Fluorimetric Tool to Discriminate Glomerular and Tubular Injuries In Vivo

The etiology and pathological complexity of acute kidney injury (AKI) pose great challenges for early diagnosis, typing, and personalized treatment. It is an important reason for poor prognosis and high mortality of AKI. In order to provide a relatively noninvasive diagnostic and typing method for AKI, we proposed the pathological changes of albumin permeability after glomerular injury and reabsorption efficiency after tubular injury as potential entry points. Thus, a renal tubule labeling fluorescent dye which features albumin concentration-related fluorescence intensity was used to fit these pathological changes. Utilizing this fluorescence assay, we realized urinary tract obstruction imaging as early as 12 h after morbidity. For glomerular and tubular injury discrimination, compared to a healthy control, membranous nephropathy as a representative glomerular injury resulted in enhanced fluorescence intensity of the kidney due to increased albumin penetration, while renal tubular injury caused insufficient dye reabsorption to exhibit weakened fluorescence intensity. The significant differences demonstrated the feasibility of this approach for fluorescence imaging-based AKI typing in vivo.

Authors

Institutions

Publication Details

Journal
Analytical Chemistry
Published
2024-08-30
DOI
https://doi.org/10.1021/acs.analchem.4c02724
Citations
1
Primary Topic
Acute Kidney Injury Research
Type
article
Field-Weighted Citation Impact
0.34

Funders

Controls
|||
ALL TIME
JAN
FEB
MAR
APR
MAY
JUN
JUL
AUG
SEP
OCT
article

Fluorimetric Tool to Discriminate Glomerular and Tubular Injuries In Vivo

Jiahong Ai, Xiaojun Chai, Yongkang Yue, Hu Shi et al.
1 citations
Analytical Chemistry
Acute Kidney Injury Research
0.34
article

Fluorimetric Tool to Discriminate Glomerular and Tubular Injuries In Vivo

Jiahong Ai, Xiaojun Chai, Yongkang Yue, Hu Shi, Fangjun Huo, Caixia Yin, Shuo Wang, Xu Zhou
article en
1 citations

Abstract

The etiology and pathological complexity of acute kidney injury (AKI) pose great challenges for early diagnosis, typing, and personalized treatment. It is an important reason for poor prognosis and high mortality of AKI. In order to provide a relatively noninvasive diagnostic and typing method for AKI, we proposed the pathological changes of albumin permeability after glomerular injury and reabsorption efficiency after tubular injury as potential entry points. Thus, a renal tubule labeling fluorescent dye which features albumin concentration-related fluorescence intensity was used to fit these pathological changes. Utilizing this fluorescence assay, we realized urinary tract obstruction imaging as early as 12 h after morbidity. For glomerular and tubular injury discrimination, compared to a healthy control, membranous nephropathy as a representative glomerular injury resulted in enhanced fluorescence intensity of the kidney due to increased albumin penetration, while renal tubular injury caused insufficient dye reabsorption to exhibit weakened fluorescence intensity. The significant differences demonstrated the feasibility of this approach for fluorescence imaging-based AKI typing in vivo.

Analytical ChemistryVol. 96(37)
Shanxi University (CN), People’s Hospital of Linqing (CN), Xian Yang Central Hospital (CN)
National Natural Science Foundation of China
Reduced inequalities
Openalex Percentile: Top 36%
Acute Kidney Injury Research
0.34
AI Navigator

Ask Laika to Summarize, Analyze, and Connect papers live on the map.

Summarize Papers & Methodologies

Extract key findings, datasets, and comparative methods across publications.

Benchmark Rankings & Visual Analytics

Rank top research institutions, authors, funders, topics, and journals by Field-Weighted Citation Impact (FWCI) and paper volume with instant charts.

Connect Distant Disciplines

Bridge topological clusters on the map to find hidden collaborative intersections.

Fluorimetric Tool to Discriminate Glomerular and Tubular Injuries In Vivo — Jiahong Ai, Xiaojun Chai, et al. · Analytical Chemistry (2024) | TGRS Research Map | TGRS