ログイン

Psychopharmacology Exam 2 (part 4)
22問 • 10ヶ月前
  • Two Clean Queens
  • 通報

    問題一覧

  • 1

    Discuss pathology and clinical features of Alzheimer's Disease

    Pathology: Amyloid/tau Clinical Features: Memory deficit, Aphasia, Apraxia, Agnosia

  • 2

    Discuss the pathology and clinical features of Dementia with Lewy Bodies and Parkinson's

    Pathology: Alpha-synuclein Clinical features: Lewy bodies- memory deficits, fluctuating attention, EPS, Psychosis (hallucinations); PD - shuffling gait, Psychosis (hallucinations), facial apices, pin-rolling

  • 3

    Discuss the pathology and clinical features of Frontotemproal Dementia

    Pathology: Tau Clinical Features: Memory deficits, Speech/language disorders, Disinhibition, Hyperorality

  • 4

    Discuss the pathology and clinical features of Huntington's Disease

    Pathology: Trinucleotide repeat Clinical features: Memory deficit, Executive dysfunction, Chorea

  • 5

    Discuss the pathology of Wilson's Disease

    Toxic/metabolic (copper)

  • 6

    Discuss the pathology of Metachromatic Leukodystrophy

    Leukodystrophy

  • 7

    Discuss the pathology and clincial features of Creutzfeldt-Jakob Disease

    Pathoogy: Prion-related pathology Clinical features: Memory deficits, Ataxia, Myoclonus, Language Disturbance

  • 8

    How do you differentiate Vascular Dementia from other Dementias?

    It is associated with a stroke (CVA)

  • 9

    What peptide is associated with Alzheimers pathology?

    AB 42

  • 10

    What is the greatest risk factor for Alzheimer's Disease?

    Age

  • 11

    Name the genetic polymorphism of Alzheimer's Disease

    Apolipoprotein E4

  • 12

    ACh's action can be terminated by two different enzymes:

    Acetylcholinesterase (AChE) and Butyrylcholinesterase (BuChE)

  • 13

    What Cholinesterase Inhibitor is available in a patch, no drug-to-drug interactions in its class r/t bypaass 1st pass metabolism, and has the most severe S/E of N/V and diarrhea in its class?

    Rivastigmine

  • 14

    While all Cholinesterase Inhibitors have GI S/E, which one is the only one that is hepatotoxic?

    Tacrine

  • 15

    Treats mild-moderate Alzheimer's Disease

    Cholinesterase Inhibitors (Donepezil, Rivastigmine, and Galantamine)

  • 16

    What drug class treats moderate-to-severe Alzheimer's Disease

    N-methyl-D-aspartate Receptor Antagonist & Combo Drug (Memantine and Donepezil + Memantine)

  • 17

    Work by reducing the breakdown of acetylcholine in the brain, a chemical which helps neurons to communicate.

    Cholinesterase Inhibitors

  • 18

    Preferentially blocks excessive extrasynaptic activity of the N-methyl-D-aspertate (NMDA) glutamate receptors in the brain, which is thought to be associated with AD. However, transmission associated with normal cell functioning is spared.

    Memantine

  • 19

    A 2nd Gen, piperidine-class, selective and reversible AChE inhibitor, and is structurally dissimilar to others in its class. It inhibits AChE activity in human erythrocytes and increases extracellular ACh levels in the cerebral cortex and the hippocampus of the rat. Its 1/2 life is approximately 70h allowing for daily dosing.

    Donepezil

  • 20

    This drug a pseudoirreversible inhibitor (it reverses itself over hours) of the enzymes acetylcholinesterase (AChE) and butyrylcholinesterase (BuChE), which are present both in the central nervous system (CNS) and peripherally. Central cholinergic neurons are important for regulation of memory; thus, in the CNS, the boost of acetylcholine caused by AChE blockade contributes to improved cognitive functioning. In particular, this drug appears to be somewhat selective for AChE in the cortex and hippocampus – two regions important for memory – over other areas of the brain. Peripheral cholinergic neurons in the gut are involved in gastrointestinal effects; thus the boost in peripheral acetylcholine caused by AChE and BuChE blockade may contribute major gastrointestinal side effects.

    Rivastigmine

  • 21

    This drug is unique among cholinesterase inhibitors in that it is also a positive allosteric modulator (PAM) at nicotinic cholinergic receptors, which means it can boost the effects of acetylcholine at these receptors. This drug's second action as a PAM at nicotinic receptors could theoretically enhance its primary action as a cholinesterase inhibitor.

