Evidence map›Paper›PMID 35120261›Full record

ArticleFASEB journal : official publication of the Federation of American Societies for Experimental Biology2022

The clock modulator Nobiletin mitigates astrogliosis-associated neuroinflammation and disease hallmarks in an Alzheimer's disease model.

Marvin Wirianto, Chih-Yen Wang, Eunju Kim, Nobuya Koike, Ruben Gomez-Gutierrez, Kazunari Nohara, Gabriel Escobedo, Jong Min Choi, Chorong Han, Kazuhiro Yagita and 6 more

Open access · hybridAbstract read
In one paragraph

Article in FASEB journal : official publication of the Federation of American Societies for Experimental Biology, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 33 papers.

0numbers the graph read from it
0cells of the map it votes in
33citing papers in PubMed
8.4field-weighted citation impact, top 2% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

33 citing papers in PubMed, 42 citations in OpenAlex.

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  16. Natural Compounds for Preventing Age-Related Diseases and Cancers.International journal of molecular sciences · 2024
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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

16 authors at 4 institutions in 4 countries.

Marvin WiriantoDepartment of Biochemistry and Molecular Biology, The University of Texas Health Science Center at Houston (UTHealth), Houston, Texas, USA.
Chih-Yen WangDepartment of Pediatrics, Baylor College of Medicine, Neurological Research Institute, Texas Children's Hospital, Houston, Texas, USA.
Eunju KimDepartment of Biochemistry and Molecular Biology, The University of Texas Health Science Center at Houston (UTHealth), Houston, Texas, USA.
Nobuya KoikeDepartment of Physiology and Systems Bioscience, Graduate School of Medicine, Kyoto Prefectural University of Medicine, Kyoto, Japan.
Ruben Gomez-GutierrezDepartment of Neurology, The University of Texas Health Science Center (UTHealth), Houston, Texas, USA.ORCID https://orcid.org/0000-0001-9134-4375
Kazunari NoharaDepartment of Biochemistry and Molecular Biology, The University of Texas Health Science Center at Houston (UTHealth), Houston, Texas, USA.
Gabriel EscobedoDepartment of Neurology, The University of Texas Health Science Center (UTHealth), Houston, Texas, USA.
Jong Min ChoiDepartment of Biochemistry and Molecular Biology, Baylor College of Medicine, Houston, Texas, USA.
Chorong HanDepartment of Biochemistry and Molecular Biology, The University of Texas Health Science Center at Houston (UTHealth), Houston, Texas, USA.
Kazuhiro YagitaDepartment of Physiology and Systems Bioscience, Graduate School of Medicine, Kyoto Prefectural University of Medicine, Kyoto, Japan.ORCID https://orcid.org/0000-0002-1889-7050
Sung Yun JungDepartment of Biochemistry and Molecular Biology, Baylor College of Medicine, Houston, Texas, USA.
Claudio SotoDepartment of Neurology, The University of Texas Health Science Center (UTHealth), Houston, Texas, USA.
Hyun Kyoung LeeDepartment of Pediatrics, Baylor College of Medicine, Neurological Research Institute, Texas Children's Hospital, Houston, Texas, USA.
Rodrigo MoralesDepartment of Neurology, The University of Texas Health Science Center (UTHealth), Houston, Texas, USA.
Seung-Hee YooDepartment of Biochemistry and Molecular Biology, The University of Texas Health Science Center at Houston (UTHealth), Houston, Texas, USA.
Zheng ChenDepartment of Biochemistry and Molecular Biology, The University of Texas Health Science Center at Houston (UTHealth), Houston, Texas, USA.ORCID https://orcid.org/0000-0002-2464-5474
The University of Texas Health Science Center · USBaylor College of Medicine · USKyoto Prefectural University · JPUniversidad Bernardo O'Higgins · CL

