• 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

犬颈椎、胸椎和腰椎血-蛛网膜屏障和血-脊髓屏障中转运体、受体和紧密连接分子的绝对丰度的区域性差异。

Regional Differences in the Absolute Abundance of Transporters, Receptors and Tight Junction Molecules at the Blood-Arachnoid Barrier and Blood-Spinal Cord Barrier among Cervical, Thoracic and Lumbar Spines in Dogs.

机构信息

Division of Membrane Transport and Drug Targeting, Graduate School of Pharmaceutical Sciences, Tohoku University, 6-3 Aoba, Aramaki, Aoba-ku, Sendai, 980-8578, Japan.

Faculty of Pharmaceutical Sciences, Tohoku University, Sendai, Japan.

出版信息

Pharm Res. 2022 Jul;39(7):1393-1413. doi: 10.1007/s11095-022-03275-1. Epub 2022 Apr 29.

DOI:10.1007/s11095-022-03275-1
PMID:35488144
Abstract

PURPOSE

The purpose of the present study was to quantitatively determine the expression of transporters, receptors and tight junction molecules at the blood-arachnoid barrier (BAB) and blood-spinal cord barrier (BSCB) in cervical, thoracic and lumbar spines from dogs.

METHODS

The expression levels of 31 transporters, 3 receptors, 1 tight junction protein, and 3 marker proteins in leptomeninges and capillaries isolated from spines (3 male and 2 female dogs) were determined by quantitative Targeted Absolute Proteomics (qTAP). The units were converted from fmol/μg protein to pmol/cm (absolute abundance at the BAB and the BSCB in a 1 cm section of spine).

RESULTS

The expression of MDR1 and BCRP were greater at the BSCB compared to the BAB (especially in the cervical cord), and the expressions at the lumbar BSCB were lower than that for the cervical BSCB. Among the organic anionic and cationic drug transporters, OAT1, OAT3, MRP1, OCT2 and MATE1/2 were detected only in the BAB, and not at the BSCB). The expression of these transporters was higher in the order: lumbar > thoracic > cervical BAB. The expressions of GLUT1, 4F2hc, EAAT1, 2, PEPT2, CTL1, and MCT1 at the BSCB of the cervical cord were higher than the corresponding values for the cervical BAB, and these values decreased in going down the spinal cord.

CONCLUSION

These results provide a better understanding of the molecular mechanisms underlying the concentration gradients of drugs and endogenous substances in the cerebrospinal fluid and parenchyma of the spinal cord.

摘要

目的

本研究旨在定量测定犬颈椎、胸椎和腰椎脑膜和毛细血管中 31 种转运体、3 种受体、1 种紧密连接分子和 3 种标记蛋白在血-蛛网膜屏障(BAB)和血-脊髓屏障(BSCB)的表达。

方法

通过定量靶向绝对蛋白质组学(qTAP)测定从脊柱(3 只雄性和 2 只雌性犬)分离的软脑膜和毛细血管中 31 种转运体、3 种受体、1 种紧密连接蛋白和 3 种标记蛋白的表达水平。单位从 fmol/μg 蛋白转换为 pmol/cm(脊柱 1cm 节段的 BAB 和 BSCB 的绝对丰度)。

结果

与 BAB 相比,BSCB 处 MDR1 和 BCRP 的表达更高(尤其是在颈髓),而腰 BSCB 的表达低于颈 BSCB。在有机阴离子和阳离子药物转运体中,OAT1、OAT3、MRP1、OCT2 和 MATE1/2 仅在 BAB 中检测到,而不在 BSCB 中检测到。这些转运体的表达顺序为:腰>胸>颈 BAB。GLUT1、4F2hc、EAAT1、2、PEPT2、CTL1 和 MCT1 在颈脊髓 BSCB 的表达高于相应的颈 BAB 值,并且这些值在脊髓向下走时降低。