    Galantamine

  • 22

    This drug is a noncompetitive, low-affinity NMDA (N-methyl-D- aspartate) receptor antagonist that binds to the magnesium site when the channel is open. Thus, blocks the downstream effects of excessive tonic glutamate release by “plugging” the NMDA ion channel, which may improve memory and prevent neuronal death due to glutamate excitotoxicity.

    Memantine

  • Patho Renal

    Patho Renal

    Two Clean Queens · 100問 · 2年前

    Patho Renal

    Patho Renal

    100問 • 2年前
    Two Clean Queens

    Pathophysiology

    Pathophysiology

    Two Clean Queens · 100問 · 2年前

    Pathophysiology

    Pathophysiology

    100問 • 2年前
    Two Clean Queens

    Patho Immunology

    Patho Immunology

    Two Clean Queens · 34問 · 2年前

    Patho Immunology

    Patho Immunology

    34問 • 2年前
    Two Clean Queens

    Patho Hematology

    Patho Hematology

    Two Clean Queens · 100問 · 2年前

    Patho Hematology

    Patho Hematology

    100問 • 2年前
    Two Clean Queens

    Patho Hematology 2

    Patho Hematology 2

    Two Clean Queens · 76問 · 2年前

    Patho Hematology 2

    Patho Hematology 2

    76問 • 2年前
    Two Clean Queens

    Patho Respiratory

    Patho Respiratory

    Two Clean Queens · 100問 · 2年前

    Patho Respiratory

    Patho Respiratory

    100問 • 2年前
    Two Clean Queens

    Patho Respiratory 2

    Patho Respiratory 2

    Two Clean Queens · 54問 · 2年前

    Patho Respiratory 2

    Patho Respiratory 2

    54問 • 2年前
    Two Clean Queens

    Patho Cardiovascular

    Patho Cardiovascular

    Two Clean Queens · 100問 · 2年前

    Patho Cardiovascular

    Patho Cardiovascular

    100問 • 2年前
    Two Clean Queens

    Patho Cardiovascular 2

    Patho Cardiovascular 2

    Two Clean Queens · 56問 · 2年前

    Patho Cardiovascular 2

    Patho Cardiovascular 2

    56問 • 2年前
    Two Clean Queens

    Patho MSK

    Patho MSK

    Two Clean Queens · 52問 · 2年前

    Patho MSK

    Patho MSK

    52問 • 2年前
    Two Clean Queens

    Patho Acid Base

    Patho Acid Base

    Two Clean Queens · 35問 · 2年前

    Patho Acid Base

    Patho Acid Base

    35問 • 2年前
    Two Clean Queens

    Renal 2

    Renal 2

    Two Clean Queens · 10問 · 2年前

    Renal 2

    Renal 2

    10問 • 2年前
    Two Clean Queens

    Fluid Balance

    Fluid Balance

    Two Clean Queens · 43問 · 2年前

    Fluid Balance

    Fluid Balance

    43問 • 2年前
    Two Clean Queens

    Patho Endocrine

    Patho Endocrine

    Two Clean Queens · 100問 · 2年前

    Patho Endocrine

    Patho Endocrine

    100問 • 2年前
    Two Clean Queens

    Patho Endocrine 2

    Patho Endocrine 2

    Two Clean Queens · 42問 · 2年前

    Patho Endocrine 2

    Patho Endocrine 2

    42問 • 2年前
    Two Clean Queens

    Infections

    Infections

    Two Clean Queens · 58問 · 2年前

    Infections

    Infections

    58問 • 2年前
    Two Clean Queens

    Patho Shock

    Patho Shock

    Two Clean Queens · 31問 · 2年前

    Patho Shock

    Patho Shock

    31問 • 2年前
    Two Clean Queens

    GI

    GI

    Two Clean Queens · 100問 · 2年前

    GI

    GI

    100問 • 2年前
    Two Clean Queens

    GI 2

    GI 2

    Two Clean Queens · 18問 · 2年前

    GI 2

    GI 2

    18問 • 2年前
    Two Clean Queens

    Cancer

    Cancer

    Two Clean Queens · 54問 · 2年前

    Cancer

    Cancer

    54問 • 2年前
    Two Clean Queens

    問題一覧

  • 1

    Discuss pathology and clinical features of Alzheimer's Disease

    Pathology: Amyloid/tau Clinical Features: Memory deficit, Aphasia, Apraxia, Agnosia

  • 2

    Discuss the pathology and clinical features of Dementia with Lewy Bodies and Parkinson's

