Outcome
    Moderate Evidence

    Pterostilbene for Antioxidant Protection

    Pterostilbene raises antioxidant capacity in preclinical work, with only indirect human confirmation.

    Overview

    Pterostilbene raises antioxidant capacity in preclinical work, with only indirect human confirmation.

    Verdict

    Mixed evidence

    How It Works

    It upregulates Nrf2-driven expression of glutathione peroxidase, catalase and superoxide dismutase, and directly scavenges reactive oxygen species.

    Dosing & Protocol

    Typical dose

    Recommended dose
    Studied at 50-250 mg/day; antioxidant marker changes in humans are inconsistent and clinically unproven
    Expected timeframe
    Not established

    Protocol

    form
    Pterostilbene, sometimes combined with grape extract
    duration
    6-8 weeks in the main human trial
    co factor
    Evidence is mixed. Pterostilbene is a potent antioxidant in vitro, scavenging free radicals, inducing Nrf2-mediated antioxidant enzyme expression including superoxide dismutase and glutathione peroxidase, and outperforming resveratrol in several assays owing to greater bioavailability and membrane permeability. Rodent studies show reduced markers of oxidative damage. Human data are thin: the Riche trials measured cardiovascular markers rather than oxidative stress endpoints directly, and no adequately powered trial has demonstrated meaningful reductions in oxidative damage markers such as F2-isoprostanes or 8-OHdG at the doses sold.
    titration
    Not applicable - no dose-response for antioxidant outcomes has been established in humans
    starting dose
    Not established for this outcome. Trials used 50-250 mg/day, typically 100 mg twice daily

    Evidence

    What the studies say

    Rodent studies consistently show reduced oxidative damage markers. Human trials report modest changes in oxidative stress biomarkers, but samples are small and outcomes surrogate.

    A review of pterostilbene antioxidant activity and disease modification

    Score: 5/10
    2013
    systematic_review
    0

    McCormack D, McFadden D

    Preclinical work shows antioxidant, anti-inflammatory and metabolic effects of pterostilbene, with greater bioavailability than resveratrol.

    View source

    Safety

    Caveats

    In vitro antioxidant potency has repeatedly failed to predict human benefit - large trials of beta-carotene, vitamin E and vitamin C found no benefit and in some cases harm, with beta-carotene increasing lung cancer risk in smokers. Reactive oxygen species also serve necessary signalling functions, including in exercise adaptation and immune defence, so suppression is not automatically good. Safety of pterostilbene: the key flag is that 250 mg/day raised LDL cholesterol in the Riche randomised trial, an effect attenuated by co-administered grape extract - relevant because people taking it for antioxidant purposes are usually pursuing cardiovascular health. Human safety data cover roughly 8 weeks only, so long-term safety is unknown and no upper intake level has been set; do not exceed the studied range. Pterostilbene inhibits cytochrome P450 enzymes in vitro and may have antiplatelet activity, so use caution with anticoagulants such as warfarin and direct oral anticoagulants, antiplatelet drugs, and medications with narrow therapeutic windows, and stop before surgery. Avoid in pregnancy and breastfeeding, as no safety data exist. For oxidative stress, a diet high in vegetables, fruit, legumes, nuts and whole grains has the evidence that isolated compounds lack.

    Less likely to help if

    Everyone - human antioxidant outcomes are unproven and higher doses raised LDL.

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