Evidence mapPaperPMID 39551771Full record

ArticleJournal of nanobiotechnology2024

Exploring the anti-inflammatory effects of curcumin encapsulated within ferritin nanocages: a comprehensive in vivo and in vitro study in Alzheimer's disease.

Carlo Morasso, Marta Truffi, Veronica Tinelli, Polychronis Stivaktakis, Rosalinda Di Gerlando, Dragoni Francesca, Giulia Perini, Mahvish Faisal, Jana Aid, Bekzod Noridov and 13 more

Abstract read
In one paragraph

Article in Journal of nanobiotechnology, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
9citing papers in PubMed, 1 pooled it
field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

9 citing papers in PubMed, 1 synthesis or guideline pooled it.

  1. Pooled it
  2. Article
  3. Review
  4. Review
  5. Review
  6. Review
  7. Review
  8. Review
  9. Review
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

23 authors.

Carlo MorassoIstituti Clinici Scientifici Maugeri IRCCS, Pavia, 27100, Italy.
Marta TruffiIstituti Clinici Scientifici Maugeri IRCCS, Pavia, 27100, Italy.
Veronica TinelliDepartment of Biotechnology and Bioscience, University of Milano-Bicocca, Piazza della Scienza 2, Milano, 20126, Italy.
Polychronis StivaktakisDepartment of Toxicology & Forensic Sciences, Faculty Medicine, University of Crete, Heraklion, Greece.
Rosalinda Di GerlandoDepartment of Biology and Biotechnology "L. Spallanzani" , University of Pavia, Pavia, Italy.
Dragoni FrancescaIRCCS Mondino Foundation, Pavia, 27100, Italy.
Giulia PeriniIRCCS Mondino Foundation, Pavia, 27100, Italy.
Mahvish FaisalDepartment of Pharmacology, Institute of Biomedicine and Translational Medicine, University of Tartu, Tartu, Estonia.
Jana AidDepartment of Pharmacology, Institute of Biomedicine and Translational Medicine, University of Tartu, Tartu, Estonia.
Bekzod NoridovDepartment of Pharmacology, Institute of Biomedicine and Translational Medicine, University of Tartu, Tartu, Estonia.
Benjamin LeeDepartment of Pharmacology, Institute of Biomedicine and Translational Medicine, University of Tartu, Tartu, Estonia.
Linda BarbieriDepartment of Biotechnology and Bioscience, University of Milano-Bicocca, Piazza della Scienza 2, Milano, 20126, Italy.
Sara NegriIstituti Clinici Scientifici Maugeri IRCCS, Pavia, 27100, Italy.
Dragana NikitovicDepartment of Histology-Embryology, School of Medicine, University of Crete, Heraklion, 71003, Greece.
Lydia-Nefeli ThrapsaniotiDepartment of Histology-Embryology, School of Medicine, University of Crete, Heraklion, 71003, Greece.
Aristides TsatsakisDepartment of Toxicology & Forensic Sciences, Faculty Medicine, University of Crete, Heraklion, Greece.
Cristina CeredaDepartment of Biomedical and Clinical Sciences, Università di Milano, Milan, 20157, Italy.
Arianna BonizziIstituti Clinici Scientifici Maugeri IRCCS, Pavia, 27100, Italy.
Serena MazzucchelliDepartment of Biomedical and Clinical Sciences, Università di Milano, Milan, 20157, Italy.
Davide ProsperiDepartment of Biotechnology and Bioscience, University of Milano-Bicocca, Piazza della Scienza 2, Milano, 20126, Italy.
Miriam A HickeyDepartment of Pharmacology, Institute of Biomedicine and Translational Medicine, University of Tartu, Tartu, Estonia. miriam.ann.hickey@ut.ee.
Fabio CorsiIstituti Clinici Scientifici Maugeri IRCCS, Pavia, 27100, Italy. fabio.corsi@icsmaugeri.it.
Stella GagliardiIRCCS Mondino Foundation, Pavia, 27100, Italy.

Funding

EuroNanoMed III JTC 2018 CurcumAgeMinistero della Salute Ricerca Corrente 2022-2024
6 · The paper itself

Abstract

backgroundThe global demographic shift towards an aging population is generating a rise in neurodegenerative conditions, with Alzheimer's disease (AD) as the most prominent problem. In this landscape, the use of natural supplements has garnered attention for their potential in dementia prevention. Curcumin (Cur), derived from Curcuma longa, has demonstrated promising pharmacological effects against AD by reducing the levels of inflammatory mediators. However, its clinical efficacy is hindered by poor solubility and bioavailability. Our study introduces the use of H-Ferritin nanocages (HFn) as a nanoformulation vehicle for Cur, aiming to enhance its therapeutic potential for AD. In this work, we characterized a nanoformulation of Cur in HFn (HFn-CUR) by evaluating its safety, stability, and its transport across the blood-brain barrier (BBB) in vitro. Moreover, we evaluated the efficacy of HFn-CUR by transcriptomic analysis of peripheral blood mononuclear cells (PBMCs) from both AD patients and healthy controls (HC), and by using the well-established 5xFAD mouse model of AD.

resultsOur data show that HFn-CUR exhibits improved water dispersibility, is non-toxic, and can traverse the BBB. Regarding its activity on PBMCs from AD patients, HFn-CUR enhances cellular responses to inflammation and reduces RAGE-mediated stress. Studies on an AD mouse model demonstrate that HFn-CUR exhibits mild beneficial effects on cognitive performance. Moreover, it effectively reduces microgliosis and astrogliosis and in vivo in mouse, suggesting potential neuroprotective benefits.

conclusionsOur data suggest that HFn-CUR is safe and effective in reducing inflammation in both in vitro and in vivo models of AD, supporting the need for further experiments to define its optimal use.

Indexed as

Alzheimer DiseaseAnti-Inflammatory AgentsBlood-Brain BarrierCurcuminDisease Models, AnimalAnimalsFemaleFerritinsHumansLeukocytes, MononuclearMaleMiceMice, TransgenicNanoparticlesAnti-Inflammatory AgentsCurcuminFerritins5xFAD miceAlzheimer’s diseaseBlood-brain barrierCurcuminH-FerritinNanoparticlesNeuroinflammationToxicity

Identifiers

PMID39551771
PMCPMC11571668

What Socratic holds

Textmetadata
LicenceCC BY-NC-ND
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the Socratic graph.