Metabolism Flashcards

exam 4 (78 cards)

1
Q

Regardless of the type of fuel; whether carbohydrates, fats, or protein, they all come into the body and have three destinations

A
STORAGE:
Limited amount of glycogen, more amount of protein, and limitless fat
GOODIES:
Cholesterol biosynthesis, FASN, etc.
ENERGY:
Consumed in oxidation
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2
Q

All type of fuel leave the body as

A

They all leave the body as CO2, UREA, H2O

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3
Q

Liver:

Donates ________ and __________(starvation) to the brain

A

GLUCOSE and KETONE BODIES

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4
Q

Liver:

Donates______ and ______ to the heart

A

FAs and KETONE BODIES

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5
Q

A HEALTHY HEART USES

A

FAT, NOT GLUCOSE

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6
Q

Liver:

Donates ______, _______ and_______ to skeletal muscle
RECYCLES _______ from muscle via Cori Cycle
RECYCLES _______ from muscle via Cahill Cycle

A

GLUCOSE + KETONE BODIES + FAs

RECYCLES Lactate from muscle via Cori Cycle
RECYCLES Alanine from muscle via Cahill Cycle

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7
Q

Liver:

Donates _______ to RBC
RECYCLES _______from RBC via Cori Cycle

A

Donates GLUCOSE

RECYCLES Lactate

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8
Q

RBCs are

A

glucose dependent

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9
Q

Cancer cells rely on

A

GLYCOLYSIS

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10
Q

CARBS ←→ FAT

________can be used to make NADPH, NADPH is NEEDED for fat synthesis

________ can be converted to GLYCEROL

______ can be split into Acetyl-CoA

A

GLUCOSE-6-P can be used to make NADPH

DHAP (glycolytic intermediate) can be converted to GLYCEROL

Pyruvate can be split into Acetyl-CoA

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11
Q

Acetyl-CoA can become {3}

A
  1. FAs
  2. Ketone Bodies
  3. Cholesterol synthesis
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12
Q

CARBS ←→ PROTEIN
_______ can turn into SERINE
REMEMBER, you can turn SERINE into GLYCINE/CYSTEINE via HOMOCYSTEINE

Pyruvate can turn into ______ (Glycine, Alanine, and Serine)
Glucose is used in the TCA cycle and those TCA cycle intermediates can enter PROTEIN

A

3-Phosphoglycerate (glycolytic intermediate) can turn into SERINE

Pyruvate can turn into PROTEIN

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13
Q

Glucose is used in the TCA cycle and those TCA cycle intermediates can enter

A

PROTEIN

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14
Q

FAT ←→ PROTEIN

Glycerol can be converted to _______which can then be used to make SERINE

Acetyl-CoA (from fat oxidation) can be turned into_____

A

GLycerol converted to DHAP

Acetyl-CoA turned into A.As

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15
Q

Separate by tissue type or even WITHIN a cell

A

Compartmental Separation

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16
Q

Regulatory proteins in pathways are the ones that ______________ the most

A

TURNOVER

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17
Q

Coordination of carbohydrate and fat metabolism occurs via _____________

A

allosteric control

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18
Q

During FASN, Acetyl-CoA (of mitochondria) must be transported to cytoplasm via

A

CITRATE SHUTTLE

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19
Q

While acetyl-CoA needs the shuttle, Citrate will just diffuse across cytoplasm; in the cytoplasm some of it will INHIBIT ____________

A

PFKI of glycolysis

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20
Q

During FASN, Malonyl-CoA is created from

A

Acetyl-CoA Carboxylase

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21
Q

Malonyl-CoA is used in FASN, but some if it will bind and INHIBIT ___________

A

the CPT-1 transporter,

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22
Q

the Carnitine Transporter that moves FAs_______matrix for oxidation and Carnitine _________ to the cytoplasm to bind FA

A

the Carnitine Transporter that moves FAs INTO matrix for oxidation
and
Carnitine OUT to the cytoplasm to bind FA

