The Many Fates of Nitrogen: Part 1 & Part 2

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Flashcards covering essential concepts of nitrogen metabolism, protein digestion, and related disorders, based on the provided lecture notes.

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60 Terms

1
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What is nitrogen balance?

The relationship between nitrogen intake and nitrogen excretion, indicating overall protein status.

2
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What are essential amino acids?

Amino acids that cannot be synthesized by the body and must be obtained from the diet.

3
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Name two conditions associated with negative nitrogen balance.

Kwashiorkor and Marasmus.

4
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What does urea represent in nitrogen metabolism?

The primary method of nitrogen excretion.

5
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Which amino acids are classified as glucogenic?

Amino acids that can be converted into glucose.

6
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What is the function of proteases?

Enzymes that break down proteins into peptides and amino acids.

7
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Which hormone stimulates the release of gastrin?

Gastrin is stimulated by the presence of food in the stomach.

8
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What is the role of trypsin in protein digestion?

It cleaves peptide bonds at lysine and arginine residues.

9
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Define Kwashiorkor.

A form of severe protein-energy malnutrition characterized by protein deficiency despite adequate caloric intake.

10
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What is the typical dietary protein intake recommended for adults?

100 g/day.

11
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What triggers the ubiquitin-proteasome degradation pathway?

Short-lived or damaged proteins are tagged for degradation.

12
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Describe the importance of vitamin B6 in amino acid metabolism.

It is a coenzyme for transaminases involved in amino acid metabolism.

13
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What are zymogens?

Inactive enzyme precursors that become active after undergoing a biochemical change.

14
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What is hyperammonemia?

A condition characterized by elevated levels of ammonia in the blood, often due to urea cycle disorders.

15
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What is the role of aspartate in the urea cycle?

Aspartate donates a nitrogen atom to urea during the cycle.

16
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How does the body regulate blood glucose levels during fasting?

Through gluconeogenesis and protein catabolism.

17
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What does the term 'aminotransferase' refer to?

Enzymes that facilitate the transfer of amino groups between amino acids and alpha-keto acids.

18
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What is the primary nitrogenous waste product?

Urea.

19
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Identify the two fates of amino acids in metabolism.

They can be used for protein synthesis or catabolized for energy.

20
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What dietary sources are recommended to meet the protein needs of children in growth phases?

Increased protein intake from sources like eggs, lean meats, and legumes.

21
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What is the significance of branched-chain amino acids?

They are essential for muscle metabolism and energy production, especially during exercise.

22
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Explain the correlation between urea cycle disorders and the central nervous system.

They can lead to neurological symptoms due to the accumulation of toxins like ammonia.

23
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What are the clinical signs of Marasmus?

Severe malnutrition characterized by weight loss and muscle wasting.

24
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How does the urea cycle contribute to nitrogen metabolism?

It converts excess nitrogen from amino acid catabolism into urea for excretion.

25
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Define the term 'glucogenic amino acids.'

Amino acids that can be converted into intermediates of the gluconeogenesis pathway.

26
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What happens during oxidative deamination?

The removal of an amino group from an amino acid, generating ammonia.

27
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List examples of ketogenic amino acids.

Leucine and lysine are classified as ketogenic.

28
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What is the effect of insulin on amino acid metabolism?

Insulin promotes the uptake of amino acids into cells and stimulates protein synthesis.

29
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Name the two enzymes involved in the conversion of glutamate to alpha-ketoglutarate.

Glutamate dehydrogenase and transaminase.

30
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What is the main metabolic fate of excess nitrogen in the body?

Excretion as urea.

31
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Describe cystinuria.

An inherited condition characterized by impaired reabsorption of cystine, leading to kidney stones.

32
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What role do hormones like CCK and secretin play in digestion?

They stimulate the secretion of digestive enzymes and bicarbonate, respectively.

33
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Explain the process of transamination.

The transfer of an amino group from one amino acid to a keto acid, forming a new amino acid.

34
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What is the principle behind dietary protein adequacy?

Dietary intake should match protein breakdown and synthesis to maintain nitrogen balance.

35
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What are the consequences of arginine deficiency in the urea cycle?

Disruption of nitrogen excretion, potentially leading to elevated blood ammonia levels.

36
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Identify the main sources of protein turnover.

Dietary proteins and body's own protein reserves.

37
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What happens in the proteasome system?

Ubiquitin-tagged proteins are degraded into their constituent amino acids.

38
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Which mechanisms are involved in protein turnover?

Synthesis and degradation of proteins occur simultaneously.

39
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What are the impacts of kwashiorkor on growth?

Children with kwashiorkor experience stunted growth and muscle wasting.

40
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Summarize the role of hydrolases in protein digestion.

Hydrolases catalyze the breakdown of proteins into smaller peptides and amino acids.

41
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What is the link between amino acid metabolism and energy production?

Catabolized amino acids contribute to TCA cycle intermediates for ATP generation.

42
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Define the amino acid pool.

A collection of free amino acids available for protein synthesis and energy production.

43
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What is the significance of the enzyme CPS I in the urea cycle?

It is the rate-limiting enzyme that initiates the urea cycle.

44
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What does the term hyperphenylalaninemia refer to?

Elevated phenylalanine levels due to impaired metabolism, notably in PKU.

45
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Explain the relationship between diet and amino acid deficiency diseases.

Dietary imbalances lead to deficiencies in specific amino acids, causing various diseases.

46
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What is unique about cysteine compared to other amino acids?

Cysteine contains a sulfur atom and can form disulfide bonds.

47
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Describe the effects of nitrogen balance during pregnancy.

Pregnancy typically results in a positive nitrogen balance due to increased protein needs.

48
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What characterizes maple syrup urine disease?

Impaired metabolism of branched-chain amino acids leading to toxic accumulation.

49
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What do alanine and glutamine transport in the body?

They transport ammonia from peripheral tissues to the liver.

50
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How does protein malnutrition manifest in adults?

Through muscle wasting, weakness, and decreased immunity.

51
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What is the main biochemical role of glutamate?

It acts as a neurotransmitter and participates in nitrogen metabolism.

52
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How does increasing dietary protein affect nitrogen balance in athletes?

Higher protein intake can support muscle synthesis and recovery in athletes.

53
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List some techniques used in proteomics.

Mass spectrometry and protein sequencing for analysis of protein expression.

54
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How can protein-energy malnutrition affect cognitive development?

Malnutrition can impair brain development and function in children.

55
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What does the term 'lactate cycle' refer to in amino acid metabolism?

A cycle involving the conversion of lactate back to glucose in the liver.

56
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Explain the significance of the kidneys in nitrogen metabolism.

The kidneys filter and excrete urea and other nitrogenous wastes from the blood.

57
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Define oxidative deamination and its impact on amino acids.

A process that converts amino acids to keto acids while releasing ammonia.

58
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What is the role of the pancreas in digestion?

It secretes digestive enzymes that break down proteins in the small intestine.

59
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What do the terms 'gain of function' and 'loss of function' refer to in metabolism?

Changes in enzyme activity that either enhance or impair metabolic processes.

60
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