Related Experiment Videos

Nicardipine: a hypotensive dihydropyridine-type calcium antagonist with a peculiar cerebrovascular profile

Francesco Amenta1, Daniele Tomassoni, Enea Traini

  • 1Centro Recherche Cliniche, Dipartimento di Medicina Sperimentale e Sanità Pubblica, Università di Camerino, Camerino, Italy. francesco.amenta@unicam.it

Insights

Nicardipine, a calcium channel blocker, shows promise in preventing stroke and treating vascular dementia (VaD). Its effectiveness in managing cerebrovascular injury suggests potential for broader clinical use.

Area of Science:

  • Neurology
  • Cardiology
  • Pharmacology

Background:

  • Cerebrovascular disease is a significant cause of cognitive impairment and dementia in the elderly.
  • Controlling blood pressure is crucial for preventing cerebrovascular lesions and stroke.
  • Nicardipine is a dihydropyridine calcium channel blocker (CCB) with a unique cerebrovascular profile.

Purpose of the Study:

  • To review controlled clinical studies on nicardipine for cerebrovascular injuries.
  • To evaluate nicardipine's efficacy in subarachnoid hemorrhage (SAH), acute stroke, and vascular dementia (VaD).
  • To assess nicardipine's potential in preventing recurrent stroke and treating cognitive impairment.

Main Methods:

  • Systematic review of controlled clinical trials involving nicardipine.
  • Analysis of studies focusing on SAH, acute stroke, and VaD.
  • Examination of nicardipine's safety and effectiveness in cognitive and cerebrovascular outcomes.

Main Results:

  • Nicardipine prolonged-release implants reduced vasospasm and improved outcomes in severe SAH.
  • Controlled trials confirm nicardipine's effectiveness in stroke prevention.
  • Over 60% of ~6,000 patients with VaD showed improved cognitive deterioration with nicardipine.

Conclusions:

  • Nicardipine demonstrates efficacy in managing SAH, preventing stroke, and improving cognitive function in VaD.
  • Its anti-hypertensive and cognitive benefits warrant reconsideration for vascular cognitive impairment and stroke risk reduction.
  • Nicardipine offers a potentially valuable therapeutic option for cerebrovascular conditions.

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,...
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...
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...
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...
Adrenergic Antagonists: ɑ and β-Receptor Blockers01:31

Adrenergic Antagonists: ɑ and β-Receptor Blockers

Third-generation β-blockers, such as labetalol and carvedilol, represent a significant advancement in managing cardiovascular conditions. Unlike conventional β-blockers, which can induce peripheral vasoconstriction, third-generation drugs block α1 adrenoceptors. This promotes vasodilation through several mechanisms, such as increased nitric oxide production, inhibition of calcium ion entry, opening of potassium ion channels, and antioxidant action. Labetalol, for instance, is clinically...
Antihypertensive Drugs: Thiazide-Class Diuretics01:15

Antihypertensive Drugs: Thiazide-Class Diuretics

Thiazide diuretics are sulfonamide derivatives featuring a benzothiadiazine ring system in their molecular structure. Based on this structure, thiazide diuretics can be categorized into two groups: thiazide-type and thiazide-like diuretics. Thiazide-type diuretics, including hydrochlorothiazide and chlorothiazide, consist of a benzothiadiazine backbone with an attached sulfonamide group. Thiazide-like diuretics, such as chlorthalidone and indapamide, lack the thiazide ring but demonstrate...