Evidence map›Paper›PMID 31201731›Full record

ArticleNeurotoxicity research2019

Influence of Tacrolimus on Depressive-Like Behavior in Diabetic Rats Through Brain-Derived Neurotrophic Factor Regulation in the Hippocampus.

Yoo Jin Shin, Yeon Tae Chun, Sun Woo Lim, Kang Luo, Yi Quan, Sheng Cui, Eun Jeong Ko, Byung Ha Chung, Jiyeong Lee, Seongno Hong and 3 more

Abstract read
PubMed Publisher
In one paragraph

Article in Neurotoxicity research, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers.

0numbers the graph read from it
0cells of the map it votes in
13citing papers in PubMed
0.5field-weighted citation impact, top 40% 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

13 citing papers in PubMed, 14 citations in OpenAlex.

  1. Article
  2. Tacrolimus and diabetic rodent models.Pharmacological reports : PR · 2025
    Review
  3. Article
  4. Review
  5. Article
  6. Review
  7. Article
  8. Histopathological efficacy of tacrolimus in an experimental head trauma study.Ulusal travma ve acil cerrahi dergisi = Turkish journal of trauma & emergency surgery : TJTES · 2023
    Article
  9. Article
  10. Article
  11. Article
  12. Article
  13. Article
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

13 authors at 5 institutions in 3 countries.

Yoo Jin ShinConvergent Research Consortium for Immunologic Disease, Seoul St. Mary's Hospital, The Catholic University of Korea, School of Medicine, 222 Banpo-daero, Seocho-gu, Seoul, 06501, Republic of Korea.
Yeon Tae ChunDepartment of Biomedical Laboratory Science, College of Health Sciences, Eulji University, Seongnam, 13135, Republic of Korea.
Sun Woo LimConvergent Research Consortium for Immunologic Disease, Seoul St. Mary's Hospital, The Catholic University of Korea, School of Medicine, 222 Banpo-daero, Seocho-gu, Seoul, 06501, Republic of Korea.
Kang LuoConvergent Research Consortium for Immunologic Disease, Seoul St. Mary's Hospital, The Catholic University of Korea, School of Medicine, 222 Banpo-daero, Seocho-gu, Seoul, 06501, Republic of Korea.
Yi QuanConvergent Research Consortium for Immunologic Disease, Seoul St. Mary's Hospital, The Catholic University of Korea, School of Medicine, 222 Banpo-daero, Seocho-gu, Seoul, 06501, Republic of Korea.
Sheng CuiConvergent Research Consortium for Immunologic Disease, Seoul St. Mary's Hospital, The Catholic University of Korea, School of Medicine, 222 Banpo-daero, Seocho-gu, Seoul, 06501, Republic of Korea.
Eun Jeong KoConvergent Research Consortium for Immunologic Disease, Seoul St. Mary's Hospital, The Catholic University of Korea, School of Medicine, 222 Banpo-daero, Seocho-gu, Seoul, 06501, Republic of Korea.
Byung Ha ChungConvergent Research Consortium for Immunologic Disease, Seoul St. Mary's Hospital, The Catholic University of Korea, School of Medicine, 222 Banpo-daero, Seocho-gu, Seoul, 06501, Republic of Korea.
Jiyeong LeeDepartment of Biomedical Laboratory Science, College of Health Sciences, Eulji University, Seongnam, 13135, Republic of Korea.
Seongno HongDepartment of Clinical Laboratory Science, Dongnam Health University, 50 Cheonchon-ro 74-Gil, Jangan-gu, Suwon-si, Gyeonggi-do, 16328, Republic of Korea.
Mun Yong LeeDepartment of Anatomy, Catholic Neuroscience Institute, Cell Death Disease Research Center, The Catholic University of Korea, School of Medicine, 222 Banpo-daero, Seocho-gu, Seoul, 06501, Republic of Korea.
Hee Gyoo KangDepartment of Biomedical Laboratory Science, College of Health Sciences, Eulji University, Seongnam, 13135, Republic of Korea. kanghg@eulji.ac.kr.
Chul Woo YangConvergent Research Consortium for Immunologic Disease, Seoul St. Mary's Hospital, The Catholic University of Korea, School of Medicine, 222 Banpo-daero, Seocho-gu, Seoul, 06501, Republic of Korea. yangch@catholic.ac.kr.ORCID http://orcid.org/0000-0001-9796-636X
The Catholic University of Korea Seoul St. Mary's Hospital · KREulji University · KRSt. Mary's Hospital · USCatholic University of Korea · KRDongnam Health University · KR

Funding

Ministry of Education NRF-2018R1D1A1B07044219Ministry of Health and Welfare HI14C3417
6 · The paper itself

Abstract

The neurotoxicity of immunosuppressive agents and diabetes mellitus are known risk factors of neurological complications in kidney transplant recipients. The aim of the present study was to investigate the influence of tacrolimus on brain-derived neurotrophic factor (BDNF), the critical protein for maintenance of neuronal functions, in the hippocampus in a diabetic condition. A diabetic rat model was established by a single streptozotocin injection (60 mg/kg). Control and diabetic rats then received daily tacrolimus (1.5 mg/kg per day) injections for 6 weeks. BDNF expression in the hippocampus was examined in the dentate gyrus (DG) and CA3 region using immunohistochemistry. There was a significant decrease of BDNF expression in the DG and CA3 region in tacrolimus-treated and diabetic rats compared with that of the control group injected with vehicle only. However, there was no difference in BDNF expression between the two experimental groups. Tacrolimus treatment in diabetic rats further decreased the BDNF expression level in the DG and CA3 region. Interestingly, mossy fiber sprouting, demonstrated by prominent punctate immunolabeling of BDNF with synaptoporin, was observed in the diabetic group treated with tacrolimus, which localized at the stratum oriens of the CA3 region. These data suggest that tacrolimus treatment or a diabetic condition decreases BDNF expression in the hippocampus, and that tacrolimus treatment in the diabetic condition further injures the CA3 region of the hippocampus. In addition to BDNF expression, decreased locomotor activity and evident depressive behavior were observed in tacrolimus-treated diabetic rats. Moreover, there were significant decreases of the mRNA levels of γ-aminobutyric acid and serotonin receptors in the diabetic hippocampus with tacrolimus treatment. This finding suggests that tacrolimus treatment may cause further psychiatric and neurological complications for patients with diabetes, and should thus be used with caution.

Indexed as

AnimalsBrain-Derived Neurotrophic FactorDepressionDiabetes Mellitus, ExperimentalHippocampusImmunosuppressive AgentsMaleRatsRats, Sprague-DawleyTacrolimusBdnf protein, ratBrain-Derived Neurotrophic FactorImmunosuppressive AgentsTacrolimusBrain-derived neurotrophic factorDiabetesHippocampal dysfunctionInterneuronMossy fiberTacrolimus

Identifiers

PMID31201731
OpenAlexW2949237641

What OpenQuestion 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 OpenQuestion graph.