Gluconeogenesis And The Control Of Blood Glucose Flashcards

1
Q

Prevent a Simple Reversal of Glycolysis

A

Thermodynamic Barriers

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2
Q

GLUCONEOGENESIS INVOLVES

A

GLYCOLYSIS

THE CITRIC ACID CYCLE,
PLUS SOME SPECIAL REACTIONS

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3
Q

Induction & Repression of Key Enzymes Requires

A

Several hours

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4
Q

is of quantitative importance only in ruminants.

A

Propionate

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5
Q

______Modification by Reversible Phosphorylation Is Rapid

A

Covalent

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6
Q

This Modification Is Instantaneous

A

allosteric

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7
Q

Plays a Unique Role in the Regulation of Glycolysis & Gluconeogenesis in Liver

A

Fructose 2,6-Bisphosphate

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8
Q

kidney may contribute up to

A

40%

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9
Q

key gluconeogenic enzymes are expressed in

A

small intestine, but it is unclear whether or not there is significant glucose production by the intestine in the fasting state.

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10
Q

Glucose is also important in maintaining adequate concentrations of intermediates of the

A

citric acid cycle

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11
Q

clears lactate produced by muscle and erythrocytes, and glycerol produced by adipose tissue.

A

gluconeogenesis

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12
Q

Hyperglycemia leads to changes in

A

osmolality of body fluids,
impaired blood flow,
intracellular acidosis and
increased superoxide radical production (see Chapter 45),

resulting in deranged endothelial and immune system function and impaired blood coagulation

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13
Q

impaired downregulation in response to insulin.

A

gluconeogenesis is also a contributory factor to hyperglycemia in type 2 diabetes

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14
Q

nonequilibrium reactions in glycolysis (see Chapter 17), catalyzed by ______3)prevent simple reversal of glycolysis for glucose synthesis

A

hexokinase, phosphofructokinase and pyruvate kinase

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15
Q

Three nonequilibrium reactions in glycolysi

A

Pyruvate & Phosphoenolpyruvate

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16
Q

catalyzes the carboxylation of pyruvate to oxaloacetate, an ATP-requiring reaction in which the vitamin biotin is the coenzyme.

A

Mitochondrial pyruvate carboxylase

17
Q

presence determines whether a tissue is capable of synthesizing glucose (or glycogen) not only from pyruvate, but also from triose phosphates

A

fructose 1,6-bisphosphatase

present in liver, kidney, and skeletal muscle, but is probably absent from heart and smooth muscle.

18
Q

present in liver and kidney, but absent from muscle, which, therefore, cannot export glucose into the bloodstream.

A

glucose-6-phosphatase

19
Q

involves a different pathway via uridine diphosphate glucose and glycogen synthase

A

Glycogen synthesis

20
Q

After transamination or deamination, glucogenic amino acids yield either pyruvate or intermediates of the citric acid cycle

A

True

21
Q

arises from the β-oxidation of odd-chain fatty acids that occur in ruminant lipids (see Chapter 22), as well as the oxidation of isoleucine and the side chain of cholesterol

A

In nonruminants, including human beings, propionate

22
Q

a vitamin B12dependent enzyme, and in deficiency methylmalonic acid is excreted in the urine

A

Methylmalonyl-CoA mutase

23
Q

Three mechanisms are responsible for regulating the activity of enzymes concerned in carbohydrate metabolism

A

1) changes in the rate of enzyme synthesis, (2) covalent modification by reversible phosphorylation, and (3) allosteric effects.

24
Q

The enzymes involved in the utilization of glucose (ie, those of glycolysis and lipogenesis) become more active when

A

there is a superfluity of glucose, and under these conditions the enzymes of gluconeogenesis have low activity.

25
Q

antagonizes the effect of the glucocorticoids and glucagon-stimulated cAMP

A

Insulin, secreted in response to increased blood glucose,

26
Q

activates cAMP-dependent protein kinase, leading to the phosphorylation and inactivation of pyruvate kinase.

A

Glucagon and epinephrine, hormones that are responsive to a decrease in blood gluco

27
Q

In gluconeogenesis, pyruvate carboxylase, which catalyzes the synthesis of oxaloacetate from pyruvate, requires acetyl-CoA as an

A

allosteric activator.

28
Q

The addition of acetyl-CoA results in a change in the

A

the tertiary structure of the protein, lower-ing the Km for bicarbonate

29
Q

as acetyl-CoA is formed from pyruvate, it automatically ensures the provision of oxaloacetate and, therefore, its further oxidation in the cit-ric acid cycle, by activating

A

pyruvate carboxylase

30
Q

explain the action of fatty acid oxida-tion in sparing the oxidation of pyruvate (and hence glucose) and in stimulating gluconeogenesis.

A

The acti-vation of pyruvate carboxylase and the reciprocal inhibition of pyruvate dehydrogenase by acetyl-CoA derived from the oxidation of fatty acids

31
Q

A major role of fatty acid oxidation in promoting gluconeogenesis is

A

supply the ATP that is required.

32
Q

inhibited by citrate and by normal intracellular concentrations of ATP and is activated by 5′ AMP.

A

Phosphofructokinase

33
Q

acts as an indicator of the energy status of the cell.

A

5′ AMP

34
Q

allows rapid equilibration of the reaction

A

adenylyl kinase in liver and many other tissue

35
Q

activity of phosphofructokinase-1 is thus regulated in response to the energy status of the cell to control the quantity of carbohydrate undergoing glycolysis prior to its entry into the citric acid cycle.

True or False

A

True

36
Q

accumulation of glucose-6-phosphate, which in turn inhibits further uptake of glucose in extrahepatic tissues by inhibition of hexokinase.

A

consequence of the inhibition of phosphofructokinase-1 by ATP

37
Q

most potent positive allosteric activator of phosphofructokinase-1 and inhibitor of fructose 1,6-bisphosphatase in liver is

A

fructose 2,6-bisphosphate

38
Q

relieves inhibition of phosphofructokinase-1 by ATP and increases the affinity for fructose-6-phosphate

inhibits fructose 1,6-bisphosphatase by increasing the Km for fructose 1,6-bisphosphate

A

fructose 2,6-bisphosphate

39
Q

also responsible for its breakdown, since it has fructose 2,6-bisphosphatase activity.

A

phosphofructokinase-2.