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Effects of Drugs and Other Agents on the Synapse Tada Obert Department of Livestock & Wildlife Management Midlands State University Contents Stimulants Sedatives Anesthetics Opiates/Opioids Tranquilizers Antidepressants Psychedelics Marijuana/Mbanje Stimulants most widely used are caffeine (in coffee, tea, and cola beverages) nicotine (in cigarettes) amphetamines cocaine these drugs mimic the stimulation provided by the sympathetic nervous system. Nicotine binds to a subset of acetylcholine (ACh) receptors. – nicotine is strongly addictive. Amphetamines and cocaine bind to — thus blocking — transporters used for the reuptake of dopamine (and noradrenaline) into presynaptic neurons. – causes the level of dopamine to rise in the synapses & appear to mediate the pleasurable effects. Stimulants cont’d chief medical uses for amphetamines to help lose weight (becoz they suppress appetite); to help with Attention Deficit/Hyperactivity Disorder to perform better in school. Cocaine been used for thousands of years in the Andes of South America. In order to achieve its effects, cocaine must cross the blood-brain barrier. If antibodies are bound to the cocaine molecule, it cannot cross. this has raised the possibility of immunizing against cocaine (works in mice). Sedatives Sedatives induce sleep & include: 1. ethanol (beverage alcohol) 2. barbiturates, such as phenobarbital secobarbital (Seconal®) 3. meprobamate (Miltown®, Equanil®) 1. Ethanol/Ethyl alcohol the sense of well-being that it induces at low doses. perhaps low doses sedate those parts of the brain involved with, for example, tension and anxiety and in this way produce a sense of euphoria. however, higher doses depress brain centers involved in such important functions as pain sensation, coordination, and balance. at sufficiently high doses, the reticular formation can be depressed enough to cause loss of consciousness. 2. Barbiturates often prescribed to prevent seizures as well as sleeping pills. mimic some of the action of alcohol – particularly in their ability to depress the reticular formation (thus promoting sleep) and, – in high doses, the medulla oblongata (thus stopping breathing). barbiturates and ethanol both bind to GABAA receptors. – ligand-gated channels that enhance the flow of chloride ions (Cl−) into the postsynaptic neuron, thus increasing its resting potential and making it less likely to fire. increase the natural inhibitory effect of GABA synapses. 3. Meprobamate prescribed as a tranquilizer, but its action is quite different from the tranquilizers discussed below. molecular activity is like that of other sedatives and in combination can produce a lethal overdose. sedatives produce two related physiological effects: tolerance — the necessity for a steadily-increasing dose to achieve the same physiological and psychological effects physical dependence — withdrawal of the drug precipitates unpleasant physical and psychological symptoms. These traits are also shared with nicotine, opiates, and other psychoactive drugs. Anesthetics Most of these are volatile hydrocarbons or ethers. They bind to GABA receptors in the spinal cord and brain decreasing the sensitivity of the postsynaptic neurons. 1,4-Butanediol is a common solvent. – when ingested, it is converted into γ-hydroxybutyrate, an increasingly-popular (and illegal) "club drug". – γ-Hydroxybutyrate acts on GABAB receptors. – Conversion of 1,4-butanediol to γ-hydroxybutyrate requires the enzyme alcohol dehydrogenase, the same enzyme used to metabolize ethanol. – Ingesting both ethanol and 1,4-butanediol delays the effects of the latter. Opiates/Opioids substances isolated from the opium poppy or synthetic relatives. Examples: Morphine, codeine, heroin, methadone, oxycodone. depress nerve transmission in sensory pathways of the spinal cord and brain that signal pain. – explains why opiates are such effective pain killers. also inhibit brain centers controlling coughing, breathing, and intestinal motility. morphine and codeine are used as pain killers. – codeine is also used in cough medicine. are exceedingly addictive, quickly producing tolerance and dependence. although heroin is even more effective as a painkiller than morphine and codeine, it is so highly addictive that its use is illegal. Opiates/Opioids cont’d Methadone is a synthetic opiate that is used to break addiction to heroin (and replace it with addiction to methadone). Opiates bind to µ receptors of the G-protein located on the subsynaptic membrane of neurons involved in the transmission of pain signals. Release of enkephalins suppresses the transmission of pain signals. By binding to enkephalin receptors, opiates like morphine enhance the pain-killing effects of enkephalin neurons. µ receptors are also found on the cells in the medulla oblongata that regulate breathing. – accounts for the suppressive effect opiates have on breathing. Opiate antagonists – such as naloxone (Narcan®) & naltrexone (ReVia®) bind to µ receptors & prevent binding of opiates themselves. Tranquilizers act like sedatives in reducing anxiety and tensions – But do not have their sleep-inducing effect. often subdivided into the major tranquilizers and minor tranquilizers. Major tranquilizers Examples: Chloropromazine & haloperidol used to treat schizophrenia, a common and devastating mental disease. act by binding to a class of receptors for the neurotransmitter dopamine. drugs block the action of dopamine, and in a homeostatic response, the neurons increase their activity. Minor tranquilizers (treat anxiety) most belong to a group called benzodiazepines, which act on interneurons that use the inhibitory neurotransmitter GABA. – bind to GABAA receptors on postsynaptic membrane & enhance the action of GABA at the synapse. Antidepressants increase the amount of serotonin at synapses that use it as a neurotransmitter. Monoamine oxidase (MAO) inhibitors – act on a mitochondrial enzyme that breaks down monoamines such as noradrenaline and serotonin. – by inhibiting the enzyme in presynaptic serotonin-releasing neurons, more serotonin is deposited in the synapse. Tricyclics and tetracyclics – block the reuptake of both noradrenaline and serotonin causing an increase in the level of these neurotransmitters in the synapse. antidepressants do not relieve the symptoms of depression until a week or more after dosing begins. – during this period, the number of serotonin receptors on the postsynaptic membranes decreases. Bupropion blocks reuptake of noradrenaline and dopamine Atomoxetine selectively interferes with the reuptake of noradrenaline Psychedelics distort sensory perceptions, especially sight and sound. some e.g. mescaline, psilocybin and dimethyltryptamine (DMT) are natural plant products. others are synthetic (lysergic acid diethylamide (LSD), dimethoxymethylamphetamine (DOM), methylenedioxymethamphetamine (MDMA or "ecstasy"). – DOM and MDMA share the stimulant qualities of amphetamines. all the psychedelics have a molecular structure that resembles serotonin and probably bind to serotonin receptors on the postsynaptic membrane. Marijuana/Mbanje active ingredient in marijuana is delta-9-tetrahydrocannabinol (Δ9-THC). binds to: CB1 receptors (G-protein-coupled receptors) that are present on presynaptic membranes in several parts of the brain; CB2 receptors that are found on cells of the immune system (e.g., B cells and T cells). THC produces: the drowsiness of sedatives like alcohol the dulling of pain (like opiates) and in high doses, the perception-distorting effects of the psychedelics. Marijuana unlike sedatives and opiates, however, tolerance to THC does not occur. drug is excreted so slowly from the body that, with repeated use, a given response is achieved by a lower dose. turn out to have multiple effects, the clearest ones so far are their effects on: – appetite • humans with cancer or AIDS find that marijuana improves their appetite. – neuronal activity in the brain. • Marijuana has been used for centuries to control epileptic seizures in humans. KETE