NIH-funded research R21 grant

Investigating how mitochondrial dysfunction affects tau pathology in Alzheimer's disease

Official title: Mitochondrial dysfunction and tau pathology in Alzheimer's disease

Funded at University of Rochester · NIH-10805120 · Data updated 2026-11-12

This study is looking at how problems with tiny energy factories in our cells, called mitochondria, might be linked to the brain changes seen in Alzheimer's disease, and it uses special light technology to see how these issues affect brain health in both lab samples and live mice.

Quick facts

Grant typeR21 grant
Study typeNIH-funded research
Funding institutionUniversity of Rochester
NIH-funded
Lab location1 site (Rochester, United States)
Project startSeptember 16, 2023
Project endSeptember 15, 2025
Funding year2023
Award (this year)$423,500
NIH project number1R21AG085324-01
Project IDNIH-10805120 on NIH RePORTER

Who could benefit from this research

Could help

Ideal candidates for this research are adults aged 21 and older who are experiencing symptoms of Alzheimer's disease or are at risk for developing it.

Less likely to help

Patients with other forms of dementia unrelated to Alzheimer's disease may not benefit from this research.

What this research studies

This research explores the relationship between mitochondrial dysfunction and tau pathology in Alzheimer's disease (AD), which is a leading cause of dementia. Using innovative optogenetic technology, the study aims to manipulate mitochondrial function and reactive oxygen species (ROS) production in real-time to determine their roles in the progression of tau pathology. By employing light-activated tools, researchers will be able to control these processes in both brain slice cultures and live mouse models, providing insights into the underlying mechanisms of AD. This approach seeks to clarify the complex interactions between these factors and their impact on neuronal health.

Why it matters

Potential benefit: If successful, this research could lead to new therapeutic strategies that slow or halt the progression of Alzheimer's disease.

How similar studies have gone: While the specific optogenetic approach is novel, previous research has shown that targeting mitochondrial function can have beneficial effects in neurodegenerative diseases.

Where this research is happening

  • University of Rochester
    Rochester, United States
    Active

Researchers

  • Principal investigator: Wojtovich, Andrew Phillip — University of Rochester
  • Study coordinator: Wojtovich, Andrew Phillip

Related research

Other NIH-funded projects on the same topics.

About this research

  1. This is an active NIH-funded research project — typically early-stage science, not a clinical trial accepting patient enrollment.
  2. Some NIH-funded labs run parallel clinical studies or seek volunteers for related work. To check, contact the principal investigator or institution listed above.
  3. For full project details, budget, and progress reports, visit the official NIH RePORTER page.
Last reviewed 2026-11-14 by the Find a Trial editorial team. Information on this page is for educational purposes and is not medical advice. Always consult qualified healthcare professionals about clinical trial participation.