* Your assessment is very important for improving the workof artificial intelligence, which forms the content of this project
Download DRUG A - University of Kentucky
NK1 receptor antagonist wikipedia , lookup
Nicotinic agonist wikipedia , lookup
Toxicodynamics wikipedia , lookup
Pharmacognosy wikipedia , lookup
Drug discovery wikipedia , lookup
Pharmacogenomics wikipedia , lookup
Prescription drug prices in the United States wikipedia , lookup
Polysubstance dependence wikipedia , lookup
Pharmaceutical industry wikipedia , lookup
Theralizumab wikipedia , lookup
Prescription costs wikipedia , lookup
Drug design wikipedia , lookup
Pharmacokinetics wikipedia , lookup
Drug interaction wikipedia , lookup
Neuropsychopharmacology wikipedia , lookup
Psychopharmacology wikipedia , lookup
Gender Differences in Alcohol and Drug Response Thomas H. Kelly, PhD Department of Behavioral Science College of Medicine University of Kentucky (859) 323-5206 [email protected] Pharmacokinetics • Bioavailability – Absorption and first-pass metabolism • Distribution – Body fat/volume of distribution – Protein binding – Body size • Metabolism – Phase I CYP450 superfamily – Phase II reactions • Excretion – Glomular filtration rate varies with body weight Pharmacodynamics • CNS drugs – Striatal dopamine release and reuptake – SSRI’s and other antidepressants – Anit-anxiety medications – Anesthetics – Seizure medications – Drug Abuse • Cardiovascular drugs • Energy drugs • Immune system drugs Neuropharmacology of Estrogen and Progesterone Hormones have powerful influences on behavior… Hormones do not “cause” behavior; they alter probabilities of responses to given stimuli One hormone can have many effects: A single hormone can affect complex behaviors Pfaff, Phillips & Rubin, 2004 Neuropharmacology of Estrogens and Progestins • Function as neurotransmitters acting at nuclear receptor sites to regulate gene activity in the neuron • Function as direct or indirect neuromodulators of neuronal membrane receptor systems that are targeted by classical neurotransmitters (e.g., dopamine, 5-HT, GABA, glutamate, etc.) Estrogens • Steroid hormones (~ 30) produced by the ovaries – Estradiol – Estrone – Estriol • Synthesized in the CNS from circulating testosterone Behavioral Effects of Estrogens • • • • Sexual Behavior Learning & Memory Mood Neural Structure/Organization • • • • • • Alzheimer’s/Dimentia Parkinson’s Disease Drug Abuse Depression Brain Injury Pain Estrogens • Nuclear Receptor – ER – ER • Neurotransmitter Modulation – – – – – – – Acetylcholine Dopamine Norepinephrine Serotonin Glutamate GABA Opioid Estrogen Modulation of Dopamine • • • • Increases DA synthesis Upregulation of DA receptors Reduced DA clearance Enhanced DA release Estrogen Modulation of Dopamine Neurotransmission Becker, 2000 Amphetamine Effects Across the Menstrual Cycle Justice & de Wit, 1999 Amphetamine Effects Across the Menstrual Cycle: A Replication White, Justice & de Wit, 2002 Drug Discrimination • Drug cues established via discrimination training appear to be mediated by drug actions at the cellular level • In vivo behavioral model of receptor function Stimulus Control R Light ON L R Light OFF L R+ (e.g., Food) S No Consequence No Consequence R+ (e.g., Food) S Drugs Exert Stimulus Control R R+ (e.g., Food) S Drug L R No Consequence No Consequence Placebo L R+ (e.g., Food) S Methods Training Phase Two DRUG A Sampling Sessions Control Phase Up to 12 Sessions to correctly identify DRUG A vs. NOT DRUG A Correct = $$$ Test Phase Test various doses of training drug during different menstrual cycle phases. Test phase only during particular menstrual cycle phase(s) with hormone pretreatment. Drug-discrimination task Drug A 60 Not Drug A 0 10 Subjects • Healthy adult females who were all using oral birth control including a 5-6 day placebo phase • Occasional stimulant use • All provided written consent prior to participation and were paid for participation • Study was