• 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

呋塞米对介导肾小管钠和钠转运的体成分和尿蛋白的影响:一项随机对照试验。

Effect of furosemide on body composition and urinary proteins that mediate tubular sodium and sodium transport-A randomized controlled trial.

机构信息

University Clinic in Nephrology and Hypertension, Department of Medicine, University of Aarhus and Gødstrup Hospital, Holstebro, Denmark.

Department of Biomedicine, Aarhus University, Aarhus, Denmark.

出版信息

Physiol Rep. 2021 Jan;8(24):e14653. doi: 10.14814/phy2.14653.

DOI:10.14814/phy2.14653
PMID:33356004
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC7757674/
Abstract

BACKGROUND

Furosemide inhibits the sodium potassium chloride cotransporter (NKCC2) in the thick ascending limb of the loop of Henle and increases urinary water and sodium excretion. This study investigates the effect of furosemide on body composition estimated with multifrequency bioimpedance spectroscopy (BIS) technique and urinary proteins from NKCC2.

METHODS

This study is a randomized, placebo-controlled, crossover study where healthy subjects received either placebo or 40 mg furosemide on two separate occasions, where body composition with BIS, renal function, proteins from tubular proteins that mediate sodium and water transport, and plasma concentrations of vasoactive hormones were measured before and after intervention.

RESULTS

We observed an expected increased diuresis with a subsequent reduction in bodyweight of (-1.51 ± 0.36 kg, p < .001) and extracellular water (ECW; -1.14 ± 0.23 L, p < .001) after furosemide. We found a positive correlation between the decrease in ECW and a decrease in bodyweight and a negative correlation between the decrease in ECW and the increase in urinary output. Intracellular water (ICW) increased (0.47 ± 0.28 L, p < .001). Urinary excretion of NKCC2 increased after furosemide and the increase in NKCC2 correlated with an increase in urine output and a decrease in ECW.

CONCLUSION

We found BIS can detect acute changes in body water content but the method may be limited to estimation of ECW. BIS demonstrated that furosemide increases ICW which might be explained by an extracellular sodium loss. Finally, urinary proteins from NKCC2 increases after furosemide with a good correlation with diuresis end the decrease in ECW.

摘要

背景

呋塞米抑制升支粗段的钠钾氯协同转运蛋白(NKCC2),增加尿水和钠排泄。本研究探讨了呋塞米对多频生物电阻抗谱(BIS)技术估计的身体成分和 NKCC2 尿蛋白的影响。

方法

这是一项随机、安慰剂对照、交叉研究,健康受试者在两次不同的时间接受安慰剂或 40mg 呋塞米,在干预前后测量身体成分(BIS)、肾功能、介导钠和水转运的管状蛋白蛋白和血管活性激素的血浆浓度。

结果

我们观察到预期的利尿作用,随后体重(-1.51±0.36kg,p<0.001)和细胞外液(ECW;-1.14±0.23L,p<0.001)减少。我们发现 ECW 减少与体重减轻呈正相关,ECW 减少与尿排量增加呈负相关。细胞内液(ICW)增加(0.47±0.28L,p<0.001)。呋塞米后 NKCC2 的尿排泄增加,NKCC2 的增加与尿排量增加和 ECW 减少相关。

结论

我们发现 BIS 可以检测到身体水分含量的急性变化,但该方法可能仅限于估计 ECW。BIS 表明,呋塞米增加了 ICW,这可能是由于细胞外钠丢失所致。最后,NKCC2 的尿蛋白在呋塞米后增加,与利尿作用和 ECW 减少呈良好相关性。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1120/7757674/19db0342a374/PHY2-8-e14653-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1120/7757674/dbe24d3c6161/PHY2-8-e14653-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1120/7757674/9df55ccb1b66/PHY2-8-e14653-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1120/7757674/19db0342a374/PHY2-8-e14653-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1120/7757674/dbe24d3c6161/PHY2-8-e14653-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1120/7757674/9df55ccb1b66/PHY2-8-e14653-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1120/7757674/19db0342a374/PHY2-8-e14653-g003.jpg

