Metabolic Pathways and Vitamin Deficiencies
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Questions and Answers

What is the result of the deficiency in cystathionase?

  • Accumulation of homocysteine
  • Deficiency of thyroxine
  • Formation of diiodotyrosine
  • Accumulation of cystathionine (correct)
  • What is the pathway of thyroxine formation?

  • Tyrosine is converted to thyroxine directly
  • Two molecules of diiodotyrosine condense together to form thyroxine (correct)
  • Homocysteine is converted to thyroxine
  • Cystathionine is converted to thyroxine
  • What is the main symptom of Homocystinuria?

  • Mental retardation
  • Osteoporosis
  • Dislocation of the lens
  • All of the above (correct)
  • What is the result of the deficiency in cystathionine synthase?

    <p>Accumulation of homocysteine</p> Signup and view all the answers

    What is the name of the pathway that involves the formation of thyroxine?

    <p>3-Pathway of thyroxine</p> Signup and view all the answers

    What is the name of the disease characterized by the accumulation of homocysteine in the urine?

    <p>Homocystinuria</p> Signup and view all the answers

    What is the main pathway of tryptophan?

    <p>1-Nicotinic acid pathway</p> Signup and view all the answers

    What is the result of the deficiency in cystathionase?

    <p>Accumulation of cystathionine</p> Signup and view all the answers

    What is the symptom of Homocystinuria that affects the eyes?

    <p>Dislocation of the lens</p> Signup and view all the answers

    What is the name of the enzyme that breaks down cystathionine?

    <p>Cystathionase</p> Signup and view all the answers

    Study Notes

    Vitamin Deficiencies

    • Vitamin B6 deficiency leads to a decrease in GABA production
    • Vitamin C is necessary for the synthesis of collagen through its interaction with proline hydroxylase
    • Hydroxylysine is involved in the synthesis of collagen

    Tyrosine Metabolism

    • Tyrosine can undergo transamination to form p-hydroxyphenyl pyruvic acid
    • p-Hydroxyphenyl pyruvic acid is converted to homogentisic acid by p-hydroxyphenyl pyruvic acid hydroxylase
    • Homogentisic acid is then acted upon by homogentisic acid oxygenase
    • A congenital deficiency of p-hydroxyphenyl pyruvic acid hydroxylase leads to Tyrosinosis
    • A congenital deficiency of homogentisic acid oxygenase leads to Alkaptonuria
    • Dopa can be converted to melanin through the formation of dopachrome
    • Melanin is a brown or black pigment that protects the skin against ultraviolet rays

    Albinism

    • Characterized by very white skin, fine white hair, and pink or light blue irises
    • No treatment available

    Neurotransmitters

    • Dopamine and norepinephrine are neurotransmitters

    Thyroxine Pathway

    • Tyrosine is iodinated in the thyroid gland to form diiodotyrosine
    • Two molecules of diiodotyrosine condense together to form thyroxine

    Phenol Pathway

    • No detailed information provided

    Amino Acid Disorders

    • Cystathioninuria: accumulation of cystathionine and its metabolites due to a deficiency in cystathionase
    • Homocystinuria: disease caused by a deficiency in cystathionine synthase, leading to accumulation of homocysteine in the urine
    • Symptoms of Homocystinuria: mental retardation, osteoporosis, myocardial infarction, and dislocation of the lens

    Tryptophan Metabolism

    • Nicotinic acid pathway: the main and most important pathway of tryptophan

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    Description

    This quiz covers the effects of vitamin deficiencies on metabolic pathways, including the synthesis of collagen and the metabolism of tyrosine.

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