Cardiovascular Drugs and Osteoarthritis: Effects of Targeting Ion Channels

Raminta Vaiciuleviciute1, Daiva Bironaite1, Ilona Uzieliene1

  • 1Department of Regenerative Medicine, State Research Institute Centre for Innovative Medicine, LT-08406 Vilnius, Lithuania.

Cells
|October 23, 2021
PubMed

Insights

Cardiovascular drugs, often targeting ion channels, may impact osteoarthritis progression by affecting cartilage and bone. Long-term use necessitates considering these potential joint tissue effects.

Area of Science:

  • Biomedical Science
  • Pharmacology
  • Rheumatology

Background:

  • Osteoarthritis (OA) and cardiovascular diseases (CVD) share risk factors and molecular pathways.
  • Cardiovascular drugs modulate ion channels, influencing cellular processes relevant to joint health.

Purpose of the Study:

  • To review the effects of cardiovascular drugs on articular tissues in OA.
  • To discuss the impact of ion channel modulation by these drugs on OA progression.

Main Methods:

  • Literature review of cardiovascular drugs affecting ion channels.
  • Analysis of drug mechanisms on chondrocytes, cartilage, and subchondral bone.
  • Focus on ion channel modulation, pain, and inflammation in OA.

Main Results:

  • Cardiovascular drugs can influence cartilage metabolism, cell function, and inflammation.
  • Specific drug classes, including channel inhibitors and receptor blockers, show potential effects.
  • Long-term cardiovascular drug use may impact OA pathogenesis.

Conclusions:

  • Cardiovascular drugs' effects on joint tissues warrant consideration in OA management.
  • Prescribing ion channel modulators requires awareness of potential implications for osteoarthritis.
  • Further research is needed to clarify the long-term impact of these drugs on joint health.

Related Concept Videos

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,...
2.0K
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...
770
Targets for Drug Action: Overview01:26

Targets for Drug Action: Overview

Drugs target macromolecules to modify ongoing cellular processes. Primary drug targets include receptors, ion channels, transporters, and enzymes.
Receptors are either membrane-spanning or intracellular proteins, which upon binding a ligand, get activated and transmit the signal downstream to elicit a response. Drugs bind receptors, either mimicking the action of endogenous ligands or blocking the receptor activity to bring about a modified response. Nearly 35% of approved drugs target the G...
8.1K
Heart Failure Drugs: Inhibitors of Renin-Angiotensin System01:26

Heart Failure Drugs: Inhibitors of Renin-Angiotensin System

The activation of the sympathetic nervous system and the renin-angiotensin-aldosterone system (RAAS) contributes to cardiac remodeling, and inhibiting the RAAS is a pharmacological target in heart failure management. As a result, neurohumoral modulation is a crucial treatment principle for managing heart failure. This approach involves using medications like ACE inhibitors (ACEIs), angiotensin receptor blockers (ARBs), β-blockers, mineralocorticoid receptor antagonists (MRAs), and neutral...
569
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,...
941
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...
1.1K