相似文献

1
Effect of furosemide on body composition and urinary proteins that mediate tubular sodium and sodium transport-A randomized controlled trial.呋塞米对介导肾小管钠和钠转运的体成分和尿蛋白的影响:一项随机对照试验。
Physiol Rep. 2021 Jan;8(24):e14653. doi: 10.14814/phy2.14653.
2
Regulation of the Na(+)-K(+)-2Cl(-) cotransporter by cGMP/cGMP-dependent protein kinase I after furosemide administration.速尿给药后环鸟苷酸/环鸟苷酸依赖蛋白激酶 I 对 Na(+)-K(+)-2Cl(-)协同转运蛋白的调节。
FEBS J. 2015 Oct;282(19):3786-98. doi: 10.1111/febs.13376. Epub 2015 Jul 30.
3
Effects of the sodium-glucose cotransporter 2 inhibitor dapagliflozin on fluid distribution: A comparison study with furosemide and tolvaptan.钠-葡萄糖协同转运蛋白 2 抑制剂达格列净对液体分布的影响:与呋塞米和托伐普坦的比较研究。
Nephrology (Carlton). 2019 Sep;24(9):904-911. doi: 10.1111/nep.13552. Epub 2019 May 2.
4
SGLT2 inhibitor and loop diuretic induce different vasopressin and fluid homeostatic responses in nondiabetic rats.SGLT2 抑制剂和袢利尿剂在非糖尿病大鼠中引起不同的血管加压素和液体稳态反应。
Am J Physiol Renal Physiol. 2022 Sep 1;323(3):F361-F369. doi: 10.1152/ajprenal.00070.2022. Epub 2022 Jul 28.
5
Inhibition of ROMK blocks macula densa tubuloglomerular feedback yet causes renal vasoconstriction in anesthetized rats.抑制ROMK可阻断致密斑肾小管-肾小球反馈,但在麻醉大鼠中会引起肾血管收缩。
Am J Physiol Renal Physiol. 2017 Jun 1;312(6):F1120-F1127. doi: 10.1152/ajprenal.00662.2016. Epub 2017 Feb 22.
6
Abundance of the Na-K-2Cl cotransporter NKCC2 is increased by high-fat feeding in Fischer 344 X Brown Norway (F1) rats.在Fischer 344×Brown Norway(F1)大鼠中,高脂喂养会增加钠-钾-2氯协同转运蛋白NKCC2的丰度。
Am J Physiol Renal Physiol. 2009 Apr;296(4):F762-70. doi: 10.1152/ajprenal.90484.2008. Epub 2009 Feb 4.
7
Tubuloglomerular and connecting tubuloglomerular feedback during inhibition of various Na transporters in the nephron.肾单位中各种钠转运体受抑制期间的球管反馈和连接管球反馈。
Am J Physiol Renal Physiol. 2015 May 1;308(9):F1026-31. doi: 10.1152/ajprenal.00605.2014. Epub 2015 Feb 25.
8
Effect of amiloride and spironolactone on renal tubular function and central blood pressure in patients with arterial hypertension during baseline conditions and after furosemide: a double-blinded, randomized, placebo-controlled crossover trial.氨氯吡咪和螺内酯对呋塞米作用下动脉高血压患者基础状态和治疗期肾小管功能及中心血压的影响:一项双盲、随机、安慰剂对照交叉试验。
Clin Exp Hypertens. 2013;35(5):313-24. doi: 10.3109/10641963.2012.721843. Epub 2012 Sep 11.
9
Sequential expression of NKCC2, TonEBP, aldose reductase, and urea transporter-A in developing mouse kidney.NKCC2、TonEBP、醛糖还原酶和尿素转运蛋白-A在发育中小鼠肾脏中的顺序表达。
Am J Physiol Renal Physiol. 2007 Jan;292(1):F269-77. doi: 10.1152/ajprenal.00145.2006. Epub 2006 Aug 22.
10
Osmoregulation requires brain expression of the renal Na-K-2Cl cotransporter NKCC2.渗透压调节需要肾脏钠-钾-2氯协同转运蛋白NKCC2在大脑中表达。
J Neurosci. 2015 Apr 1;35(13):5144-55. doi: 10.1523/JNEUROSCI.4121-14.2015.

