# Focused ultrasound enhances targeted curcumin delivery and alleviates behavioral and neuropathological deficits in a Parkinson’s disease mouse model

**Authors:** Shu-Mei Yang, Sen-Hi Yeoh, Meng-Ting Lin, Ming-Yen Hsiao, Chueh-Hung Wu, Sung-Jan Lin, Wen-Shiang Chen

PMC · DOI: 10.3389/fnagi.2026.1740256 · Frontiers in Aging Neuroscience · 2026-02-09

## TL;DR

Using focused ultrasound to open the blood-brain barrier improves curcumin delivery and reduces Parkinson's symptoms in mice.

## Contribution

This is the first study to show unmodified curcumin with focused ultrasound improves Parkinson's disease outcomes in a mouse model.

## Key findings

- FUS combined with curcumin improved motor coordination and exploratory activity in early-stage Parkinson's mice.
- FUS increased curcumin accumulation in the brain without causing tissue damage or adverse effects.
- Combined treatment preserved dopaminergic neurons and reduced astrocytic activation compared to curcumin alone.

## Abstract

Curcumin exhibits potent neuroprotective properties but is limited by poor blood-brain barrier (BBB) permeability. This study aimed to evaluate whether focused ultrasound (FUS)-mediated BBB opening enhances curcumin delivery and therapeutic efficacy in a 6-hydroxydopamine (6-OHDA) mouse model of Parkinson’s disease (PD).

Male C57BL/6 mice with unilateral 6-OHDA lesions received intravenous curcumin with or without FUS targeted to the lesioned striatum for 4 weeks. Behavioral performance was assessed using rotarod and open-field tests. Postmortem analyses included tyrosine hydroxylase (TH) immunostaining in the striatum and substantia nigra pars compacta (SNpc), glial fibrillary acidic protein expression, and fluorescence quantification of curcumin accumulation. Microglial activation and pro-inflammatory cytokine expression were evaluated using ionized calcium-binding adaptor molecule 1 (Iba1) and interleukin-6 (IL-6) staining. Safety was evaluated by histological examination for hemorrhage or necrosis.

Significant improvements in motor coordination and exploratory activity were observed in the FUS + curcumin group, particularly during early stages of degeneration. Histologically, combined treatment was associated with greater preservation of TH-positive dopaminergic neurons in the SNpc and reduced astrocytic activation in the striatum compared with curcumin alone, whereas striatal TH fiber density did not differ between curcumin-treated groups. No significant differences were observed in striatal Iba1 or IL-6 expression across groups at the 4-week time point. Enhanced curcumin accumulation in the brain was observed following FUS, as demonstrated by fluorescence quantification. No tissue damage or adverse effects were observed after repeated sonications.

This is the first study to demonstrate the efficacy of unmodified curcumin combined with FUS in a 6-OHDA PD model. The findings support FUS as a safe and effective strategy to transiently disrupt the BBB and enhance the central nervous system delivery of small-molecule therapeutic agents, offering translational potential for regionally targeted, non-invasive treatment of PD.

## Linked entities

- **Proteins:** IL6 (interleukin 6)
- **Chemicals:** curcumin (PubChem CID 969516), 6-hydroxydopamine (PubChem CID 4624)
- **Diseases:** Parkinson’s disease (MONDO:0005180)

