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Questions:
This category covers a lot of drugs and a lot of questions. They can be categorized as:
1. Questions asking about which drug from a list might be used to treat a certain condition:
hypertension:
1) Diuretics such as the high ceiling or loop-acting diuretic, furosemide;
2) Beta-blockers such as propranolol or the cardioselective beta blocker metoprololor atenolol
3) Alpha-1 blockers such as prazosin,
4) Centrally acting adrenergic drugs such as methyldopa or clonidine
5) Neuronal blockers such as guanethidine (reserved for severe hypertension)
6) Angiotensin converting enzyme inhibitors such as Captopril, lisinopril angina: Nitroglycerin, sometimes propranolol, calcium channel blockers such as verapamil
arrhythmias:
1) Lidocaine (ventricular arrhythmias),
2) Phenytoin (to reverse digitalis induced arrhythmias),
3) Quinidine (supraventricular tachyarrhythmias, atrial fibrillation),
4) Verapamil (supraventricular tachyarrhythmias, paroxysmal tachycardia, atrial fibrillation),
5) Digitalis (atrial fibrillation, paroxysmal tachycardia)
6) Propranolol (paroxysmal tachycardia)
angina: Nitroglycerin, sometimes propranolol, calcium channel blockers such as verapamil
Congestive heart failure: Glycosides such as digitalis, digoxin, ACE inhibitors such as captopril
2. The second major category of questions concerns mechanism of action of the various agents:
Antiarrhythmics: Remember problem is that the heart beats irregularity
a. Type 1A agents such as quinidine: acts by increasing the refractory period of cardiac muscle
b. Type 1B agents such as lidocaine decrease cardiac excitability
c. When digitalis is used for atrial fibrillation it acts by decreasing the rate of A-V conduction
Antiangina drugs: problem is insufficient oxygen to meet demands of myocardium
a. Nitroglycerin increases oxygen supply to the heart by a direct vasodilatory action on the smooth muscle in coronary arteries
b. Propranolol reduces oxygen demand by preventing chronotropic responses to endogenous epinephrine, emotions and exercise.
c. Calcium channel blockers decrease oxygen demand by reducing afterload by reducing peripheral resistance via vasodilation
Antihypertensives: Remember, most drugs have the ultimate effect of reducing peripheral resistance via vasodilation
ACE inhibitors: Captopril blocks the enzyme which converts angiotensin I to angiotensin II. The latter is a potent vasoconstrictor (administration of angiotensin will result in an elevation of blood pressure).
Adrenergic Agents:
a. Prazosin: selective alpa-1 blocker, inhibits binding of nerve induced release of NE resulting in vasodilation
b. Methyldopa: acts centrally as a false neurotransmitter stimulating alpha receptors to reduce sympathetic outflow resulting in vasodilation
c. Clonidine: selective agonist stimulates alpha-2receptors in the CNS to reduce sympathetic outflow to peripheral vessels resulting in vasodilation
d. Propranolol: nonselective beta blocker reduces cardiac output and inhibits renin secretion
e. Metoprolol: selective beta-1 blocker, reduces cardiac output
Diuretics: decrease the renal absorption of sodium, thus resulting in fluid loss and a reduction in blood volume. This decreases the work the heart has to pump. Also have weak dilatory action. Types of diuretics which may be mentioned include:
a. Thiazides: chlorothiazide
b. High-ceiling or loop acting: furosemide
c. Potassium sparing: spironolactone
Congestive heart failure drugs:
a. Cardiac glycosides such as digitalis or digitoxin are effective because they have a positive inotropic effect, increasing the force of contraction of the myocardium. This is achieved by an inhibition of Na+, K+ ATPASE leading to increased calcium influx. Digitalis therapy reduces the compensatory changes that are associated with congestive heart failure such as increased heart size, rate, edema, etc.
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Quinidine is principally used to treat
(d) by elimination. Hypertension ((a)) is treated primarily with beta blockers such as propranolol. Angina is primarily treated with nitroglycerin, while digoxin (digitalis) is the drug of choice for congestive heart failure. Quinidine is classed as an antiarrthymic drug (Type I-blocks sodium channels). It reduces automaticity and responsiveness and increases refractoriness. It also has an antimuscarinic action preventing the bradycardia that follows vagal stimulation.
(d) by elimination. Hypertension ((a)) is treated primarily with beta blockers such as propranolol. Angina is primarily treated with nitroglycerin, while digoxin (digitalis) is the drug of choice for congestive heart failure. Quinidine is classed as an antiarrthymic drug (Type I-blocks sodium channels). It reduces automaticity and responsiveness and increases refractoriness. It also has an antimuscarinic action preventing the bradycardia that follows vagal stimulation.
Quinidine is used to treat
(c) same question as above, just gave you a different type of arrythmia
(c) same question as above, just gave you a different type of arrythmia
Verapamil is most efficacious in the treatment of
(a) memorize
(a) memorize
Which of the following drugs is most useful in treating or preventing angina pectoris?
Each of the following drugs can be used in the prevention and treatment of angina pectoris EXCEPT
All of the following drugs are useful in the treatment of hypertension EXCEPT
Digitalis is useful in the treatment of which of the following conditions?