引用本文的文献

1
Solid Self-Nanoemulsifying Drug Delivery Systems of Furosemide: In Vivo Proof of Concept for Enhanced Predictable Therapeutic Response.呋塞米固体自纳米乳化药物递送系统:增强可预测治疗反应的体内概念验证
Pharmaceuticals (Basel). 2024 Apr 14;17(4):500. doi: 10.3390/ph17040500.
2
SGLT2 inhibitor and loop diuretic induce different vasopressin and fluid homeostatic responses in nondiabetic rats.SGLT2 抑制剂和袢利尿剂在非糖尿病大鼠中引起不同的血管加压素和液体稳态反应。
Am J Physiol Renal Physiol. 2022 Sep 1;323(3):F361-F369. doi: 10.1152/ajprenal.00070.2022. Epub 2022 Jul 28.
3
Effect of 0.9% NaCl compared to plasma-lyte on biomarkers of kidney injury, sodium excretion and tubular transport proteins in patients undergoing primary uncemented hip replacement - a randomized trial.

本文引用的文献

1
Comparison of Chronic Hemodialysis Patients under Strict Volume Control with respect to Cardiovascular Disease.严格容量控制下慢性血液透析患者心血管疾病的比较
Int J Nephrol. 2019 Jul 3;2019:6430947. doi: 10.1155/2019/6430947. eCollection 2019.
2
Effect of 3% saline and furosemide on biomarkers of kidney injury and renal tubular function and GFR in healthy subjects - a randomized controlled trial.3%生理盐水和呋塞米对健康受试者肾损伤和肾小管功能及肾小球滤过率生物标志物的影响——一项随机对照试验。
BMC Nephrol. 2019 Jun 3;20(1):200. doi: 10.1186/s12882-019-1342-x.
3
Classification of Hydration in Clinical Conditions: Indirect and Direct Approaches Using Bioimpedance.
0.9%氯化钠与血浆代用品对初次非骨水泥髋关节置换术后患者肾损伤生物标志物、钠排泄和管状转运蛋白的影响:一项随机试验。
BMC Nephrol. 2021 Mar 26;22(1):111. doi: 10.1186/s12882-021-02310-4.
临床条件下的水合分类:使用生物阻抗的间接和直接方法。
Nutrients. 2019 Apr 10;11(4):809. doi: 10.3390/nu11040809.
4
Different Effects on Fluid Distribution between Tolvaptan and Furosemide in a Liver Cirrhosis Patient with Chronic Kidney Disease.托伐普坦和呋塞米对一名肝硬化合并慢性肾脏病患者液体分布的不同影响
Intern Med. 2019 Jun 1;58(11):1587-1591. doi: 10.2169/internalmedicine.2174-18. Epub 2019 Feb 1.
5
Effects of the sodium-glucose cotransporter 2 inhibitor dapagliflozin on fluid distribution: A comparison study with furosemide and tolvaptan.钠-葡萄糖协同转运蛋白 2 抑制剂达格列净对液体分布的影响:与呋塞米和托伐普坦的比较研究。
Nephrology (Carlton). 2019 Sep;24(9):904-911. doi: 10.1111/nep.13552. Epub 2019 May 2.
6
Fluid Overload in Critically Ill Children.危重症患儿的液体超负荷
Front Pediatr. 2018 Oct 29;6:306. doi: 10.3389/fped.2018.00306. eCollection 2018.
7
A Comprehensive Review of Bioelectrical Impedance Analysis and Other Methods in the Assessment of Nutritional Status in Patients with Liver Cirrhosis.生物电阻抗分析及其他方法在肝硬化患者营养状况评估中的综合综述
Gastroenterol Res Pract. 2017;2017:6765856. doi: 10.1155/2017/6765856. Epub 2017 Aug 13.
8
Effect of tolvaptan on renal handling of water and sodium, GFR and central hemodynamics in autosomal dominant polycystic kidney disease during inhibition of the nitric oxide system: a randomized, placebo-controlled, double blind, crossover study.在一氧化氮系统受抑制期间,托伐普坦对常染色体显性遗传性多囊肾病患者肾脏对水和钠的处理、肾小球滤过率及中心血流动力学的影响:一项随机、安慰剂对照、双盲、交叉研究
BMC Nephrol. 2017 Aug 15;18(1):268. doi: 10.1186/s12882-017-0686-3.
9
Pharmacodynamics of intravenous frusemide bolus in critically ill patients.危重症患者静脉注射速尿推注的药效学
Crit Care Resusc. 2017 Jun;19(2):142-149.
10
Functional assessment of sodium chloride cotransporter NCC mutants in polarized mammalian epithelial cells.极化哺乳动物上皮细胞中氯化钠共转运体NCC突变体的功能评估
Am J Physiol Renal Physiol. 2017 Aug 1;313(2):F495-F504. doi: 10.1152/ajprenal.00088.2017. Epub 2017 May 17.