Evidence map›Paper›PMID 38612681›Full record

ArticleInternational journal of molecular sciences2024

Integrated Transcriptomic and Proteomic Study of the Mechanism of Action of the Novel Small-Molecule Positive Allosteric Modulator 1 in Targeting PAC1-R for the Treatment of D-Gal-Induced Aging Mice.

Lili Liang, Shang Chen, Wanlin Su, Huahua Zhang, Rongjie Yu

Open access · goldAbstract read
In one paragraph

Article in International journal of molecular sciences, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
1.0field-weighted citation impact, top 26% 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

1 citing paper in PubMed, 3 citations in OpenAlex.

  1. 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

5 authors at 2 institutions in 1 country.

Lili LiangDepartment of Cell Biology, College of Life Science and Technology, Jinan University, Guangzhou 510632, China.ORCID 0000-0001-9296-8155
Shang ChenDepartment of Cell Biology, College of Life Science and Technology, Jinan University, Guangzhou 510632, China.
Wanlin SuDepartment of Cell Biology, College of Life Science and Technology, Jinan University, Guangzhou 510632, China.
Huahua ZhangDepartment of Medical Genetics, Guangdong Medical University, Dongguan 523808, China.
Rongjie YuDepartment of Cell Biology, College of Life Science and Technology, Jinan University, Guangzhou 510632, China.
Jinan University · CNGuangdong Medical College · CN

Funding

National Natural Science Foundation of China No. 31100545National Natural Science Foundation of China No. 31670848Natural Science Foundation of Guangdong Province 2022A1515011158Natural Science Foundation of Guangdong Province No. 2016A030313087
6 · The paper itself

Abstract

Small-molecule positive allosteric modulator 1 (SPAM1), which targets pituitary adenylate cyclase-activating polypeptide receptor 1 (PAC1-R), has been found to have a neuroprotective effect, and the underlying mechanism was explored in this study. First, using a D-galactose (D-gal)-induced aging mouse model, we confirmed that SPAM1 improves the structure of the hippocampal dentate gyrus and restores the number of neurons. Compared with D-gal model mice, SPAM1-treated mice showed up-regulated expression of Sirtuin 6 (SIRT6) and Lamin B1 and down-regulated expression of YinYang 1 (YY1) and p16. A similar tendency was observed in senescent RGC-5 cells induced by long-term culture, indicating that SPAM1 exhibits significant in vitro and in vivo anti-senescence activity in neurons. Then, using whole-transcriptome sequencing and proteomic analysis, we further explored the mechanism behind SPAM1's neuroprotective effects and found that SPAM is involved in the longevity-regulating pathway. Finally, the up-regulation of neurofilament light and medium polypeptides indicated by the proteomics results was further confirmed by Western blotting. These results help to lay a pharmacological network foundation for the use of SPAM1 as a potent anti-aging therapeutic drug to combat neurodegeneration with anti-senescence, neuroprotective, and nerve regeneration activity.

Indexed as

ProteomicsTranscriptomeAgingAnimalsGalactoseGene Expression ProfilingLongevityMiceGalactoseanti-agingneuroprotective effectspituitary adenylate cyclase-activating polypeptide (PACAP)pituitary adenylate cyclase-activating polypeptide receptor 1 (PAC1-R)proteomictranscriptomic

Identifiers

PMID38612681
PMCPMC11011505
OpenAlexW4393356389

What Socratic holds

Textmetadata
LicenceCC BY
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 Socratic graph.