Evidence map›Paper›PMID 42719278›Full record

Review3 Biotech2026

Advances in phytochemical modulation of protein aggregation in neurodegenerative diseases.

Nitu Kumari, Santosh Anand

Abstract readReview
In one paragraph

Review in 3 Biotech, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
–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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

2 authors.

Nitu KumariDepartment of Biotechnology, School of Applied Sciences, REVA University, Bengaluru, 560064 Karnataka India.
Santosh AnandDepartment of Biotechnology, School of Applied Sciences, REVA University, Bengaluru, 560064 Karnataka India.ORCID 0000-0002-2445-8118

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Protein aggregation and misfolding are central pathological events underlying major neurodegenerative disorders, including Alzheimer's disease, Parkinson's disease, and related proteinopathies. The aberrant aggregation of amyloid-β, tau, and α-synuclein generates toxic oligomeric and fibrillar species that disrupt proteostasis, impair synaptic function, promote oxidative stress and neuroinflammation, and ultimately drive progressive neuronal loss. This review critically summarizes recent advances in plant-derived secondary metabolites with anti-aggregation properties, emphasizing their structural diversity, molecular mechanisms, structure-activity relationships, and translational potential. Current findings demonstrate that polyphenols, flavonoids, terpenoids, alkaloids, curcuminoids, and secoiridoids inhibit protein aggregation through multiple complementary mechanisms, including direct modulation of amyloidogenic proteins and restoration of proteostasis via molecular chaperones, the ubiquitin-proteasome system, autophagy-lysosomal pathways, mitochondrial protection, and suppression of neuroinflammatory signaling. Emerging evidence further demonstrates that rational structural optimization, hybrid molecule design, and nanotechnology-based delivery systems can substantially improve the pharmacokinetic limitations of these compounds. Overall, the accumulated evidence indicates that phytochemicals possess multitarget therapeutic potential by simultaneously reducing protein aggregation, oxidative stress, mitochondrial dysfunction, and neuroinflammation, thereby offering broader neuroprotection than single-target approaches. Nevertheless, limited bioavailability, poor blood-brain barrier penetration, interspecies variability, and insufficient clinical validation continue to impede translation. By integrating mechanistic evidence with recent advances in medicinal chemistry and drug delivery, this review highlights promising strategies to accelerate the development of phytochemical-based therapeutics for protein aggregation-associated neurodegenerative diseases. Unlike previous studies that primarily summarize anti-amyloid phytochemicals, this review integrates recent mechanistic insights into protein aggregation, proteostasis regulation, medicinal chemistry optimization, structural biology, and translational challenges across multiple neurodegenerative proteinopathies.

Indexed as

Amyloid-βNeurodegenerationPhytochemicalsPolyphenolsProtein aggregationα-Synuclein

Identifiers

PMID42719278
PMCPMC13554045

What OpenQuestion holds

Textmetadata
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 OpenQuestion graph.