Rhizolutin, a Novel 7/10/6‐Tricyclic Dilactone, Dissociates Misfolded Protein Aggregates and Reduces Apoptosis/Inflammation Associated with Alzheimer's Disease
Rhizolutin (1) was discovered as a natural product of ginseng‐rhizospheric Streptomyces sp. WON17. Its structure features an unprecedented 7/10/6‐tricyclic dilactone carbon skeleton composed of dimethylcyclodecatriene flanked by a 7‐membered and a 6‐membered lactone ring based on spectroscopic analy...
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Published in | Angewandte Chemie International Edition Vol. 59; no. 51; pp. 22994 - 22998 |
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Main Authors | , , , , , , , , , , , , , , , |
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Abstract | Rhizolutin (1) was discovered as a natural product of ginseng‐rhizospheric Streptomyces sp. WON17. Its structure features an unprecedented 7/10/6‐tricyclic dilactone carbon skeleton composed of dimethylcyclodecatriene flanked by a 7‐membered and a 6‐membered lactone ring based on spectroscopic analysis. During an unbiased screening of natural product libraries, this novel compound was found to dissociate amyloid‐β (Aβ) plaques and tau tangles, which are key pathological hallmarks of Alzheimer's disease (AD). Rhizolutin treatment of APP/PS1 double transgenic mice with AD significantly dissociated hippocampal plaques. In vitro, rhizolutin substantially decreased Aβ‐induced apoptosis and inflammation in neuronal and glial cells. Our findings introduce a unique chemical entity that targets Aβ and tau concurrently by mimicking misfolded protein clearance mechanisms of immunotherapy, which is prominently investigated in clinical trials.
Rhizolutin was discovered from a ginseng‐rhizospheric Streptomyces strain and structurally characterized as an unprecedented 7/10/6‐tricyclic dilactone based on spectroscopic analysis and chemical derivatizations. Rhizolutin was found to dissociate Aβ and tau aggregates and reduced Alzheimer's disease (AD)‐like pathology in APP/PS1 transgenic mice. |
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AbstractList | Rhizolutin (1) was discovered as a natural product of ginseng-rhizosphericStreptomycessp. WON17. Its structure features an unprecedented 7/10/6-tricyclic dilactone carbon skeleton composed of dimethylcyclodecatriene flanked by a 7-membered and a 6-membered lactone ring based on spectroscopic analysis. During an unbiased screening of natural product libraries, this novel compound was found to dissociate amyloid-beta (A beta) plaques and tau tangles, which are key pathological hallmarks of Alzheimer's disease (AD). Rhizolutin treatment of APP/PS1 double transgenic mice with AD significantly dissociated hippocampal plaques. In vitro, rhizolutin substantially decreased A beta-induced apoptosis and inflammation in neuronal and glial cells. Our findings introduce a unique chemical entity that targets A beta and tau concurrently by mimicking misfolded protein clearance mechanisms of immunotherapy, which is prominently investigated in clinical trials. Rhizolutin (1) was discovered as a natural product of ginseng‐rhizospheric Streptomyces sp. WON17. Its structure features an unprecedented 7/10/6‐tricyclic dilactone carbon skeleton composed of dimethylcyclodecatriene flanked by a 7‐membered and a 6‐membered lactone ring based on spectroscopic analysis. During an unbiased screening of natural product libraries, this novel compound was found to dissociate amyloid‐β (Aβ) plaques and tau tangles, which are key pathological hallmarks of Alzheimer's disease (AD). Rhizolutin treatment of APP/PS1 double transgenic mice with AD significantly dissociated hippocampal plaques. In vitro, rhizolutin substantially decreased Aβ‐induced apoptosis and inflammation in neuronal and glial cells. Our findings introduce a unique chemical entity that targets Aβ and tau concurrently by mimicking misfolded protein clearance mechanisms of immunotherapy, which is prominently investigated in clinical trials. Rhizolutin was discovered from a ginseng‐rhizospheric Streptomyces strain and structurally characterized as an unprecedented 7/10/6‐tricyclic dilactone based on spectroscopic analysis and chemical derivatizations. Rhizolutin was found to dissociate Aβ and tau aggregates and reduced Alzheimer's disease (AD)‐like pathology in APP/PS1 transgenic mice. Rhizolutin (1) was discovered as a natural product of ginseng-rhizospheric Streptomyces sp. WON17. Its structure features an unprecedented 7/10/6-tricyclic dilactone carbon skeleton composed of dimethylcyclodecatriene flanked by a 7-membered and a 6-membered lactone ring based on spectroscopic analysis. During an unbiased screening of natural product libraries, this novel compound was found to dissociate amyloid-β (Aβ) plaques and tau tangles, which are key pathological hallmarks of Alzheimer's disease (AD). Rhizolutin treatment of APP/PS1 double transgenic mice with AD significantly dissociated hippocampal plaques. In vitro, rhizolutin substantially decreased Aβ-induced apoptosis and inflammation in neuronal and glial cells. Our findings introduce a unique chemical entity that targets Aβ and tau concurrently by mimicking misfolded protein clearance mechanisms of immunotherapy, which