结论

这些结果提供了对药物和内源性物质在脑脊液和脊髓实质中浓度梯度的分子机制的更好理解。

相似文献

1
Regional Differences in the Absolute Abundance of Transporters, Receptors and Tight Junction Molecules at the Blood-Arachnoid Barrier and Blood-Spinal Cord Barrier among Cervical, Thoracic and Lumbar Spines in Dogs.犬颈椎、胸椎和腰椎血-蛛网膜屏障和血-脊髓屏障中转运体、受体和紧密连接分子的绝对丰度的区域性差异。
Pharm Res. 2022 Jul;39(7):1393-1413. doi: 10.1007/s11095-022-03275-1. Epub 2022 Apr 29.
2
A human blood-arachnoid barrier atlas of transporters, receptors, enzymes, and tight junction and marker proteins: Comparison with dog and pig in absolute abundance.人类血脑屏障转运体、受体、酶、紧密连接和标记蛋白图谱:与犬和猪的绝对丰度比较。
J Neurochem. 2022 Apr;161(2):187-208. doi: 10.1111/jnc.15599. Epub 2022 Mar 17.
3
Abundant Expression of OCT2, MATE1, OAT1, OAT3, PEPT2, BCRP, MDR1, and xCT Transporters in Blood-Arachnoid Barrier of Pig and Polarized Localizations at CSF- and Blood-Facing Plasma Membranes.在猪的血-蛛网膜屏障中大量表达 OCT2、MATE1、OAT1、OAT3、PEPT2、BCRP、MDR1 和 xCT 转运体,并在 CSF-和血液-面对的质膜上呈现极化定位。
Drug Metab Dispos. 2020 Feb;48(2):135-145. doi: 10.1124/dmd.119.089516. Epub 2019 Nov 26.
4
Drug Clearance from Cerebrospinal Fluid Mediated by Organic Anion Transporters 1 (Slc22a6) and 3 (Slc22a8) at Arachnoid Membrane of Rats.有机阴离子转运体 1(Slc22a6)和 3(Slc22a8)介导的药物从大鼠蛛网膜脑脊液清除。
Mol Pharm. 2018 Mar 5;15(3):911-922. doi: 10.1021/acs.molpharmaceut.7b00852. Epub 2018 Feb 21.
5
Comparison of Absolute Protein Abundances of Transporters and Receptors among Blood-Brain Barriers at Different Cerebral Regions and the Blood-Spinal Cord Barrier in Humans and Rats.比较不同脑区血脑屏障和血脊髓屏障中转运体和受体的绝对蛋白含量在人类和大鼠中的差异。
Mol Pharm. 2020 Jun 1;17(6):2006-2020. doi: 10.1021/acs.molpharmaceut.0c00178. Epub 2020 Apr 29.
6
[Molecular Mechanism Underlying the Function and Disintegration of the Central Nerve System Barrier Unraveled by Proteo-typing of Membrane Proteins].[通过膜蛋白蛋白质组学揭示中枢神经系统屏障功能与解体的分子机制]
Brain Nerve. 2021 Jan;73(1):59-78. doi: 10.11477/mf.1416201712.
7
Inner Blood-Retinal Barrier Dominantly Expresses Breast Cancer Resistance Protein: Comparative Quantitative Targeted Absolute Proteomics Study of CNS Barriers in Pig.内在血-视网膜屏障主要表达乳腺癌耐药蛋白:猪中枢神经系统屏障的比较定量靶向绝对蛋白质组学研究。
Mol Pharm. 2017 Nov 6;14(11):3729-3738. doi: 10.1021/acs.molpharmaceut.7b00493. Epub 2017 Oct 12.
8
Organic Anion-Transporting Polypeptide 1a4 (Oatp1a4/Slco1a4) at the Blood-Arachnoid Barrier is the Major Pathway of Sulforhodamine-101 Clearance from Cerebrospinal Fluid of Rats.血脑屏障上的有机阴离子转运多肽 1a4(Oatp1a4/Slco1a4)是大鼠脑脊液中磺罗丹明 101 清除的主要途径。
Mol Pharm. 2019 May 6;16(5):2021-2027. doi: 10.1021/acs.molpharmaceut.9b00005. Epub 2019 Apr 22.
9
Quantitative targeted absolute proteomics of rat blood-cerebrospinal fluid barrier transporters: comparison with a human specimen.大鼠血脑脊髓液屏障转运蛋白的定量靶向绝对蛋白质组学:与人类样本的比较。
J Neurochem. 2015 Sep;134(6):1104-15. doi: 10.1111/jnc.13147. Epub 2015 Jun 8.
10
Involvement of Claudin-11 in Disruption of Blood-Brain, -Spinal Cord, and -Arachnoid Barriers in Multiple Sclerosis.Claudin-11 在多发性硬化症中血脑、脊髓和蛛网膜屏障破坏中的作用。
Mol Neurobiol. 2019 Mar;56(3):2039-2056. doi: 10.1007/s12035-018-1207-5. Epub 2018 Jul 8.

引用本文的文献

1
Cerebrospinal fluid draining lymphatics in health and disease: advances and controversies.健康与疾病状态下的脑脊液引流淋巴管:进展与争议
Nat Cardiovasc Res. 2025 Sep 8. doi: 10.1038/s44161-025-00705-2.
2
The canine blood-brain barrier in health and disease: focus on brain protection.健康与疾病状态下的犬血脑屏障:聚焦脑保护
Vet Q. 2025 Dec;45(1):12-32. doi: 10.1080/01652176.2025.2450041. Epub 2025 Jan 10.
3
Breaking boundaries: role of the brain barriers in metastatic process.突破界限:脑屏障在转移过程中的作用。

