one of the principal curcuminoids in turmeric, exhibits a broad spectrum of therapeutic effects. It shows strong anti-inflammatory and antioxidant activities by inhibiting TNF‑α-induced NF‑κB signaling and promoting Nrf2-mediated expression of heme oxygenase-1 (HO‑1), which boosts cellular antioxidant capacity.
Bisdemethoxycurcumin (BDMC), one of the principal curcuminoids in turmeric, exhibits a broad spectrum of therapeutic effects. It shows strong anti-inflammatory and antioxidant activities by inhibiting TNF‑α-induced NF‑κB signaling and promoting Nrf2-mediated expression of heme oxygenase-1 (HO‑1), which boosts cellular antioxidant capacity. Compared to other curcuminoids, BDMC demonstrates higher radical-scavenging activity and is particularly effective in reducing oxidative stress.
BDMC also provides cardioprotective effects, notably by activating the PI3K/AKT-Nrf2/HO‑1 pathway in cardiomyocytes. This action helps protect heart cells from apoptosis and oxidative injury. Blocking these pathways reduces BDMC’s protective effects, highlighting its critical role in stress adaptation of heart tissue.
In the central nervous system, BDMC has been shown to offer neuroprotection in Alzheimer’s disease models by countering β‑amyloid-induced cytotoxicity. It reduces oxidative damage and modulates apoptosis-related proteins, ultimately improving neuronal survival and cognitive function in animal models.
BDMC also displays potent anticancer properties, where it inhibits cancer cell proliferation, induces apoptosis, suppresses metastasis, and disrupts key signaling pathways such as NF‑κB and MAPK. Its efficacy in halting tumor progression has been reported to surpass that of curcumin in certain cell lines.
In addition, BDMC offers chondroprotective effects, especially in osteoarthritis models. It suppresses inflammatory mediator production and inhibits cartilage degradation by activating Nrf2/HO‑1 signaling and modulating NLRP3 inflammasome activity. Moreover, BDMC has been found to permeate human skin effectively in ex vivo studies, suggesting its potential for topical applications targeting inflammatory joint conditions.
References
Yang K. et al., Journal of Agricultural and Food Chemistry, 2022 – Anti-inflammatory action via Nrf2/HO‑1 activation.
Li Y. et al., Oxidative Medicine and Cellular Longevity, 2021 – Cardioprotective effects in oxidative stress models.
Zhang L. et al., Molecular Neurobiology, 2023 – Neuroprotection in Alzheimer’s disease models.
Lin M. et al., Cancer Letters, 2022 – BDMC-induced apoptosis in cancer cell lines.
Huang J. et al., International Journal of Molecular Sciences, 2023 – Chondroprotection through Nrf2/NLRP3 pathway.
Wang H. et al., Pharmaceutical Research, 2021 – Skin permeation study of BDMC for topical use.
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Bisdemethoxycurcumin
one of the principal curcuminoids in turmeric, exhibits a broad spectrum of therapeutic effects. It shows strong anti-inflammatory and antioxidant activities by inhibiting TNF‑α-induced NF‑κB signaling and promoting Nrf2-mediated expression of heme oxygenase-1 (HO‑1), which boosts cellular antioxidant capacity.
Health Benefits of Bisdemethoxycurcumin (BDMC)
Bisdemethoxycurcumin (BDMC), one of the principal curcuminoids in turmeric, exhibits a broad spectrum of therapeutic effects. It shows strong anti-inflammatory and antioxidant activities by inhibiting TNF‑α-induced NF‑κB signaling and promoting Nrf2-mediated expression of heme oxygenase-1 (HO‑1), which boosts cellular antioxidant capacity. Compared to other curcuminoids, BDMC demonstrates higher radical-scavenging activity and is particularly effective in reducing oxidative stress.
BDMC also provides cardioprotective effects, notably by activating the PI3K/AKT-Nrf2/HO‑1 pathway in cardiomyocytes. This action helps protect heart cells from apoptosis and oxidative injury. Blocking these pathways reduces BDMC’s protective effects, highlighting its critical role in stress adaptation of heart tissue.
In the central nervous system, BDMC has been shown to offer neuroprotection in Alzheimer’s disease models by countering β‑amyloid-induced cytotoxicity. It reduces oxidative damage and modulates apoptosis-related proteins, ultimately improving neuronal survival and cognitive function in animal models.
BDMC also displays potent anticancer properties, where it inhibits cancer cell proliferation, induces apoptosis, suppresses metastasis, and disrupts key signaling pathways such as NF‑κB and MAPK. Its efficacy in halting tumor progression has been reported to surpass that of curcumin in certain cell lines.
In addition, BDMC offers chondroprotective effects, especially in osteoarthritis models. It suppresses inflammatory mediator production and inhibits cartilage degradation by activating Nrf2/HO‑1 signaling and modulating NLRP3 inflammasome activity. Moreover, BDMC has been found to permeate human skin effectively in ex vivo studies, suggesting its potential for topical applications targeting inflammatory joint conditions.
References
Yang K. et al., Journal of Agricultural and Food Chemistry, 2022 – Anti-inflammatory action via Nrf2/HO‑1 activation.
Li Y. et al., Oxidative Medicine and Cellular Longevity, 2021 – Cardioprotective effects in oxidative stress models.
Zhang L. et al., Molecular Neurobiology, 2023 – Neuroprotection in Alzheimer’s disease models.
Lin M. et al., Cancer Letters, 2022 – BDMC-induced apoptosis in cancer cell lines.
Huang J. et al., International Journal of Molecular Sciences, 2023 – Chondroprotection through Nrf2/NLRP3 pathway.
Wang H. et al., Pharmaceutical Research, 2021 – Skin permeation study of BDMC for topical use.
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