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Developmental changes in endothelium-dependent pulmonary vasodilatation in pigs
S F Liu1, A A Hislop, S G Haworth
1Department of Thoracic Medicine, National Heart and Lung Institute, London.
British Journal of Pharmacology
|June 1, 1992
Summary
The nitric oxide pathway is not active in neonatal pig pulmonary arteries but becomes crucial for vasodilation during the transition to stable postnatal circulation. Responses to sodium nitroprusside increase with age.
Area of Science:
- Cardiovascular Physiology
- Neonatal Circulation
- Vascular Biology
Background:
- Pulmonary artery (PA) vasodilation is critical for successful transition to extrauterine life.
- Endothelium-dependent vasodilation mediated by nitric oxide (NO) plays a key role in regulating vascular tone.
Purpose of the Study:
- To investigate the developmental changes in endothelium-dependent and independent vasorelaxant responses in porcine pulmonary arteries.
- To elucidate the role of the nitric oxide pathway in neonatal and adult pulmonary artery function.
Main Methods:
- In vitro assessment of vasorelaxant responses to acetylcholine (endothelium-dependent) and sodium nitroprusside (endothelium-independent) in porcine PA rings.
- Comparison across different age groups: neonatal, juvenile, and adult.
- Pharmacological inhibition of nitric oxide synthesis using NG-monomethyl-L-arginine.
Main Results:
- Vasodilation to acetylcholine was negligible in neonatal pigs but present and highest in 3-10 day old pigs, decreasing with age.
- Vasodilation to sodium nitroprusside was present in all age groups and increased significantly with age.
- Endothelium removal abolished acetylcholine-induced relaxation, while NG-monomethyl-L-arginine inhibited it, confirming NO mediation.
Conclusions:
- The nitric oxide pathway is functionally immature at birth in pig pulmonary arteries but becomes vital postnatally.
- Developmental changes in pulmonary artery vasodilation are linked to the maturation of the nitric oxide pathway and potentially smooth muscle contractility.