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新生儿慢性肺病中肺的建模与重塑:对治疗的启示。

Modeling and remodeling of the lung in neonatal chronic lung disease: implications for therapy.

作者信息

Sweet David G, Halliday Henry L

机构信息

Regional Neonatal Unit, Royal Maternity Hospital, Belfast, Northern Ireland.

出版信息

Treat Respir Med. 2005;4(5):347-59. doi: 10.2165/00151829-200504050-00006.

Abstract

Neonatal chronic lung disease (CLD) is the major long-term pulmonary complication of preterm birth affecting about 20% of infants who need mechanical ventilation. CLD is the result of abnormal repair processes following inflammatory lung injury that lead to remodeling of the lung. Inflammation may be initiated by a variety of stimuli including mechanical ventilation, oxygen toxicity and infection. The resultant neutrophil chemotaxis and degranulation leads to the release of enzymes such as matrix metalloproteinases that can cause proteolysis of the lung extracellular matrix. Abnormal healing with remodeling leads to poorly compliant lungs with reduced capacity for gas exchange. Drugs can influence the normal process of lung modeling or remodeling. Fetal lung development can be influenced by glucocorticosteroids and inflammation. Both can cause abnormal lung modeling with fewer, larger alveoli and accelerated lung maturation, which confers benefits in terms of reduced morbidity and mortality from respiratory distress syndrome but potentially increases the risk of subsequent lung injury. Antioxidants, such as retinol (vitamin A), administered post-natally may reduce the effects of oxidative stress leading to a modest reduction in CLD but they require repeated intramuscular injections. Postnatal glucocorticosteroid therapy can modify the lung inflammatory response and reduce CLD but it can also have detrimental effects on the developing brain and lung, thereby creating a clinical dilemma for neonatologists. Proteinase inhibitors may be a rational therapy but more research is needed before they can be accepted as a treatment for preterm neonates.'Modeling' is defined as planning or forming that follows a set pattern. The term is used to describe the normal process of lung growth and development that culminates in mature branching alveolar air spaces surrounded by a network of capillaries. Normal lung modeling occurs under a variety of genetic and hormonal influences that can be altered, leading to abnormal patterns of growth. 'Remodeling' is defined as altering the structure of or re-making and, in the case of the lung, is used to describe the abnormal patterns of lung growth that occur after lung injury. Modeling and remodeling of the lungs occur to an extent throughout life but never more rapidly than during the fetal and early neonatal periods, and factors that influence this process may lead to development of neonatal CLD. Some of the factors involved in normal and abnormal lung modeling and inflammation and glucocorticosteroid-induced remodeling in the perinatal period, in the context of neonatal CLD, are reviewed with considerations of how various drugs may influence these processes.

摘要

新生儿慢性肺疾病(CLD)是早产的主要长期肺部并发症,影响约20%需要机械通气的婴儿。CLD是肺部炎症性损伤后异常修复过程导致肺重塑的结果。炎症可能由多种刺激引发,包括机械通气、氧中毒和感染。由此产生的中性粒细胞趋化和脱颗粒导致诸如基质金属蛋白酶等酶的释放,这些酶可引起肺细胞外基质的蛋白水解。伴有重塑的异常愈合导致肺顺应性差,气体交换能力降低。药物可影响肺建模或重塑的正常过程。胎儿肺发育可受糖皮质激素和炎症影响。两者均可导致肺建模异常,肺泡数量减少、体积增大,肺成熟加速,这在降低呼吸窘迫综合征的发病率和死亡率方面有好处,但可能增加随后肺损伤的风险。出生后给予的抗氧化剂,如视黄醇(维生素A),可能会降低氧化应激的影响,导致CLD略有减少,但需要反复肌肉注射。出生后糖皮质激素治疗可改变肺部炎症反应并减少CLD,但也可能对发育中的脑和肺产生有害影响,从而给新生儿科医生带来临床难题。蛋白酶抑制剂可能是一种合理的治疗方法,但在被接受用于早产新生儿治疗之前还需要更多研究。“建模”被定义为遵循既定模式的规划或形成。该术语用于描述肺生长和发育的正常过程,最终形成由毛细血管网络包围的成熟分支肺泡气腔。正常的肺建模在多种遗传和激素影响下发生,这些影响可能改变,导致异常的生长模式。“重塑”被定义为改变结构或重新制造,就肺而言,用于描述肺损伤后发生的异常肺生长模式。肺的建模和重塑在一生中都会在一定程度上发生,但从未比胎儿期和新生儿早期更快,影响这一过程的因素可能导致新生儿CLD的发生。本文回顾了围生期正常和异常肺建模以及炎症和糖皮质激素诱导的重塑过程中涉及的一些因素,这些因素与新生儿CLD相关,并考虑了各种药物如何影响这些过程。

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