    Pathology: Alpha-synuclein Clinical features: Lewy bodies- memory deficits, fluctuating attention, EPS, Psychosis (hallucinations); PD - shuffling gait, Psychosis (hallucinations), facial apices, pin-rolling

  • 3

    Discuss the pathology and clinical features of Frontotemproal Dementia

    Pathology: Tau Clinical Features: Memory deficits, Speech/language disorders, Disinhibition, Hyperorality

  • 4

    Discuss the pathology and clinical features of Huntington's Disease

    Pathology: Trinucleotide repeat Clinical features: Memory deficit, Executive dysfunction, Chorea

  • 5

    Discuss the pathology of Wilson's Disease

    Toxic/metabolic (copper)

  • 6

    Discuss the pathology of Metachromatic Leukodystrophy

    Leukodystrophy

  • 7

    Discuss the pathology and clincial features of Creutzfeldt-Jakob Disease

    Pathoogy: Prion-related pathology Clinical features: Memory deficits, Ataxia, Myoclonus, Language Disturbance

  • 8

    How do you differentiate Vascular Dementia from other Dementias?

    It is associated with a stroke (CVA)

  • 9

    What peptide is associated with Alzheimers pathology?

    AB 42

  • 10

    What is the greatest risk factor for Alzheimer's Disease?

    Age

  • 11

    Name the genetic polymorphism of Alzheimer's Disease

    Apolipoprotein E4

  • 12

    ACh's action can be terminated by two different enzymes:

    Acetylcholinesterase (AChE) and Butyrylcholinesterase (BuChE)

  • 13

    What Cholinesterase Inhibitor is available in a patch, no drug-to-drug interactions in its class r/t bypaass 1st pass metabolism, and has the most severe S/E of N/V and diarrhea in its class?

    Rivastigmine

  • 14

    While all Cholinesterase Inhibitors have GI S/E, which one is the only one that is hepatotoxic?

    Tacrine

  • 15

    Treats mild-moderate Alzheimer's Disease

    Cholinesterase Inhibitors (Donepezil, Rivastigmine, and Galantamine)

  • 16

    What drug class treats moderate-to-severe Alzheimer's Disease

    N-methyl-D-aspartate Receptor Antagonist & Combo Drug (Memantine and Donepezil + Memantine)

  • 17

    Work by reducing the breakdown of acetylcholine in the brain, a chemical which helps neurons to communicate.

    Cholinesterase Inhibitors

  • 18

    Preferentially blocks excessive extrasynaptic activity of the N-methyl-D-aspertate (NMDA) glutamate receptors in the brain, which is thought to be associated with AD. However, transmission associated with normal cell functioning is spared.

    Memantine

  • 19

    A 2nd Gen, piperidine-class, selective and reversible AChE inhibitor, and is structurally dissimilar to others in its class. It inhibits AChE activity in human erythrocytes and increases extracellular ACh levels in the cerebral cortex and the hippocampus of the rat. Its 1/2 life is approximately 70h allowing for daily dosing.

    Donepezil

  • 20

    This drug a pseudoirreversible inhibitor (it reverses itself over hours) of the enzymes acetylcholinesterase (AChE) and butyrylcholinesterase (BuChE), which are present both in the central nervous system (CNS) and peripherally. Central cholinergic neurons are important for regulation of memory; thus, in the CNS, the boost of acetylcholine caused by AChE blockade contributes to improved cognitive functioning. In particular, this drug appears to be somewhat selective for AChE in the cortex and hippocampus – two regions important for memory – over other areas of the brain. Peripheral cholinergic neurons in the gut are involved in gastrointestinal effects; thus the boost in peripheral acetylcholine caused by AChE and BuChE blockade may contribute major gastrointestinal side effects.

    Rivastigmine

  • 21

    This drug is unique among cholinesterase inhibitors in that it is also a positive allosteric modulator (PAM) at nicotinic cholinergic receptors, which means it can boost the effects of acetylcholine at these receptors. This drug's second action as a PAM at nicotinic receptors could theoretically enhance its primary action as a cholinesterase inhibitor.

    Galantamine

  • 22

    This drug is a noncompetitive, low-affinity NMDA (N-methyl-D- aspartate) receptor antagonist that binds to the magnesium site when the channel is open. Thus, blocks the downstream effects of excessive tonic glutamate release by “plugging” the NMDA ion channel, which may improve memory and prevent neuronal death due to glutamate excitotoxicity.

    Memantine