City
Epaper

JNCASR’s new autism therapy to help patients become more self-sufficient

By IANS | Updated: April 4, 2025 18:06 IST

New Delhi, April 4 Researchers from Jawaharlal Nehru Centre for Advanced Scientific Research (JNCASR), an autonomous institute of ...

Open in App

New Delhi, April 4 Researchers from Jawaharlal Nehru Centre for Advanced Scientific Research (JNCASR), an autonomous institute of the Department of Science and Technology (DST) have developed a new therapy that may help patients suffering from autism or intellectual disability to lead a life less dependent on others.

Current therapeutics prescribed to treat autism spectrum disorder (ASD) or intellectual disability are mostly related to alleviating the symptoms. These do not correct the phenotypes observed in neurodevelopmental disorders, especially after brain development.

In a study on mice, the team led by Tapas K Kundu and James Clement from JNCASR, found that a gene that gets repressed in the brain of patients with autism.

“In mice with mutated syngap gene -- which resembles humans with mutated syngap gene (present in autistic patients) -- the acetylation of DNA-associated proteins, histones, or proteins that provide structural support for chromosomes is repressed in the brain,” said the team. The epigenetic enzyme behind this acetylation seems to be KAT3B or p300, they said.

Kundu’s group had previously discovered an activator of this enzyme, TTK21.

Upon conjugating this activator with glucose-derived nanosphere (CSP-TTK21) and feeding to the Syngap1 autistic mice, the researchers could induce acetylation in the brain.

In the research, published recently in the journal Aging Cell, the CSP-TTK21 was found to restore neuronal function, learning, and memory, and induce neuronal rearrangements in Syngap1 mice, mainly when administered after the brain is considered to be developed (adolescents in human beings).

This report not only directly connects histone acetylation with autism, for the first time, but also opens a very optimistic door for ASD therapy, said the researchers.

The study provides a new potential therapeutic option by targeting epigenetic modifications in Syngap1-related intellectual disability /ASD that can restore the deficits to an extent that will enable the patient to lead a life less dependent on others.

Disclaimer: This post has been auto-published from an agency feed without any modifications to the text and has not been reviewed by an editor

Open in App

Related Stories

NationalPM Modi pledges to end Macaulay’s 200-year legacy of mental slavery in next decade

InternationalTrying to keep Awami League followers calm: Former Bangladesh minister

NationalTrying to keep Awami League followers calm: Former Bangladesh minister

NationalPM Modi urges governance over 'jungle raj' in Bihar, calls for emotional commitment beyond elections

CricketFrom Pietersen's blizzard to Stokes' early signs of greatness: Top individual performances by England in Australia in 21st century

Health Realted Stories

HealthNadda and Norwegian counterpart discuss healthcare partnership

HealthRajasthan: 65,490 animals treated via ‘unique’ initiative

HealthNurses are backbone of healthcare system: Govt officials

HealthEPFO ensuring that PF services reach every worker with speed, dignity: Dr Mansukh Mandaviya

HealthResearchers use AI to create first 100-billion-star Milky Way simulation