Evidence map›Paper›PMID 32528023›Full record

ArticleScientific reports2020

Vagus nerve stimulation even after injury ameliorates cisplatin-induced nephropathy via reducing macrophage infiltration.

Rie Uni, Tsuyoshi Inoue, Yasuna Nakamura, Daichi Fukaya, Sho Hasegawa, Chia-Hsien Wu, Rie Fujii, Bongkod Surattichaiyakul, Wachirasek Peerapanyasut, Atsuko Ozeki and 4 more

Abstract read
In one paragraph

Article in Scientific reports, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 16 papers.

0numbers the graph read from it
0cells of the map it votes in
16citing 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

16 citing papers in PubMed.

  1. Article
  2. Article
  3. Neuroimmune interactions in cardiovascular homeostasis and disease.American journal of physiology. Cell physiology · 2026
    Review
  4. Article
  5. Cholinergic system in patients with chronic kidney disease: cognitive and renal implications.Nephrology, dialysis, transplantation : official publication of the European Dialysis and Transplant Association - European Renal Association · 2025
    Review
  6. Article
  7. Article
  8. Article
  9. Article
  10. Clinical perspectives on vagus nerve stimulation: present and future.Clinical science (London, England : 1979) · 2022
    Review
  11. Review
  12. Cholinergic immunomodulation in inflammatory bowel diseases.Brain, behavior, & immunity - health · 2022
    Review
  13. Neuroimmune system-mediated renal protection mechanisms.Clinical and experimental nephrology · 2021
    Review
  14. Article
  15. Septic acute kidney injury: a review of basic research.Clinical and experimental nephrology · 2020
    Review
  16. 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

14 authors.

Rie UniDivision of Nephrology and Endocrinology, The University of Tokyo Graduate, School of Medicine, Bunkyo-ku, Tokyo, 113-8655, Japan.
Tsuyoshi InoueDivision of CKD, Pathophysiology, The University of Tokyo Graduate School of Medicine, Bunkyo-ku, Tokyo, 113-8655, Japan. tsinoue-tky@umin.ac.jp.
Yasuna NakamuraDivision of Nephrology and Endocrinology, The University of Tokyo Graduate, School of Medicine, Bunkyo-ku, Tokyo, 113-8655, Japan.
Daichi FukayaDivision of CKD, Pathophysiology, The University of Tokyo Graduate School of Medicine, Bunkyo-ku, Tokyo, 113-8655, Japan.
Sho HasegawaDivision of Nephrology and Endocrinology, The University of Tokyo Graduate, School of Medicine, Bunkyo-ku, Tokyo, 113-8655, Japan.
Chia-Hsien WuDivision of Nephrology and Endocrinology, The University of Tokyo Graduate, School of Medicine, Bunkyo-ku, Tokyo, 113-8655, Japan.
Rie FujiiDivision of Nephrology and Endocrinology, The University of Tokyo Graduate, School of Medicine, Bunkyo-ku, Tokyo, 113-8655, Japan.
Bongkod SurattichaiyakulDivision of CKD, Pathophysiology, The University of Tokyo Graduate School of Medicine, Bunkyo-ku, Tokyo, 113-8655, Japan.
Wachirasek PeerapanyasutMahidol University, Nakhonsawan Campus, Nakhonsawan, 60130, Thailand.
Atsuko OzekiIsotope Science Center, The University of Tokyo, Bunkyo-ku, Tokyo, 113-0032, Japan.
Nobuyoshi AkimitsuIsotope Science Center, The University of Tokyo, Bunkyo-ku, Tokyo, 113-0032, Japan.
Youichiro WadaIsotope Science Center, The University of Tokyo, Bunkyo-ku, Tokyo, 113-0032, Japan.
Masaomi NangakuDivision of Nephrology and Endocrinology, The University of Tokyo Graduate, School of Medicine, Bunkyo-ku, Tokyo, 113-8655, Japan.
Reiko InagiDivision of CKD, Pathophysiology, The University of Tokyo Graduate School of Medicine, Bunkyo-ku, Tokyo, 113-8655, Japan.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The efficacy of prior activation of an anti-inflammatory pathway called the cholinergic anti-inflammatory pathway (CAP) through vagus nerve stimulation (VNS) has been reported in renal ischemia-reperfusion injury models. However, there have been no reports that have demonstrated the effectiveness of VNS after injury. We investigated the renoprotective effect of VNS in a cisplatin-induced nephropathy model. C57BL/6 mice were injected with cisplatin, and VNS was conducted 24 hours later. Kidney function, histology, and a kidney injury marker (Kim-1) were evaluated 72 hours after cisplatin administration. To further explore the role of the spleen and splenic macrophages, key players in the CAP, splenectomy, and adoptive transfer of macrophages treated with the selective α7 nicotinic acetylcholine receptor agonist GTS-21 were conducted. VNS treatment significantly suppressed cisplatin-induced kidney injury. This effect was abolished by splenectomy, while adoptive transfer of GTS-21-treated macrophages improved renal outcomes. VNS also reduced the expression of cytokines and chemokines, including CCL2, which is a potent chemokine attracting monocytes/macrophages, accompanied by a decline in the number of infiltrating macrophages. Taken together, stimulation of the CAP protected the kidney even after injury in a cisplatin-induced nephropathy model. Considering the feasibility and anti-inflammatory effects of VNS, the findings suggest that VNS may be a promising therapeutic tool for acute kidney injury.

Indexed as

Acute Kidney Injuryalpha7 Nicotinic Acetylcholine ReceptorAnimalsAnti-Inflammatory AgentsBenzylidene CompoundsCisplatinCytokinesInflammationKidneyMacrophagesMaleMiceMice, Inbred C57BLPyridinesReperfusion InjurySpleen3-(2,4-dimethoxybenzylidene)anabaseinealpha7 Nicotinic Acetylcholine ReceptorAnti-Inflammatory AgentsBenzylidene CompoundsCisplatinCytokinesPyridines

Identifiers

PMID32528023
PMCPMC7290038

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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.