Key result
A two-week intervention with Magnolia officinalis L. bark extract-fortified chewing gum attenuated ex vivo LPS-stimulated TNF-alpha release by 73.4% compared to regular control gum.
Why the study?
Does Magnolia officinalis L. bark extract (MBE)-fortified chewing gum reduce LPS-induced inflammation in oral epithelial cells of healthy volunteers?
RCT (n=40)
Does Magnolia officinalis L. bark extract (MBE)-fortified chewing gum reduce LPS-induced inflammation in oral epithelial cells of healthy volunteers?
MBE-fortified chewing gum attenuates ex vivo LPS-induced pro-inflammatory cytokine release in oral epithelial cells, suggesting in vivo anti-inflammatory activity.
Supports short-term anti-inflammatory effects of MBE gum; extends RCT evidence for botanical modulation of oral epithelial responses.
Inflammatory diseases of the periodontal tissues are known health problems worldwide. Therefore, anti-inflammatory active compounds are used in oral care products to reduce long-term inflammation. In addition to inducing inflammation, pathogen attack leads to an increased production of reactive oxygen species (ROS), which may lead to oxidative damage of macromolecules. Magnolia officinalis L. bark extract (MBE) has been shown to possess antioxidant and anti-inflammatory potential in vitro. In the present study, the influence of MBE-fortified chewing gum on the resistance against lipopolysaccharide (LPS)-induced inflammation and oxidative stress of oral epithelial cells was investigated in a four-armed parallel designed human intervention trial with 40 healthy volunteers. Ex vivo stimulation of oral epithelial cells with LPS from Porphyromonas gingivalis for 6[Formula: see text]h increased the mRNA expression and release of the pro-inflammatory cytokines IL-1[Formula: see text], IL-[Formula: see text], IL-8, MIP-1[Formula: see text], and TNF[Formula: see text]. Chewing MBE-fortified gum for 10[Formula: see text]min reduced the ex vivo LPS-induced increase of IL-8 release by 43.8 [Formula: see text] 17.1% at the beginning of the intervention. In addition, after the two-week intervention with MBE-fortified chewing gum, LPS-stimulated TNF[Formula: see text] release was attenuated by 73.4 [Formula: see text] 12.0% compared to chewing regular control gum. This increased resistance against LPS-induced inflammation suggests that MBE possesses anti-inflammatory activity in vivo when added to chewing gum. In contrast, the conditions used to stimulate an immune response of oral epithelial cells failed to induce oxidative stress, measured by catalase activity, or oxidative DNA damage.
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Walker et al. (2016) conducted an RCT in Healthy volunteers (n=40). Magnolia officinalis L. bark extract (MBE)-fortified chewing gum vs. Regular control gum was evaluated on Ex vivo LPS-induced increase of pro-inflammatory cytokines (IL-8 and TNF-alpha release). A two-week intervention with Magnolia officinalis L. bark extract-fortified chewing gum attenuated ex vivo LPS-stimulated TNF-alpha release by 73.4% compared to regular control gum.
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