Structure Of Carbohydrates And Carbohydrate Metabolism Flashcards
(42 cards)
What is needed to activate the glucose transporters in adipose tissues and striated muscles?
Insulin
Which glucose transporter is activated on an insulin-dependent mechanism?
GLUT4 transporters
Which glucose transporter facilitates the absorption of fructose?
GLUT5 transporters
What are the glucose transporters that require sodium-dependent active uptake of glucose against a concentration gradient?
SGLT1/2 transporters
What vitamins are essential in the citric acid cycle?
Vitamin B1, Vitamin B2, Vitamin B3, Vitamin B5
What are the processes that replenish the intermediates of the citric acid cycle called?
Anaplerotic reactions
Which enzyme is important in maintaining the adequate concentration of oxaloacetate in the citric acid cycle?
Pyruvate carboxylase
What are the major sites of gluconeogenesis in the body?
Liver (90%), Kidney (10%)
What process occurs when lactate formed by glycolysis in skeletal muscle is transported to the liver?
Cori cycle
This substance is important in the attachment of glucose to the glycogen substrate
Uridine diphosphate
It serves as a primer for glycogen synthesis when glycogen is completely depleted
. glycogenin
What enzyme is deficient in Von Gierke disease?
Glucose-6-phosphatase.
What enzyme is deficient in Pompe disease?
Lysosomal acid maltase.
What enzyme is deficient in Cori disease?
Debranching enzyme.
What enzyme is deficient in Andersen disease?
Branching enzyme.
What enzyme is deficient in McArdle syndrome?
Muscle phosphorylase.
What enzyme is deficient in Hers disease?
Liver phosphorylase.
What enzyme is deficient in essential fructosuria?
Fructokinase.
What enzyme is deficient in hereditary fructose intolerance?
Aldolase B.
What enzyme is lacking in the retina, lens, kidneys, and Schwann cells in uncontrolled diabetes?
Sorbitol dehydrogenase.
This pentose is increased in the urine of patients with essential pentosuria?
Xylulose.
What is the most common disease producing enzyme abnormality in humans?
Glucose-6-phosphate dehydrogenase deficiency.
Altered hemoglobin precipitating in the red blood cells of patients with G6PD deficiency.
Heinz bodies
These are abnormally shaped red blood cells occurring due to the phagocytic removal of Heinz bodies in the spleen
Degmacytes (Bite Cells)