approved by the UK Medical IRB Daily Schedule • • • • • 9:00 Check In 9:10 Assessment 9:15 Snack 9:45 Dose 10:15 Assessment • • • • • 10:45 Assessment 11:15 Assessment 11:45 Assessment 12:15 Assessment 12:45 Assessment Assessment: ARS, VAS, ARCI, DSST, Drug Discrimination and cardiovascular measures. placebo 15 mg/70 kg d-amphetamine % Drug-Appropriate Responding % Drug-Appropriate Responding d-Amphetamine Discrimination 100 80 60 40 100 80 60 40 20 20 0 0 30 60 90 120 Time (min) 150 180 PL 3.125 7.5 15 d-amphetamine (mg/70 kg) d-amphetamine d-amphetamine + estradiol 100 % Drug-Appropriate Responding % Drug-Appropriate Responding % Drug-Appropriate Responding d-Amphetamine Discrimination: Estradiol Pretreatment 80 60 40 20 0 PL 3.125 7.5 15 d-amphetamine (mg/70 kg) d-amphetamine d-amphetamine + estradiol 100 % Drug-Appropriate Responding % Drug-Appropriate Responding % Drug-Appropriate Responding d-Amphetamine Discrimination: Estradiol Pretreatment 3.125 mg/70 kg d-amphetamine 80 60 40 20 0 30 60 90 120 Time (min) 150 180 Subject Ratings Like Drug Subject Ratings Like Drug VAS: Like Drug Subject Ratings Like Drug Subject Ratings Like Drug ARS: Stimulated Estrogen modulates the neuropharmacological and behavioral effects of d-amphetamine • Extracellular dopamine increased • Stereotypical behaviors enhanced • Self-report of stimulant drug effects enhanced • Self-report effects are not easily replicated • Discriminative stimulus effects enhanced Progestins • Steroid hormones produced by the ovaries, placenta and adrenals – Progesterone – Progesterone Metabolites • Progestins are also synthesized in the CNS Biosynthesis of Neurosteroids Allopregnanolone Pisu & Serra, 2004 Behavioral Effects of Progestins • Sexual Behavior • Learning & Memory • Mood • • • • • • • Epilepsy Depression Sleep Anxiety Stress Alcohol/Drug Abuse Brain Injury Progestins • Nuclear Receptor – PRA – PRB • Neurotransmitter Modulation – GABAA Receptors – Nicotinic Acetylcholine Receptors – Sigma • NMDA Progesterone Regulation of GABA • Upregulate GABA receptors • Modulate GABA binding (?) • Direct Agonist (?) Progesterone Modulation of Triazolam Effects in Postmenopausal Women • 16 healthy postmenopausal women not using HRT • Random Assignment – Placebo + Triazolam (0.5 mg IV) – Progesterone (300 mg PO) + Triazolam (0.5 mg IV) • Lower doses administered to progesterone group • Behavioral effects adjusted to triazolam levels Progesterone Modulation of Triazolam Effects in Postmenopausal Women McAuley et al., 1995 Discriminative Stimulus Effects of Alcohol and Allopregnanolone Across the Menstrual Cycle Grant et al., 1997 Discriminative Stimulus Effects of Alcohol and Allopregnanolone Across the Menstrual Cycle Grant et al., 1997 Discriminative Stimulus Effects of Alcohol and Allopregnanolone Across the Menstrual Cycle Grant et al., 1997 Progesterone Modulates the Behavioral Effects of GABA Agonists • Progesterone enhances the performance impairment engendered by Triazolam • Enhanced discriminative stimulus effects of GABAA agonists • Alcohol • Triazolam • Allopregnanolone Estrogens and progestins can have powerful influences on behavior… These hormones do not “cause” behavior; they can modulate behavior via both genomic and nongenomic neuropharmacological mechanisms Estrogens and progestins can affect many complex behaviors Adverse Consequences: Alcohol • Men vs. Women – Women consistently achieve higher BAL’s for drinking the same amount as men • Due to body water? • Due to differential enzyme activity? – Other factors • Women progress to alcoholism more rapidly • Effects of estrogen and progesterone • Cycling of women’s hormones Gender Differences: Alcohol • Pharmacology – Differential activity of alcohol dehydrogenase in men and women – Women have a lower proportion of body water – Women have a lower first pass metabolism – Combined, these factors allow women to achieve consistently higher BALs even when drinking the same amount as men