Phosphodiesterase III Flashcards

1
Q

Which enzyme metabolizes cyclic adenosine monophosphate (cAMP)?

A

Study on!!!

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2
Q

What molecule is considered the energy of life?

A

ATP

(adenosine triphosphate)

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3
Q

Through its high energy —– bonds, ATP stores energy that we obtain from food

A

phosphate bonds,

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4
Q

Through its high energy phosphate bonds, ATP stores energy that we obtain from food and acts as the molecular unit of currency of —– transfer.

A

energy transfer

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5
Q

In the presence of oxygen, —– moles of ATP can be produced from 1 mole of glucose.

A

38 moles of ATP

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6
Q

Beta —– receptors are present in the heart

A

Beta-1 receptors

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7
Q

Beta-1 receptors are present in the heart, while —– receptors are present in skeletal muscle and other vascular beds, such as the myocardium

A

beta-2 receptors

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8
Q

Beta receptor stimulation activates a —– G-protein

A

Stimulatory G-protein

(Gs)

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9
Q

Beta receptor stimulation activates a stimulatory G-protein (Gs) and instructs —– to convert ATP into —–.

A

Adenylate cyclase

cAMP

(cyclic adenosine monophosphate)

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10
Q

cAMP is responsible for “turning on” a variety of —– that instruct the cell to perform a specific function.

A

protein kinases

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11
Q

—– metabolizes cAMP to AMP (adenosine monophosphate).

A

Phosphodiesterase Ill

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12
Q

Phosphodiesterase Ill metabolizes cAMP to AMP (adenosine monophosphate). This “—–” these protein kinases, and the cell is no longer instructed to perform that specific function

A

turns off

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13
Q

By inhibiting the “turn off” mechanism, inhibition of phosphodiesterase Ill indirectly increases —–.

A

intracellular cAMP

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14
Q

By inhibiting the “turn off” mechanism, inhibition of phosphodiesterase Ill indirectly increases intracellular cAMP and maintains the protein kinases in the “—–” state

A

“turned on”

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15
Q

In the cardiac muscle cell, cAMP augments myocardial performance by increasing intracellular —– and the force of —–.

A

intracellular calcium and the

force of contraction

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16
Q

In the cardiac muscle cell, cAMP increases the rate of myocardial relaxation by accelerating the return of —– to the sarcoplasmic reticulum

A

Calcium

17
Q

The process of increasing the rate of myocardial relaxation by accelerating the return of calcium to the sarcoplasmic reticulum is called —–.

A

Lusitropy

18
Q

In the vascular smooth muscle cell, cAMP inhibits —– kinase

A

myosin light chain kinase

19
Q

In the vascular smooth muscle cell, cAMP inhibits myosin light chain kinase. This causes

A

Vasodilation

Decreased SVR

20
Q

Which drug is an example of a PDE Ill inhibitors?

A

Milrinone

21
Q

PDE Ill inhibitors, such as milrinone, are also called —–.

A

Inodilators

22
Q

PDE Ill inhibitors, such as milrinone, are also called inodilators. They augment myocardial performance independently of the

—– nervous system

A

Sympathetic nervous system

23
Q

PDE Ill inhibitors, such as milrinone, are also called inodilators. They augment myocardial performance independently of the sympathetic nervous system. This feature makes PDE Ill inhibitors useful in which drug-induced myocardial depression

A

Beta-blocker induced myocardial depression

24
Q

PDE Ill inhibitors, such as milrinone, are also called inodilators. They augment myocardial performance independently of the sympathetic nervous system. This feature makes PDE Ill inhibitors useful in —– heart failure

A

Acute heart failure

25
Q

PDE Ill inhibitors, such as milrinone, are also called inodilators. They augment myocardial performance independently of the sympathetic nervous system. This feature makes PDE Ill inhibitors useful in unresponsiveness to IV —–.

A

Catecholamines

26
Q

PDE Ill inhibitors, such as milrinone, are also called inodilators. They augment myocardial performance independently of the sympathetic nervous system. This feature makes PDE Ill inhibitors useful anytime the combination of increased —– and reduced —– would be desirable

A

increased inotropy and

reduced afterload

27
Q

In case you were wondering, there are —– different varieties of phosphodiesterase

A

Five

Phosphodiesterase (I-V).

28
Q

PDE Ill is specific to which intracellular second messenger?

A

cAMP

29
Q

While PDE Ill is specific for cAMP, the other forms of PDE are

—– specific to cAMP

A

Not specific to cAMP

30
Q

—– is the prototype nonselective phosphodiesterase inhibitor

A

Theophylline

31
Q

Which enzyme metabolizes cyclic adenosine monophosphate?

A

Phosphodiesterase III

32
Q

—– is an effector that converts ATP to cAMP (the second messenger).

A

Adenylate Cyclase

33
Q

cAMP activates —–, which initiates a variety of phosphorylation reactions inside the cell

A

protein kinase A

34
Q

Phosphodiesterase Ill essentially “—–” cAMP by metabolizing it to AMP

A

“turns off”

35
Q

References:

A
  • Barash. Clinical Anesthesia. 8th ed**.* 2017. p. 321-322.
  • Hemmings* . Pharmacology and Physiology for Anesthesia: Foundations and Clinical Application . 1st ed.* *2013. p.* *391. Flood. Stoel**ting’s Pharmacology & Physiology in Anesthetic Practice. 5th ed. 2015. p. 468-469, 684.