• 文献检索
  • 文档翻译
  • 深度研究
  • 学术资讯
  • Suppr Zotero 插件Zotero 插件
  • 邀请有礼
  • 套餐&价格
  • 历史记录
应用&插件
Suppr Zotero 插件Zotero 插件浏览器插件Mac 客户端Windows 客户端微信小程序
定价
高级版会员购买积分包购买API积分包
服务
文献检索文档翻译深度研究API 文档MCP 服务
关于我们
关于 Suppr公司介绍联系我们用户协议隐私条款
关注我们

Suppr 超能文献

核心技术专利:CN118964589B侵权必究
粤ICP备2023148730 号-1Suppr @ 2026

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验

妊娠早期人类胎儿胆汁中的胆汁酸成分。

Biliary bile acid composition of the human fetus in early gestation.

作者信息

Colombo C, Zuliani G, Ronchi M, Breidenstein J, Setchell K D

出版信息

Pediatr Res. 1987 Feb;21(2):197-200. doi: 10.1203/00006450-198702000-00017.

DOI:10.1203/00006450-198702000-00017
PMID:3822601
Abstract

Using analytical techniques, which included capillary column gas-liquid chromatography and mass spectrometry, detailed bile acid profiles were obtained for 24 fetal bile samples collected after legal abortions were performed between the 14th and 20th wk of gestation. Qualitatively, the bile acid profiles of all fetal bile samples were similar. The predominant bile acids identified were chenodeoxycholic and cholic acid. The presence of small but variable amounts of deoxycholic acid and traces of lithocholic acid suggested placental transfer of these bile acids from the maternal circulation. 3 beta-Hydroxy-5-cholenoic acid was detected at higher levels than lithocholic acid. A conspicuous feature of the profiles was the presence of bile acids with hydroxyl groups at positions C-1 and C-6, and one other nuclear position of unknown origin, indicating fetal hepatic synthesis via pathways different from those normally seen in the adult. Quantitatively total biliary bile acid concentrations were extremely low (less than 0.05 mM) before wk 17 of gestation, but thereafter concentrations markedly increased reflecting a possible surge in bile acid synthesis; however, the ratio of cholic:chenodeoxycholic acids remained relatively constant over this period (mean +/- SD = 0.85 +/- 0.36) and different from that reported for the healthy newborn (ca. 2.5) and adult (ca. 1.6). These data indicate an immaturity in hepatic 12 alpha-hydroxylation of bile acids during early development and may explain why other pathways, in particular 1 beta and 6 alpha-hydroxylation, are activated at this stage of life.

摘要

运用包括毛细管柱气液色谱法和质谱分析法在内的分析技术,对妊娠第14至20周进行合法堕胎后收集的24份胎儿胆汁样本进行了详细的胆汁酸谱分析。定性分析显示,所有胎儿胆汁样本的胆汁酸谱相似。鉴定出的主要胆汁酸为鹅去氧胆酸和胆酸。少量但含量各异的脱氧胆酸以及痕量的石胆酸的存在表明这些胆汁酸可从母体循环经胎盘转运。检测到的3β-羟基-5-胆烯酸水平高于石胆酸。这些胆汁酸谱的一个显著特征是在C-1和C-6位以及另一个未知来源的核位置存在羟基胆汁酸,这表明胎儿肝脏通过与成人通常所见不同的途径进行合成。定量分析表明,妊娠第17周前总胆汁胆汁酸浓度极低(低于0.05 mM),但此后浓度显著增加,这反映出胆汁酸合成可能激增;然而,在此期间胆酸与鹅去氧胆酸的比例相对保持恒定(平均值±标准差 = 0.85±0.36),且与健康新生儿(约2.5)和成人(约1.6)报道的比例不同。这些数据表明在早期发育过程中胆汁酸的肝脏12α-羟化不成熟,这可能解释了为何在生命的这个阶段其他途径,特别是1β和6α-羟化途径被激活。