All of the following drugs are useful in the treatment of cardiac arrhythmias EXCEPT
The drug of choice for initial therapy for mild hypertension is
Which of the following antihypertensives are usually reserved for treatment of severe hypertension?
Which of the following beta-adrenergic receptor blocking agents is thought to be cardioselective?
Antiarrhythmic drugs, such as quinidine, suppress certain cardiac arrhythmias by
Most drugs useful in the treatment of cardiac arrhythmias act primarily by
The most important pharmacologic action of drugs that suppress cardiac arrhythmias is
Lidocaine produces its antiarrhythmic effects by
(b) arrhythmias are defined as any abnormality of the normal sinus rhythm of the heart due to disease or injury induced damage to the impulse conducting systems. They also result from the development of ectopic pacemakers or abnormal pacemaker rhythms. Drugs such as lidocaine are used to normalize these rhythms. Lidocaine, a local anesthetic, depresses cardiac excitability, answer (b). The refractory period of cardiac muscle is increased, thus slowing the heart down. All of the other alternatives given would exacerbate the arrhythmia.
(b) arrhythmias are defined as any abnormality of the normal sinus rhythm of the heart due to disease or injury induced damage to the impulse conducting systems. They also result from the development of ectopic pacemakers or abnormal pacemaker rhythms. Drugs such as lidocaine are used to normalize these rhythms. Lidocaine, a local anesthetic, depresses cardiac excitability, answer (b). The refractory period of cardiac muscle is increased, thus slowing the heart down. All of the other alternatives given would exacerbate the arrhythmia.
When digitalis is used in atrial fibrillation, the therapeutic objective is to
Nitroglycerin dilates the coronary arteries in angina pectoris by
Propranolol is of value in treating angina pectoris because it
Administration of angiotensin results in
The primary antihypertensive effect of captopril (Capoten) is due to accumulation of
(b) Captopril is an angiotension-converting enzyme inhibitor that blocks the activation of angiotension I to angiotension II. The decreased blood concentration of angiotension II reduces blood pressure, because angiotension II is a potent vasoconstrictor. Thus (c) is wrong, accumulation of angiotension I is the usual effect. Captopril also maintains lowered BP by elevating bradykinin (which has potent vasodilatory action) in the blood by blocking its metabolism. Thus (d) is wrong, bradykinin metabolites do not accumulate.
(b) Captopril is an angiotension-converting enzyme inhibitor that blocks the activation of angiotension I to angiotension II. The decreased blood concentration of angiotension II reduces blood pressure, because angiotension II is a potent vasoconstrictor. Thus (c) is wrong, accumulation of angiotension I is the usual effect. Captopril also maintains lowered BP by elevating bradykinin (which has potent vasodilatory action) in the blood by blocking its metabolism. Thus (d) is wrong, bradykinin metabolites do not accumulate.
Administration of angiotensin results in
(c) I guess because more angiotensin II would be formed, and that is a potent vasoconstrictor
(c) I guess because more angiotensin II would be formed, and that is a potent vasoconstrictor
Which of the following is NOT characteristic of the thiazide diuretics?
(f) first off, how can you have an option (f)?! (a) is how diuretics lower BP, (b) is why they can cause hypokalemia, which is conveniently option (e), and hypokalemia can potentiate digitalis induced arrhythmias option(c). They apparently can also cause hyperglycemia, which would relate to option (d). How the heck are you supposed to remember all of this?
(f) first off, how can you have an option (f)?! (a) is how diuretics lower BP, (b) is why they can cause hypokalemia, which is conveniently option (e), and hypokalemia can potentiate digitalis induced arrhythmias option(c). They apparently can also cause hyperglycemia, which would relate to option (d). How the heck are you supposed to remember all of this?
The most useful diuretic drugs act by
(b) people with high BP are always told to reduce salt intake, since high sodium levels cause fluid retention which can increase BP, so ipso facto, reducing renal reabsorption of sodium makes BP go down
(b) people with high BP are always told to reduce salt intake, since high sodium levels cause fluid retention which can increase BP, so ipso facto, reducing renal reabsorption of sodium makes BP go down
Which of the following drugs act by inhibiting renal reabsorption of sodium?
(b) same question as above, just reversed.
(b) same question as above, just reversed.
Digoxin exerts its positive inotropic effect by
Answer is (d)- Remember, cardiac glycosides such as digoxin are used in the treatment of congestive heart failure, which is the failure of the heart to function adequately as a pump and thus maintain an adequate circulation. Cardiac glycosides are thought to act by altering calcium ion movement, with a desired effect of increasing the force of contraction of the myocardium (e.g. the inotropic effect). While several of the alternatives involve calcium, the way digoxin does it is via (d), inhibition of Na+, K+ ATPase, resulting in an increase of calcium ion influx into the cardiac cells, and a subsequent enhancement of the contractile mechanism. (a) is the way epinephrine works.
