Re-energizing mitochondria to treat Alzheimer’s disease

Alzheimer's nerve cells manifest a decrease in the connections between nerve cells, called synapses, shown here within the blue circles. Half the synapse is marked with a red fluorescent stain and the other half with a yellow stain.
Credit: Scripps Research

Scripps Research team restored neuron-to-neuron connections in human cells.

Nerve cells in the brain demand an enormous amount of energy to survive and maintain their connections for communicating with other nerve cells. In Alzheimer’s disease, the ability to make energy is compromised, and the connections between nerve cells (called synapses) eventually come apart and wither, causing new memories to fade and fail.

A Scripps Research team, reporting in the journal Advanced Science on January 18, 2024, has now identified the energetic reactions in brain cells that malfunction and lead to neurodegeneration. By using a small molecule to address the malfunction, which occurred in the mitochondria—the cell’s major energy producers—the researchers showed that many neuron-to-neuron connections were successfully restored in nerve cell models derived from human Alzheimer’s patient stem cells. These findings highlight that improving mitochondrial metabolism could be a promising therapeutic target for Alzheimer’s and related disorders.

“We thought that if we could repair metabolic activity in the mitochondria, maybe we could salvage the energy production,” says senior author Stuart Lipton, MD, PhD, Step Family Foundation Endowed Professor and Co-Director of the Neurodegeneration New Medicines Center at Scripps Research, and a clinical neurologist in La Jolla, Calif. “In using human neurons derived from people with Alzheimer’s, protecting the energy levels was sufficient to rescue a large number of neuronal connections.”

In the new study, Lipton and his team found a block in the enzymes that make energy due to an abnormal tag of nitrogen (N) and oxygen (O) atoms onto a sulfur (S) atom, all together forming a dysfunctional “SNO” enzyme. This reaction is termed S-nitrosylation, and the team demonstrated that a virtual “SNO-Storm” of these reactions occurred in the Alzheimer’s brain neurons.

Lipton and his colleagues initially made the discovery of the “SNO-tag” on energy enzymes by comparing human brains (obtained at autopsy from people with Alzheimer’s disease) to those with no brain disease. The researchers subsequently generated nerve cells from stem cells derived from skin biopsies of people with and without a genetic mutation that causes Alzheimer’s disease. Then, using a series of metabolic labels and an oxygen-measuring apparatus, they calculated cellular energy production and identified unique deficits in the Alzheimer’s nerve cells compared to controls.

The researchers found the neurons had a disrupted Krebs cycle—the cellular process in mitochondria that produces most of the body’s crucial molecular power source, ATP. The team pinpointed a bottleneck (or block) in the step where a key molecule is formed: succinate, which drives much of the subsequent production of ATP. In the study, the bottleneck inhibited the mitochondria’s ability to produce the energy needed to sustain neurons and their numerous connections.

The researchers hypothesized that if they could supply some of the missing succinate molecules, they might be able to restore energy production—essentially jumpstarting the stalled mitochondrial Krebs cycle. Since succinate does not easily travel in or out of cells, they used an analog that could better pass through nerve cell membranes. The strategy worked, repairing up to three quarters of the synapses that had been lost, while preventing further decline.

“Succinate is not a compound that people can now take as a treatment, but it’s proof-of-principle that you can re-energize the Krebs cycle,” says Lipton. “The beauty of the study is that we were able to show this in living nerve cells derived from Alzheimer’s patients, but we still have to come up with a much better compound in order to develop an effective drug for humans to take.”

Lipton has a history of developing FDA-approved drugs for Alzheimer’s disease, such as Namenda®, and acknowledges that much more work is needed here to produce an additional energy-preserving drug that is both safe and effective in humans. His lab will continue to pursue the mitochondrial Krebs cycle as a promising therapeutic target in the hopes they can restore neuronal connectivity in patients with Alzheimer’s, thereby stopping disease progression and enhancing cognitive function.

In addition to Lipton, authors of the study, “Metabolic Bypass Rescues Aberrant S-Nitrosylation-Induced TCA Cycle Inhibition and Synapse Loss in Alzheimer’s Disease Human Neurons,” include Alexander Andreyev, Nima Dolatabadi, Xu Zhang, Melissa Luevanos, Mayra Blanco, Christine Baal, Ivan Putra, and Tomohiro Nakamura of Scripps Research; Hongmei Yang and Steven Tannenbaum of MIT; and Paschalis-Thomas Doulias and Harry Ischiropoulos of the Perelman School of Medicine at the University of Pennsylvania.

This work was supported in part by funding from the National Institutes of Health (R01 AG061845, R61 NS122098, RF1 NS123298, R35 AG071734, RF1 AG057409, R56 AG065372, R01 DA048882, DP1 DA041722, and R01 AG056259).

About Scripps Research

Scripps Research is an independent, nonprofit biomedical institute ranked one of the most influential in the world for its impact on innovation by Nature Index. We are advancing human health through profound discoveries that address pressing medical concerns around the globe. Our drug discovery and development division, Calibr, works hand-in-hand with scientists across disciplines to bring new medicines to patients as quickly and efficiently as possible, while teams at Scripps Research Translational Institute harness genomics, digital medicine and cutting-edge informatics to understand individual health and render more effective healthcare. Scripps Research also trains the next generation of leading scientists at our Skaggs Graduate School, consistently named among the top 10 US programs for chemistry and biological sciences. Learn more at www.scripps.edu.

Journal: Advanced Science
DOI: 10.1002/advs.202306469

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