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新生儿持续性肺动脉高压的病理生理机制

Pathophysiologic mechanisms of persistent pulmonary hypertension of the newborn.

作者信息

Dakshinamurti S

机构信息

Department of Pediatrics, University of Manitoba, Manitoba Institute of Child Health, Winnipeg, Canada.

出版信息

Pediatr Pulmonol. 2005 Jun;39(6):492-503. doi: 10.1002/ppul.20201.

Abstract

Persistent pulmonary hypertension of the newborn (PPHN), among the most rapidly progressive and potentially fatal of vasculopathies, is a disorder of vascular transition from fetal to neonatal circulation, manifesting as hypoxemic respiratory failure. PPHN represents a common pathway of vascular injury activated by numerous perinatal stresses: hypoxia, hypoglycemia, cold stress, sepsis, and direct lung injury. As with other multifactorial diseases, a single inciting event may be augmented by multiple concurrent/subsequent phenomena that result in differing courses of disease progression. I review the various mechanisms of vascular injury involved in neonatal pulmonary hypertension: endothelial dysfunction, inflammation, hypoxia, and mechanical strain, in the context of downstream effects on pulmonary vascular endothelial-myocyte interactions and myocyte phenotypic plasticity.

摘要

新生儿持续性肺动脉高压(PPHN)是血管病变中进展最迅速且可能致命的疾病之一,是一种从胎儿循环向新生儿循环转变的血管疾病,表现为低氧性呼吸衰竭。PPHN代表了由多种围产期应激因素激活的血管损伤的常见途径:缺氧、低血糖、寒冷应激、败血症和直接肺损伤。与其他多因素疾病一样,单一的诱发事件可能会因多种同时发生/随后发生的现象而加剧,从而导致疾病进展的不同过程。我将在对肺血管内皮-肌细胞相互作用和肌细胞表型可塑性的下游影响的背景下,综述新生儿肺动脉高压中涉及的血管损伤的各种机制:内皮功能障碍、炎症、缺氧和机械应变。

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