Evidence map›Paper›PMID 38584970›Full record

ArticleJournal of toxicologic pathology2024

Induction of lung lesions by bronchial administration using bronchoscope technique in mice.

Takako Hiyoshi, Chiyoko Nishime, Eiko Nishinaka, Fumiko Seki, Kenji Kawai, Misa Mochizuki, Koji Urano, Toshio Imai, Taichi Yamamoto, Masami Suzuki

Abstract read
In one paragraph

Article in Journal of toxicologic pathology, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
–field-weighted citation impact
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

1 citing paper in PubMed.

  1. 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

10 authors.

Takako HiyoshiTranslational Research Division, Central Institute for Experimental Medical and Life Science, 25-12-3 Tonomachi, Kawasaki-ku, Kawasaki, Kanagawa 210-0821, Japan.
Chiyoko NishimeTranslational Research Division, Central Institute for Experimental Medical and Life Science, 25-12-3 Tonomachi, Kawasaki-ku, Kawasaki, Kanagawa 210-0821, Japan.
Eiko NishinakaTranslational Research Division, Central Institute for Experimental Medical and Life Science, 25-12-3 Tonomachi, Kawasaki-ku, Kawasaki, Kanagawa 210-0821, Japan.
Fumiko SekiBioimaging Center, Central Institute for Experimental Medical and Life Science, 25-12-3 Tonomachi, Kawasaki-ku, Kawasaki, Kanagawa 210-0821, Japan.
Kenji KawaiTranslational Research Division, Central Institute for Experimental Medical and Life Science, 25-12-3 Tonomachi, Kawasaki-ku, Kawasaki, Kanagawa 210-0821, Japan.
Misa MochizukiTranslational Research Division, Central Institute for Experimental Medical and Life Science, 25-12-3 Tonomachi, Kawasaki-ku, Kawasaki, Kanagawa 210-0821, Japan.
Koji UranoTranslational Research Division, Central Institute for Experimental Medical and Life Science, 25-12-3 Tonomachi, Kawasaki-ku, Kawasaki, Kanagawa 210-0821, Japan.
Toshio ImaiTranslational Research Division, Central Institute for Experimental Medical and Life Science, 25-12-3 Tonomachi, Kawasaki-ku, Kawasaki, Kanagawa 210-0821, Japan.
Taichi YamamotoTranslational Research Division, Central Institute for Experimental Medical and Life Science, 25-12-3 Tonomachi, Kawasaki-ku, Kawasaki, Kanagawa 210-0821, Japan.
Masami SuzukiTranslational Research Division, Central Institute for Experimental Medical and Life Science, 25-12-3 Tonomachi, Kawasaki-ku, Kawasaki, Kanagawa 210-0821, Japan.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

This study aimed to establish an exposure method that can induce homogeneous lesions with minimal inter-individual variability. The distribution of lesions induced by bleomycin (BLM) administration was also analyzed. C57BL mice were intrabronchially administered 20 µL of BLM (3 mg/mL) using a bronchoscope in the left or right bronchus. The mice were sacrificed 14 days after administration, and their lungs were evaluated histopathologically. BLM-induced inflammatory lesions were widely observed in the lungs. In the left bronchus-treated group, lesions were uniformly observed throughout the lobe, and no individual differences were noted. Meanwhile, in the right bronchus-treated group, individual differences in the distribution of the pulmonary lesions were observed. The distribution of lesions differed among the four lobes of the right lung owing to their anatomical features. Administration into the left bronchus is recommended for highly homogeneous lung exposure and for establishing models that contribute to highly accurate toxicity and efficacy evaluations.

Indexed as

bleomycinbronchibronchoscopesinflammationmice

Identifiers

PMID38584970
PMCPMC10995434

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.