63 μM (0.36 to 9.0 μg/mL). VPA concentration ranges investigated in previous in vitro studies were substantially higher (500 μM to 15 mM; [5] and 100 μM to 20 mM; [6]. In the current study, we performed an enzyme kinetics experiment using pooled cryoperserved hepatocytes over a concentration range that not only covered the observed unbound VPA concentration range but extended ~13 fold higher (5 to 800 μM or 0.72 to 115 μg/mL). The extension of the upper incubation concentration to 800 μM was based upon our observations that the kinetics of VPAglucuronide formation was not fully characterized in vivo (Figure 2). It must be noted that the 800 μM incubation concentration is still closer to the lower end of VPA concentrations used in previous in vitro investigations.

Our in vitro enzyme kinetics study using human hepatocytes clearly show that the in vitro formation kinetics of VPA-glucuronide is atypical in nature over a more clinically relevant concentration range (Figure 1). The Eadie-Hofstee Plot exhibits the characteristic “curved” shape that is associated with atypical sigmoidal/autoactivation kinetics and provides evidence that this phenomenon occurs in vitro in humans. Finally, the estimated CLmax (15 mL/hr/kg) based upon kinetic parameters from the hepatocyte study is in line with reported estimates of VPA-glucuronide formation clearance observed in humans (12-22 ml/hr/kg) [11].

Enhanced rates of in vivo glucuronidation in humans at high doses of VPA have previously been described in the literature. Granneman et al. [9] reported that an increase in VPA dose from 250 mg to 1000 mg resulted in a 13.6 fold increase in the dose normalized urinary excretion rate of VPA-glucuronide. Increases in VPA unbound fraction (i.e. 10% unbound at 250 mg versus 40% unbound at 1000 mg) could at most account for a four-fold increase in glucuronidation, leaving much of the change unexplained. A second report by Anderson et al. [12] showed dose-dependent increases in the intrinsic formation clearance of VPA-glucuronide in healthy volunteers treated with consecutive 4 day regimens of VPA at daily oral doses of 250, 500, and 1000 mg. Data were also presented showing increases in VPA-glucuronide formation clearance with increasing dose for patients undergoing chronic VPA therapy. As multiple-dose regimens were involved, possible inductive effects of VPA may have contributed to the observations of Anderson et al. [12]. Nevertheless, human data presented in both reports described above are consistent with our previous observations of in vivo autoactivation kinetics of VPA glucuronidation in sheep [3].

Observations of in vivo sigmoidal/autoactivation kinetics reported in literature are rare. Compounds exhibiting sigmoidal/autoactivation kinetics in vitro, often do not achieve the range of concentrations required to characterize the phenomenon in vivo. Alternatively, the design of in vivo studies to characterize autoactivation kinetics may not be feasible for many of these compounds due to the complexity of their disposition in an in vivo system. Our ability to observe and characterize the in vivo autoactivation kinetics of VPA glucuronidation in sheep previously was in part due to the in vivo tolerability of VPA at high doses [3]. Intravenous doses of 100 mg/kg administered to sheep provided a large concentration range of unbound drug in plasma, thus allowing for reliable estimation of in vivo enzyme kinetic parameters from modeling of unbound plasma concentration-time profiles [3]. Similar characterization in humans is not feasible since doses normally administered are far less than those employed in our previous studies in sheep. In addition, although a major pathway in humans (i.e. 10-70%; [4], glucuronidation does not consistently contribute to the elimination of VPA to the same extent as in sheep (i.e. 70-80%; [3]. Therefore, our approach of characterizing sigmoidal/autoactivation kinetics of VPA glucuronidation using unbound VPA plasma-concentration time profiles in sheep is not possible in humans since pathways other than glucuronidation can play a major role in VPA elimination from plasma.

An alternative approach to detect in vivo sigmoidal/autoactivation kinetics of VPA glucuronidation is through the use of diagnostic in vivo Eadie-Hofstee Plots [3]. Figure 3 illustrates the distinct shapes of Eadie-Hofstee Plots resulting from classical Michaelis-Menten kinetics and atypical sigmoidal/autoactivation kinetics. In our previous manuscript [3], we presented in vivo Eadie-Hofstee Plots generated from VPA-glucuronide urinary excretion data and unbound VPA plasma concentrations from five sheep dosed at 100 mg/kg iv. All in vivo Eadie-Hofstee plots presented had the characteristic “curved” shape associated with autoactivation kinetics. Figure 4 is an in vivo Eadie-Hofstee Plot from a single animal dosed at 10 mg/kg iv, a dose closer in range to that used clinically in humans. At this lower dose, only the bottom portion of the characteristic “curved” Eadie-Hofstee plot is evident due to a more limited range of concentrations achieved in vivo. At low non-saturating substrate concentrations, the slope of the Eadie-Hofstee Plot is positive due to increasing unbound intrinsic clearance with increasing unbound VPA concentrations (Figure 3 and Figure 1B). The linear regression line through the data from sheep in figure 4 has a positive slope consistent with what would be expected for atypical sigmoidal/autoactivation kinetics. Eadie-Hofstee Plots from four human subjects given a single oral dose of 1000 mg VPA show a similar positive slope reflective of atypical in vivo kinetics in humans (Figure 2).

pharmaceutica-analytica-acta-associated-equation

Figure 4: Representative in vivo Eadie-Hofstee Plot for individual sheep dosed at 10 mg/kg iv (V = urinary excretion rate of VPA-glucuronide; Cmidu = unbound VPA concentration in plasma at the midpoint of the urine collection interval). Regression line and associated equation is presented. Data extracted from Wong et al. [13].

In summary, we have shown that the in vitro kinetics of VPA in human hepatocytes is atypical in nature under clinically relevant concentrations. In addition, based upon our analysis of existing data, the in vivo kinetics of VPA glucuronidation in humans are consistent with atypical sigmoidal/autoactivation kinetics.

References

Citation: Wong H, Xia B, Tong V, Kumar S, Kenny JR (2012) Atypical Kinetics of Valproic Acid Glucuronidation In vitro and In vivo in Humans. Pharmaceut Anal Acta S11:006.

Copyright: © 2012 Wong H, et al. This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.