本文引用的文献

1
Impact of P-Glycoprotein-Mediated Active Efflux on Drug Distribution into Lumbar Cerebrospinal Fluid in Nonhuman Primates.P-糖蛋白介导的主动外排对非人类灵长类动物腰椎脑脊液中药物分布的影响。
Drug Metab Dispos. 2020 Nov;48(11):1183-1190. doi: 10.1124/dmd.120.000099. Epub 2020 Aug 29.
2
Efficient isolation of brain capillary from a single frozen mouse brain for protein expression analysis.从单个冷冻小鼠大脑中高效分离脑毛细血管用于蛋白质表达分析。
J Cereb Blood Flow Metab. 2021 May;41(5):1026-1038. doi: 10.1177/0271678X20941449. Epub 2020 Jul 23.
3
Comparison of Absolute Protein Abundances of Transporters and Receptors among Blood-Brain Barriers at Different Cerebral Regions and the Blood-Spinal Cord Barrier in Humans and Rats.
Fluids Barriers CNS. 2025 Jan 8;22(1):3. doi: 10.1186/s12987-025-00618-z.
4
MCT1-mediated endothelial cell lactate shuttle as a target for promoting axon regeneration after spinal cord injury.MCT1 介导线粒体细胞乳酸穿梭作为促进脊髓损伤后轴突再生的靶点。
Theranostics. 2024 Sep 3;14(14):5662-5681. doi: 10.7150/thno.96374. eCollection 2024.
5
How Much is Enough? Impact of Efflux Transporters on Drug delivery Leading to Efficacy in the Treatment of Brain Tumors.究竟多少才算足够?外排转运体对药物传递的影响对治疗脑肿瘤的疗效至关重要。
Pharm Res. 2023 Nov;40(11):2731-2746. doi: 10.1007/s11095-023-03574-1. Epub 2023 Aug 17.
6
Proton-Coupled Oligopeptide Transport (Slc15) in the Brain: Past and Future Research.质子偶联寡肽转运体(Slc15)在大脑中的作用:过去和未来的研究。
Pharm Res. 2023 Nov;40(11):2533-2540. doi: 10.1007/s11095-023-03550-9. Epub 2023 Jun 12.
7
A year in review: brain barriers and brain fluids research in 2022.年度回顾:2022 年的脑屏障和脑液研究。
Fluids Barriers CNS. 2023 Apr 21;20(1):30. doi: 10.1186/s12987-023-00429-0.
比较不同脑区血脑屏障和血脊髓屏障中转运体和受体的绝对蛋白含量在人类和大鼠中的差异。
Mol Pharm. 2020 Jun 1;17(6):2006-2020. doi: 10.1021/acs.molpharmaceut.0c00178. Epub 2020 Apr 29.
4
Abundant Expression of OCT2, MATE1, OAT1, OAT3, PEPT2, BCRP, MDR1, and xCT Transporters in Blood-Arachnoid Barrier of Pig and Polarized Localizations at CSF- and Blood-Facing Plasma Membranes.在猪的血-蛛网膜屏障中大量表达 OCT2、MATE1、OAT1、OAT3、PEPT2、BCRP、MDR1 和 xCT 转运体,并在 CSF-和血液-面对的质膜上呈现极化定位。
Drug Metab Dispos. 2020 Feb;48(2):135-145. doi: 10.1124/dmd.119.089516. Epub 2019 Nov 26.
5
Involvement of Claudin-11 in Disruption of Blood-Brain, -Spinal Cord, and -Arachnoid Barriers in Multiple Sclerosis.Claudin-11 在多发性硬化症中血脑、脊髓和蛛网膜屏障破坏中的作用。
Mol Neurobiol. 2019 Mar;56(3):2039-2056. doi: 10.1007/s12035-018-1207-5. Epub 2018 Jul 8.
6
Drug Clearance from Cerebrospinal Fluid Mediated by Organic Anion Transporters 1 (Slc22a6) and 3 (Slc22a8) at Arachnoid Membrane of Rats.有机阴离子转运体 1(Slc22a6)和 3(Slc22a8)介导的药物从大鼠蛛网膜脑脊液清除。
Mol Pharm. 2018 Mar 5;15(3):911-922. doi: 10.1021/acs.molpharmaceut.7b00852. Epub 2018 Feb 21.
7
The cerebrospinal fluid and barriers - anatomic and physiologic considerations.脑脊液与屏障——解剖学和生理学考量
Handb Clin Neurol. 2017;146:21-32. doi: 10.1016/B978-0-12-804279-3.00002-2.
8
Inner Blood-Retinal Barrier Dominantly Expresses Breast Cancer Resistance Protein: Comparative Quantitative Targeted Absolute Proteomics Study of CNS Barriers in Pig.内在血-视网膜屏障主要表达乳腺癌耐药蛋白:猪中枢神经系统屏障的比较定量靶向绝对蛋白质组学研究。
Mol Pharm. 2017 Nov 6;14(11):3729-3738. doi: 10.1021/acs.molpharmaceut.7b00493. Epub 2017 Oct 12.
9
Quantification of Transporter and Receptor Proteins in Dog Brain Capillaries and Choroid Plexus: Relevance for the Distribution in Brain and CSF of Selected BCRP and P-gp Substrates.犬脑毛细血管和脉络丛中转运体和受体蛋白的定量:对选定的 BCRP 和 P-糖蛋白底物在脑和 CSF 中分布的相关性。
Mol Pharm. 2017 Oct 2;14(10):3436-3447. doi: 10.1021/acs.molpharmaceut.7b00449. Epub 2017 Sep 19.
10
Dynamic dual-isotope molecular imaging elucidates principles for optimizing intrathecal drug delivery.动态双示踪分子影像学阐明了优化鞘内药物递送的原则。
JCI Insight. 2016 Feb 25;1(2):e85311. doi: 10.1172/jci.insight.85311.