Proteins, Enzymes, Membranes and Signal Transduction EC Flashcards

1
Q

Cystinuria

A

Autosomal Recessive
Defect in basic amino acid transporter (Cystine, Lysine, Arginine) in renal tubules
Excessive excretion and formation of cystine kidney stones

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2
Q

Hartnup’s Disease

A
Autosomal Recessive
Pellagra like (diarrhea, dermatitis, dementia)
Defective absorption of tryptophan
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3
Q

Gs Receptor function and coupled receptors

A

Stimulate Adenylate Cyclase (increase cAMP –> PKA)

Dopamine (D1)
Epinephrine (B1,B2)
Glucagon histamine (H2)
Vasopressin (V2)

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4
Q

Gi Receptor function and coupled receptors

A

Inhibit adenylate cyclase (decrease cAMP)

Dopamine (D2)
Epinephrine (a2)

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5
Q

Gq Receptor function and coupled receptors

A

Stimulates phospholipase C (increased IP3 & DAG)

Angiotensin II
Epinephrine (a1)
Oxytosin
Vasopressin (V1)

phosphorylated myosin light chains –> SM contraction

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6
Q

Gt receptor function and coupled receptors

A

Stimulate cGMP phosphodiesterase (increase cGMP)

Rhodopsin (light sensitive)

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7
Q

Tyrosine Kinase overview (insulin receptor as example)

A

Insulin binds TK–> autophosphorylation
IRS-1 activates . . .
RAS/MAP kinase (long-term effects-gene expression) and
PKB (short term effects-increased GLUT-4)

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8
Q

Cholera/EHEC toxins

A

Permanently activate Gs (ADP-ribosylation)
Increased cAMP
Loss of isotonic fluid
Diarrhea

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9
Q

Pertussis toxin

A

Permanently inactivates Gi (ADP-ribosylation)
Increased cAMP
Increased mucus secretion in respiratory tract (whooping cough)

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10
Q

Ephedrine MOA and use

A

alpha-1 agonist

Vasoconstriction (decongestant)

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11
Q

Albuterol and Terbutaline MOA and use

A

Beta-2 agonists

Bronchodilation (asthma)

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12
Q

Beta blockers MOA and use

A

decrease BP

precipitate asthma

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13
Q

Losarton MOA and use

A

Angiotensin II antagonist

Lowers BP

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14
Q

Chlorpromazine/Haloperidol MOA and use

A

D2 antagonists

Antipsychotics

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15
Q

Niacin as a co-enzyme

A
NAD+ (nicotine adenine dinucleotide) 
REDOX reactions (ie. glycolytic pathway)
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16
Q

Pyridoxine as a co-enzyme

A
Pyridoxal phosphate
TRANSAMINATION reactions (ie. alanine to pyruvic acid)
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17
Q

Thiamine as a co-enzyme

A

DECARBOXYLATION (ie. degradation of branched chain amino acids)

Transketolase (2-carbon transfer in pentose-phosphate-pathway)

18
Q

Biotin as a co-enzyme

A

CARBOXYLATION

19
Q

Folic acid as a co-enzyme

A

THF (tetra-hydro-folate)

One carbon transfers (ie. serine –> glycine)

20
Q

Magnesium as co-factor

21
Q

Zinc as a co-factor

A

Carbonic anhydrase
Collagen
Alcohol dehydrogenase
Superoxide dismutase

22
Q

Copper as a co-factor

A

Oxidases (lysyl oxidase in collagen cross-linking)
Ferroxidase (Fe3+–>Fe2+)
Cytochrome c oxidase (electrons to O2 to make water)

23
Q

Iron as a co-factor

A

Cytochromes

24
Q

Selenium as a co-factor

A

Glutathione peroxidase

25
Zero-Order Reaction
Velocity independent of [Substrate] Saturated
26
First-Order Reaction
Velocity dependent on [Substrate] Below Km
27
Alanine aminotransferase (ALT) diagnostic use
Viral hepatitis (ALT>AST)
28
Aspartate aminotransferase (AST) diagnostic use
Alcoholic hepatitis (AST>ALT) MI (AST only)
29
Alkaline phosphatase diagnostic use
Osteoblastic bone disease Metastatic prostate cancer Obstructive liver disease
30
Amylase diagnostic use
``` Acute pancreatitis (lipase more specific) Mumps (parotitis) ```
31
Creatine Kinase (CK) diagnostic use
MI (CK-MB) | DMD (CK-MM)
32
gamma-glutamyl transferase (GGT) diagnostic use
Obstructive liver disease | Alcoholics (increased)
33
Lactate dehydrogenase (LDH)
MI
34
Lipase
Acute pancreatitis (more specific than amylase)
35
What form of Fe binds O2?
Fe2 binds O2
36
What is methemoglobin?
Hgb with Fe3+ | CANNOT BIND O2
37
What does a left shift in the O2 binding curve mean?
Increased Hgb affinity for O2 (loading)
38
What does a right shift in the O2 binding curve mean?
Decreased Hgb affinity for O2 (UNloating) ``` Causes: decreased O2 binding 2,3 BPG (response to high altitude) H+/CO2 Increased tempterature ```
39
What is the mechanism by which CO2 effects hemoglobin binding?
Conversion by carbonic anhydrase decreases pH Protonation of histidine residues DECREASED AFFINITY FOR O2
40
Slate grey cyanosis in infant without pulmonary or cardiac disease
Hereditary methemoglobinemia (HgM)