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Drugs of Addiction. Elizabeth McQueen, LMHC Clinical Director Stewart-Marchman Center NET Training Institute Freedom Series. Course Objectives. To define psycho active chemicals To examine the routes that drugs take to the brain and the ways in which they affect brain chemistry
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Drugs of Addiction Elizabeth McQueen, LMHC Clinical Director Stewart-Marchman Center NET Training Institute Freedom Series
Course Objectives • To define psycho active chemicals • To examine the routes that drugs take to the brain and the ways in which they affect brain chemistry • To present a system for classifying these psychoactive substances. • To detail the physiological effects of uppers, downers and other commonly abused drugs • To outline the principles of effective prevention and treatment
The Addictive Process: Psychoactive drugs: Substances that affect the central nervous system to cause physical and mental changes to take place
3 Factors that determine the effects a chemical will have • The methods by which people put psychoactive chemicals into their bodies • The speed of transmission to the brain • The attraction of the drug for nerve cells, neurotransmitters and other brain chemicals
Routes of Administration 1. Inhaling 2. Injecting 3. Mucous Membrane Absorption 4. Oral Ingestion 5. Contact Absorption
Inhaling The vaporized drug enters the lungs and is rapidly absorbed through tiny blood vessels in the lungs called capillaries. It travels back to the veins and then the heart where it is pumped directly to the brain and the rest of the body. Time of transmission: 7-10 seconds for change to begin
Inhaled drugs • Marijuana • Freebase cocaine • Glue • Aerosols • Cigarettes
Characteristics of Inhaled drugs • Effects felt quickly • Easy to regulate the amount of the drug used • Only small amount absorbed with each inhalation
Injecting • Intravenous injecting – “Slamming” Injected directly into the blood stream by way of a vein • Intramuscular injecting – “muscling” Injecting into a muscle mass • Subcutaneous – “Skin popping” Injecting just under the skin Time of transmission: 15-30 seconds in the vein
Time of transmission for injected drugs: • 15-30 seconds in the vein • 3-5 minutes in the muscle or under the skin
Injected Drugs • Heroin • Cocaine • methamphetamines
Characteristics of Injected Drugs • Large amount absorbed at once • Instant “RUSH” • Nothing of the drug is wasted
Snorting and Mucosal absorption • Insufflation – absorption into the muscosa membranes in the nasal passages • Sublingual – absorption into the mucosa under the tongue • Buccally – between the gums and the cheek • Rectally – absorption into the mucosa in the rectum • Vaginally – absorption into the mucosa in the vagina
Time of Transmission • From 3 to 15 minutes depending on the place of administration
Drugs of Mucosal Absorption • Cocaine • Herion • nitroglycerin • Chewing tobacco • Morphione
Characteristics of Mucosal Absorbed Drugs • Results more rapid • High more intense • Bypasses the digestive acids, enzymes and liver
ORAL • Swallowed • Passes through the esophagus into stomach • Absorbed in to the capillaries and enters the vein and liver • Pumped back to the heart and on to the rest of the body
Time of transmission • 20-30 minutes from administration
Drugs of Oral Admission • Oxycontin • Xanax • Valium • Loratab • Robotussin • Alcohol
Characteristics of Oral Ingested Drugs • Low Concentration at Absorption • First Pass metabolism (first absorbed) drugs are most potent
Transdermal Absorption • Absorbed through the skin • Lotions • Eye drops • Patches • Stamps
Time of Transmission • 1-2 days for effects to be noticed • Up to 7 days of absorption in the average patch
Drugs of transdermal absorption • Nicotine • Fentanyl • Clonidine • LSD • Cocaine
Characteristics of Transdermal Administration • Usually by prescription • Measured amount of the drug • Seldom used for illegal drugs
Drug Distribution: GETTING TO THE BRAIN • Distribution depends on Blood volume and characteristics of the drug • Less blood volume, increased potency • MOST PSYCHOACTIVE DRUGS ARE FAT SOLUABLE • THEY CAN CROSS THE BLOOD BRAIN BARRIER
The Blood Brain Barrier • The Gateway to the central nervous system • The wall of the capillary in the brain which is sealed to act as a barrier to the brain. • Only Fat soluble drugs can cross the blood brain barrier
The Nervous System • The Central Nervous System – half of the complete nervous system, includes the brain and the spinal cord • The Peripheral Nervous System –the Other part of the nervous system which connects the CNS with the internal and external systems Includes the autonomic nervous system and the somatic nervous system
The Central Nervous System • The Brain – Computer of the body, receiving, analyzing and responding to messages from the peripheral nervous system • Controls circulatory response • Respiration • Digestion • Excretory function • Endocrine function • Reproductive function • Enables us to reason and make judgments
Autonomic Nervous System • Controls involuntary functions such as • Circulation • Digestion • Respiration • Glandular outputs • Genital reactions • Sympathetic responses
Somatic Nervous System • Includes sensory neurons that reach the skin, muscles and joints. Responsible for relaying information about muscle and limb position • Transmits instructions back to skeletal muscles • Provides for voluntary response
Understanding how nervous system processes messages • Neurons - nerve cells that act as the building blocks of the nervous system
Parts of a neuron: (see handout) • Dendrites- finger like bodies that receive signals from other cells and then relay them to the cell body • Soma – the cell body • Axon – the finger like bodies that carry the signals away from the cell • Terminals – the pathway that carries the signal from one cell to the dendrites of the next cell.
