Psychopharm & PhsyioPsych

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Description and Tags

parts of the brain, neurotransmitters, SSRI's

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117 Terms

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Medulla

Regulates involuntary functions such as respiration and heart rate. involuntary mouth movements (coughing, sneezing, swallowing), respiration, heart rate, blood pressure

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Pons

Involved in movements on both sides of the body and plays a role in sleep. Serves as a communication bridge.

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Cerebellum

Coordinates balance and fine motor skills.

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Reticular Formation

Controls muscle tone, eye movement, and sleep-wake cycles.

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Substantia Nigra

Produces dopamine; low levels associated with Parkinson's disease.

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Hypothalamus

Regulates hormones, hunger, thirst, temperature, and circadian rhythms.

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Thalamus

Acts as a sensory relay station for motor signals (except smell).

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Amygdala

Processes emotions and attaches them to memories.

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Basal Ganglia

Involved in motor control, habit formation, and procedural learning.

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Pituitary Gland

Regulates hormones related to growth, stress, and reproduction.

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Cingulate Cortex

Involved in emotional reactions to pain and motivation.

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Hippocampus

Essential for memory formation and spatial navigation.

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Temporal Lobe

Responsible for auditory processing and language comprehension.

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Parietal Lobe

Processes sensory information and spatial awareness.

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Occipital Lobe

Responsible for visual processing.

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Frontal Lobe

Involved in higher-order thinking, decision-making, and motor control.

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Broca’s Area

Responsible for speech production and grammar.

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Prefrontal Cortex

Involves executive functions like working memory and social judgment.

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Dorsolateral PFC

Associated with executive functions and working memory.

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Ventromedial Prefrontal Cortex

Handles decision-making and emotion regulation.

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Serotonin Reuptake Inhibitors (SSRIs)

Medications for depression that increase serotonin availability.

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Dopamine

A neurotransmitter involved in movement, mood, and reward.

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Acetylcholine

Involved in movement, attention, and early memory.

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Glutamate

An excitatory neurotransmitter; excessive levels can cause excitotoxicity.

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Norepinephrine

Involved in arousal, attention, and mood regulation.

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Serotonin

Regulates mood, sleep, and appetite.

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GABA

An inhibitory neurotransmitter that regulates anxiety and arousal.

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Tricyclic Antidepressants (TCAs)

Medications that inhibit serotonin and norepinephrine reuptake.

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Monoamine Oxidase Inhibitors (MAOIs)

Medications that prevent the breakdown of neurotransmitters due to oxidization for depression.

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First Generation anti-psychotics

Medications primarily used to treat schizophrenia and other severe mental disorders by blocking dopamine receptors.

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Second generation anti psychotics treatment purposes

Medications used to treat schizophrenia and bipolar disorder, often with fewer side effects than first generation drugs, and they also affect serotonin receptors.

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anticholinergic side effects

are unintended effects caused by medications that block the action of acetylcholine, leading to symptoms such as dry mouth, blurred vision, constipation, and urinary retention.

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Low potency first generation anti-psychotics side effects

anticholinergic side effects: urinary retention, constipation, blurred vision, dry mouth

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Types of low potency first generation anti-psychotics

Chlopromazine (throazine) and Thioridazine (mellari)

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Types of high potency first generation anti-psychotics

Haloperidol (Haldol) and Fluphenazine (Prolixin).

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side effects for first generation high potency side effects

extrapyramidal symptoms, akathisia, tardive dyskinesia, and neuroleptic malignant syndrome.

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extrapyramidal symptoms

movement disorders such as tremors, rigidity, and bradykinesia caused by antipsychotic medication. These symptoms result from dopamine receptor blockade in the basal ganglia.

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Second generation anti-psychotics

medications that primarily target serotonin receptors and are used to treat schizophrenia and other mental disorders.

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side effects of second generation anti-psychotics

weight gain, metabolic syndrome, sedation, and increased risk of diabetes.

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which generation of anti-psychotics has the least side effects?

Second generation anti-psychotics

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Disorder that affects the medulla

characterized by respiratory issues and cardiovascular disturbances.

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Drugs that affect the medulla

Opioids disrupt functioning and can lead to death.

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Drugs that affect the pons

Benzodiaziapians and barbiturates to improve sleep

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Disorders that affect the pons

Sleep disorders

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Disorders that affect the cerebellum

Ataxia, symptoms of Parkinsonism

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Ataxia

A neurological sign consisting of lack of voluntary coordination of muscle movements, which can affect walking, hand movements, speech, and eye movements.

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Drugs that affect the cerebellum

Benzodiazaiapins and anti convulsants

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Disorders that affect the Reticular Formation

Coma or sleep disturbances

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Drugs that affect the reticular formation

stimulants can enhance arousal and attention by increasing activity in this area, while depressants may inhibit activity, leading to drowsiness or coma

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Drugs that affect the Substantia Nigra

Ledova (increases dopamine), antipsychotics, stimulants (increase of dopamine in reward pathways)

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Disorders that affect the Substantia Nigra

Parkinson's disease and other movement disorders.

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Disorders that affect the Hypothalamus

Disorders related to abnormal hormone regulation, eating disorders, sleep disorders, and temperature regulation issues.

