プロカインアミド 化学特性,用途語,生産方法
用途
ナトリウムチャネル抑制薬（Ⅰa群）抗不整脈薬
効能
抗不整脈薬, ナトリウムチャネル遮断薬
説明
Procainamide and its analogs were employed by Dr Claude
Beck in a series of cardiac surgeries during the early 1930s. The
compound was used to alleviate arrhythmias that present
during the procedures, and was selected for its favorable tissue
absorption properties. Procainamide’s central amide provides
it protection from inactivating esterase action and allows oral
administration of the compound. Procainamide was approved
for use in the United States in 1950.
使用
Procainamide is intended for treating paroxysmal atrial tachycardia, atrial fibrillation, premature ventricular contraction, and ventricular tachycardia. For quickly reaching therapeutic concentrations, parenternal introduction of procainamide is preferred over cynidine.
定義
ChEBI: 4-Aminobenzamide substituted on the amide N by a 2-(diethylamino)ethyl group. It is a pharmaceutical antiarrhythmic agent used for the medical treatment of cardiac arrhythmias.
生物学の機能
Procainamide (Pronestyl, Procan SR) is a derivative of
the local anesthetic agent procaine. Procainamide has a
longer half-life, does not cause CNS toxicity at therapeutic
plasma concentrations, and is effective orally.
Procainamide is a particularly useful antiarrhythmic
drug, effective in the treatment of supraventricular, ventricular,
and digitalis-induced arrhythmias.
作用機序
The chemical difference between procainamide and procaine lies in the replacement of the ester group with an amide group. The action of procainamide is qualitatively similar to the action of procaine. Its effect on the heart is identical to that of quinidine. As an antiarrhythmic, procainamide is preferred over procaine because unlike procaine, it is better absorbed when taken orally and it is more difficult for the esterases of the plasma to hydrolyze it, which results in long-lasting action.
臨床応用
Procainamide is an effective antiarrhythmic agent when
given in sufficient doses at relatively short (3–4 hours)
dosage intervals. Procainamide is useful in the treatment
of premature atrial contractions, paroxysmal atrial tachycardia,
and atrial fibrillation of recent onset. Procainamide
is only moderately effective in converting atrial flutter or
chronic atrial fibrillation to sinus rhythm, although it has value in preventing recurrences of these arrhythmias
once they have been terminated by direct current (DC)
cardioversion.
Procainamide can decrease the occurrence of all
types of active ventricular dysrhythmias in patients with
acute myocardial infarction who are free from A-V dissociation,
serious ventricular failure, and cardiogenic
shock. About 90% of patients with ventricular premature
contractions and 80% of patients with ventricular
tachycardia respond to procainamide administration.
Although the spectrum of action and electrophysiological
effects of quinidine and procainamide are similar,
the relatively short duration of action of procainamide
has tended to restrict its use to patients who
are intolerant of or unresponsive to quinidine.
副作用
Acute cardiovascular reactions to procainamide administration
include hypotension, A-V block, intraventricular
block, ventricular tachyarrhythmias, and complete
heart block. The drug dosage must be reduced or even
stopped if severe depression of conduction (severe prolongation
of the QRS interval) or repolarization (severe
prolongation of the QT interval) occurs.
Long-term drug use leads to increased antinuclear
antibody titers in more than 80% of patients; more than
30% of patients receiving long-term procainamide therapy
develop a clinical lupus erythematosus–like syndrome.
The symptoms may disappear within a few days
of cessation of procainamide therapy, although the tests
for antinuclear factor and lupus erythematosus cells
may remain positive for several months.
Procainamide, unlike procaine, has little potential to
produce CNS toxicity. Rarely, patients may be confused
or have hallucinations.
薬物相互作用
The inherent anticholinergic properties of procainamide
may interfere with the therapeutic effect of cholinergic
agents. Patients receiving cimetidine and procainamide
may exhibit signs of procainamide toxicity, as cimetidine
inhibits the metabolism of procainamide. Simultaneous use of alcohol will increase the hepatic clearance of procainamide.
Procainamide may enhance or prolong the
neuromuscular blocking activity of the aminoglycosides
with the potential of producing respiratory depression.
The simultaneous administration of quinidine or amiodarone
may increase the plasma concentration of procainamide.
代謝
Metabolites of
procainamide include p-aminobenzoic acid and N-acetylprocainamide. Interestingly, the acetylated
metabolite is also active as an antiarrhythmic. Its formation accounts for up to one-third of the
administered dose and is catalyzed by the liver enzyme N-acetyl transferase. Because acetylation is
strongly influenced by an individual's genetic background, marked variability in the amounts of this
active metabolite may be observed from patient to patient. Renal excretion dominates, with
approximately 90% of a dose excreted as unchanged drug and metabolites. The elimination half-life
is approximately 3.5 hours. A substantial percentage (60–70%) of patients on procainamide show
elevated levels of antinuclear antibodies after a few months. Of these patients, between 20 and 30%
develop a drug-induced lupus syndrome if therapy is continued. These adverse effects, which are
attributed to
the aromatic amino group, are observed more frequently and more rapidly in “slow acetylators.”
Usually, the symptoms associated with procainamide-induced lupus syndrome subside fairly rapidly
after the drug is discontinued. These problems, however, have discouraged long-term procainamide
therapy.
予防処置
Contraindications to procainamide are similar to those
for quinidine. Because of its effects on A-V nodal and
His-Purkinje conduction, procainamide should be administered
with caution to patients with second-degree
A-V block and bundle branch block. Procainamide
should not be administered to patients who have shown
procaine or procainamide hypersensitivity and should
be used with caution in patients with bronchial asthma.
Prolonged administration should be accompanied by
hematological studies, since agranulocytosis may occur.
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