Integrated Metabolism Flashcards

1
Q

What are the primary ingested and absorbed macronutrients during the fed state (3 hours after a meal)?

A

Glucose, fatty acids, and amino acids, depending on food intake.

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2
Q

Describe the postabsorptive or early fasting state (3 – 18 hours).

A

Sources of fuel shift from ingested glucose, amino acids, and fatty acids to liver glycogenolysis, providing glucose released into the blood and delivered to tissues.

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3
Q

What characterizes the fasting state (18 hours – 2 days without food intake)?

A

Glycogen stores are depleted, and de novo glucose formation occurs in the liver using precursors such as amino acids, glycerol, and lactate.

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4
Q

Explain the key pathways in the postabsorptive state.

A

After the initial phase of liver glycogenolysis, gluconeogenesis becomes vital, utilizing precursors like lactate and the glucose-alanine cycle. Muscle glycogenolysis provides glucose for muscles, and lipolysis releases fatty acids.

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5
Q

What happens to liver and muscle glycogen stores after an overnight fast, and what remains the main fuel source?

A

Liver and muscle glycogen stores are depleted, and glucose remains the main fuel source through glycolysis or gluconeogenesis.

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6
Q

Outline the key pathways in the fasting state (18 – 48 hours of no food intake).

A

Glycogen stores are depleted, and de novo glucose formation occurs in the liver using precursors such as amino acids, glycerol, and lactate. Increased glucagon secretion stimulates lipolysis, leading to fatty acids as an energy source.

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7
Q

How does the body utilize proteins during the fasting state, and what is the role of glucagon?

A

Amino acids from muscle protein breakdown contribute to de novo glucose formation, stimulated by increased glucagon secretion, leading to large losses of nitrogen through urine.

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8
Q

What are the key pathways during starvation (long-term fast)?

A

A metabolic shift spares body proteins, relying on gluconeogenesis and lipolysis. Plasma fatty acids become a major fuel for the heart, liver, and skeletal muscle, leading to the formation of ketones for brain energy.

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9
Q

Explain the role of glycerol during starvation and the organ responsible for gluconeogenesis after several weeks.

A

Glycerol from lipolysis serves as a precursor for gluconeogenesis, and the kidney becomes the organ for gluconeogenesis after several weeks.

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10
Q

Describe the key pathways during continued starvation and the role of TCA cycle intermediates.

A

Continued starvation leads to the depletion of TCA cycle intermediates for gluconeogenesis, with an accumulation of acetyl-CoA from fatty acid degradation. This results in increased ketone body formation in the liver.

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11
Q

What happens to ketone bodies in the blood during continued starvation, and how are they utilized in the body?

A

Ketone bodies in the blood increase, leading to ketosis. They serve as a source of fuel in skeletal muscle, heart, and brain, sparing amino acids for essential proteins.

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12
Q

How does the duration of starvation vary based on body fat levels?

A

3 months for adults with normal weight and body fat, and 1 year for obese adults, with potential physiological damage due to ketosis.

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13
Q

What occurs after the depletion of fat reserves during prolonged starvation?

A

Essential proteins are used to form glucose, leading to the loss of liver and muscle function.

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14
Q

Explain the fuel use by the brain during starvation.

A

The brain switches from relying on glucose to ketones as a source of fuel during starvation.

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15
Q

Describe the fuel metabolization during starvation, focusing on reliance on adipose tissue lipolysis.

A

During starvation, there is a higher reliance on adipose tissue lipolysis, leading to increased muscle protein degradation.

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16
Q

What is the fuel output of the liver during starvation, and how does it change?

A

The liver switches from mostly producing glucose to producing both glucose and ketones during starvation.

17
Q

How does gluconeogenesis in the kidney contribute to continued starvation?

A

The kidney produces NH3 (ammonia) during continued starvation, which neutralizes ketosis.

18
Q

Explain the concept of ketosis during continued starvation.

