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DOI 10.1111/aji.13402

Медицинская библиотека · American journal of reproductive immunology (New York, N.Y. : 1989) · 2021

Melatonin for the prevention of fetal injury associated with intrauterine inflammation.

Kim Jang Mee, Lee Seung-Yun, Lee Ji Yeon

СтатьяПоддержка исследования: вне правительства СШАОбзорПеревод в очереди

Аннотация

Intrauterine inflammation is shown to be associated with preterm birth, fetal inflammatory response syndrome, and other pregnancy-related comorbidities such as central nervous system diseases including cerebral palsy and periventricular leukomalacia, pulmonary diseases such as bronchopulmonary dysplasia and respiratory distress syndrome, and necrotizing enterocolitis, to name a few. Many animal studies on intrauterine inflammation demonstrate that ascending infection of reproductive organs or the production of proinflammatory cytokines by some stimuli in utero results in such manifestations. Melatonin, known for its primary function in maintaining circadian rhythm, is now recognized as one of the most potent antioxidant and anti-inflammatory drugs. In some studies, melatonin injection in pregnant animals with intrauterine inflammation significantly reduced the number of preterm births, the severity of structural disintegration of the fetal lungs observed in bronchopulmonary dysplasia, and perinatal brain injuries with improvement in neuromotor function. These implicated benefits of melatonin in pregnant women with intrauterine inflammation seem promising in many research studies, strongly supporting the hypothesis that melatonin has antioxidative and anti-inflammatory properties that can potentially be taken by pregnant women who are at risk of having intrauterine inflammation. In this review, the potential of melatonin for improving outcomes of the pregnancies with intrauterine inflammation will be discussed.

Для цитирования: Kim Jang Mee, Lee Seung-Yun, Lee Ji Yeon. Melatonin for the prevention of fetal injury associated with intrauterine inflammation.. American journal of reproductive immunology (New York, N.Y. : 1989). 2021. DOI: 10.1111/aji.13402.

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