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Nicotine Troy Hanson, Betsy Casey, Levi Kellogg
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Topics Covered Background and History Pharmacology Route of Administration Biotransformation Pharmacological and Physiological Effects Addiction and Kicking the Habit
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Background and History Two major sources of nicotine – Large leaf tobacco plants (Nicotiana tabacum) – Small leaf tobacco plants (Nicotiana rustica) Initially administered through chewing and the smoking of pipes and cigars. – Finely powdered tobacco leaves (snuff) were also snorted. 1610- first attempts to commercialize tobacco in Virginia by the English. Cigarettes were first used around 1850 in England and over the next 30 years in America. Image from: agecon.vt.edu
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Why Do Plants Make Nicotine? No role in pollination, storage, or photosynthesis. Toxic to vertebrates and insects. – Causes paralysis in insects. – Believed to be an evolutionary response to insect predation. Nicotine containing insecticides have largely been replaced by safer alternatives. Image from: marketeo.com
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Basic Pharmacology and Smoking Nicotine was isolated in 1828 by Posselt and Reimann. Typical cigarette- 6 to 11 mg of nicotine. Vaporized at 800⁰ Celsius in cigarettes. – Attaches to tar molecules which contribute to the unique smell and taste of cigarettes. Average smoker takes 10 total puffs from a cigarette at intervals of 30-60 seconds. – Nicotine reaches brain in only 7 seconds.
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Smoking Facts Most common mode of transport for nicotine. Yearly consumption is highly variable. 2002- 70 million Americans used tobacco. Consumption is related to many social factors. Cigarettes cause a large reduction in the activities of MAO-A and MAO-B. – Not caused by nicotine. – Slows the breakdown of DA. Textbook Image p. 313
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Biotransformation 70-80% is transformed to cotinine by cytochrome P450 2A6. – Amount of CYP2A6 activity varies from person to person. – Cotinine and other metabolites are mainly secreted in urine. Half-Life of about two hours. Textbook Image p.304
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Pharmacokinetics Activates nicotinic cholinergic receptors. – nAChRs found in the cerebral cortex, thalamus, striatum, hippocampus, autonomic ganglia, and monoamine- containing nuclei. Produces a sodium influx creating an excitatory response. – Some nAChRs also open calcium channels and act on presynaptic nerve terminals. High doses produce continuous depolarization leading to nicotine poisoning. Textbook Image p.306
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Nicotine and the Mesolimbic System Reinforcing affects mediated by the mesolimbic dopamine pathway from the VTA to the NA. Animals and humans will self-administer nicotine. – Not as reinforcing as cocaine, amphetamine, or opioids. Adolescents who use the drug have an increased chance of addiction. Image from: treatobacco.net
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Pharmacological Effects Different effects in smokers and nonsmokers. – Smokers- increases calmness and relaxation. – Nonsmokers- increases attention, tension, produces nausea, dizziness. Has been shown to increase cognitive function in both smokers and nonsmokers. – Possibly affects the α 4 ß 2 receptor. – Supported by studies of ß 2 knockout mice. Image from: myquit.net
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Nicotine’s Physiological Effects Activates the sympathetic and parasympathetic nervous systems. – Release of adrenaline and noradrenaline. – Release of HCl in the stomach. – Increases metabolic rate and decreases appetite. Produces an increased risk of cardiovascular disease and strokes. Fatal at doses as low as 60 mg. – Causes respiratory failure due to depolarization block of the breathing muscles.
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Nicotine Poisoning Can occur through accidental swallowing and absorption through the skin. – Usually the result of exposure to insecticides or contact with wet tobacco leaves. Symptoms – Nausea, salivation, stomach pain, vomiting, diarrhea, cold sweat, headache, dizziness, confusion, and weakness. Treatment – Induce vomiting (if swallowed) – artificial respiration – shock treatment.
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Tolerance and Dependence Short Term Tolerance – Tolerance can occur over the course of one day. – Dissipates over night. Smokers wake up in the morning craving a cigarette. Long Term Tolerance – First indicated by green-tobacco illness. – Large doses of nicotine produce no symptoms in long time smokers and produce toxic effects in nonsmokers. Dependence – Withdrawal is characterized in rats by gasps, shakes, tremors, and reduced locomotor activity. – Decreased ability to experience reward. – Role of DA release in the NA.
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Formation of Nicotine Dependence 5 Step Process described by Mayhew et al. – 1A: Nonsmoking – 1B: Nonsmoking-contemplation and preparation. – 2: Initiation – 3:Experimentation – 4:Regular smoker – 5:Established smoker Image from: decodeme.com
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“Kicking the Habit” Nicotine replacement – Focuses on: Nicotine withdrawal symptoms, maintaining a level of nicotine circulating in the blood, utilizing safer ways to administer nicotine. First accomplished in 1984. – Gum, patch, nasal spray, inhaler, lozenges. – Combinations with supportive therapy are most successful. Images from: medicineworld.org; bupropion-150mg.com; and mayoclinic.com
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References Meyer, J. S., & Quenzer, L. F. (2005). Psychopharmacology, drugs, the brain, and behavior. (pp. 304-318). Sunderland, MA: Sinauer Associates Inc.
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