Evidence map›Paper›PMID 37386058›Full record

ArticleMolecular psychiatry2023

SIRT1 in the BNST modulates chronic stress-induced anxiety of male mice via FKBP5 and corticotropin-releasing factor signaling.

Pu Hu, Yu Wang, Xiu-Hong Qi, Qing-Hong Shan, Zhao-Huan Huang, Peng Chen, Xiao Ma, Yu-Peng Yang, Dick F Swaab, Benjamin A Samuels and 2 more

Abstract read
PubMed Publisher
In one paragraph

Article in Molecular psychiatry, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers.

0numbers the graph read from it
0cells of the map it votes in
11citing papers in PubMed
3.7field-weighted citation impact, top 6% 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

11 citing papers in PubMed, 21 citations in OpenAlex.

  1. Article
  2. Review
  3. Article
  4. Article
  5. Neurobiology of stress · 2025
    Review
  6. Prefrontal corticotropin-releasing factor promotes resilience to social stress.Neuropsychopharmacology : official publication of the American College of Neuropsychopharmacology · 2025
    Article
  7. Review
  8. Article
  9. Review
  10. Review
  11. 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

12 authors at 4 institutions in 3 countries.

Pu Hu *Hefei National Research Center for Physical Sciences at the Microscale, Chinese Academy of Sciences Key Laboratory of Brain Function and Diseases, Division of Life Sciences and Medicine, University of Science and Technology of China, Hefei, 230027, PR China. phu@ustc.edu.cn.ORCID 0000-0003-2467-9049
Yu Wang *Institute of Brain Science, The First Affiliated Hospital of Anhui Medical University, Hefei, 230022, Anhui, China.
Xiu-Hong QiHefei National Research Center for Physical Sciences at the Microscale, Chinese Academy of Sciences Key Laboratory of Brain Function and Diseases, Division of Life Sciences and Medicine, University of Science and Technology of China, Hefei, 230027, PR China.
Qing-Hong ShanInstitute of Brain Science, The First Affiliated Hospital of Anhui Medical University, Hefei, 230022, Anhui, China.ORCID 0000-0002-3709-8094
Zhao-Huan HuangNational Engineering Laboratory for Brain-inspired Intelligence Technology and Application, School of Information Science and Technology, University of Science and Technology of China, Hefei, 230026, Anhui, China.
Peng ChenInstitute of Brain Science, The First Affiliated Hospital of Anhui Medical University, Hefei, 230022, Anhui, China.
Xiao MaHefei National Research Center for Physical Sciences at the Microscale, Chinese Academy of Sciences Key Laboratory of Brain Function and Diseases, Division of Life Sciences and Medicine, University of Science and Technology of China, Hefei, 230027, PR China.
Yu-Peng YangHefei National Research Center for Physical Sciences at the Microscale, Chinese Academy of Sciences Key Laboratory of Brain Function and Diseases, Division of Life Sciences and Medicine, University of Science and Technology of China, Hefei, 230027, PR China.
Dick F SwaabDepartment of Neuropsychiatric Disorders, Netherlands Institute for Neuroscience, An Institute of the Royal Netherlands Academy of Arts and Sciences, Meibergdreef 47, 1105 BA, Amsterdam, The Netherlands.
Benjamin A SamuelsDepartment of Psychology, Rutgers University, Piscataway, NJ, 08854, USA.ORCID 0000-0003-2535-0376
Zhi ZhangHefei National Research Center for Physical Sciences at the Microscale, Chinese Academy of Sciences Key Laboratory of Brain Function and Diseases, Division of Life Sciences and Medicine, University of Science and Technology of China, Hefei, 230027, PR China.ORCID 0000-0002-4205-3181
Jiang-Ning ZhouInstitute of Brain Science, The First Affiliated Hospital of Anhui Medical University, Hefei, 230022, Anhui, China. jnzhou@ustc.edu.cn.ORCID 0000-0003-1225-2873
University of Science and Technology of China · CNAnhui Medical University · CNNetherlands Institute for Neuroscience · NLRutgers, The State University of New Jersey · US

Funding

National Natural Science Foundation of China (National Science Foundation of China) 32000716National Natural Science Foundation of China (National Science Foundation of China) 32030046National Natural Science Foundation of China (National Science Foundation of China) 82201671National Natural Science Foundation of China (National Science Foundation of China) 82271554
6 · The paper itself

Abstract

Although clinical reports have highlighted association of the deacetylase sirtuin 1 (SIRT1) gene with anxiety, its exact role in the pathogenesis of anxiety disorders remains unclear. The present study was designed to explore whether and how SIRT1 in the mouse bed nucleus of the stria terminalis (BNST), a key limbic hub region, regulates anxiety. In a chronic stress model to induce anxiety in male mice, we used site- and cell-type-specific in vivo and in vitro manipulations, protein analysis, electrophysiological and behavioral analysis, in vivo MiniScope calcium imaging and mass spectroscopy, to characterize possible mechanism underlying a novel anxiolytic role for SIRT1 in the BNST. Specifically, decreased SIRT1 in parallel with increased corticotropin-releasing factor (CRF) expression was found in the BNST of anxiety model mice, whereas pharmacological activation or local overexpression of SIRT1 in the BNST reversed chronic stress-induced anxiety-like behaviors, downregulated CRF upregulation, and normalized CRF neuronal hyperactivity. Mechanistically, SIRT1 enhanced glucocorticoid receptor (GR)-mediated CRF transcriptional repression through directly interacting with and deacetylating the GR co-chaperone FKBP5 to induce its dissociation from the GR, ultimately downregulating CRF. Together, this study unravels an important cellular and molecular mechanism highlighting an anxiolytic role for SIRT1 in the mouse BNST, which may open up new therapeutic avenues for treating stress-related anxiety disorders.

Indexed as

AnxietyCorticotropin-Releasing HormoneMice, Inbred C57BLSeptal NucleiSignal TransductionSirtuin 1Stress, PsychologicalTacrolimus Binding ProteinsAnimalsAnxiety DisordersDisease Models, AnimalMaleMiceNeuronsReceptors, GlucocorticoidTacrolimus Binding Protein 5Corticotropin-Releasing HormoneReceptors, GlucocorticoidSirt1 protein, mouseSirtuin 1Tacrolimus Binding Protein 5Tacrolimus Binding Proteins

Identifiers

PMID37386058
OpenAlexW4382560253

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.