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Related Concept Videos

Antihypertensive Drugs: Action of Calcium Channel Blockers01:18

Antihypertensive Drugs: Action of Calcium Channel Blockers

Calcium ions are essential to contract smooth muscle cells in blood vessels. They enter these cells through voltage-dependent calcium channels, specifically L-type calcium channels in the cell membrane. These L-type calcium channels are integral to the excitation-contraction coupling process in smooth muscle. When a stimulus is received by smooth muscle cells, their membrane depolarizes. This alteration in membrane potential instigates the opening of L-type calcium channels. As a result,...
Antihypertensive Drugs: Vasodilators01:23

Antihypertensive Drugs: Vasodilators

Vasodilators, primarily affecting the smooth muscles within arterial and venous walls, are commonly used for hypertension treatment. Medications such as minoxidil and hydralazine primarily target arteries and arterioles, while sodium nitroprusside acts on arterioles and venules. Minoxidil, functioning as a prodrug, is metabolized by hepatic sulfotransferase into its active form, minoxidil sulfate, after oral administration. This metabolite binds to the sulfonylurea receptor (SUR) component of...
Antiarrhythmic Drugs: Class I Agents as Sodium Channel Blockers01:22

Antiarrhythmic Drugs: Class I Agents as Sodium Channel Blockers

Class I antiarrhythmic drugs are used to treat various types of arrhythmias or irregular heart rhythms. These drugs block the sodium (Na+) channels in the cardiac cells, thereby affecting the movement of electrical impulses across the heart. Class I antiarrhythmic drugs are divided into three subgroups: Class IA, Class IB, and Class IC, each with distinct mechanisms of action and effects on the heart.
Class 1A Antiarrhythmic Drugs: These drugs work by moderately blocking sodium channels,...
Antiarrhythmic Drugs: Class IV Agents as Calcium Channel Blockers01:20

Antiarrhythmic Drugs: Class IV Agents as Calcium Channel Blockers

Class IV antiarrhythmic drugs, such as verapamil and diltiazem, block calcium channels. They primarily affect the heart, slowing the conduction in calcium-dependent tissues like the SA and AV nodes. These drugs manage reentrant supraventricular tachycardia (SVT) and reduce ventricular rate in atrial flutter/fibrillation.
Verapamil, a calcium channel blocker, inhibits calcium movement across myocardial cell membranes and vascular smooth muscle. This results in the dilation of coronary and...
Antianginal Drugs: Calcium Channel Blockers and Ranolazine01:25

Antianginal Drugs: Calcium Channel Blockers and Ranolazine

Angina pectoris, a primary symptom of ischemic heart disease, requires careful pharmacological interventions. In this context, calcium channel blockers (CCBs) and ranolazine have emerged as crucial pharmacotherapeutic agents, providing deep insights into the complexities of angina management.
CCBs, a diverse class that includes dihydropyridines (nifedipine) and diphenylalkylamines (verapamil and diltiazem), exert their effect by blocking calcium channels in cardiac and smooth muscle cells. This...
Antiepileptic Drugs: Calcium Channel Blockers01:17

Antiepileptic Drugs: Calcium Channel Blockers

Calcium channel blockers, a class of antiepileptic drugs, regulate the flow of calcium ions within neurons.
Calcium channel blockers exert their antiepileptic effects by targeting T-type calcium channels, which are integral to transmitting nerve signals in the central nervous system. These channels allow the passage of calcium ions, which are vital for neuronal communication. By inhibiting T-type calcium channels, calcium channel blockers effectively reduce the release of neurotransmitters and...

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Calcium entry blocking agents in digital vasospasm (Raynaud's phenomenon).

A Kahan, S Weber, B Amor

    European Heart Journal
    |May 1, 1983
    PubMed
    Summary

    Nifedipine effectively treats Raynaud's phenomenon and idiopathic digital vasospasm by reducing cold-induced vasospastic attacks. This calcium channel blocker offers significant therapeutic benefits for patients with these conditions.

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    Area of Science:

    • Cardiology
    • Rheumatology
    • Pharmacology

    Background:

    • Raynaud's phenomenon (RP) and idiopathic digital vasospasm are conditions characterized by digital vasospasm.
    • Connective tissue diseases like progressive systemic sclerosis (PSS), systemic lupus erythematosus (SLE), and rheumatoid arthritis (RA) can be associated with RP.

    Purpose of the Study:

    • To evaluate the therapeutic efficacy of nifedipine, a calcium entry blocker, in patients with Raynaud's phenomenon and idiopathic digital vasospasm.
    • To assess nifedipine's protective effect against cold-induced vasospasm.

    Main Methods:

    • A preliminary study involved 16 patients receiving 20 mg oral nifedipine before cold water immersion.
    • A double-blind, randomized, placebo-controlled trial included 30 patients (10 PSS, 5 SLE, 3 RA, 12 idiopathic) treated with nifedipine (20 mg TID) or placebo for two weeks each.

    Main Results:

    • Nifedipine protected 14 out of 16 patients from cold-induced vasospasm in the preliminary study.
    • In the ambulatory study, nifedipine significantly reduced weekly vasospastic attacks from 27.3 to 5.8 (P<0.01).
    • Improvement was greatest in idiopathic cases (90.9%), followed by SLE/RA (78.6%), and PSS (64.0%).

    Conclusions:

    • Nifedipine is an effective treatment for Raynaud's phenomenon and idiopathic digital vasospasm.
    • The drug demonstrates significant efficacy in reducing the frequency of vasospastic attacks.
    • Treatment outcomes varied by underlying condition, with idiopathic cases showing the most pronounced improvement.