# Quantification of Kidney Inflammation Using Nanobubble-mediated Contrast Enhanced Ultrasound

**Authors:** Niloufar Rostam Shirazi, Xiaolin He, Dana Dranka, Omar Falou, Eno Hysi, Agata A. Exner, Darren Yuen, Michael C. Kolios

PMC · DOI: 10.7150/ntno.126443 · 2026-02-11

## TL;DR

This study introduces a non-invasive ultrasound method using nanobubbles to measure kidney inflammation, offering a potential alternative to biopsies.

## Contribution

The novel use of Cy5-labeled nanobubbles with contrast-enhanced ultrasound to quantify kidney inflammation in a preclinical model.

## Key findings

- CEUS imaging with nanobubbles revealed impaired microvascular perfusion and increased retention in inflamed kidneys.
- Decorrelation time mapping showed prolonged nanobubble retention, indicating increased capillary permeability in injured kidneys.
- Imaging metrics correlated with histological injury scores, validating the non-invasive method's accuracy.

## Abstract

Kidney inflammation is a central driver of acute kidney injury (AKI) and its progression to chronic kidney disease (CKD). While several imaging and biomarker-based approaches are under development, clinically validated non-invasive methods to directly quantify renal inflammation remain limited. This study introduces a novel approach using contrast-enhanced ultrasound (CEUS) with Cy5-labeled nanobubbles (NBs) to address this critical knowledge gap. Using a murine ischemia-reperfusion injury (IRI) model, CEUS imaging enabled real-time visualization of inflammation-induced changes in kidney perfusion and vascular integrity. Parametric analyses of non-linear imaging revealed delayed time-to-peak (TTP) and increased area under the falling curve (AUfC) in IRI kidneys, suggesting impaired microvascular perfusion and NB retention. Decorrelation time (DT) mapping further identified prolonged NB retention in the IRI group, indicating increased capillary permeability and NB extravasation. These findings correlated with histological and immunofluorescent analyses, which confirmed the presence of tubular injury, extravascular Cy5 signal localization, and increased neutrophil infiltration in inflamed kidney tissues. This study is the first to establish CEUS with NBs as a non-invasive, quantitative method for measuring kidney inflammation. With strong correlations between imaging metrics and histologic injury scores, this technology provides an accessible and non-invasive tool for monitoring renal inflammation and reducing reliance on invasive renal biopsies.

## Linked entities

- **Diseases:** acute kidney injury (MONDO:0002492), chronic kidney disease (MONDO:0005300)
- **Species:** Mus musculus (taxon 10090)

## Full-text entities

- **Genes:** Nr3c1 (nuclear receptor subfamily 3, group C, member 1) [NCBI Gene 14815] {aka GR, Grl-1, Grl1}, Havcr1 (hepatitis A virus cellular receptor 1) [NCBI Gene 171283] {aka KIM-1, TIM-1, Tim1, Timd1}, Il18 (interleukin 18) [NCBI Gene 16173] {aka Igif, Il-18}, Numb (NUMB endocytic adaptor protein) [NCBI Gene 18222] {aka Nb}, Selp (selectin, platelet) [NCBI Gene 20344] {aka CD62P, GMP-140, Grmp, LECAM3, PADGEM}, Vcam1 (vascular cell adhesion molecule 1) [NCBI Gene 22329] {aka CD106, Vcam-1}, Proc (protein C) [NCBI Gene 19123] {aka PC}, Pecam1 (platelet and endothelial cell adhesion molecule 1) [NCBI Gene 29583] {aka CD31, Pecam}, Pecam1 (platelet/endothelial cell adhesion molecule 1) [NCBI Gene 18613] {aka Cd31, PECAM-1, Pecam}, Lcn2 (lipocalin 2) [NCBI Gene 16819] {aka 24p3, NRL, Sip24}
- **Diseases:** ischemic (MESH:D002545), Tubular injury (MESH:D000230), cancer (MESH:D009369), declines (MESH:D060825), tubular necrosis (MESH:D007683), CKD (MESH:D051436), edema (MESH:D004487), atrophy (MESH:D001284), fibrosis (MESH:D005355), Inflammation (MESH:D007249), ischemia (MESH:D007511), renal (MESH:D006030), organ injury (MESH:D009102), AKI (MESH:D058186), dilation (MESH:D002311), vascular damage (MESH:D057772), microvascular damage (MESH:D017566), thrombosis (MESH:D013927), IRI (MESH:D015427), necrosis (MESH:D009336), radiation injury (MESH:D011832), endothelial (MESH:D005642), Kidney Inflammation (MESH:D007674), type 1 diabetes (MESH:D003922), TTP (MESH:D000377), pancreatic islet inflammation (MESH:D007516)
- **Chemicals:** paraffin (MESH:D010232), oxygen (MESH:D010100), water (MESH:D014867), isoflurane (MESH:D007530), Alexa Fluor 488 (MESH:C000711379), propylene glycol (MESH:D019946), H&amp;E (MESH:D006371), -8C5 (-), glycerol (MESH:D005990), hematoxylin (MESH:D006416), DPPE (MESH:C043062), buprenorphine (MESH:D002047), eosin (MESH:D004801), PBS (MESH:D007854), Cy5 (MESH:C085321), formalin (MESH:D005557), DAPI (MESH:C007293), DPPA (MESH:C007523), chloroform (MESH:D002725), lipid (MESH:D008055)
- **Species:** Mus musculus (house mouse, species) [taxon 10090], Rattus norvegicus (brown rat, species) [taxon 10116], Homo sapiens (human, species) [taxon 9606]

## Figures

12 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12923311/full.md

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Source: https://tomesphere.com/paper/PMC12923311