Answer is (d)- Remember, cardiac glycosides such as digoxin are used in the treatment of congestive heart failure, which is the failure of the heart to function adequately as a pump and thus maintain an adequate circulation. Cardiac glycosides are thought to act by altering calcium ion movement, with a desired effect of increasing the force of contraction of the myocardium (e.g. the inotropic effect). While several of the alternatives involve calcium, the way digoxin does it is via (d), inhibition of Na+, K+ ATPase, resulting in an increase of calcium ion influx into the cardiac cells, and a subsequent enhancement of the contractile mechanism. (a) is the way epinephrine works.
Digitoxin is effective in the treatment of cardiac failure because it
The primary action of therapeutic doses of digitalis on cardiac muscle is an increase in
The beneficial effects of digitalis in congestive heart failure result in part from the fact that digitalis causes
a. A decrease in end-diastolic volume
b. A decrease in end-diastolic pressure
c. An increase in stroke volume and cardiac output
d. A decrease in central venous pressure
e. A decrease in rate of the hear where tachycardia exists
The cardiac glycosides will increase the concentration of which ion in an active heart muscle?
Which of the following ions augments the inotropic effect of digitalis?
.
In the treatment of congestive heart failure, digitalis glycosides generally decrease all of the following EXCEPT
The mechanism of action of prazosin, an antihypertensive agent is to
Which of the following owes a significant amount of its antihypertensive effect to a central action?
(a) All of these drugs are used to treat hypertension, but act by different mechanisms. (a), methyldopa, is the drug with central action- it alters CNS control of blood pressure by acting on cardioregulatory and vasomotor systems of the brain by stimulating alpha2 receptors in the brain stem. Clonidine is the usual drug that is involved in this particular question. (b) metropolol is a selectively blocks beta-1 receptors in the heart to reduce cardiac output. (c) hydralazine has a direct action on vascular smooth muscle to reduce hypertension via vasodilation. (d) propranolol blocks beta receptors in the heart, while (e) guanethidine prevents the release and causes depletion of catecholamines taken up into storage vesicles and is released like a false transmitter. It does not cross the bloodbrain barrier.
(a) All of these drugs are used to treat hypertension, but act by different mechanisms. (a), methyldopa, is the drug with central action- it alters CNS control of blood pressure by acting on cardioregulatory and vasomotor systems of the brain by stimulating alpha2 receptors in the brain stem. Clonidine is the usual drug that is involved in this particular question. (b) metropolol is a selectively blocks beta-1 receptors in the heart to reduce cardiac output. (c) hydralazine has a direct action on vascular smooth muscle to reduce hypertension via vasodilation. (d) propranolol blocks beta receptors in the heart, while (e) guanethidine prevents the release and causes depletion of catecholamines taken up into storage vesicles and is released like a false transmitter. It does not cross the bloodbrain barrier.
Which of the following drugs is thought to reduce arterial blood pressure by activating alpha receptors in the vasomotor center of the medulla?
(b)- see above explanation
(b)- see above explanation
Propranolol (Inderal) can be useful in the treatment of hypertension because it blocks
(v) Answer is (v)- You should immediately recognize that propranolol is the prototypic beta-adrenergic receptor blocker, thus any answer with alternative a (i and ii) is wrong. Similarly, d is wrong as well-propranolol is a competitive beta- receptor blocker- it has no effect on NE release. Another drug used for hypertension, Clonidine, acts via this mechanism by stimulating alpha-2 autoreceptors. Thus ii, iii, and iv are wrong. This leaves (v) as the only possible right answer. Indeed, aside from blocking beta-1 receptors, blocking of renin release is thought to be the other mechanism whereby beta-blockers alter hypertension.
(v) Answer is (v)- You should immediately recognize that propranolol is the prototypic beta-adrenergic receptor blocker, thus any answer with alternative a (i and ii) is wrong. Similarly, d is wrong as well-propranolol is a competitive beta- receptor blocker- it has no effect on NE release. Another drug used for hypertension, Clonidine, acts via this mechanism by stimulating alpha-2 autoreceptors. Thus ii, iii, and iv are wrong. This leaves (v) as the only possible right answer. Indeed, aside from blocking beta-1 receptors, blocking of renin release is thought to be the other mechanism whereby beta-blockers alter hypertension.
One of the proposed mechanisms of the antihypertensive effect of beta-adrenergic receptor blocking agents is
Selective beta-1 adrenergic agonists will produce which of the following effects?
Ototoxicity with deafness may encountered occasionally in patients taking which of the following diuretic agents?
(d) answer is (d)- straight memorization- deafness is typically associated with use of ethacrynic acid, a loop or high-ceiling diuretic.
(d) answer is (d)- straight memorization- deafness is typically associated with use of ethacrynic acid, a loop or high-ceiling diuretic.
Symptoms of digitalis toxicity include all of the following EXCEPT
Administration of which of the following drugs increases the likelihood of a toxic response to digitalis?
(d) Chlorthiazide is a diuretic which causes potassium loss or hypokalemia. This results in greater penetration of digitalis into the myocardium, and thus potential toxicity.
(d) Chlorthiazide is a diuretic which causes potassium loss or hypokalemia. This results in greater penetration of digitalis into the myocardium, and thus potential toxicity.