Funding

Role of the circadian oscillator in AD neuropathological and behavioral alterationsRF1AG061901 · NIA · UNIVERSITY OF TEXAS HLTH SCI CTR HOUSTON · PI CHEN, ZHENG, SOTO, CLAUDIO · 2019 to 2019
$3.6M
Deciphering the mechanisms of glia development and white matter injuryR01NS110859 · NINDS · BAYLOR COLLEGE OF MEDICINE · PI Hyun Kyoung Lee · 2019 to 2026
$3.2M
Role of circulating Abeta seeds and peripheral tissue damage in Alzheimer's disease pathogenesisRF1AG059321 · NIA · UNIVERSITY OF TEXAS HLTH SCI CTR HOUSTON · PI MORALES, RODRIGO, SOTO, CLAUDIO · 2020 to 2020
$2.9M
Concerted Enhancement Of Core And Output Rhythms To Promote Healthy AgingR01AG065984 · NIA · UNIVERSITY OF TEXAS HLTH SCI CTR HOUSTON · PI CHEN, ZHENG · 2019 to 2023
$2.3M
Infection-driven mechanisms associated with Alzheimer's disease pathologyRF1AG072491 · NIA · UNIVERSITY OF TEXAS HLTH SCI CTR HOUSTON · PI BARICHELLO, TATIANA, MORALES, RODRIGO · 2021 to 2021
$2.0M
Regulation and function of the circadian factor Period2R01GM114424 · NIGMS · UNIVERSITY OF TEXAS HLTH SCI CTR HOUSTON · PI YOO, SEUNG-HEE · 2015 to 2019
$1.6M
Role of circulating Abeta seeds and peripheral tissue damage in Alzheimer's disease pathogenesisR01AG059321 · NIA · UNIVERSITY OF TEXAS HLTH SCI CTR HOUSTON · PI MORALES, RODRIGO, SOTO, CLAUDIO · 2024 to 2024
$718k
Role of RORs in age-related circadian and metabolic alterationsR56AG063746 · NIA · UNIVERSITY OF TEXAS HLTH SCI CTR HOUSTON · PI CHEN, ZHENG · 2019 to 2019
$510k
Functional crosstalk between brain circadian oscillators and AD pathology in mouse models.R03AG063286 · NIA · UNIVERSITY OF TEXAS HLTH SCI CTR HOUSTON · PI YOO, SEUNG-HEE · 2019 to 2020
$309k
NIA NIH HHS R01 AG059321NIA NIH HHS R01 AG065984NIA NIH HHS R03 AG063286NIA NIH HHS R56 AG063746NIA NIH HHS RF1 AG059321NIA NIH HHS RF1 AG061901NIA NIH HHS RF1 AG072491NIGMS NIH HHS R01 GM114424NINDS NIH HHS R01 NS110859
6 · The paper itself

Abstract

Alzheimer's disease (AD) is a devastating neurodegenerative disorder, and there is a pressing need to identify disease-modifying factors and devise interventional strategies. The circadian clock, our intrinsic biological timer, orchestrates various cellular and physiological processes including gene expression, sleep, and neuroinflammation; conversely, circadian dysfunctions are closely associated with and/or contribute to AD hallmarks. We previously reported that the natural compound Nobiletin (NOB) is a clock-enhancing modulator that promotes physiological health and healthy aging. In the current study, we treated the double transgenic AD model mice, APP/PS1, with NOB-containing diets. NOB significantly alleviated β-amyloid burden in both the hippocampus and the cortex, and exhibited a trend to improve cognitive function in these mice. While several systemic parameters for circadian wheel-running activity, sleep, and metabolism were unchanged, NOB treatment showed a marked effect on the expression of clock and clock-controlled AD gene expression in the cortex. In accordance, cortical proteomic profiling demonstrated circadian time-dependent restoration of the protein landscape in APP/PS1 mice treated with NOB. More importantly, we found a potent efficacy of NOB to inhibit proinflammatory cytokine gene expression and inflammasome formation in the cortex, and immunostaining further revealed a specific effect to diminish astrogliosis, but not microgliosis, by NOB in APP/PS1 mice. Together, these results underscore beneficial effects of a clock modulator to mitigate pathological and cognitive hallmarks of AD, and suggest a possible mechanism via suppressing astrogliosis-associated neuroinflammation.

Indexed as

Alzheimer DiseaseAmyloid beta-PeptidesAnimalsAnti-Inflammatory AgentsCerebral CortexCytokinesFlavonesGliosisHippocampusMiceNeuroprotective AgentsAmyloid beta-PeptidesAnti-Inflammatory AgentsCytokinesFlavonesNeuroprotective AgentsnobiletinAlzheimer's diseaseAβ pathologycircadian clockneuroinflammationNobiletin (NOB)ROR nuclear receptors

Identifiers

PMID35120261
PMCPMC8887996
OpenAlexW4210374823

What OpenQuestion holds

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LicenceCC BY
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.