# Ultrasound combined with microbubble enhanced renoprotective effects of NLRP3 inflammasome inhibitor MCC950 in CKD model

**Authors:** Wen Wen, Bin Tu, Xiaomei Ren, Yangli Liu, Rufang Jiang, Xiaofeng Wu, Jian Liu

PMC · DOI: 10.3389/fphar.2025.1616542 · 2025-07-31

## TL;DR

Combining ultrasound and microbubbles with the drug MCC950 improves kidney function and reduces damage in a rat model of chronic kidney disease.

## Contribution

The study shows that ultrasound and microbubbles enhance the effectiveness of MCC950 in treating CKD.

## Key findings

- US + MBs + MCC950 reduced kidney damage and improved function as effectively as a higher MCC950 dose alone.
- The combination therapy significantly lowered markers of kidney dysfunction and inflammation.
- NLRP3 inflammasome activity was inhibited more with the combination treatment.

## Abstract

This study evaluated the effectiveness of the NLRP3 inflammasome inhibitor MCC950 combined with ultrasound (US) and microbubbles (MBs) on kidney function and fibrosis in a rat model of chronic kidney disease (CKD).

After establishing the model, SD rats were divided into eight groups (n = 5): Control, CKD, MCC950 (10 mg/kg), MCC950 (5 mg/kg), US + MCC950 (5 mg/kg), US + MBs + MCC950 (5 mg/kg), US and US + MBs. MCC950 was administered at high (10 mg/kg) or low (5 mg/kg) doses, and 200 μL of sulfur hexafluoride microbubbles was delivered via tail vein injection. Ultrasound (mechanical index 0.99) was applied over the kidneys for 10 min every 2 days for six sessions post-injection. Renal function was assessed from urine and blood samples. Kidney tissues were examined using HE and Masson staining, while mRNA and protein levels of NLRP3, caspase-1, ASC, IL-1β, and IL-18 were quantified via RT-qPCR, immunohistochemistry, and ELISA.

Treatment with MCC950 (10 mg/kg), US + MCC950 (5 mg/kg), and US + MBs + MCC950 (5 mg/kg) significantly reduced serum creatinine, blood urea nitrogen, and albumin-to-creatinine ratios, and alleviated kidney damage and fibrosis compared to untreated CKD rats. Notably, US + MBs + MCC950 (5 mg/kg) was as effective as 10 mg/kg MCC950 treatment, with US + MBs further enhancing MCC950’s inhibitory effects on NLRP3 inflammasome activity in renal tissues, manifesting as reductions in the mRNA and protein expression of NLRP3, caspase-1, ASC, IL-1β and IL-18.

The combination of US and MB therapy with MCC950 improves renal function and reduces fibrosis in CKD rats, providing promising evidence for its potential in renal protection and the treatment of inflammatory disorders.

## Linked entities

- **Genes:** NLRP3 (NLR family pyrin domain containing 3) [NCBI Gene 114548], Caspase1 (caspase-1) [NCBI Gene 692604], STS (steroid sulfatase) [NCBI Gene 412], IL1B (interleukin 1 beta) [NCBI Gene 3553], IL18 (interleukin 18) [NCBI Gene 3606]
- **Chemicals:** MCC950 (PubChem CID 9910393), sulfur hexafluoride (PubChem CID 17358)
- **Diseases:** chronic kidney disease (MONDO:0005300)

## Full-text entities

- **Genes:** Nlrp3 (NLR family, pyrin domain containing 3) [NCBI Gene 287362] {aka Cias1}, Casp1 (caspase 1) [NCBI Gene 25166] {aka Ice, Il1bc, p45}, Pycard (PYD and CARD domain containing) [NCBI Gene 282817] {aka Asc}, Alb (albumin) [NCBI Gene 24186] {aka Alb1, Albza}, Il1b (interleukin 1 beta) [NCBI Gene 24494] {aka IL-1F2}, Il18 (interleukin 18) [NCBI Gene 29197] {aka IL-1 gamma, IL-18}
- **Diseases:** inflammatory disorders (MESH:D007249), CKD (MESH:D051436), fibrosis (MESH:D005355), kidney damage (MESH:D007674)
- **Chemicals:** sulfur hexafluoride (MESH:D013459), MCC950 (MESH:C000597426), urea nitrogen (MESH:C530477), creatinine (MESH:D003404)
- **Species:** Rattus norvegicus (brown rat, species) [taxon 10116]

## Figures

6 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12350275/full.md

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Source: https://tomesphere.com/paper/PMC12350275