Terminals of one cell do not touch the dendrites of the next cell • Synaptic Gap – the microscopic space between the terminals of one cell and the dendrites of the next cell A message jumps the synaptic gap in the form of neurotransmitters.
Neurotransmitters – bits of chemicals that are synthesized electrical signals that jump the synaptic gap Vesticles – tiny sacs that store neurotransmitters Synapse – the transmission process across the synaptic gap
Receptor Sites – Protein molecules that are activated by neurotransmitters. • When receptor sites are activated, they open a molecular gate that allow electrical charges in or out
The process of message transmission (see handout) • Incoming electrical signals force the release of neurotransmitters • From the vesticles • And send them across the synaptic gap • On the other side the neurotranmitters “fit themselves” into • receptor sites • The receptor sites open the ion molecule gate
Allowing the electrical charges in or out • When enough electrical charge is achieved, the next signal fires • Once the job is done, neurotranmitters return to the synaptic gap and are reabsorbed by reuptake ports • Auto receptors monitor the amount of neurotransmitter needs for the transmission
Psychoactive drugs disrupt the process of message transmission Drugs that enhance the activity of the neurotransmitters and receptor sites are called agonists Drugs that block activity are called antagonists
AGONISTS: Cocaine - forces the release of extra neurotranmitters and blocks their reabsorption ANTAGONISTS: Heroin – inhibits the release of neurotransmitters and therefore blocks a message of pain from reaching the brain Specific Drug Examples:
The body regards any drug as a toxin, but ifthe use continues over a long time, it is forced to adapt and and develop a tolerancefor the drug Tolerance – the need to use increase amounts to get the same effect!
Types of Tolerance • Dispositional Tolerance – the speeding up of metabolism in order to eliminate the drug • Pharmacodynamic Tolerance – nerve cells become less sensitive to the drugs • Reverse Tolerance – when the body systems are no longer able to metabolize drugs and the body can no longer tolerate the drug (alcohol absorption after liver destruction)
Acute tolerance – an automatic acceptance of a drug by the body Select Tolerance- When increased quantities of a drug are taken to overcome acute tolerance in order to produce a high Inverse Tolerance – When a person becomes more sensitive to the effects pf a drug as the brain’s chemistry changes
Withdrawal – the bodies attempt to rebalance itself Nonpurposive Withdrawal – Physical withdrawal -objective physical signs that are directly observable when a drug is stopped. EXAMPLES: • Seizures Sweating • Goosebumps Vomiting • Diarrhea Tremors
Purposive Withdrawal-psychological withdrawal Resulting behavior exhibited by an addict when the drug stops EXAMPLES: • Manipulation • Psychic Conversion (anticipated nonexistent symptoms of withdrawal) • Malingering
Protracted Withdrawal: Environmental Influence • Withdrawal stimulated by environmental triggers or cues EXAMPLE: Any white powder may trigger a cocaine addict
Body Effect vs Withdrawal See hand out on opioids
Metabolism - the body’s mechanism for processing foreign substances • Excretion – the process of eliminating foreign substances
What effects Metabolism • Age – after 30 the body produces less enzymes • Race – different ethnic groups have different levels of enzymes • Sex – males and females metabolize at different rates • Health – certain conditions affect metabolism
Emotional Health – Metabolism is affected by preexisting chemical imbalance Other Drugs – two or more drugs will have the body fighting for metabolism attention making the process slower
Desired Effects of Drug Use • Curiosity Satisfaction • To “get high” and be in dreamlike state • To self –medicate • To have confidence • To have energy • Pain Relief • Anxiety Control • Peer influence • Social Confidence • Boredom Relief