Evidence map›Paper›PMID 42875680›Full record

ReviewMolecular neurobiology2026

Restoring Neural Homeostasis via Class II HDAC Modulation: Mechanistic Insights and Therapeutic Opportunities.

Rohan Gupta, Reetesh Kumar, Bhargav Shreevatsa K S, Deepak Kumar Modi, Smita Kumari, Naveen Kumar, Pallavi Singh, Karthikeyan Ravi, Mosleh Mohammad Abomughaid

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In one paragraph

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

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0citing papers in PubMed
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1 · What the graph read from it

What it found

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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

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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

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0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

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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

9 authors.

Rohan GuptaDepartment of Biotechnology & Bioengineering, School of Biosciences & Technology, Galgotias University, Greater Noida, Uttar Pradesh, 203201, India. rohan.gupta@galgotiasuniversity.edu.in.ORCID http://orcid.org/0000-0002-6635-6558
Reetesh KumarDepartment of Biotechnology & Bioengineering, School of Biosciences & Technology, Galgotias University, Greater Noida, Uttar Pradesh, 203201, India.
Bhargav Shreevatsa K SDepartment of Microbiology, JSS Academy of Higher Education and Research, Mysuru, Karnataka, India.
Deepak Kumar ModiKusuma School of Biological Sciences, Indian Institute of Technology, New Delhi, Delhi, India.
Smita KumariCollege of Pharmacy, The Ohio State University, Columbus, OH, USA.
Naveen KumarDepartment of Physics, School of Basic and Applied Sciences, Galgotias University, Greater Noida, 203201, Uttar Pradesh, India.
Pallavi SinghDepartment of Biotechnology, Graphic Era Deemed to Be University, Dehradun, 248002, Uttarakhand, India.
Karthikeyan RaviCentre for Herbal Pharmacology and Environmental Sustainability, Chettinad Hospital and Research Institute, Chettinad Academy of Research and Education, Kelambakkam, 603103, Tamil Nadu, India.
Mosleh Mohammad AbomughaidDepartment of Medical Laboratory Sciences, College of Applied Medical Sciences, University of Bisha, Bisha, 61922, Saudi Arabia.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Class II histone deacetylases (HDACs) comprise class IIa enzymes HDAC4, HDAC5, HDAC7, and HDAC9 and class IIb enzymes HDAC6 and HDAC10, which differ substantially in structure, catalytic activity, subcellular localization, and neural function. Class IIa HDACs exhibit weak intrinsic deacetylase activity and function predominantly as signal-responsive scaffolds that couple calcium and kinase signaling to transcription through nucleocytoplasmic shuttling, recruitment of HDAC3-containing NCoR/SMRT corepressor complexes, and interactions with MEF2, CREB, and FOXO. Conversely, HDAC6 is a predominantly cytoplasmic deacetylase that regulates α-tubulin acetylation, cytoskeletal dynamics, axonal transport, autophagy, and proteostasis. Dysregulated class II HDAC signaling contributes to neurodegenerative diseases through convergent mechanisms involving synaptic dysfunction, maladaptive transcriptional repression, mitochondrial impairment, oxidative stress, neuroinflammation, blood-brain barrier disruption, and defective clearance of pathological proteins. Disease-associated substrates include amyloid-β and tau in Alzheimer's disease, α-synuclein in Parkinson's disease, mutant huntingtin in Huntington's disease, and TDP-43/SOD1 in amyotrophic lateral sclerosis. Emerging evidence additionally links aberrant HDAC4/5 signaling to neurodevelopmental disorders through altered synaptic maturation, excitation-inhibition balance, and circuit development. This review integrates the structural and mechanistic biology of class II HDACs with their disease-specific roles and evaluates therapeutic approaches to restore neural homeostasis. Particular emphasis is placed on selective HDAC6 inhibitors, modulation of class IIa protein-protein interactions and subcellular trafficking, natural compounds, and RNA-based strategies. Finally, we discuss major translational challenges, including isoform specificity, brain penetration, context-dependent functions, and the need to distinguish catalytic from non-enzymic mechanisms when developing disease-modifying interventions for neurological disorders while preserving normal essential HDAC functions and minimizing off-target toxicity.

Indexed as

Histone DeacetylasesHomeostasisNeuronsAnimalsHistone Deacetylase InhibitorsHumansNeurodegenerative DiseasesSignal TransductionHistone Deacetylase InhibitorsHistone DeacetylasesHistone deacetylases (HDACs)Natural compoundsNeurodegenerative diseases (NDDs)NeuroinflammationProtein aggregationSelective inhibitors

Identifiers

PMID42875680

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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.