Evidence map›Paper›PMID 42510608›Full record

ArticleAntioxidants (Basel, Switzerland)2026

Kampo Medicines Modulate Angiogenic, Antioxidant, and Inflammatory Pathways in Human Preclinical Models: Implications for Preeclampsia.

Natalie K Binder, Kenji Onda, Sally Beard, Kei Uchiyama, Chika Ohi, Natasha de Alwis, Lydia Baird, Tu'uhevaha J Kaitu'u-Lino, Toshihiko Hirano, Haruki Yamada and 2 more

Abstract read
In one paragraph

Article in Antioxidants (Basel, Switzerland), 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

12 authors.

Natalie K BinderTherapeutic Discovery and Vascular Function in Pregnancy Group, University of Melbourne and Mercy Hospital for Women, Heidelberg 3084, Australia.ORCID 0000-0002-8943-2269
Kenji OndaDepartment of Clinical Pharmacology, Tokyo University of Pharmacy and Life Sciences, Tokyo 192-0392, Japan.
Sally BeardTherapeutic Discovery and Vascular Function in Pregnancy Group, University of Melbourne and Mercy Hospital for Women, Heidelberg 3084, Australia.ORCID 0000-0003-2322-0471
Kei UchiyamaDepartment of Clinical Pharmacology, Tokyo University of Pharmacy and Life Sciences, Tokyo 192-0392, Japan.
Chika OhiDepartment of Clinical Pharmacology, Tokyo University of Pharmacy and Life Sciences, Tokyo 192-0392, Japan.
Natasha de AlwisTherapeutic Discovery and Vascular Function in Pregnancy Group, University of Melbourne and Mercy Hospital for Women, Heidelberg 3084, Australia.ORCID 0000-0001-8376-0096
Lydia BairdTherapeutic Discovery and Vascular Function in Pregnancy Group, University of Melbourne and Mercy Hospital for Women, Heidelberg 3084, Australia.
Tu'uhevaha J Kaitu'u-LinoMercy Perinatal, Mercy Hospital for Women, Heidelberg 3084, Australia.
Toshihiko HiranoDepartment of Clinical Pharmacology, Tokyo University of Pharmacy and Life Sciences, Tokyo 192-0392, Japan.
Haruki YamadaDepartment of Kampo Medicine, Tokyo University of Pharmacy and Life Sciences, Tokyo 192-0392, Japan.
Toshihiro SakuraiDepartment of Pharmaceutical Sciences, Ohu University, Koriyama 963-8611, Japan.
Natalie J HannanTherapeutic Discovery and Vascular Function in Pregnancy Group, University of Melbourne and Mercy Hospital for Women, Heidelberg 3084, Australia.

Funding

National Health and Medical Research Council NJH #1146128; TJKL #1159261
6 · The paper itself

Abstract

Preeclampsia is a serious pregnancy complication characterised by maternal vascular dysfunction, placental dysfunction, and organ injury, with no effective treatment currently available. Kampo, a system of Japanese traditional medicine comprising standardised herbal formulations, could target pathophysiological pathways driving preeclampsia. We evaluated the effects of select Kampo formulations on markers of preeclampsia using primary human trophoblasts, placental explants, human umbilical vein endothelial cells (HUVECs), and uterine microvascular endothelial cells (UtMVECs). Twelve formulations were initially screened in HUVECs, and six formulations advanced for further study. TNFα was used to induce endothelial dysfunction, and angiogenic, antioxidant, inflammatory, and vascular dysfunction markers were assessed. Overall, Kampo formulations had minimal effect on sFlt-1 expression and only modest effects on sFlt-1 secretion by primary human trophoblast. In contrast, several formulations consistently increased placental growth factor (PlGF) expression and secretion, upregulated HMOX1 in trophoblasts, and enhanced PlGF secretion from placental explants. In endothelial cells, Kampo treatment partially reversed TNFα-induced dysfunction, demonstrated by reduced VCAM1 expression, and additional endothelial cell type-dependent effects on ET-1 and inflammatory pathways. These findings indicate that selected Kampo formulations modulate key pathways involved in the pathophysiology underpinning preeclampsia and warrant further investigation as potential therapeutic candidates.

Indexed as

angiogenesisendothelial dysfunctionherbal medicineoxidative stressplacenta

Identifiers

PMID42510608
PMCPMC13403422

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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.