Evidence map›Paper›PMID 36555497›Full record

ArticleInternational journal of molecular sciences2022

A Dietary Oxysterol, 7-Ketocholesterol, Exacerbates Imiquimod-Induced Psoriasis-like Dermatitis in Steatohepatitic Mice.

Ayami Saga, Masahiro Koseki, Kotaro Kanno, Jiuyang Chang, Tomoaki Higo, Daisuke Okuzaki, Takeshi Okada, Hiroyasu Inui, Masumi Asaji, Katsunao Tanaka and 14 more

Open access · goldAbstract read
In one paragraph

Article in International journal of molecular sciences, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
0.5field-weighted citation impact, top 38% 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

2 citing papers in PubMed, 7 citations in OpenAlex.

  1. Article
  2. Review
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

24 authors at 5 institutions in 1 country.

Ayami SagaDepartment of Cardiovascular Medicine, Osaka University Graduate School of Medicine, Osaka 565-0871, Japan.
Masahiro KosekiDepartment of Cardiovascular Medicine, Osaka University Graduate School of Medicine, Osaka 565-0871, Japan.
Kotaro KannoDepartment of Cardiovascular Medicine, Osaka University Graduate School of Medicine, Osaka 565-0871, Japan.
Jiuyang ChangDepartment of Cardiovascular Medicine, Osaka University Graduate School of Medicine, Osaka 565-0871, Japan.ORCID 0000-0001-9644-0737
Tomoaki HigoDepartment of Cardiovascular Medicine, Osaka University Graduate School of Medicine, Osaka 565-0871, Japan.
Daisuke OkuzakiGenome Information Research Center, Research Institute for Microbial Diseases, Osaka University, Osaka 565-0871, Japan.ORCID 0000-0002-4552-783X
Takeshi OkadaDepartment of Cardiovascular Medicine, Osaka University Graduate School of Medicine, Osaka 565-0871, Japan.
Hiroyasu InuiDepartment of Cardiovascular Medicine, Osaka University Graduate School of Medicine, Osaka 565-0871, Japan.
Masumi AsajiDepartment of Cardiovascular Medicine, Osaka University Graduate School of Medicine, Osaka 565-0871, Japan.
Katsunao TanakaDepartment of Cardiovascular Medicine, Osaka University Graduate School of Medicine, Osaka 565-0871, Japan.
Takashi OmatsuDepartment of Cardiovascular Medicine, Osaka University Graduate School of Medicine, Osaka 565-0871, Japan.
Sae NishiharaDepartment of Cardiovascular Medicine, Osaka University Graduate School of Medicine, Osaka 565-0871, Japan.
Yinghong ZhuDepartment of Cardiovascular Medicine, Osaka University Graduate School of Medicine, Osaka 565-0871, Japan.ORCID 0000-0002-9987-073X
Kaori ItoDepartment of Advanced Medical Technology and Development, BML, Inc., Kawagoe TX 79608, Japan.
Hiroaki HattoriDepartment of Advanced Medical Technology and Development, BML, Inc., Kawagoe TX 79608, Japan.
Ikuyo IchiInstitute for Human Life Innovation, Ochanomizu University, Tokyo 112-8610, Japan.
Yoshihiro KamadaDepartment of Advanced Metabolic Hepatology, Osaka University Graduate School of Medicine, Osaka 565-0871, Japan.
Masafumi OnoDivision of Innovative Medicine for Hepatobiliary & Pancreatology, Faculty of Medicine, Kagawa University, Kagawa 760-0016, Japan.
Toshiji SaibaraDepartment of Gastroenterology and Hepatology, Kochi Medical School, Kochi 783-8505, Japan.
Tohru OhamaDepartment of Cardiovascular Medicine, Osaka University Graduate School of Medicine, Osaka 565-0871, Japan.
Shungo HikosoDepartment of Cardiovascular Medicine, Osaka University Graduate School of Medicine, Osaka 565-0871, Japan.ORCID 0000-0003-2284-1970
Makoto NishidaHealth Care Division, Health and Counseling Center, Osaka University, Osaka 565-0871, Japan.
Shizuya YamashitaRinku General Medical Center, Osaka 598-8577, Japan.
Yasushi SakataDepartment of Cardiovascular Medicine, Osaka University Graduate School of Medicine, Osaka 565-0871, Japan.
The University of Osaka · JPKagawa University · JPKochi Medical School Hospital · JPOchanomizu University · JPOsaka Health Science University · JP

Funding

Japan Society for the Promotion of Science (JSPS) KAKENHI grants 18H03532, 17H02100, 18K11020, 18K16026, 18H06222, 19K11766, 20K08383, 20K17149, and 21K20870the Japan Agency for Medic al Research and Development (AMED) JP19fk0210031
6 · The paper itself

Abstract

Patients with psoriasis are at a higher risk of developing nonalcoholic fatty liver disease. We previously identified an oxidized derivative of cholesterol, 7-ketocholesterol (7KC), in diet-induced steatohepatitic mice. Here, we investigated whether 7KC exacerbates psoriasis-like dermatitis by accelerating steatohepatitis in mice. A high-fat/high-cholesterol/high-sucrose/bile salt diet (nonalcoholic steatohepatitis (NASH) diet) with or without 0.0125% 7KC was fed to C57BL/6 mice (7KC or control group) for three weeks to induce steatohepatitis. A 5% imiquimod cream was then applied to the ears and dorsal skin for four days to induce psoriasis-like dermatitis. Hepatic lipid accumulation and inflammatory cell infiltration were exacerbated in the 7KC group compared with the control group after three weeks. Serum tumor necrosis factor-α (TNF-α) levels were also elevated in the 7KC group (108.5 ± 9.8 vs. 83.1 ± 13.1 pg/mL, p < 0.005). Imiquimod cream increased the psoriasis area severity index (PASI) score in mice in the 7KC group (9.14 ± 0.75 vs. 5.17 ± 1.17, p < 0.0001). Additionally, Tnfa, Il23a, Il17a, and Il22 mRNA levels in the dorsal lesion were significantly upregulated. Finally, Th17 cell differentiation and the TNF signaling pathway were enhanced in the dorsal lesions and liver of mice in the 7KC group. These data suggest that steatohepatitis and psoriasis are linked by a potent, diet-related factor.

Indexed as

DermatitisNon-alcoholic Fatty Liver DiseaseOxysterolsPsoriasisAnimalsDiet, High-FatDisease Models, AnimalImiquimodKetocholesterolsMiceMice, Inbred C57BL7-ketocholesterolImiquimodKetocholesterolsOxysterols7-ketocholesterolinterleukin-17psoriasissteatohepatitistumor necrosis factor-α

Identifiers

PMID36555497
PMCPMC9785382
OpenAlexW4311480368

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Registered trials

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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.