Neurobehavioral and molecular neuroplasticity differences in stress response circuitry for resilience and vulnerability for post-traumatic stress disorder
Implementing Organization
National Institute Of Pharmaceutical Education And Research (NIPER), Raebareli, Uttar Pradesh
Principal Investigator
Dr. Ashok Kumar Datusalia
National Institute Of Pharmaceutical Education And Research (NIPER), Raebareli, Uttar Pradesh
Project Overview
Stressful life events impact on brain and bodily function and represent a major risk factor for the development of neuropsychiatric disorders such as depression and PSTD. Neuroimaging studies have shown volumetric reduction/remodelling of neuronal architecture in limbic/cortical brain areas of patients and animal models of chronic stress, thus suggesting that stress-induced maladaptive changes have a primary role in the chain of events leading to development of psychopathology. Although genetic vulnerability may represent a moderating factor, it is not clear what mechanisms address the individual responses towards pro-adaptive or maladaptive course. Aim of this project is the identifications of key factors responsible for both functional synaptic changes and architectural changes induced by acute stress in mPFC-BLA-HPC pathways, to understand better the dynamics of the stress response and identify molecular changes that may trigger stress-related psychopathology. This project will investigate short/long-term cellular/molecular changes in the aftermath of acute stress, linked to functional and architectural changes in the brain, to understand better the dynamics of the stress response. This will help to identify epigenetic changes that may trigger stress-related psychopathology. In this proposed work, we first plan to identify key factors responsible for acute footshock-stress induced differential changes in stress response circuit linked with vulnerable and resilient behavior. We will use qPCR assessment of miRNAs and expression of their target genes at short- and long-term after stress in stress response circuits. Finally, rescue experiments in-vivo will be carried out using pharmacological agents (antidepressant ketamine) to validate the neurobehavioral and molecular differences in PTSD resilient and vulnerable rats. This will establish early understanding about individual differences in stress response as vulnerable and resilient. The long term goal of PI revolves around the possibility of conversion from stress vulnerable to stress resilient.
Source
Source
Science and Engineering Research Board (SERB), DST 2022-23
Science and Engineering Research Board (SERB), New Delhi
Quick Information
Area of Research
Life Sciences & Biotechnology
Start Date
2022
End Date
2024
Status
Completed
Contact
ashokdatusalia@gmail.com
Output
No. of Research Paper
00
Technologies (If Any)
00
No. of PhD Produced
00
Publications
00
No. of Patents
Filed :00
Grant :00
Disclaimer:
Information available on this portal is sourced from various organizations and is provided for informational purposes only. Users are advised to verify details from the respective official sources.
Please enter your details
Please provide your name and email to continue. Your details are saved in this browser for future use.
Latest Updates
Loading…
⚠️
You are leaving this website
You are about to be redirected to an external website that is not operated by
India Science, Technology & Innovation (ISTI) Portal.