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23
Q

Binding of Malonyl-CoA will inhibit the transporter and thus

A

stop β-Oxidation

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24
Q

NET EFFECT IS THAT FASN will inhibit __________ and __________

A

GLYCOLYSIS and β-Oxidation

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25
G-6-P will immediately bind and inhibit
Hexokinase
26
Acetyl-CoA will bind to ___________and stop production of more Acetyl-CoA
PDH
27
Glucagon will cause the formation of ______ which activates PKA; PKA will phosphorylate __________ and HSL
Glucagon will cause the formation of cAMP which activates PKA; PKA will phosphorylate PFKII and HSL
28
p-PFKII will act as a PHOSPHATASE to cleave F-2,6-BP and __________
turn off glycolysis
29
F-2,6-BP is the strongest promoter of
PFKI
30
covalent modification: | Thus, in the starved state removing F-2,6-BP will inactivate glycolysis and will allow ___________to run
GLUCONEOGENESIS
31
HSL will break down TAGs
TAGs into FAs and Glycerol
32
Regulation of Amount of Enzyme: | Upregulation of UREA, A.A Catabolism, and Gluconeogenic enzyme
HIGH PROTEIN
33
Regulation of Amount of Enzyme: | Upregulation of glucose uptake, increase in PPS proteins, and increase in FASN proteins
HIGH CHO
34
Regulation of Amount of Enzyme: | Inhibition of PPS (don’t need NADPH if you have fat) and upregulation of gluconeogenic enzymes
HIGH FAT
35
Within cells: | β-Oxidation occurs in _____________ and FASN occurs in ________
β-Oxidation occurs in mitochondria and FASN occurs in cytoplasm
36
Promotes fuel storage | Promotes growth
insulin
37
Mobilizes fuel | Helps mobilize glucose
Glucagon
38
Mobilizes fuel during ACUTE STRESS
Epinephrine
39
Provides fuel over long-term case
Cortisol
40
Glycogenesis in muscle and liver FASN A.A uptake and protein synthesis
Insulin
41
Stimulates gluconeogenesis Releases FAs from adipose Stimulates A.A. mobilization
Cortisol
42
Activates glycogenolysis to release glucose | Releases FAs from adipose tissues
Epinephrine
43
Activates glycogenolysis and gluconeogenesis | Releases FAs from adipose tissues
Glucagon
44
inhibits cAMP Phosphodiesterase
CAFFEINE
45
Heterotrimeric G-Protein Receptors or G-Protein Coupled Receptors (GPCR) will span across the membrane 7 times Transmembrane areas are hydrophobic Intracellular domain has G-Protein machinery; extracellular domain is different and provides specificity Summary 1.Receptor will be activated 2. G-Protein will activate 3. G-Protein will activate _________ and form cAMP 4. cAMP will activate PKA 5. cAMP Phosphodiesterase will degrade cAMP to________
Summary 1. Receptor will be activated 2. G-Protein will activate 3. G-Protein will activate Adenylate Cyclase and form cAMP 4. cAMP will activate PKA 5. cAMP Phosphodiesterase will degrade cAMP to 5’-AMP
46
In the ________ form, GDP is bound to the G𝜶; while Gβ and GƔ bind to G𝜶 and keep it
INACTIVE for both parts
47
Ligand binds to GPCR; receptor has GEF that swaps out GDP for GTP on G𝜶 and now G𝜶 becomes
active.
48
Cholera Toxin will ADP-Ribsoylate G𝜶s and thus it will be kept permanently in the
ACTIVE STATE
49
G𝜶 has natural GATPase activity to hydrolyze GTP TO GDP and inactivate it, its activity is helped by __________which will hydrolyze GTP to GDP.
GTPase Activating Proteins
50
G𝜶i will______ adenylate cyclase and thus ________ cAMP
inhibit and reduce
51
Pertussis Toxin exploits G𝜶i by ADP-Ribosylating it and thus permanently __________; leads to continuous adenylate cyclase activity and thus buildup of cAMP
INACTIVATING IT
52
Remember, in general INSULIN will _____________enzymes and GLUCAGON will cause _______________
Remember, in general INSULIN will DEPHOSPHORYLATE enzymes and GLUCAGON will cause PHOSPHORYLATION
53
