Porto Scientists Target Vitamin C Gateway to Delay Alzheimer’s

Portugal’s swiftly greying population has been anxiously awaiting a scientific breakthrough capable of slowing Alzheimer’s disease. A research team in Porto now offers fresh hope: by restoring vitamin C uptake inside the brain’s own immune sentinels, they believe the clock on cognitive decline can be wound back.
Why this matters for an ageing Portugal
With nearly 200,000 Portuguese already living with some form of dementia, the country shoulders one of Europe’s highest per-capita burdens. Longer life expectancy, however welcome, is stretching family carers and the National Health Service alike. The new findings from the i3S centre at the University of Porto suggest that fine-tuning a single nutrient pathway could postpone both the onset and progression of Alzheimer’s—a tantalising prospect for communities in the interior where specialist care is scarce. Researchers emphasise that the benefit lies not in swallowing more ascorbic acid, but in ensuring that the molecule crosses into microglia, those tiny yet powerful cells responsible for clearing toxic debris in the brain. Failure of this step appears to accelerate the neuroinflammation that fuels memory loss.
Inside the Porto lab: unlocking the SVCT2 gateway
Working with mouse models, the group led by João Relvas and first author Camila Portugal genetically dialled up a transporter called SVCT2—the protein that ferries vitamin C across the cell membrane. Enhanced expression restored normal microglial activity, delayed plaque formation and stalled cognitive deterioration in animals already showing Alzheimer-like symptoms. These pre-clinical results, published in the journal Redox Biology, position SVCT2 as a drug target with global implications. The team also observed that ageing brains typically show a sharp drop in intracellular ascorbate, even when blood levels remain adequate, underscoring that transport, not supply, is the bottleneck.
Beyond oranges: the limits of simple supplementation
Portugal’s culture of fresh fruit and winter-time citrus might suggest plentiful vitamin C, yet epidemiological snapshots reveal that older adults—especially those in residential homes—often fall below optimal intake. Even so, the Porto scientists warn that “more pills” is not a silver bullet. Oral or intravenous supplements flood the bloodstream, but unless SVCT2 is active, little reaches the brain’s immune cells. That insight aligns with earlier international studies linking poor transporter performance to elevated oxidative stress and faster amyloid-beta build-up. In short, diet alone may ease scurvy but it will not recalibrate the delicate redox balance inside neurons unless the molecular door is propped open.
From petri dish to pharmacy shelves
The immediate challenge is translating genetic tinkering into a therapy suitable for people. The i3S group is screening thousands of small-molecule compounds, hunting for candidates that boost SVCT2 activity without unwanted side-effects. If successful, a future tablet could complement existing drugs such as donepezil, offering dual protection—symptom relief plus slowed disease biology. Investors are watching closely; Portugal’s biomedical sector views the project as a potential flagship for innovation-led export. Yet researchers caution that human trials remain at least two years away, and any intervention will likely work best when started early, before extensive neuronal damage sets in.
What clinicians recommend today
Until those trials materialise, neurologists advise sticking with evidence-backed lifestyle measures: regular aerobic exercise, Mediterranean-style eating rich in natural antioxidants, and strict control of vascular risk factors such as hypertension and diabetes. For patients already diagnosed, physicians do not oppose moderate vitamin C supplementation, but they stress it should never replace prescribed medication. More importantly, families are urged to enrol loved ones in Portugal’s expanding network of memory clinics, where participation in upcoming SVCT2-focused studies could grant early access to the most promising advances. In the words of Renato Socodato, another member of the Porto team, “we’re not chasing a miracle fruit; we’re fine-tuning a molecular gateway that may keep the brain’s own defenders on duty longer.”

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