相似文献

1
Biliary bile acid composition of the human fetus in early gestation.妊娠早期人类胎儿胆汁中的胆汁酸成分。
Pediatr Res. 1987 Feb;21(2):197-200. doi: 10.1203/00006450-198702000-00017.
2
Hepatic bile acid metabolism during early development revealed from the analysis of human fetal gallbladder bile.通过对人类胎儿胆囊胆汁的分析揭示早期发育过程中的肝脏胆汁酸代谢
J Biol Chem. 1988 Nov 15;263(32):16637-44.
3
Effect of 7-ketolithocholic acid on bile acid metabolism in humans.7-酮石胆酸对人体胆汁酸代谢的影响。
Gastroenterology. 1982 Aug;83(2):341-7.
4
Comparative effects of ursodeoxycholic acid and chenodeoxycholic acid on bile acid kinetics and biliary lipid secretion in humans. Evidence for different modes of action on bile acid synthesis.熊去氧胆酸和鹅去氧胆酸对人体胆汁酸动力学及胆汁脂质分泌的比较效应。关于胆汁酸合成不同作用模式的证据。
Gastroenterology. 1983 Dec;85(6):1248-56.
5
Bile acid pattern in human amniotic fluid.人羊水的胆汁酸模式
Eur J Clin Invest. 1978 Feb;8(1):41-5. doi: 10.1111/j.1365-2362.1978.tb00807.x.
6
Bile acid metabolism during development: metabolism of lithocholic acid in human fetal liver.
Pediatr Res. 1987 Jan;21(1):99-103. doi: 10.1203/00006450-198701000-00021.
7
Correlation between fetal and maternal serum bile acid concentrations.
Pediatr Res. 1985 Feb;19(2):227-31. doi: 10.1203/00006450-198502000-00018.
8
Bile acids in porcine fetal bile.猪胎儿胆汁中的胆汁酸。
Biol Pharm Bull. 2000 Oct;23(10):1143-6. doi: 10.1248/bpb.23.1143.
9
Bile acid synthesis in cultured human hepatocytes: support for an alternative biosynthetic pathway to cholic acid.培养的人肝细胞中的胆汁酸合成:对胆酸替代生物合成途径的支持。
Hepatology. 2000 Jun;31(6):1305-12. doi: 10.1053/jhep.2000.7877.
10
Determination of fetal bile acids in biological fluids from neonates by gas chromatography-negative ion chemical ionization mass spectrometry.采用气相色谱-负离子化学电离质谱法测定新生儿生物体液中的胎儿胆汁酸。
J Chromatogr B Biomed Sci Appl. 1997 Mar 28;691(1):13-22. doi: 10.1016/s0378-4347(96)00384-2.

引用本文的文献

1
Bile acid metabolism in type 2 diabetes mellitus.2型糖尿病中的胆汁酸代谢
Nat Rev Endocrinol. 2025 Apr;21(4):203-213. doi: 10.1038/s41574-024-01067-8. Epub 2025 Jan 6.
2
Biliary atresia.先天性胆道闭锁。
Nat Rev Dis Primers. 2024 Jul 11;10(1):47. doi: 10.1038/s41572-024-00533-x.
3
In Utero Extrahepatic Bile Duct Damage and Repair: Implications for Biliary Atresia.子宫内肝外胆管损伤与修复:对胆道闭锁的影响。
Pediatr Dev Pathol. 2024 Jul-Aug;27(4):291-310. doi: 10.1177/10935266241247479. Epub 2024 May 19.
4
Revisited role of the placenta in bile acid homeostasis.胎盘在胆汁酸稳态中的作用再探讨。
Front Physiol. 2023 Jul 21;14:1213757. doi: 10.3389/fphys.2023.1213757. eCollection 2023.
5
Meconium-stained amniotic fluid.胎粪污染的羊水。
Am J Obstet Gynecol. 2023 May;228(5S):S1158-S1178. doi: 10.1016/j.ajog.2022.11.1283. Epub 2023 Apr 1.
6
Cholestasis impairs gut microbiota development and bile salt hydrolase activity in preterm neonates.胆汁淤积症会损害早产儿肠道微生物群落的发育和胆汁盐水解酶活性。
Gut Microbes. 2023 Jan-Dec;15(1):2183690. doi: 10.1080/19490976.2023.2183690.
7
Placental Expression of Bile Acid Transporters in Intrahepatic Cholestasis of Pregnancy.胎盘内胆汁酸转运体在妊娠肝内胆汁淤积症中的表达。
Int J Mol Sci. 2021 Sep 28;22(19):10434. doi: 10.3390/ijms221910434.
8
Pediatric Cholestatic Liver Disease: Review of Bile Acid Metabolism and Discussion of Current and Emerging Therapies.小儿胆汁淤积性肝病:胆汁酸代谢综述及当前和新兴治疗方法的讨论
Front Med (Lausanne). 2020 May 5;7:149. doi: 10.3389/fmed.2020.00149. eCollection 2020.
9
Clinical and molecular characterization of four patients with NTCP deficiency from two unrelated families harboring the novel SLC10A1 variant c.595A>C (p.Ser199Arg).两名无关联家系中 4 名 NTCP 缺陷患者的临床和分子特征,携带新型 SLC10A1 变异 c.595A>C(p.Ser199Arg)。
Mol Med Rep. 2019 Dec;20(6):4915-4924. doi: 10.3892/mmr.2019.10763. Epub 2019 Oct 23.
10
Transcriptome Profiling of Placenta through Pregnancy Reveals Dysregulation of Bile Acids Transport and Detoxification Function.通过妊娠对胎盘进行转录组谱分析揭示了胆汁酸转运和解毒功能的失调。
Int J Mol Sci. 2019 Aug 22;20(17):4099. doi: 10.3390/ijms20174099.