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Emerging Evidence for the Role of Polymorphic Drug Metabolizing Enzymes in Smoking Behavior and Treatment. Caryn Lerman & Rachel Tyndale University of Pennsylvania & University of Toronto. Polymorphic Drug Metabolizing Enzymes CYP2A6 and CYP2B6. Genetic polymorphisms Ethnic variation
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Emerging Evidence for the Role of Polymorphic Drug Metabolizing Enzymes in Smoking Behavior and Treatment Caryn Lerman & Rachel Tyndale University of Pennsylvania & University of Toronto
Polymorphic Drug Metabolizing EnzymesCYP2A6 and CYP2B6 Genetic polymorphisms • Ethnic variation • Association with nicotine metabolism • Association with smoking behavior Therapeutic approaches • Traditional NRTs • Novel treatments
Nicotine removal (i.e. metabolism) Nicotine intake (i.e. smoking) 80% NICOTINECOTININE CYP2A6 Nicotine Dependent Individuals Adjust Smoking Behavior to Maintain Nicotine Levels
Centromere Telomere Chromosome 19 Gene cluster CYP2A and CYP2B 350bp 2A6 2A7 2B7 2B6 94% homologous
Frequencies of CYP2A6 variant alleles vary among ethnic groups WHO statistics African Americans Caucasians Chinese Japanese Canadian Natives
Genetic Variation in CYP2A6 alters nicotine and cotinine plasma levels Nicotine 4 mg base, oral Japanese subjects (Xu et al., 2001) Nicotine inactive Cotinine *4/*4 reduced *1/*1 plasma (ng/ml) *1/*4 *1/*4 *1/*1 *4/*4 active Time (min) Time (min) People with 1 or 2 inactive (*4) alleles have significantly higher NIC (2.3x, 2.8x) and lower COT (7x, 12x)
CYP2A6 slow metabolizers are at lower risk for becoming tobacco dependent • Caucasians with an inactive alleles (*2, *4, *10) or low activity alleles (*7) are “slow” nicotine metabolizers • Allelic variants less frequent in smokers vs non-smokers: Odds Ratio = 0.46 ( 95% CI: 0.22-0.95) • indicates slow nicotine inactivators are less likely to become smokers Caucasians OR 0.46 (0.22-0.95) P = 0.034 Slow metabolizer frequency (%) Non-smokers Smokers TND (N=334) TD (N=365) Tyndale et al, 2001
CYP2A6 Genotype Alters Smoking (n=296 Caucasians) Carbon Monoxide Levels (ppm)* Plasma Cotinine Levels (ng/ml) P<0.05 P<0.05 *1/*1 (n=277) *1/null (n=14) *1/dup (n=5) *1/*1 (n=277) *1/null (n=14) *1/dup (n=5) Rao et al., 2000 *dose and timing not controlled
Summaryof 2A6 Epidemiological Data CYP2A6 ( activity variant) • Decreased nicotine metabolism • Decreased risk for tobacco dependence • Decreased smoking rate and exposure • Increased success quitting (Gu et al., 2000)
Human Brain CYP2B6 (and rat CYP2B1) Alters Local Drug and Metabolite concentrations • Inactivate Drugs: Nicotine (central metabolic tolerance?) • Activate Drugs: Bupropion (greater efficacy?) • Endogenous Substrates: metabolizes Testosterone Mutagenicity and Genotoxicity • Activate tobacco-smoke procarcinogens (i.e. NNK)
6 4 2 0 Nicotine Induces Increase in Brain Levels of CYP2B6 Enzyme Brain Stem Protein *** ** Relative Density Units ** Brain Stem Protein Saline 0.1 0.3 1.0 mg/kg Nicotine S Miksys et al., Biochem Pharmacol 59(12): 1501-1511, 2000.
17 14 13 12 11 10 9 8 7 6 5 20 23 16 17 15 21 22 24 Nonsmokers Smokers CYP2B6 is found at higher levels in specific brain regions of smokers, compared with nonsmokers Non-Smokers (n=10) Smokers (N=14) Density Units 4 2 0 FC TC CG OC HC EC CD PT NA GP SN CV CH
Interactions between environment and genotype on Hippocampal CYP2B6 P=0.03 x3.9 P=0.07 x2.5 2 CYP2B6 Denisty P=0.07x1.7 1 0 Miksys, Lerman, Shields, Mash, Tyndale, 2003 Wt Wt Mut Mut NS SMK NS SMK
Bupropion Male Female n=88 n=109 n=106 n=123 P<.05 for sex x geno x trt CYP2B6 and Smoking Cessation Lerman, Shields et al. Pharmacogenetics, 2002 Placebo Male Female
QUIT P<.05
CYP2B6( activity variant) • Lower brain 2B6 levels • Decreased induction of enzyme by smoking • (Slower nicotine clearance &increased tolerance)? • Increased cigarette cravings • Decreased success quitting • Therapeutic application? Summary: CYP2B6
CYP2A6 inhibitors & oral nicotine pills (4 mg) increasebioavailability & decreasedesire to smoke in deprived smokers during 90 minute ad-lib period Mean plasma nicotine Mean of “desire to smoke” 8 0 p = 0.0001 p = 0.0001 7 -5 6 -10 5 -15 4 Mean (ng/ml), baseline adjusted -20 Mean Score, baseline adjusted 3 -25 2 -30 1 p = 0.007 p = 0.02 -35 0 -40 Placebo Methox- salen Tranyl- cypromine Placebo Methox- salen Tranyl- cypromine Sellers & Tyndale, 2000
40 p = 0.01 p = 0.01 30 20 Mean (±SEM) (min) 10 0 2A6 In & Nic 2A6 In & Plac Plac & Nic Plac & Plac CYP2A6 inhibitors & oral nicotine pills (4 mg) leads to reduction in smoking Latency Between Cigarettes Number of cigarettes smoked decreased Total cigarette puffs decreased Time between cigarettes increased Sellers & Tyndale, 2000
Inhibition of CYP2A6 Increases Nicotine from Nicorette (4mg) n=11 *1/*1 genotype 52% Increase in Nicotine Concentration with Methoxsalen 35 * 30 * * 25 * * 20 15 Day 3 Nicotine (ng/mL) 10 5 0 8:00 9:00 10:00 11:00 12:00 13:00 14:00 15:00 16:00 17:00 Time Methoxsalen Placebo
Therapeutic Implications Systemic Inhibition of 2A6* • Increase nicotine from tobacco & decrease smoking • Increase nicotine from NRTs & improve efficacy Induction of Brain 2B6? *Sellers & Tyndale, 2000
Acknowledgements! University of Toronto: Rachel Tyndale, Sharon Miksys, Ewa Hoffman, Chun Xu, Yushi Rao, Bo Xu, Edward Sellers University of Pennsylvania : Janet Audrain, Paul Wileyto, Angela Pinto, Vyga Kaufmann, Sue Kucharski, Mike Burdick, Freda Patterson Georgetown University: Peter Shields Brown University: Ray Niaura UCSF: Neal Benowitz Tyndale Lab: Canadian Research Chair in Pharmacogenetics NIDA: DA06889 Centre for Addiction and Mental Health CIHR: MT-14173; MT-14719, training grant and doctoral awards NCIC: 010271, Ontario Mental Health Foundation, Nicogen Res.