Evidence map›Paper›PMID 36404863›Full record

ArticleJournal of diabetes and metabolic disorders2022

Primaquine activates Keratin 7 to treat diabetes and its complications.

Tongyu Wu, Chun Li, Jing Zhou, Liang Han, Shaojia Qiang, Zhuozhou Hu, Jingjing Liu, Xiangxiang Li, Wenyang Zhao, Xinping Chen

Open access · greenAbstract read
In one paragraph

Article in Journal of diabetes and metabolic disorders, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
–field-weighted citation impact, top 88% 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

0 citing papers in PubMed, 0 citations in OpenAlex.

No citing paper in PubMed yet.

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.

Tongyu Wu *Department of Pharmacy, Lanzhou University, Lanzhou, 730000 People's Republic of China.
Chun Li *Department of Pharmacy, Lanzhou University, Lanzhou, 730000 People's Republic of China.
Jing Zhou *Department of Pharmacy, Lanzhou University, Lanzhou, 730000 People's Republic of China.
Liang HanDepartment of Pharmacy, Lanzhou University, Lanzhou, 730000 People's Republic of China.
Shaojia QiangDepartment of Pharmacy, Lanzhou University, Lanzhou, 730000 People's Republic of China.
Zhuozhou HuDepartment of Pharmacy, Lanzhou University, Lanzhou, 730000 People's Republic of China.
Jingjing LiuDepartment of Pharmacy, Lanzhou University, Lanzhou, 730000 People's Republic of China.
Xiangxiang LiDepartment of Pharmacy, Lanzhou University, Lanzhou, 730000 People's Republic of China.
Wenyang ZhaoDepartment of Pharmacy, Lanzhou University, Lanzhou, 730000 People's Republic of China.
Xinping ChenDepartment of Pharmacy, Lanzhou University, Lanzhou, 730000 People's Republic of China.ORCID 0000-0002-7490-9036
Lanzhou University · CNLanzhou Veterinary Research Institute · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background: The global prevalence of type 2 diabetes mellitus (T2DM) raises the rates of its complications, such as diabetic nephropathy and cardiovascular diseases. To conquer the complications, new strategies to reverse the deterioration of T2DM are urgently needed. In this project, we aimed to examine the hypoglycemic effect of primaquine and explore its specific target. Methods: In vitro T2DM insulin resistance model was built in HepG2 cells to screen the potential anti-diabetic chemicals. On the other hand, the potential protein targets were explored by molecular docking. Accordingly, we chose C57BL/6 N mice to establish T2DM model to verify the effect of the chemicals on anti-hyperglycemia and diabetic complications. Results: By targeting the Keratin 7 (K7) to activate EGFR/Akt glucose metabolism signaling pathway, primaquine poses a potent hypoglycemic effect. The level of acetyl-CoA is enhanced markedly, supporting that primaquine upregulates the aerobic glycolysis. Moreover, primaquine ameliorates kidney function by reducing the secretion of urinary proteins and creatinine, especially for the urea nitrogen which is significantly decreased compared to no-treatment T2DM mice. Notably, primaquine restores the level of plasma low-density lipoprotein cholesterol (LDL-C) nearly to normal, minimizing the incidence of cardiovascular diseases. Conclusions: We find that primaquine may reverse the dysregulated metabolism to prevent diabetic complications by stimulating EGFR/Akt signaling axis, shedding new light on the therapy of T2DM. Graphical abstract: Insulin resistance is characterized by reduced p-Akt and glucose metabolism, dominated by anaerobic glycolysis. Primaquine activates the complex made of K7 and EGFR, further stimulating Akt phosphorylation. Then, p-Akt promotes the aerobic glucose metabolism and upregulates Ac-CoA to mobilize TCA cycle, improving insulin sensitivity. Supplementary Information: The online version contains supplementary material available at 10.1007/s40200-022-01135-8.

Indexed as

Aerobic glycolysis, oncologicDiabetes mellitus, type 2Keratin 7Primaquine

Identifiers

PMID36404863
PMCPMC9672200
OpenAlexW4297989953

What Socratic 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 Socratic graph.