Evidence map›Paper›PMID 38671979›Full record

ArticleBrain sciences2024

Hippocampal Lactate-Infusion Enhances Spatial Memory Correlated with Monocarboxylate Transporter 2 and Lactylation.

Yuhan Wu, Hui Hu, Weiwei Liu, Yun Zhao, Fang Xie, Zhaowei Sun, Ling Zhang, Huafeng Dong, Xue Wang, Lingjia Qian

Open access · goldAbstract read
In one paragraph

Article in Brain sciences, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 15 papers.

0numbers the graph read from it
0cells of the map it votes in
15citing papers in PubMed
5.4field-weighted citation impact, top 4% 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

15 citing papers in PubMed, 20 citations in OpenAlex.

  1. Review
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  8. Lactate and cognition: a dual modulator.Frontiers in molecular neuroscience · 2026
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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

10 authors at 2 institutions in 1 country.

Yuhan WuBeijing Institute of Basic Medical Sciences, Academy of Military Medical Sciences, Beijing 100039, China.
Hui HuBeijing Institute of Basic Medical Sciences, Academy of Military Medical Sciences, Beijing 100039, China.
Weiwei LiuBeijing Institute of Basic Medical Sciences, Academy of Military Medical Sciences, Beijing 100039, China.
Yun ZhaoBeijing Institute of Basic Medical Sciences, Academy of Military Medical Sciences, Beijing 100039, China.
Fang XieBeijing Institute of Basic Medical Sciences, Academy of Military Medical Sciences, Beijing 100039, China.ORCID 0000-0002-6573-035X
Zhaowei SunBeijing Institute of Basic Medical Sciences, Academy of Military Medical Sciences, Beijing 100039, China.
Ling ZhangBeijing Institute of Basic Medical Sciences, Academy of Military Medical Sciences, Beijing 100039, China.
Huafeng DongBeijing Institute of Basic Medical Sciences, Academy of Military Medical Sciences, Beijing 100039, China.
Xue WangInstitute of Military Cognition and Brain Sciences, Beijing 100850, China.
Lingjia QianBeijing Institute of Basic Medical Sciences, Academy of Military Medical Sciences, Beijing 100039, China.
Academy of Military Medical Sciences · CNNorth China University of Science and Technology · CN

Funding

National Natural Science Foundation of China 82201685National Natural Science Foundation of China 82271553
6 · The paper itself

Abstract

Lactate has emerged as a key player in regulating neural functions and cognitive processes. Beyond its function as an energy substrate and signal molecule, recent research has revealed lactate to serve as an epigenetic regulator in the brain. However, the molecular mechanisms by which lactate regulates spatial memory and its role in the prevention of cognitive disorders remain unclear. Herein, we injected L-lactate (10 μmol/kg/d for 6 d) into the mouse's hippocampus, followed by the Morris water maze (MWM) test and molecular analyses. Improved spatial memory performances were observed in mice injected with lactate. Besides, lactate upregulated the expression of synaptic proteins post-synaptic density 95 (PSD95), synaptophysin (SYP), and growth associated protein 43 (GAP43) in hippocampal tissues and HT22 cells, suggesting a potential role in synaptic transmission and memory formation. The facilitative role of monocarboxylate transporter 2 (MCT2), a neuron-specific lactate transporter, in this process was confirmed, as MCT2 antagonists attenuated the lactate-induced upregulation of synaptic proteins. Moreover, lactate induced protein lactylation, a post-translational modification, which could be suppressed by MCT2 inhibition. RNA sequencing of lactated-injected hippocampal tissues revealed a comprehensive gene expression profile influenced by lactate, with significant changes in genes associated with transcriptional progress. These data demonstrate that hippocampal lactate injection enhances spatial memory in mice, potentially through the upregulation of synaptic proteins and induction of protein lactylation, with MCT2 playing a crucial role in these processes. Our findings shed light on the multi-faceted role of lactate in neural function and memory regulation, opening new avenues for therapeutic interventions targeting cognitive disorders.

Indexed as

HT22lactatelactylationMCT2spatial memory

Identifiers

PMID38671979
PMCPMC11048250
OpenAlexW4393253953

What OpenQuestion holds

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LicenceCC BY
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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.