Mariana Babayeva MD, PhD Touro College of Pharmacy, New ... · New York, NY, USA. Compound...
Transcript of Mariana Babayeva MD, PhD Touro College of Pharmacy, New ... · New York, NY, USA. Compound...
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Mariana Babayeva MD, PhDMariana Babayeva MD, PhD
Touro College of Pharmacy,Touro College of Pharmacy,
New York, NY, USANew York, NY, USA
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� Compound extracted from plant Aristolochia
� Nephrotoxin and carcinogen
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Chinese herbs
nephropathy Herbal remedies
� AA-I is an organic anion eliminated by the kidney
� Produces nephrotoxic effect to S3 segment of renal proximal tubule
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nephropathy
(CHN)
Herbal remedies
Belgian
nephropathy
Slimming pills:
Aristolochia
fangchi
Balkan endemic
nephropathy
(BEN)
Bread
contaminated by
Aristolochia
clematitis
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� Glomerular Filtration
• GFR: glomerular filtration rate
� Tubular Secretion
• Active transport
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• Secretion transporters: OATs, OCTs, etc.
� Tubular Reabsorption
• Active transport
• Reabsorptive transporters
• Passive transport
� Glomerular Filtration (1)
� Tubular Secretion (2)
� Tubular Reabsorption (3)
� Renal Excretion (4)
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• OAT system plays an important role in tubular secretion and reabsorption of
compounds (organic anions)
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Human:
OAT1 OAT2
OAT3 OAT4
Rodent:
Oats1 Oat2
Oat3 Oat4
Oat5
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� The overall goal of the research was to assess
transport mechanism of renal excretion of AA-I.
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� Further identify potential strategies to mitigate
drug toxicity by reducing renal uptake
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Step 1 Step 2 Step 3
HPLC Method
Protein
Binding
Studies
IPK Stuides
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� Assessment of renal drug excretion mechanism- Dose-linearity- Inhibition studies
� Drug interaction screening
� Model for nephrotoxicity
� Probing renal drug metabolism
� Gender differences in renal function and drug excretion
� Correlation between drug excretion and membrane transporter expression
� Model for aging
� Studies in mutant strains (genetic “knockout” animals)
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cannulate forurine collection
cannulate forkidney perfusion
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� Krebs-Henseleit buffer (KHS buffer)
� Bovine serum albumin (BSA)
� Dextran
� Glucose
� Inulin
� Amino acids
◦ Mixture of 20 amino acids
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Treatment
Group
Compound(s)
(Concentration)Justification
Control
PerfusionNone
Establish viability of preparation and allow
for evaluating of drug effects on kidney
function
AA-I Aristolochic acid I Obtain baseline parameter values of renal AA-I
Excretion
Aristolochic acid I
(20uM)
Obtain baseline parameter values of renal
excretion and of AA-I
AA-I
Transport
Inhibition
Aristolochic acid I
(20uM)
+
Probenecid (1mM)
Study mechanisms of AA-I renal transport
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Viability Parameters Minimum Acceptable Value
GFR > 0.5 ml/min
Glucose Reabsorption (FRGlu) > 90%Glucose Reabsorption (FRGlu) > 90%
Sodium Reabsorption (FRNa) > 85%
Urine Flow Rate > 0.03 ml/min
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p
U
rC
dtdX
Cl =
• dXU/dt = urinary drug excretion rate • Cp = perfusate drug concentration
• XR = excretion ratio• CLr = clearance• fu = fraction unbound• GFR = glomerular filtration rate
GFRf
ClXR
u
r
×
=
XR > 1 = net secretion process
XR < 1 = net reabsorption process
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� Protein Binding of AA-I
� IPK Viability Parameters
� AA-I Renal Excretion Parameters
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Ultrafiltration technique was used for the protein binding studies
Table 1. Summary of AAI Protein Binding Studies in Perfusate
There were no significant differences in protein binding among the different concentrations of AA-I (ANOVA, p >0.05)
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Table 2. Effect of Probenecid on AAI Protein Binding in Perfusate
There was no significant difference in protein binding between
the two study groups (ANOVA, p >0.05)
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Kidney function was well maintained across all study groups
The IPK technique has been successfully applied
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Table 5. Summary of AAI Renal Excretion Parameters in IPK
The renal excretion parameters ~ 2-fold higher in studies with PBC
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Effect of Effect of ProbenecidProbenecid on AAon AA--I I Excretion in the IPK.Excretion in the IPK.
Plot of Cumulative Amount of AA-I Excreted in Urine vs Time.
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� XR of AA-I < 1 (0.08 and 0.17) for both study groups
� The results suggest net reabsorption
� XR of AA-I was more than 2-fold higher in the presence of probenecid
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� Probenecid inhibited the tubular reabsorption of AA-I most probably by
interaction with renal organic anion transport system
� The amount of unrecovered AA-I in Phase I studies was 3-fold higher
than in Phase II
� Probenecid decreased accumulation of AA-I in the kidney cells
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Bidirectional Transport:
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Bidirectional Transport:
Oat2 / Oat5
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• The S3 segment of proximal tubule is the most vulnerable part to AA-I toxicity
• Rat Oat2 and Oat5 are localized to the apical membrane of S3 segment of proximal tubules
• Oat2 and Oat5may take part in active renal reabsorption of AA-I
• Reabsorption of AA-I by Oat2 and Oat5 may cause tubular injury of S3 segments of proximal tubules
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proximal tubules
• AA-I has a high affinity to Oat2
Previous findings
• Inhibition of reabsorption can decrease nephrotoxicity of AA I
Assumption
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� The present study described the transport mechanism of
Aristolochic acid I renal excretion
� The observation suggested that the renal apical transporters (Oat2
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and Oat5) may function as reabsorptive pathway during renal
elimination of AA-I.
� Inhibition of AA-I reabsorption can decrease nephrotoxicity of AA-I.
This assumption requires further investigation
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