A

Ketosis occurs due to the accumulation of acetyl-CoA from fatty acid degradation and the lacking oxaloacetate for entry into the TCA cycle.

19
Q

What are the physiological implications of prolonged starvation?

A

Prolonged starvation can lead to essential protein utilization, loss of liver and muscle function, and potential physiological damage due to ketosis.

20
Q

What are the primary macronutrients that serve as sources of energy in the human body?

A

Carbohydrates, proteins, and fats are the main macronutrients that provide energy.

21
Q

How is energy used in the human body, and what are the key processes involved?

A

Energy is utilized for ATP formation through the oxidation of macronutrients, including glucose, amino acids, and fatty acids.

22
Q

What is the significance of sleep in diurnal energy supply, and what functions does sleep perform in the body?

A

Sleep is essential for repairing, restoring, and maintaining bodily functions.

23
Q

How do dietary choices impact the fed-fast cycle, and what is the irrelationship of pathways during this cycle?

A

Dietary choices influence the availability of glucose, amino acids, and fatty acids during different stages of the fed-fast cycle.
The irrelationship refers to the dynamic interplay of pathways during this cycle.

24
Q

Describe the fed state and its energy sources, emphasizing the priority of energy usage.

A

The fed state occurs during and after a meal, with energy sources being carbohydrates, fats, and proteins.
Priority: Carbohydrates > Fats > Proteins.

25
Q

What happens during the postabsorptive or early fasting state, and what are the key pathways for energy sources?

A

This stage occurs 3-18 hours after a meal.
Energy sources: Glycogenolysis, gluconeogenesis, and lipolysis.

26
Q

Define the fasting state (18 hours - 2 days) and its pathways for energy sources.

A

Glycogen stores are depleted.
Energy sources: Gluconeogenesis and lipolysis.

27
Q

Explain the starvation state (long-term fast) and its characteristics.

A

Fully adapted state of food deprivation lasting several weeks.
Protein sparing, gluconeogenesis in kidneys, lipolysis, and ketone body formation in the liver.

28
Q

Describe the glucose metabolism pathway in the fed state after a mixed meal.

A

Glucose, amino acids, and fatty acids are digested and absorbed.
Glucose is taken up for glycolysis and the TCA cycle.
Special users include the brain, central nervous system, erythrocytes, and adipose tissue.

29
Q

Detail the lipid metabolism pathway in the fed state, including fatty acid storage and utilization.

A

Fatty acids are taken up by tissues, especially adipose tissue.
Insulin stimulates fatty acid uptake for storage.
Liver plays a key role in triacylglycerol and VLDL formation.
Fatty acid synthesis from excess glucose and amino acids in the liver and adipose tissue.

30
Q

Illustrate nitrogen balance and protein turnover in the body.

A

30-50% of amino acids retained in enterocytes.
20% retained in the liver for energy production and protein formation.
Excess amino acids used for gluconeogenesis or converted to fatty acids.

31
Q

Explain the amino acid metabolism pathway in the fed state, emphasizing the fate of amino acids.

A

Amino acids retained in the liver for energy, protein formation, and nitrogen-containing compounds.
Excess and certain amino acids used for gluconeogenesis or converted to fatty acids.

32
Q

What are the primarypathways for sources of energy during different stages of the fed-fast cycle?

A

Post-absorptive/early fasting: Glycogenolysis, gluconeogenesis, lipolysis.
Fasting state: Gluconeogenesis, lipolysis.
Starvation/long-term fast: Protein sparing, gluconeogenesis, lipolysis, ketone body formation.

33
Q

Summarize the key processes in glucose metabolism during the fed state after a mixed meal.

A

Glucose is taken up for glycolysis and the TCA cycle.
Special users include the brain, central nervous system, erythrocytes, and adipose tissue.
Excess glucose is stored as glycogen or used for fatty acid synthesis when glycogen stores are replete.