Glucagon results in the formation of cAMP, cAMP accumulates and activates PKA; PKA will cause the regulation of many metabolic enzymes: _________GLYCOLYSIS (PFKII) ___________GLYCOGENESIS _________GLUCONEOGENESIS ___________ LIPOLYSIS (HSL) __________ GLYCOGENOLYSIS (Glycogen Phosphorylase)
``` DECREASES GLYCOLYSIS (PFKII) DECREASES GLYCOGENESIS INCREASES GLUCONEOGENESIS INCREASES LIPOLYSIS (HSL) INCREASES GLYCOGENOLYSIS (Glycogen Phosphorylase) ```
54
Remember steroid hormones (cortisol) bind to receptors IN the
cytoplasm
55
steroid hormones once bound to ligand
will be moved to the nucleus and affect transcription
56
A fetal heart is DEPENDENT
on GLYCOLYSIS
57
A healthy adult heart can use ALL FORMS of ENERGY, but primarily uses
Fas
58
A failing heart shows _______ use of GLYCOLYSIS and thus _____ ATP formation
increased use of glycolysis and less ATP formation
59
ter birth, the conditions of the neonate change and for a brief period of time _____________ is the primary source of ENERGY
LACTATE OXIDATION
60
After some time, the heart of the child changes and takes on _________ as the primary ENERGY form
β-Oxidation
61
The switch from GLYCOLYSIS to β-Oxidation occurs due to changes in___________
transcriptional regulators
62
Fetal Heart, Pathology, Hypertrophy, Hypoxia, Ischemia ALL cause a _________ in transcription factors PGC-1𝜶, PPAR𝜶, and ERR𝜶
DECREASE
63
Adult Heart, Exercise, Fasting, and Diabetes will promote an ___________ in transcription factors transcription factors PGC-1𝜶, PPAR𝜶, and ERR𝜶
INCREASE
64
The changes in transcription allow for the creation of Malonyl-CoA Decarboxylase (MCD) which turns Malonyl-CoA to Acetyl-CoA; thus STOPPING _____
INHIBITIION β-Oxidation
65
In a diseased heart, ATP comes from Glycolysis and thus results in LESS ATP: LESS ATP means MORE is used in maintaining ion homeostasis and LESS is used in generating force →
REDUCED CARDIAC EFFICIENCY
66
Overall nutritional deficiency associated with WASTING OF MUSCLE and SUBCUTANEOUS FAT; seen in children
Marasmus
67
Protein deficiency characterized by edema in extremities, dermatitis, and bloating Calories are sufficient, but PROTEIN IS INSUFFICIENT
Kwashiorkor
68
Complex hypercatabolic state associated with illness and characterized by muscle loss either WITH or WITHOUT the loss of fat Cytokine related Leads to loss of weight in adults and DEVELOPMENTAL FAILURE in children
Cachexia
69
Exogenous phase
all glucose is derived from diet
70
During hours of 4-16hr, glucose mostly from
glycogen breakdown liver uses FA and sends out glucose protein used for gluconeogenesis
71
During hours 16hr to 28hr, we start using ________ from protein as the main glucose source
gluconeogenesis
72
During hours 28hr to 30 days, ____ drops to conserve it and brains starts to use mostly
Protein usage and brains start to use ketone bodies
73
After 30 days, ________ remains low and brains just uses
GLuconegenesis is low and brains just uses Ketone bodies
74
LIVER is the common area of gluconeogenesis; only small amounts can be made by the kidneys AS STARVATION CONTINUES, the AMOUNT of glucose made by
kidneys WIILL INCREASE
75
Early starvation: The ______ is releasing FAs to send to tissues such as the HEART, LIVER (glycerol for gluconeogenesis), KIDNEY, and MUSCLES
adipose
76
Early Starvation: The __________ are releasing A.As to the liver
muscles
77
Metabolites during fast: 1. ________KB 2. Nitrogen _______ 3. ______Ammonia
Metabolites during fast: 1. increase KB 2. Nitrogen rises, then falls 3. increases Ammonia to conserve cations and prevent ketoacidosis
78
The sudden uptake of minerals while already in a DEPLETED STATE results in a _________ of serum electrolytes, minerals, causes hypophosphatemia, and will manifest with fluid retention
REDUCTION