6459901
Descripción
Fichas por Madeline Luedke, actualizado hace más de 1 año
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Creado por Madeline Luedke
hace más de 7 años
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| Pregunta | Respuesta |
| Pharmacology | The scientific study of the actions of drugs, and their effects on living organisms |
| Neuropharmacology | drug-induced changes in the functioning of cells in the nervous system |
| Psychopharmacology | Drug-induced changes in mood, thinking or behavior |
| Neuropsychopharmacology | Identify substances that act on nervous system, to help alter behavior for hurt or disease |
| Drug Actions | Refer to the biological changes or the specific molecular changes produces when a drug binds to particular target site or receptor |
| Drug Effects | the widespread physiological or psychological changes that occur as a result of drug action |
| Specific Drug Effects | based on physical and biochemical actions of drug at target site on the body |
| Non-specific drug effects | not based on chemical action, but unique characteristics of person (previous drug experience, present mood, environment, expectation, attitudes) |
| Bioavailability | the amount of drug in the blood that is free to bind at target sites and causes actions |
| Pharmacokinetics | the dynamic other factors that contribute to drug action (absorption, distribution, elimination) |
| Absorption | movement of drug from site of administration to blood circulation |
| Drug Map | 1. Route of administration 2. Absorption/Distribution 3. Binding 4. Inactivation 5. Excretion |
| Different routes of administration | 1. oral 2. intravenous 3. intramuscular 4. intraperitoneal 5. subcutaneous 6. inhalation 7. topical 8. transdermal |
| Oral (PO) | • easy, painless • must dissolve in stomach fluid • be able to pass through stomach walls to blood • resist destruction by stomach fluids • most drugs are not fully absorbed until in small intestine |
| First-pass metabolism (first-pass effect) | PO drugs goes to the liver before the blood which reduce the amount of bioavailability • PO drugs produce blood levels that are irregular, unpredictable, and rise slowly |
| Intravenous (IV) | • placed directly into blood stream • Pros: rapid & accurate • Cons: easy to overdose |
| Intramuscular (IM) | • into muscle •Pro: slower and even absorption (slower if in vegetable oil suspension) • Con: irritation at injection site |
| Intraperitoneal (IP) | • into abdominal cavity • Pro: Rapid (less than IV) • Con: Rarely used in humans |
| Subcutaneous (SC) | • inject below the skin • Pro: slow and steady absorbtion |
| Inhalation | • inhaled directly into lungs • Pro: rapid • lungs have large surface area with capillaries, blood goes directly to brain (no liver first) • surpasses first-pass metabolism |
| T | • applied to mucus membrane • provides local drug effect, but can go system wide |
| Transdermal | • through skin • skin blocks water soluble drugs, but fat soluble can pass • Pro: controlled, sustained passage, at given rate |
| phospholipids | complex lipid molecules • look like Y • single head is negatively charged & hydrophilic (likes water) • two tails are uncharged, fatty & hydrophobic (hates water) |
| hydrophollic | • single head of phospholipid that likes water • touches intra and extra cellular fluids |
| hydrophobic | • two-tail fatty ends stick together |
| Lipid-soluble drugs | • can pass through membranes • move from high concentration to low |
| passive diffusion | move from higher concentration to lower concentration |
| concentration gradient | differences in concentration • the steeper the gradient, the faster the diffusion |
| Ionization | Dissolve into charged ion particles when in water • ionized stuff doesn't pass through membranes easily |
| pH scale and ionization | Strong acids: low numbers, ionize completely in water | battery acid weak acids: kinda ionize | tomatoes Neutral: 7 Weak Bases: kinda ionize | SLC Strong bases: high numbers, ionize completely completely in water | drain cleaner |
| Weak | • tends to dissolve into charged ions • weak doesn't mean not concentrated • most drugs are weak acids/bases |
| Environmental factors and Ionization | • depends on ionizeability of drug (pH) • pH of place drug is being dissolved in • same pH = less ionization • acid <3 base = baby ions • lack of charge means more lipid soluble so it can pass through into blood |
| Ion trapping | drugs can't go back into blood |
| Absorption Factors | 1. Rate: at which stomach empties into small intestine 2. Size: of person, dosages based on 18-65 at 150 lb 3. Sex: of person, women have more fat, less water volume = higher drug concentrations |
| Blood Brain Barrier | • Protects blood-borne substances by dense network of blood vessels • "net" |
| Blood flow and concentration | • most blood flow have higher concentration • heart, brain, kidneys, liver • brain gets 20% of blood that leaves the heart |
| Cerebral Spinal Fluid (CSF) | • made by choroid plexus • fills "spaces" • cushions brain against injury • blood vessels pass through subarachnoid space |
| Typical Capillaries | • Nutrients in/waste out • small openings (intercellular clefts) • big openings (fenestrations) • pinocytotic vesicles (transport stuff through/elevator) |
| Intercellular Clefts | small openings in capillaries |
| Fenestrations | big openings in capillaries |
| Pinocytotic Vesicles | • like an elevator • transports stuff through |
| Brain Capillaries | • Cleft closed with tight junctions • no fenestrations • rare pinocytotic vesicles • surrounded by glial feet of astrocytes |
| Area Postrema | Chemical Trigger Zone (CTZ) | • in medulla of brain stem • detects toxic substances in blood • vomiting center |
| Median Eminence | • of hypothalamus • has fenestrations that let hormones made in hypothalamus move to pituitary gland |
| Placental Barrier | seperates blood circulation of pregnant mother and fetus • lipid-soluble drugs pass easily |
| Drug Depots | reservoirs of drug at inactive sites which trigger no biological effects • plasma protein, muscle, fat |
| Depot Binding | • drug binding at depot sites • displaced drug gets dumped back into circulation |
| Biotransformation | metabolically transformed |
| First-Order Kinetics | • elimination is exponential: constant faction of drug is removed from blood at each time interval |
| Half-life | amount of time needed to remove 50% of drug in blood • after 6 half-lives the drug is gone |
| Zero-Order Kinetics | • drug molecules cleared at constant rate, regardless of concentration • alcohol |
| Microsomal Enzymes | • in the liver • most drugs metabolize through this |
| Two kinds of biotransformation | 1. Phase 1, Nonsynthetic 2. Phase 2, Synthetic |
| Phase 1, Nonsynthetic | • by oxidation • resulting metabolite is less lipid soluble and often less active |
| Phase 2, Synthetic | • required combination of drug with another small molecule (gulcoronide, sulfate, or methyl group) • Resulting metabolite is less lipid soluble, always inactive |
| Cytochrome P450 | • 30 enzymes in this family oxidize a majority of psychoactive drugs |
| Notes on biotransformation | both create metabolites which are more water soluble and easier to excrete • metabolites are returned to the bloodstream • metabolites eliminated by kidneys or bile/feces |
| Factors Influencing Drug Metabolism | • Can affect the magnitude and duration of drug effects • responsible for drug interactions, and individual responses 1. Enzyme Induction 2. Enzyme Inhibition 3. Drug Competition 4. Genetic Polymorphisms |
| Enzyme Induction | repeated use increases liver enzymes = faster metabolism for that drug and all others that need that enzyme • tolerance & cross-tolerance |
| Enzyme Inhibition | some drugs block enzymes = slower metabolism for that and all other drugs needing that enzyme |
| Drug Competition | for same enzymes • can't metabolize both, so levels of one get out of control |
| Genetic Polymorphisms | people vary in metabolism |
| Acetaldehyde | metabolite of alcohol • effects 50% of Asians when this builds up |
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