## Full-text entities

- **Genes:** Gfap (glial fibrillary acidic protein) [NCBI Gene 14580], Fus (fused in sarcoma) [NCBI Gene 233908] {aka D430004D17Rik, D930039C12Rik, Fus1, Tls}, Alb (albumin) [NCBI Gene 11657] {aka Alb-1, Alb1, BCL001, BCL002, BPL001}, Tjp1 (tight junction protein 1) [NCBI Gene 21872] {aka ZO1}, IL1B (interleukin 1 beta) [NCBI Gene 3553] {aka IL-1, IL1-BETA, IL1F2, IL1beta}, NOS2 (nitric oxide synthase 2) [NCBI Gene 4843] {aka HEP-NOS, INOS, NOS, NOS2A}, Th (tyrosine hydroxylase) [NCBI Gene 21823], Gdnf (glial cell line derived neurotrophic factor) [NCBI Gene 14573] {aka ATF}, Il6 (interleukin 6) [NCBI Gene 16193] {aka Il-6}, Bdnf (brain derived neurotrophic factor) [NCBI Gene 12064], Ocln (occludin) [NCBI Gene 18260] {aka Ocl}, Iba1 (induction of brown adipocytes 1) [NCBI Gene 114737], Cldn5 (claudin 5) [NCBI Gene 12741] {aka MBEC1, Tmvcf}, Syp (synaptophysin) [NCBI Gene 20977] {aka A230093K24Rik, Syn, p38}, Dlg4 (discs large MAGUK scaffold protein 4) [NCBI Gene 13385] {aka Dlgh4, PSD-95, PSD95, SAP90, SAP90A}, TNF (tumor necrosis factor) [NCBI Gene 7124] {aka DIF, IMD127, TNF-alpha, TNFA, TNFSF2, TNLG1F}
- **Diseases:** motor performance deficits (MESH:D009461), neurotoxic (MESH:D020258), rigidity (MESH:D009127), necrosis (MESH:D009336), cognitive decline (MESH:D003072), dopaminergic (MESH:D009422), BBB disruption (MESH:C536830), toxicity (MESH:D064420), tissue injury (MESH:D017695), striatal degeneration (MESH:C537500), edema (MESH:D004487), Neuroinflammation (MESH:D000090862), autonomic dysfunction (MESH:D001342), motor impairment (MESH:D000068079), anxiety (MESH:D001007), neurodegeneration (MESH:D019636), degeneration of dopaminergic (MESH:D009410), inflammatory (MESH:D007249), mood disorders (MESH:D019964), deficits in locomotion (MESH:D020233), astrogliosis (MESH:D005911), lesions (MESH:D009059), dopamine deficiency (MESH:C567730), neurological diseases (MESH:D020271), bleeding (MESH:D006470), postural instability (MESH:D054972), fatigue (MESH:D005221), PD (MESH:D010300), bradykinesia (MESH:D018476), resting tremor (MESH:D014202), mitochondrial dysfunction (MESH:D028361)
- **Chemicals:** 3,3'-diaminobenzidine (MESH:D015100), xylene (MESH:D014992), desipramine (MESH:D003891), eosin (MESH:D004801), dopamine (MESH:D004298), Tween 20 (MESH:D011136), alcohol (MESH:D000438), prostaglandin (MESH:D011453), ascorbic acid (MESH:D001205), Alexa Fluor 555 (MESH:C000608607), Xylazine (MESH:D014991), polyethylene glycol (MESH:D011092), Sonazoid (MESH:C069727), formalin (MESH:D005557), ethanol (MESH:D000431), DMSO (MESH:D004121), nitric oxide (MESH:D009569), 4',6-diamidino-2-phenylindole (MESH:C007293), 1-methyl-4-phenylpyridinium (MESH:D015655), polyvinyl chloride (MESH:D011143), polyethylene glycol 300 (MESH:C000595211), PBST (-), water (MESH:D014867), EB (MESH:D005070), Paraffin (MESH:D010232), Zoletil (MESH:C006131), citrate (MESH:D019343), Curcumin (MESH:D003474), saline (MESH:D012965), 6-OHDA (MESH:D016627), H&amp;E (MESH:D006371), 1-methyl-4-phenyl-1,2,3,6-tetrahydropyridine (MESH:D015632), iron (MESH:D007501), pargyline hydrochloride (MESH:D010293), Hematoxylin (MESH:D006416)
- **Species:** Rattus norvegicus (brown rat, species) [taxon 10116], Mus musculus (house mouse, species) [taxon 10090], Homo sapiens (human, species) [taxon 9606], Curcuma longa (turmeric, species) [taxon 136217]

## Full text

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## Figures

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## References

68 references — full list in the complete paper: https://tomesphere.com/paper/PMC12926497/full.md

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Source: https://tomesphere.com/paper/PMC12926497