Evidence map›Paper›PMID 41917401›Full record

ReviewAdvances in experimental medicine and biology2026

Sialidase Activity Imaging of Different Organs with BTP3-Neu5Ac.

Shota Hata, Azliza Mad Anuar, Yuuki Kurebayashi, Tadanobu Takahashi, Hideyuki Takeuchi, Tadamune Otsubo, Akira Minami

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In one paragraph

Review in Advances in experimental medicine and biology, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing 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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

7 authors.

Shota HataDepartment of Biochemistry, School of Pharmaceutical Sciences, University of Shizuoka, Shizuoka, Japan.
Azliza Mad AnuarDepartment of Biochemistry, School of Pharmaceutical Sciences, University of Shizuoka, Shizuoka, Japan.
Yuuki KurebayashiDepartment of Biochemistry, School of Pharmaceutical Sciences, University of Shizuoka, Shizuoka, Japan.
Tadanobu TakahashiDepartment of Biochemistry, School of Pharmaceutical Sciences, University of Shizuoka, Shizuoka, Japan.
Hideyuki TakeuchiDepartment of Biochemistry, School of Pharmaceutical Sciences, University of Shizuoka, Shizuoka, Japan.
Tadamune OtsuboDepartment of Organic Chemistry, School of Pharmaceutical Sciences, Hiroshima International University, Hiroshima, Japan. t-ootubo@ps.hirokoku-u.ac.jp.
Akira MinamiDepartment of Biochemistry, School of Pharmaceutical Sciences, University of Shizuoka, Shizuoka, Japan. a.minami.da@juntendo.ac.jp.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

This chapter offers an overview of the development of BTP3-Neu5Ac and the functions of sialidase, as revealed through its use. Imaging of sialidase activity in the brain with BTP3-Neu5Ac has demonstrated that high sialidase activity is primarily detected in the white matter. In the hippocampus, a region critical for memory, glutamatergic nerve terminals exhibit particularly high sialidase activity. Based on the sialidase activity atlas, it was found that sialidase plays a crucial role in cognitive function within the hippocampus. Real-time imaging of changes in brain sialidase activity using BTP3-Neu5Ac has shown that sialidase activity at nerve terminals can rapidly increase within seconds in response to neural activity. This rapid fluctuation in sialidase activity contributes to a negative feedback mechanism on excitatory neurotransmission by sialidase. Additionally, studies on the distribution of sialidase activity in the pancreas have shown that the sialidase inhibitor 2,3-dehydro-2-deoxy-N-acetylneuraminic acid (DANA) promotes insulin secretion. Importantly, DANA does not induce insulin secretion during hypoglycemia, suggesting its potential for diabetes treatment with a lower risk of hypoglycemic side effects. Moreover, research into the distribution of sialidase activity in the skin has revealed that the sialidase isozyme NEU2 promotes elastin production. Thus, information on the distribution of sialidase activity in tissues provides valuable insights into the function of sialidase and supports the development of sialidase-targeted drugs.

Indexed as

BrainMolecular ImagingNeuraminidaseAnimalsHumansPancreasNeuraminidaseBrainEnzyme activityImagingOrganic chemistryPancreasSialidaseSkin

Identifiers

What Socratic holds

Textmetadata
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 Socratic graph.