Evidence map›Paper›PMID 33448325›Full record

ArticleInternational journal of molecular medicine2021

Inhibition of aerobic glycolysis alleviates sepsis‑induced acute kidney injury by promoting lactate/Sirtuin 3/AMPK‑regulated autophagy.

Chuyi Tan, Jia Gu, Tao Li, Huan Chen, Ke Liu, Meidong Liu, Huali Zhang, Xianzhong Xiao

Open access · hybridAbstract read
In one paragraph

Article in International journal of molecular medicine, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 99 papers.

0numbers the graph read from it
0cells of the map it votes in
99citing papers in PubMed
7.9field-weighted citation impact, top 2% 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

99 citing papers in PubMed, 146 citations in OpenAlex.

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  16. Lactate Metabolism and Protein Lactylation in Diabetic Kidney Disease: A Narrative Review.Diabetes, metabolic syndrome and obesity : targets and therapy · 2026
    Review
  17. Article
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  20. Article

39 more citing papers are in PubMed but not listed here.

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

8 authors at 1 institution in 1 country.

Chuyi TanDepartment of Pathophysiology, Xiangya School of Medicine, Central South University, Changsha, Hunan 410078, P.R. China.
Jia GuDepartment of Pathophysiology, Xiangya School of Medicine, Central South University, Changsha, Hunan 410078, P.R. China.
Tao LiDepartment of Pathophysiology, Xiangya School of Medicine, Central South University, Changsha, Hunan 410078, P.R. China.
Huan ChenDepartment of Pathophysiology, Xiangya School of Medicine, Central South University, Changsha, Hunan 410078, P.R. China.
Ke LiuDepartment of Pathophysiology, Xiangya School of Medicine, Central South University, Changsha, Hunan 410078, P.R. China.
Meidong LiuDepartment of Pathophysiology, Xiangya School of Medicine, Central South University, Changsha, Hunan 410078, P.R. China.
Huali ZhangDepartment of Pathophysiology, Xiangya School of Medicine, Central South University, Changsha, Hunan 410078, P.R. China.
Xianzhong XiaoDepartment of Pathophysiology, Xiangya School of Medicine, Central South University, Changsha, Hunan 410078, P.R. China.
Central South University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Metabolism reprogramming influences the severity of organ dysfunction, progression to fibrosis, and development of disease in acute kidney injury (AKI). Previously we showed that inhibition of aerobic glycolysis improved survival rates and protected septic mice from kidney injury. However, the underlying mechanisms remain unclear. In the present study, it was revealed that sepsis or lipopolysaccharide (LPS) enhanced aerobic glycolysis as evidenced by increased lactate production and upregulated mRNA expression of glycolysis‑related genes in kidney tissues and human renal tubular epithelial (HK‑2) cells. The aerobic glycolysis inhibitor 2‑deoxy‑D‑glucose (2‑DG) downregulated glycolysis, and improved kidney injury induced by sepsis. 2‑DG treatments increased the expression of sirtuin 3 (SIRT3) and phosphorylation‑AMP‑activated protein kinase (p‑AMPK), following promoted autophagy and attenuated apoptosis of tubular epithelial cells in septic mice and in LPS‑treated HK‑2 cells. However, the glycolysis metabolite lactate downregulated SIRT3 and p‑AMPK expression, inhibited autophagy and enhanced apoptosis in LPS‑treated HK‑2 cells. Furthermore, pharmacological blockade of autophagy with 3‑methyladenine (3‑MA) partially abolished the protective effect of 2‑DG in sepsis‑induced AKI. These findings indicated that inhibition of aerobic glycolysis protected against sepsis‑induced AKI by promoting autophagy via the lactate/SIRT3/AMPK pathway.

Indexed as

Acute Kidney InjuryAMP-Activated Protein KinasesAnimalsAutophagyDeoxyglucoseGlycolysisLactic AcidMaleMiceMice, Inbred BALB CSepsisSirtuin 3AMP-Activated Protein KinasesDeoxyglucoseLactic AcidSirt3 protein, mouseSirtuin 32‑deoxy‑D‑glucoseacute kidney injuryaerobic glycolysisautophagysepsis

Identifiers

PMID33448325
PMCPMC7849980
OpenAlexW3120238688

What OpenQuestion holds

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LicenceCC BY-NC-ND
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.