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

TechnologyDefence firms report strong H1 earnings on large export deals in S. Korea

Other SportsHaaland scores brace as Man City route Wolves

BusinessDefence firms report strong H1 earnings on large export deals in S. Korea

TechnologyS. Korean large firms' combined operating profit drops 1.7 pc in H1 2025

BusinessS. Korean large firms' combined operating profit drops 1.7 pc in H1 2025

Health Realted Stories

HealthIIT Kharagpur launches healthcare and technology school to train youth as health professionals

HealthNovel live type 1, 3 oral polio vaccines show promise in phase 1 trial

HealthStudy explains why loss of smell is associated with Alzheimer's disease

HealthHighly sensitive people more likely to experience depression, anxiety: Study

HealthGenes, binge drinking, stress behind surging heart-related deaths in young adults