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Medications that affect the hypothalamus

Hormone therapies

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Disorders that affect the thalamus

sensory processing issues, movement disorders, and alterations in consciousness

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Disorders that affect the Amygdala

PTSD, anxiety disorders, depression and Kluver-Bucy syndrome

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Kluver-Bucy syndrome

characterized by symptoms such as excessive eating, hypersexuality, and changes in emotional responses

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Kluver-Bucy syndrome is caused by

damage to the amygdala

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Disorders that affect the basal ganglia

Conditions such as Parkinson's disease, Huntington's disease, and Wilson's disease that impact motor control, movement regulation, and other neurological functions.

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Drugs that affect the basal ganglia

Medications such as antipsychotics and dopaminergic agents that influence motor control and neurological functions.

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Disorders that affect the Pituitary Gland

Conditions that can involve hormonal imbalances such as pituitary tumors, acromegaly, Cushing's disease, and diabetes insipidus.

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Drugs that influence the pituitary gland

Hormone therapies that address hormonal imbalances and conditions related to the pituitary gland, such as growth hormone deficiencies and disorders affecting hormone regulation.

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Drugs that are associated with the cingulate cortex

CBT increases the volume of the cingulate cortex

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Disorders associated with the Cingulate Cortex

Conditions such as depression, anxiety, and chronic pain that affect emotional regulation.

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Disorders that affect the hippocampus

Alzheimer's, amnesia, PTSD (reduction in hippocampal volume

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Drugs that affect the hippocampus

NMDA receptor antagonists

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Diseases that impact the temporal lobe

Epilepsy, Alzheimer's disease, auditory processing disorder, Wernicke's aphasia

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Wernicke's Aphasia

Fluent speech: Speech is smooth and grammatically correct but often nonsensical or meaningless ("word salad").

Poor comprehension: Difficulty understanding spoken or written language.

Paraphasias: Use of incorrect or made-up words (e.g., calling a pen a "flim").

Unawareness: Individuals are often unaware of their language difficulties.

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Broca’s Aphasia

Non-fluent speech, intact comphrension, difficulty repeating

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Causes of Wernike’s aphasia

Stroke (most common), Traumatic brain injury, Brain tumor or infection affecting the left temporal lobe

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What is the primary difference between Wernicke's Aphasia and Broca's Aphasia?

Wernicke’s aphasia = speech is fluent

Broca’s aphasia = speech is non fluent, intact comprehension

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Causes of Broca’s aphasia

Stroke (most common), Traumatic brain injury, Brain tumor or infection affecting the left frontal lobe

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Pariatal Lobe disorders

Stroke, sensory processing disorder, spatial neglect, somatosensory agnosias, Gerstmann’s syndrome

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Gerstmann’s syndrome cause

caused by damage to the left parietal lobe

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Gerstmann’s syndrome symptoms

Agraphia/Dysgraphia: Difficulty writing, Acalculia: Difficulty performing simple math calculations, Finger Agnosia: Inability to identify or distinguish fingers on oneself or others, and Left-Right Disorientation

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Occipital Lobe Disorders

visual agnosia, visual hallucinations, achromatopsia (loss of color vision), cortical blindness, prosopagnosia

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Occipital Lobe Drugs

Hallucinogens (e.g., LSD), anti-migraine drugs (e.g., triptans)

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Frontal lobe disorders

ADHD, schizophrenia, traumatic brain injury (TBI), stroke

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Drugs that affect the frontal lobe

Stimulants (e.g., Adderall), antipsychotics (e.g., Haloperidol)

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Dorsolateral PFC disorders

MDD, GAD, OCD

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Ventrolateral PFC disorders

Social anxiety disorder and GAD

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Ventromedial prefrontal cortex disorders

MDD, OCD, GAD, PTSD & schizophrenia

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Orbital Cortex Disorders

MDD, bipolar, OCD, PTSD, schizophrenia, substance disorders

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Primary motor cortex deficits

range from weakness to paralysis in one or more muscles in the opposite side of the body

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Orbital cortex deficits

Impulsivity, social inappropriateness, aggressive behaviors

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Ventromedial prefrontal cortex deficits

impaired decision-making, moral judgment, confabulation, social cognition, blunted emotions

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Ventrolateral PFC deficits

impairments in decision-making, behavioral and emotional self-control

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Dorsolateral PFC deficits

deficits in working memory, judgment, perseverative responses, and apathy.

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Low amounts of dopamine

Parkinsons and ADHD

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High amounts of dopamine

Tourette’s and Schizophrenia

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Low amounts of acetylcholine

Early memory loss in Alzheimer's

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High amounts of Glutamate

glutamate excitotoxicity (cell damage and death)

stroke, seizures, Huntington’s, Parkinson’s

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Low amounts of norephrine

catecholamine hypothesis and depression

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High amounts of norephrine

mania

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Low amounts of serotonin

Depression, bulimia, OCD, migraines

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High amounts of serotonin

ASD and Schizophrenia

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Low amounts of GABA

anxiety and insomnia

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High amounts of GABA

memory impairment and daytime drowsiness

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SSRI use

First line treatment for MDD & PDD

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SSRI side effects

fewer side effects that other antidepressants, less cardiotoxic, and safer in overdose

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Discontinuation syndrome

flu like symptoms, sleep disturbances, lack of concentration, mood liability