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调控出生后动脉导管闭合的分子机制。

Molecular Mechanisms for Regulating Postnatal Ductus Arteriosus Closure.

机构信息

Graduate Institute of Medicine, College of Medicine, Kaohsiung Medical University, Kaohsiung 807, Taiwan.

Department of Pediatrics, St. Joseph Hospital, Kaohsiung 807, Taiwan.

出版信息

Int J Mol Sci. 2018 Jun 25;19(7):1861. doi: 10.3390/ijms19071861.

Abstract

The ductus arteriosus (DA) connects the main pulmonary artery and the aorta in fetal circulation and closes spontaneously within days after birth in normal infants. Abnormal patent DA (PDA) causes morbidities and mortality, especially in preterm infants. Closure of the DA is a complex interactive process involving two events: functional and anatomic closure. Functional closure by smooth muscle contraction was achieved through the regulatory factors of vaso-reactivity. These factors include oxygen sensing system, glutamate, osmolality, prostaglandin E₂, nitric oxide, and carbon monoxide. Anatomic closure by vascular remodeling involved several vascular components including endothelium, extracellular matrix, smooth muscle cells, and intraluminal blood cells. Despite advances in understanding of PDA pathogenesis, the molecular mechanism for regulation of DA closure is complex and not fully understood. In this article we review recent evidence regarding the molecular mechanisms of DA closure.

摘要

动脉导管(DA)在胎儿循环中连接肺动脉主干和主动脉,在正常婴儿出生后数天内会自然闭合。异常持续开放的动脉导管(PDA)会导致发病率和死亡率增加,尤其是在早产儿中。DA 的闭合是一个复杂的相互作用过程,涉及两个事件:功能性和解剖学闭合。平滑肌收缩引起的功能性闭合是通过血管反应性的调节因子实现的。这些因子包括氧感应系统、谷氨酸、渗透压、前列腺素 E₂、一氧化氮和一氧化碳。血管重塑引起的解剖学闭合涉及几个血管成分,包括内皮细胞、细胞外基质、平滑肌细胞和管腔内血细胞。尽管对 PDA 发病机制的理解有所进展,但调节 DA 闭合的分子机制很复杂,尚未完全了解。本文综述了有关 DA 闭合分子机制的最新证据。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c805/6073350/ab5649dd2442/ijms-19-01861-g001.jpg

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