{"title":"Vitamin D Supplementation Reduces Functional Impairment of Hippocampus Caused by Dexamethasone.","authors":"Qiaoer Su, Minjie Pan, Qiu Wang, Weimin Yang","doi":"10.1620/tjem.2024.J122","DOIUrl":null,"url":null,"abstract":"<p><p>The use of dexamethasone in premature infants has adverse effects on neurological function. Vitamin D is considered to be vital nutrient for neurological diseases. Pups were randomly divided into the control, model and treated groups. Treated group received vitamin D on postnatal day1 (60,000 IU/kg). Following, model and treated group received dexamethasone from postnatal day 2 to postnatal day 4 following tapering doses (0.5, 0.3, and 0.1 mg/kg.d, respectively). Pups' neurological function was assessed by wire-hanging test and Morris water maze task. And apoptotic cells in hippocampus were counted. Vitamin D effectively improved spatial learning and memory impairment induced by dexamethasone. The protective effects of vitamin D may be related to the modulation of apoptosis. Vitamin D may therefore have a role in bronchopulmonary dysplasia treatment process.</p>","PeriodicalId":23187,"journal":{"name":"Tohoku Journal of Experimental Medicine","volume":" ","pages":"127-134"},"PeriodicalIF":1.6000,"publicationDate":"2025-06-25","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Tohoku Journal of Experimental Medicine","FirstCategoryId":"3","ListUrlMain":"https://doi.org/10.1620/tjem.2024.J122","RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"2024/11/7 0:00:00","PubModel":"Epub","JCR":"Q2","JCRName":"MEDICINE, GENERAL & INTERNAL","Score":null,"Total":0}
引用次数: 0
Abstract
The use of dexamethasone in premature infants has adverse effects on neurological function. Vitamin D is considered to be vital nutrient for neurological diseases. Pups were randomly divided into the control, model and treated groups. Treated group received vitamin D on postnatal day1 (60,000 IU/kg). Following, model and treated group received dexamethasone from postnatal day 2 to postnatal day 4 following tapering doses (0.5, 0.3, and 0.1 mg/kg.d, respectively). Pups' neurological function was assessed by wire-hanging test and Morris water maze task. And apoptotic cells in hippocampus were counted. Vitamin D effectively improved spatial learning and memory impairment induced by dexamethasone. The protective effects of vitamin D may be related to the modulation of apoptosis. Vitamin D may therefore have a role in bronchopulmonary dysplasia treatment process.
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