Evidence map›Paper›PMID 28181829›Full record

ArticleDrug delivery2017

Marked augmentation of PLGA nanoparticle-induced metabolically beneficial impact of γ-oryzanol on fuel dyshomeostasis in genetically obese-diabetic ob/ob mice.

Chisayo Kozuka, Chigusa Shimizu-Okabe, Chitoshi Takayama, Kaku Nakano, Hidetaka Morinaga, Ayano Kinjo, Kotaro Fukuda, Asuka Kamei, Akihito Yasuoka, Takashi Kondo and 3 more

Open access · goldAbstract read
In one paragraph

Article in Drug delivery, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 17 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
17citing papers in PubMed, 1 pooled it
3.2field-weighted citation impact, top 8% 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

17 citing papers in PubMed, 1 synthesis or guideline pooled it, 41 citations in OpenAlex.

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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

13 authors at 4 institutions in 2 countries.

Chisayo Kozukaa Division of Endocrinology , Diabetes and Metabolism, Hematology, Rheumatology (Second Department of Internal Medicine), Graduate School of Medicine and.
Chigusa Shimizu-Okabeb Department of Molecular Anatomy , Graduate School of Medicine, University of the Ryukyus , Okinawa , Japan.
Chitoshi Takayamab Department of Molecular Anatomy , Graduate School of Medicine, University of the Ryukyus , Okinawa , Japan.
Kaku Nakanoc Department of Cardiovascular Medicine and.
Hidetaka Morinagae SENTAN Pharma Inc. , Fukuoka , Japan.
Ayano Kinjoe SENTAN Pharma Inc. , Fukuoka , Japan.
Kotaro Fukudae SENTAN Pharma Inc. , Fukuoka , Japan.
Asuka Kameif Kanagawa Academy of Science and Technology , Kanagawa , Japan , and.
Akihito Yasuokaf Kanagawa Academy of Science and Technology , Kanagawa , Japan , and.
Takashi Kondof Kanagawa Academy of Science and Technology , Kanagawa , Japan , and.
Keiko Abef Kanagawa Academy of Science and Technology , Kanagawa , Japan , and.
Kensuke Egashirac Department of Cardiovascular Medicine and.
Hiroaki Masuzakia Division of Endocrinology , Diabetes and Metabolism, Hematology, Rheumatology (Second Department of Internal Medicine), Graduate School of Medicine and.
Kanagawa Academy of Science and Technology · JPDiabetes Australia · AUKyushu University · JPUniversity of the Ryukyus · JP

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Our previous works demonstrated that brown rice-specific bioactive substance, γ-oryzanol acts as a chaperone, attenuates exaggerated endoplasmic reticulum (ER) stress in brain hypothalamus and pancreatic islets, thereby ameliorating metabolic derangement in high fat diet (HFD)-induced obese diabetic mice. However, extremely low absorption efficiency from intestine of γ-oryzanol is a tough obstacle for the clinical application. Therefore, in this study, to overcome extremely low bioavailability of γ-oryzanol with super-high lipophilicity, we encapsulated γ-oryzanol in polymer poly (DL-lactide-co-glycolide) (PLGA) nanoparticles (Nano-Orz), and evaluated its metabolically beneficial impact in genetically obese-diabetic ob/ob mice, the best-known severest diabetic model in mice. To our surprise, Nano-Orz markedly ameliorated fuel metabolism with an unexpected magnitude (∼1000-fold lower dose) compared with regular γ-oryzanol. Furthermore, such a conspicuous impact was achievable by its administration once every 2 weeks. Besides the excellent impact on dysfunction of hypothalamus and pancreatic islets, Nano-Orz markedly decreased ER stress and inflammation in liver and adipose tissue. Collectively, nanotechnology-based developments of functional foods oriented toward γ-oryzanol shed light on the novel approach for the treatment of a variety of metabolic diseases in humans.

Indexed as

Drug CarriersNanoparticlesAdministration, OralAnimalsBehavior, AnimalBlood GlucoseDiabetes MellitusDisease Models, AnimalDose-Response Relationship, DrugDrug Administration ScheduleDrug CompoundingEndoplasmic Reticulum StressEnergy MetabolismFood PreferencesGastrointestinal MicrobiomeHypoglycemic AgentsBlood GlucoseDrug Carriersgamma-oryzanolHypoglycemic AgentsHypolipidemic AgentsLactic AcidLipidsPhenylpropionatesPolyglycolic AcidPolylactic Acid-Polyglycolic Acid Copolymerbrown ricenanotechnologyobesitypoly (DL-lactide-co-glycolide)therapeutic modalityType 2 diabetes mellitusγ-oryzanol

Identifiers

PMID28181829
PMCPMC8241037
OpenAlexW2586453239

What OpenQuestion holds

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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.