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  Ceylon cinnamon and its major compound Cinnamaldehyde can limit overshooting inflammatory signaling and angiogenesis in vitro: implications for COVID-19 treatment

Lucas, K., Ackermann, M., Leifke, A. L., Li, W. W., Pöschl, U., & Fröhlich-Nowoisky, J. (2021). Ceylon cinnamon and its major compound Cinnamaldehyde can limit overshooting inflammatory signaling and angiogenesis in vitro: implications for COVID-19 treatment. doi:10.1101/2021.06.16.448642.

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アイテムのパーマリンク: https://hdl.handle.net/21.11116/0000-0008-B936-B 版のパーマリンク: https://hdl.handle.net/21.11116/0000-000D-823A-F
資料種別: Preprint

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 作成者:
Lucas, Kurt, 著者
Ackermann, Maximilian, 著者
Leifke, Anna Lena, 著者
Li, William W., 著者
Pöschl, Ulrich1, 著者           
Fröhlich-Nowoisky, Janine1, 著者           
所属:
1Multiphase Chemistry, Max Planck Institute for Chemistry, Max Planck Society, ou_1826290              

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 要旨: Overshooting immune reactions can occur during inflammatory responses that accompany severe infections, such as COVID-19. Cytokines, damage-associated molecular patterns (DAMPs), and reactive oxygen and nitrogen species can generate positive feedback loops of inflammation, leading to long-term complications such as vascular endothelialitis, thrombosis, endothelial dysfunction, neurological impairments, and chronic fatigue. Dexamethasone can limit inflammation by inhibiting the activation of pro-inflammatory transcription factors. High dose dexamethasone, however, has undesirable side effects. Here, we show that Ceylon cinnamon and its major compound cinnamaldehyde can mitigate inflammatory signaling in vitro. Cinnamaldehyde interferes with the dimerization of toll-like receptor 4 (TLR4), which can be activated by DAMPs like HSP60 and HMGB1. Our results suggest that supplementary treatment with Ceylon cinnamon may allow administration of lower doses of dexamethasone to avoid high dose steroid side effects. Moreover, preliminary results indicate that Ceylon cinnamon modulates angiogenesis, which is a reactive phenomenon in COVID-19.

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言語: eng - English
 日付: 2021-06-16
 出版の状態: オンラインで出版済み
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 識別子(DOI, ISBNなど): DOI: 10.1101/2021.06.16.448642
その他: bioRxiv 2021.06.16.448642v1
 学位: -

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