4.7 Article

Extracts from Chinese herbs with anti-amyloid and neuroprotective activities

Journal

INTERNATIONAL JOURNAL OF BIOLOGICAL MACROMOLECULES
Volume 179, Issue -, Pages 475-484

Publisher

ELSEVIER
DOI: 10.1016/j.ijbiomac.2021.03.013

Keywords

Amyloid beta(42) peptide; Fibrils destruction; Chinese herbs; Neuroprotection

Funding

  1. Slovak Research and Development Agency [APVV-18-0284, APVV SK-CN-2017-0033]
  2. Slovak Grant Agency VEGA [02/0145/17, 02/0176/21, 02/0030/18]
  3. Operational Programme Integrated Infrastructure (OPII) - ERDF [ITMS2014+ 313011T553 DIAGNAD]
  4. China 111 Project [BP0719034]
  5. Exchange project of the 8th regular meeting of China Slovak intergovernmental cooperation, Chinese Ministry of Science and Technology ([2017]) [21]

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Chinese herbs such as Salvia miltiorrhiza and Anemarrhenae asphodeloides have been found to possess neuroprotective and anti-oxidant properties. Compounds like tanshinone IIA and salvianolic acid B were effective in dissociating A beta(42) peptide fibrils. Derivatives of sarsasapogenin also showed potential for treating Alzheimer's disease by interacting with specific regions of A beta(42) responsible for fibril stabilization. These findings suggest a promising avenue for developing novel treatment agents.
Many Chinese herbs are well known for their neuroprotective and anti-oxidant properties. Extracts of Salvia miltiorrhiza and Anemarrhenae asphodeloides, tanshinone IIA (tanIIA), salvianolic acid B (Sal B) and sarsasapogenin (ML-1), were selected to study their dissociation potential towards A beta(42) peptide fibrils and neuroprotective effect on cells. Moreover, derivatives of sarsasapogenin (ML-2, ML-3 and ML-4) have been prepared by the addition of modified carbamate moiety. TanIIA and Sal B have shown to possess a strong ability to dissociate A beta(42) fibrils. The dissociation potential of ML-1 increased upon the introduction of carbamate moiety with N-heterocycles. In silico data revealed that derivatives ML-4 and Sal B interact with A beta(42) regions responsible for fibril stabilization through hydrogen bonds. Contrary, tanIIA binds close to a central hydrophobic region, which may lead to destabilization of fibrils. Sarsasapogenin derivative ML-2 decreased nitride oxide production, and derivative ML-4 enhanced the growth of neurites. The reported data highlight the possibility of using active compounds to design novel treatment agents for Alzheimer's disease. (C) 2021 Elsevier B.V. All rights reserved.

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