Jove
Visualize
Contact Us
JoVE
x logofacebook logolinkedin logoyoutube logo
ABOUT JoVE
OverviewLeadershipBlogJoVE Help Center
AUTHORS
Publishing ProcessEditorial BoardScope & PoliciesPeer ReviewFAQSubmit
LIBRARIANS
TestimonialsSubscriptionsAccessResourcesLibrary Advisory BoardFAQ
RESEARCH
JoVE JournalMethods CollectionsJoVE Encyclopedia of ExperimentsArchive
EDUCATION
JoVE CoreJoVE BusinessJoVE Science EducationJoVE Lab ManualFaculty Resource CenterFaculty Site
Terms & Conditions of Use
Privacy Policy
Policies

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,...
Heart Valves01:16

Heart Valves

The human heart is a complex organ with an intricate system of valves that regulate blood flow. There are two main types of valves: atrioventricular (AV) valves and semilunar valves.
The AV valves prevent the backflow of blood from the ventricles to the atria during ventricular contraction. These valves function with the assistance of the chordae tendineae and papillary muscles. When the ventricles are relaxed, the chordae tendineae are slack, allowing blood to flow from the atria into the...
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...
Imaging Studies for Cardiovascular System VI: Calcium -Scoring CT01:25

Imaging Studies for Cardiovascular System VI: Calcium -Scoring CT

Calcium-Scoring CT ScanA calcium-scoring CT scan, also known as coronary artery calcium (CAC) scan, detects calcium deposits in the coronary arteries. This test assesses the risk of coronary artery disease (CAD), which can lead to cardiovascular events such as angina, heart failure, and sudden cardiac arrest.A calcium-scoring CT scan is generally recommended for individuals at intermediate risk of CAD without symptoms. It includes:Men aged 40-75 and women aged 50-75: Especially those with a...

You might also read

Related Articles

Articles linked to this work by shared authors, journal, and citation graph.

Sort by
Same author

Identification of genetic variants in m<sup>6</sup>A modification genes associated with pancreatic cancer risk in the Chinese population.

Archives of toxicology·2021
Same author

HOMEODOMAIN PROTEIN8 mediates jasmonate-triggered trichome elongation in tomato.

The New phytologist·2021
Same author

BUB1B promotes extrahepatic cholangiocarcinoma progression via JNK/c-Jun pathways.

Cell death & disease·2021
Same author

3D Printed Fe Scaffolds with HA Nanocoating for Bone Regeneration.

ACS biomaterials science & engineering·2021
Same author

Design of a biofluid-absorbing bioactive sandwich-structured Zn-Si bioceramic composite wound dressing for hair follicle regeneration and skin burn wound healing.

Bioactive materials·2020
Same author

The Genetic Status of the Critically Endangered Hainan Gibbon (<i>Nomascus hainanus</i>): A Species Moving Toward Extinction.

Frontiers in genetics·2020

Related Experiment Video

Updated: Jun 24, 2026

Isolation of Mouse Interstitial Valve Cells to Study the Calcification of the Aortic Valve In Vitro
05:47

Isolation of Mouse Interstitial Valve Cells to Study the Calcification of the Aortic Valve In Vitro

Published on: May 10, 2021

Procyanidins-crosslinked heart valve matrix: anticalcification effect.

Wanyin Zhai1, Jiang Chang, Xiqin Lü

  • 1Biomaterials and Tissue Engineering Research Center, Shanghai Institute of Ceramics, Chinese Academy of Sciences, Shanghai, People's Republic of China.

Journal of Biomedical Materials Research. Part B, Applied Biomaterials
|April 9, 2009
PubMed
Summary

Procyanidins (PC) effectively inhibit calcification in bioprosthetic heart valves, improving durability. This study shows PC-crosslinked valves prevent mineral deposition and cellular calcification, offering a promising alternative to glutaraldehyde.

More Related Videos

Isolation of Human Primary Valve Cells for In vitro Disease Modeling
07:31

Isolation of Human Primary Valve Cells for In vitro Disease Modeling

Published on: April 16, 2021

Isolation and Characterization of Primary Rat Valve Interstitial Cells: A New Model to Study Aortic Valve Calcification
08:55

Isolation and Characterization of Primary Rat Valve Interstitial Cells: A New Model to Study Aortic Valve Calcification

Published on: November 20, 2017

Related Experiment Videos

Last Updated: Jun 24, 2026

Isolation of Mouse Interstitial Valve Cells to Study the Calcification of the Aortic Valve In Vitro
05:47

Isolation of Mouse Interstitial Valve Cells to Study the Calcification of the Aortic Valve In Vitro

Published on: May 10, 2021

Isolation of Human Primary Valve Cells for In vitro Disease Modeling
07:31

Isolation of Human Primary Valve Cells for In vitro Disease Modeling

Published on: April 16, 2021

Isolation and Characterization of Primary Rat Valve Interstitial Cells: A New Model to Study Aortic Valve Calcification
08:55

Isolation and Characterization of Primary Rat Valve Interstitial Cells: A New Model to Study Aortic Valve Calcification

Published on: November 20, 2017

Area of Science:

  • Biomaterials Science
  • Cardiovascular Research
  • Tissue Engineering

Background:

  • Glutaraldehyde crosslinking limits bioprosthetic heart valve durability due to calcification.
  • Procyanidins (PC) offer a potential alternative crosslinking agent with promising preliminary results.

Purpose of the Study:

  • To investigate the anticalcification efficacy of procyanidins (PC) and PC-crosslinked heart valves.
  • To evaluate the impact of PC on valvular matrix mineralization and cellular calcification.

Main Methods:

  • Decellularized porcine aortic valve leaflets were crosslinked with PC solution.
  • Valves were incubated in simulated body fluid to assess matrix calcification.
  • Valvular cells were cultured with PC to evaluate cellular anticalcification effects.

Main Results:

  • PC-crosslinked valves demonstrated inhibited matrix mineralization compared to non-crosslinked and glutaraldehyde-crosslinked valves.
  • PC significantly suppressed alkaline phosphatase activity and mineral deposition in valvular cells.
  • PC exhibited a dose-dependent inhibition of both matrix and cellular calcification.

Conclusions:

  • Procyanidins effectively inhibit bioprosthetic heart valve calcification by preventing mineral deposition and suppressing cellular osteodifferentiation.
  • PC-crosslinked heart valve matrix presents a viable candidate for improved durability in bioprosthetic implants.
  • This research highlights procyanidins as a promising strategy to enhance the longevity of artificial heart valves.