Related Experiment Videos
Flow-induced responses in cat isolated pulmonary arteries
L A Shimoda1, N A Norins, J A Madden
1Department of Biomedical Engineering, Marquette University, Milwaukee, Wisconsin 53233, USA.
Journal of Applied Physiology (Bethesda, Md. : 1985)
|January 7, 1998
Summary
Pulmonary arteries constrict when blood flow increases. This response involves endothelin-1, intracellular calcium release, and protein kinase C activation, but not extracellular calcium.
Area of Science:
- Cardiovascular Physiology
- Pulmonary Circulation Research
- Endothelial Function Studies
Background:
- The pulmonary arteries' response to intraluminal flow is not fully understood.
- Investigating the mechanisms behind flow-induced changes in pulmonary artery diameter is crucial for understanding pulmonary vascular regulation.
Purpose of the Study:
- To investigate the constrictive response of cat pulmonary arteries to increased intraluminal flow.
- To elucidate the signaling pathways involved in flow-induced pulmonary artery constriction.
Main Methods:
- Isolated, cannulated, endothelium-intact cat pulmonary arteries were used.
- Transmural pressure was maintained at 10 mmHg while intraluminal flow was increased stepwise.
- Constriction was assessed using a video system, and the effects of various inhibitors (ryanodine, phosphoramidon, BQ-123, staurosporine) and Ca2+ removal were evaluated.
Main Results:
- Pulmonary arteries demonstrated constriction in response to increased intraluminal flow.
- This constriction was independent of extracellular calcium but was abolished by ryanodine, phosphoramidon, BQ-123, staurosporine, and glutaraldehyde.
- These findings implicate endothelin-1, intracellular calcium release, and protein kinase C in the flow-induced response.
Conclusions:
- Isolated pulmonary arteries exhibit flow-induced constriction.
- The constriction mechanism involves endothelin-1 signaling, intracellular calcium release, and protein kinase C activation.
- Endothelial cell deformability also plays a role in this response.