Lamotrigine Metabolism in the Human Placenta Lindsay Samuel Mentor: Phillip M. Gerk, PharmD, PhD...
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Transcript of Lamotrigine Metabolism in the Human Placenta Lindsay Samuel Mentor: Phillip M. Gerk, PharmD, PhD...
![Page 1: Lamotrigine Metabolism in the Human Placenta Lindsay Samuel Mentor: Phillip M. Gerk, PharmD, PhD Department of Pharmaceutics Joseph K. Ritter, PhD Department.](https://reader035.fdocuments.us/reader035/viewer/2022062716/56649de55503460f94add96e/html5/thumbnails/1.jpg)
Lamotrigine Metabolism in the Human Placenta
Lindsay Samuel
Mentor: Phillip M. Gerk, PharmD, PhD Department of Pharmaceutics
Joseph K. Ritter, PhDDepartment of Pharmacology/Toxicology
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Introduction
Many pregnant women have to take medication during pregnancy.
For many different reasons Example: Women
with seizure disorders
http://www.dsf.health.state.pa.us/health/cwp/view.asp?a=179&Q=237058&
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Clinical Problem and Drug Development Medications may have adverse effects on
the fetus. There are safety concerns of including
pregnant women in clinical drug trials. Pharmaceutical companies study animal
pharmaceutical toxicology and test drugs in pregnant rats and mice,
The data from these studies cannot be directly transferred over to human patients Human placenta anatomically differs from
rats and mice
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In the lab…
In Dr. Gerk’s and Dr. Ritter’s lab, we are studying Lamotrigine metabolism.
Lamotrigine is an anti-seizure medication, which is somewhat safe in pregnancies
The objective in the lab is to determine how the placenta handles Lamotrigine.
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Placenta
“Before We Are Born: Basic Embryology and Birth Defects”, Moore, 1974.
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Enzymes
UDP-glucuronosyltransferase (UGT) family of enzymes found in the liver and other tissuesUGT2B7 is also expressed in the placenta
Glucuronidation of drugsExamples:
• Morphine: In a baboon model, the placenta makes major contributions to morphine clearance.
• Lamotrigine LTGLTG-Gluc
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Lamotrigine
Indications Bipolar disorder Epilepsy
Mechanism Unknown, but may have an effect on sodium
channels Pharmacokinetics
Absorption: 98% bioavailability Distribution: mean apparent volume of distribution
following oral administration 0.9-1.3 L/kg Metabolism: glucuronidation is the major elimination
pathway (86% of dose) Excretion: 94% urine, 2% feces
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Metabolism
UGT1A4 and UGT2B7 are the major isoforms involved
UGT2B7 is expressed in the placenta Clearance of lamotrigine is doubled in
pregnant women Clearance is also increased when
used with hormonal contraceptives UGT2B7 is inhibited by valproic acid
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Research Questions
1. What role does placental UGT play in detoxifying drugs (like LTG)?
2. To what extent do anti-seizure drugs (like LTG) inhibit UGT activity?
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My Research Proposal
Use 4-MU to establish UGT2B7 glucuronidation activity4-MU 4-MUG using UGT-2B7
Probe used to set up a procedure to detect LTG-Gluc formation in placental samples
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Methods: Setup
4-MU 4-MUG Microplate detection method to
quantitatively determine the disappearance of 4-MU through diminishing fluorescence over time
4-MUG does not fluoresce with as much intensity and at a different wavelengths as 4-MU
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Methods: Procedure
Variables: +/- protein (expressed UGT 2B7, rat liver microsomes,
human placental microsomes) +/- uridine diphosphoglucuronic acid (UDPGA), magnesium chloride, alamethicin 4-methylumbelliferone (4-MU) Buffer Time temperature
Taken from: http://www.bdbiosciences.com/discovery_labware/products/display_product.php?keyID=515
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Results
Emission Spectra
300 350 400 450 500 550 6000
50
100
150
200Blank4-MUG4-MU
wavelength (nm)
Inte
nsi
ty
Excitation Spectra
275 300 325 350 375 400 425 450 4750
50
100
150
2004-MU4-MUG
Wavelength (nm)
Inte
nsity
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Results
Human placenta Microsomes
0 10 20 30 40 50 60 700
250
500
750
1000
1250
With UDPGAWithout UDPGA
*
Time
Flu
ore
scen
ce
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Methods: Setup
LTG LTG-Gluc Detection by reversed phase HPLC UV monitoring at 254 nm
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Methods: Procedure
Variables: +/- protein (expressed UGT 2B7, rat liver
microsomes, human placental microsomes) +/- uridine diphosphoglucuronic acid
(UDPGA), magnesium chloride alamethicin Lamotrigine Buffer Time Temperature
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Results
Standard Curve 070629
0 25 50 75 100 1250
50000
100000
150000
200000
250000
300000
350000
r2=0.9995
[Lamotrigine] (M)
Pea
k A
rea
(254
nm
)
Standard Curve 070629
0 25 50 75 100 1250
10000
20000
30000
40000
r2=0.9988
[Lamotrigine] (M)P
eak
Hei
gh
t (2
54n
m)
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Results254 Peak Height
0
1000
2000
3000
4000
Protein
Pe
ak H
eig
ht
(25
4n
m)
at
tim
e=
2.2
-2.4
min
ute
s
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Results254 Peak Height
0
1000
2000
3000
4000
Peak H
eig
ht
(254n
m)
at
tim
e=
2.2
-2.4
min
ute
s
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Future Study
Improve HPLC method- to remove interfering peaks (background)
14C-UDPGA LTG-Gluc*Confirm HPLC resultsABC transporter substrate?
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Goals
To hopefully understand how the human placenta handles drugs
To clinically determine which medications will be safe for women without dangerous clinical trials
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References
Tatum, Expert Rev Neurother 2006; 6: 1077-86. Rowland et al, Drug Metab Disp 2006; 34: 1055-62 "Lamotrigine." Facts & Comparisons 4.0. 2007. Wolters Kulwer
Health INC.. 19 Jul 2007 <http://online.factsandcomparisons.com/monodisp.aspx?book=dfc&monoid=fandc-hcp11195&searched=lamotrigine>.
Christensen et al. Epilesia 2007; 48: 484-9
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Acknowledgements
Dr. Phillip Gerk Dr. Joseph Ritter Fay Kessler
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QUESTIONS?