is prominently investigated in clinical trials. Abstract Rhizolutin ( 1 ) was discovered as a natural product of ginseng‐rhizospheric Streptomyces sp. WON17. Its structure features an unprecedented 7/10/6‐tricyclic dilactone carbon skeleton composed of dimethylcyclodecatriene flanked by a 7‐membered and a 6‐membered lactone ring based on spectroscopic analysis. During an unbiased screening of natural product libraries, this novel compound was found to dissociate amyloid‐β (Aβ) plaques and tau tangles, which are key pathological hallmarks of Alzheimer's disease (AD). Rhizolutin treatment of APP/PS1 double transgenic mice with AD significantly dissociated hippocampal plaques. In vitro, rhizolutin substantially decreased Aβ‐induced apoptosis and inflammation in neuronal and glial cells. Our findings introduce a unique chemical entity that targets Aβ and tau concurrently by mimicking misfolded protein clearance mechanisms of immunotherapy, which is prominently investigated in clinical trials. |
Author | Nam, Kwangho Shin, Jongheon An, Joon Soo Hong, Seong‐Heon Bae, Munhyung Kwon, Yun Shin, Jisu Kim, Byung‐Yong Moon, Kyuho Woo, Jiwan Kim, Kyeonghwan Kim, YoungSoo Yang, Seung‐Hoon Park, Keunwan Oh, Dong‐Chan Cho, Yakdol |
Author_xml | – sequence: 1 givenname: Yun surname: Kwon fullname: Kwon, Yun organization: Seoul National University – sequence: 2 givenname: Jisu surname: Shin fullname: Shin, Jisu organization: Yonsei University – sequence: 3 givenname: Kwangho surname: Nam fullname: Nam, Kwangho organization: University of Texas at Arlington – sequence: 4 givenname: Joon Soo surname: An fullname: An, Joon Soo organization: Seoul National University – sequence: 5 givenname: Seung‐Hoon surname: Yang fullname: Yang, Seung‐Hoon organization: Dongguk University – sequence: 6 givenname: Seong‐Heon surname: Hong fullname: Hong, Seong‐Heon organization: Seoul National University – sequence: 7 givenname: Munhyung surname: Bae fullname: Bae, Munhyung organization: Seoul National University – sequence: 8 givenname: Kyuho surname: Moon fullname: Moon, Kyuho organization: Seoul National University – sequence: 9 givenname: Yakdol surname: Cho fullname: Cho, Yakdol organization: Korea Institute of Science and Technology (KIST) – sequence: 10 givenname: Jiwan surname: Woo fullname: Woo, Jiwan organization: Korea Institute of Science and Technology (KIST) – sequence: 11 givenname: Keunwan surname: Park fullname: Park, Keunwan organization: Korea Institute of Science and Technology (KIST) – sequence: 12 givenname: Kyeonghwan surname: Kim fullname: Kim, Kyeonghwan organization: Yonsei University – sequence: 13 givenname: Jongheon surname: Shin fullname: Shin, Jongheon organization: Seoul National University – sequence: 14 givenname: Byung‐Yong surname: Kim fullname: Kim, Byung‐Yong organization: ChunLab, Inc – sequence: 15 givenname: YoungSoo orcidid: 0000-0001-5029-7082 surname: Kim fullname: Kim, YoungSoo email: y.kim@yonsei.ac.kr organization: Yonsei University – sequence: 16 givenname: Dong‐Chan surname: Oh fullname: Oh, Dong‐Chan email: dongchanoh@snu.ac.kr organization: Seoul National University |
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Keywords | natural products lactones Alzheimer's disease tau protein THERMOCHEMISTRY amyloid beta amyloid β |
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Snippet | Rhizolutin (1) was discovered as a natural product of ginseng‐rhizospheric Streptomyces sp. WON17. Its structure features an unprecedented 7/10/6‐tricyclic... Rhizolutin (1) was discovered as a natural product of ginseng-rhizosphericStreptomycessp. WON17. Its structure features an unprecedented 7/10/6-tricyclic... Rhizolutin (1) was discovered as a natural product of ginseng-rhizospheric Streptomyces sp. WON17. Its structure features an unprecedented 7/10/6-tricyclic... Abstract Rhizolutin ( 1 ) was discovered as a natural product of ginseng‐rhizospheric Streptomyces sp. WON17. Its structure features an unprecedented... |
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SubjectTerms | Alzheimer Disease - drug therapy Alzheimer Disease - pathology Alzheimer's disease Amyloid Amyloid beta-Peptides - antagonists & inhibitors Amyloid beta-Peptides - metabolism amyloid β Animals Apoptosis Apoptosis - drug effects Chemistry Chemistry, Multidisciplinary Clinical trials Ginseng Glial cells Hippocampus Immunotherapy Inflammation - drug therapy Inflammation - pathology lactones Medical treatment Mice Mice, Transgenic Mimicry Natural products Neurodegenerative diseases Neuroglia - drug effects Neuronal-glial interactions Neurons - drug effects Neuroprotective Agents - chemistry Neuroprotective Agents - isolation & purification Neuroprotective Agents - pharmacology Physical Sciences Plaque, Amyloid - drug therapy Plaque, Amyloid - pathology Presenilin 1 Protein Aggregates - drug effects Protein folding Proteins Science & Technology Senile plaques Streptomyces - chemistry Tau protein tau Proteins - antagonists & inhibitors tau Proteins - metabolism Transgenic mice |
Title | Rhizolutin, a Novel 7/10/6‐Tricyclic Dilactone, Dissociates Misfolded Protein Aggregates and Reduces Apoptosis/Inflammation Associated with Alzheimer's Disease |
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