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Related Concept Videos

Anastomoses01:19

Anastomoses

In human anatomy, anastomosis refers to a connection or opening between two things, particularly between blood vessels or other tubular structures. The term is derived from the Greek term 'anastomosis,' which means 'outlet' or 'opening.' This natural network of connections plays a critical role in the survival and functionality of the human body.
Anastomoses can be formed at arterial, venous, and lymphatic vessels.
Arterial Anastomosis: These occur between arteries. They are most common in...
Arteries and Arterioles01:16

Arteries and Arterioles

Arteries, the vasculature responsible for transporting blood from the heart, possess robust walls capable of enduring the elevated pressures exerted by the heartbeat. Arteries near the heart are especially thick-walled and enriched with elastic fibers across their three tunics, classifying them as elastic or conducting arteries. These arteries, usually with a diameter exceeding 10 mm, are characterized by their ability to dilate in response to the blood pumped from the heart's ventricles and...
Arteries of the Upper Limbs01:12

Arteries of the Upper Limbs

The subclavian artery transitions into the axillary artery as it exits the chest and enters the axillary region. This artery is critical for supplying blood to the shoulder area, including the head of the humerus, through the humeral circumflex arteries. As the vessel continues into the upper arm or brachium, it becomes the brachial artery. This artery plays a key role in vascularizing the brachial region and bifurcates at the elbow into several branches. These branches include the deep...
Mechanism of Angiogenesis01:10

Mechanism of Angiogenesis

Blood vessel formation starts early during embryonic development, around day 7. In the extraembryonic yolk sac, mesodermal precursor cells called hemangioblast proliferate and differentiate into angioblast. Angioblasts express vascular endothelial growth factor receptor 2 or VEGFR2, which binds VEGF-A, a proangiogenic factor, guiding blood vessel formation. VEGF signaling promotes angioblasts to form a blood island in the developing embryo. Angioblasts further differentiate, giving rise to...
The Arch of Aorta01:10

The Arch of Aorta

The coronary arteries, originating from the ascending aorta, bifurcate from two sinuses located within the ascending aorta. Positioned just above the aortic semilunar valve, these sinuses house essential aortic baroreceptors and chemoreceptors, crucial for maintaining cardiac function. The left coronary artery and the right coronary artery branch off from the left posterior and anterior aortic sinuses, respectively.
Encircling the heart, the coronary arteries form a ring-like structure before...
Coronary Circulation01:21

Coronary Circulation

The heart, an organ critical to survival, gets nourishment not from the blood it pumps but from a separate circulation system known as coronary circulation. This is the shortest circulation in the body and is responsible for supplying the heart with the nutrients it needs to function effectively.
Coronary circulation begins at the base of the aorta, where two main arteries arise—the left and right coronary arteries. These arteries encircle the heart in the coronary sulcus and supply the...

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Related Experiment Video

Updated: May 30, 2026

Direct Re-implantation of Left Coronary Artery into the Aorta in Adults with Anomalous Origin of Left Coronary Artery from the Pulmonary Artery (ALCAPA)
13:10

Direct Re-implantation of Left Coronary Artery into the Aorta in Adults with Anomalous Origin of Left Coronary Artery from the Pulmonary Artery (ALCAPA)

Published on: April 24, 2017

Growing collateral arteries on demand.

Charles C Oh1, Jason D Klein, Raymond Q Migrino

  • 1Phoenix Veterans Affairs Health Care System, Phoenix AZ 85022, USA. charles.oh@va.gov

Recent Patents on Cardiovascular Drug Discovery
|August 25, 2011
PubMed
Summary
This summary is machine-generated.

Therapies targeting arteriogenesis, the growth of collateral arteries, show promise for ischemic diseases. Increased shear stress activates platelet endothelial cell adhesion molecule (PECAM-1) and the Rho pathway, crucial for this process.

More Related Videos

Assessing Therapeutic Angiogenesis in a Murine Model of Hindlimb Ischemia
07:48

Assessing Therapeutic Angiogenesis in a Murine Model of Hindlimb Ischemia

Published on: June 8, 2019

Related Experiment Videos

Last Updated: May 30, 2026

Direct Re-implantation of Left Coronary Artery into the Aorta in Adults with Anomalous Origin of Left Coronary Artery from the Pulmonary Artery (ALCAPA)
13:10

Direct Re-implantation of Left Coronary Artery into the Aorta in Adults with Anomalous Origin of Left Coronary Artery from the Pulmonary Artery (ALCAPA)

Published on: April 24, 2017

Assessing Therapeutic Angiogenesis in a Murine Model of Hindlimb Ischemia
07:48

Assessing Therapeutic Angiogenesis in a Murine Model of Hindlimb Ischemia

Published on: June 8, 2019

Area of Science:

  • Vascular Biology
  • Molecular Medicine
  • Biomedical Engineering

Background:

  • Arteriogenesis, the formation of new collateral arteries, is a critical process for restoring blood flow in ischemic conditions.
  • Understanding the molecular mechanisms triggering arteriogenesis is key to developing new therapies for ischemic diseases.
  • Shear stress on the endothelium is a primary initiator of arteriogenesis.

Purpose of the Study:

  • To investigate the role of platelet endothelial cell adhesion molecule (PECAM-1) and the Rho pathway in shear stress-induced arteriogenesis.
  • To explore the potential of Actin-binding Rho protein (Abra) as a therapeutic target for enhancing collateral artery formation.

Main Methods:

  • Studied the effect of increased shear stress on endothelial cells, focusing on PECAM-1 phosphorylation.
  • Investigated the involvement of the Rho pathway in the arteriogenic response.
  • Examined the impact of overexpressing Actin-binding Rho protein (Abra) on collateral perfusion in an ischemic model.

Main Results:

  • Increased shear stress leads to tyrosine-phosphorylation of PECAM-1, suggesting its role as a mechanoreceptor.
  • The Rho pathway is activated early and is essential for the arteriogenic response to shear stress.
  • Overexpression of Abra resulted in a significant increase (60%) in collateral perfusion.

Conclusions:

  • PECAM-1 and the Rho pathway are critical mediators of shear stress-induced arteriogenesis.
  • Abra represents a promising therapeutic target for promoting collateral artery growth in ischemic vascular disease.
  • The findings suggest a future where therapeutic arteriogenesis could effectively treat ischemic conditions.