胃泌素在促进小胎龄婴儿追赶生长和维持代谢平衡中的作用

Li Zhang, Jingfei Liu, Dianyong Gao, Dong Li
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引用次数: 0

摘要

围产期小于胎龄(SGA)一直是一个备受关注的问题,因为它会导致不良的围产期结局,增加新生儿的发病率和死亡率,影响长期的健康结果,并增加成年后患代谢紊乱、心血管和内分泌疾病的风险。作为生长激素分泌调节器(GHS-R)的内源性配体,胃泌素可能在调节胎儿至成年期的生长和能量代谢平衡中发挥重要作用。我们回顾了近年来胃泌素在 SGA 追赶生长和能量代谢中的作用。除了促进SGA追赶生长外,胃泌素还可能参与SGA能量代谢,维持代谢平衡。小胎龄婴儿的成因非常复杂,可能与多种代谢途径紊乱有关。胰高血糖素调控的相关信号通路有助于识别SGA代谢紊乱的高危人群,并制定有针对性的干预措施,预防成人侏儒症、胰岛素抵抗相关代谢综合征等疾病的发生。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Role of ghrelin in promoting catch-up growth and maintaining metabolic homeostasis in small-for-gestational-age infants
Small-for-gestational age (SGA) has been a great concern in the perinatal period as it leads to adverse perinatal outcomes and increased neonatal morbidity and mortality, has an impact on long-term health outcomes, and increases the risk of metabolic disorders, cardiovascular, and endocrine diseases in adulthood. As an endogenous ligand of the growth hormone secretagotor (GHS-R), ghrelin may play an important role in regulating growth and energy metabolic homeostasis from fetal to adult life. We reviewed the role of ghrelin in catch-up growth and energy metabolism of SGA in recent years. In addition to promoting SGA catch-up growth, ghrelin may also participate in SGA energy metabolism and maintain metabolic homeostasis. The causes of small gestational age infants are very complex and may be related to a variety of metabolic pathway disorders. The related signaling pathways regulated by ghrelin may help to identify high-risk groups of SGA metabolic disorders and formulate targeted interventions to prevent the occurrence of adult dwarfism, insulin resistance-related metabolic syndrome and other diseases.
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