A review on the relationship between Arachidonic acid 15-Lipoxygenase (ALOX15) and diabetes mellitus.

Arachidonic acid 15-Lipoxygenase Diabetes mellitus Diabetic kidney disease Ferroptosis Inflammatory response Oxidative stress

Journal

PeerJ
ISSN: 2167-8359
Titre abrégé: PeerJ
Pays: United States
ID NLM: 101603425

Informations de publication

Date de publication:
2023
Historique:
received: 13 03 2023
accepted: 14 09 2023
medline: 23 10 2023
pubmed: 18 10 2023
entrez: 18 10 2023
Statut: epublish

Résumé

Arachidonic acid 15-lipoxygenase (ALOX15), as one of the lipoxygenase family, is mainly responsible for catalyzing the oxidation of various fatty acids to produce a variety of lipid components, contributing to the pathophysiological processes of various immune and inflammatory diseases. Studies have shown that ALOX15 and its related products are widely distributed in human tissues and related to multiple diseases such as liver, cardiovascular, cerebrovascular diseases, diabetes mellitus and other diseases. Diabetes mellitus (DM), the disease studied in this article, is a metabolic disease characterized by a chronic increase in blood glucose levels, which is significantly related to inflammation, oxidative stress, ferroptosis and other mechanisms, and it has a high incidence in the population, accompanied by a variety of complications. Figuring out how ALOX15 is involved in DM is critical to understanding its role in diseases. Therefore, ALOX15 inhibitors or combination therapy containing inhibitors may deliver a novel research direction for the treatment of DM and its complications. This article aims to review the biological effect and the possible function of ALOX15 in the pathogenesis of DM.

Identifiants

pubmed: 37849828
doi: 10.7717/peerj.16239
pii: 16239
pmc: PMC10578307
doi:

Substances chimiques

Arachidonate 15-Lipoxygenase EC 1.13.11.33
Fatty Acids 0
ALOX15 protein, human EC 1.13.11.33

Types de publication

Review Journal Article Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

e16239

Informations de copyright

©2023 He et al.

Déclaration de conflit d'intérêts

The authors declare there are no competing interests.

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Auteurs

Kaiying He (K)

Lanzhou University, Lanzhou, Gansu, China.
Lanzhou University Second Hospital, Lanzhou University, LanZhou, Gansu, China.

Xiaochun Zhou (X)

Lanzhou University Second Hospital, Lanzhou University, LanZhou, Gansu, China.

Hongxuan Du (H)

Lanzhou University, Lanzhou, Gansu, China.
Lanzhou University Second Hospital, Lanzhou University, LanZhou, Gansu, China.

Jing Zhao (J)

Lanzhou University, Lanzhou, Gansu, China.
Lanzhou University Second Hospital, Lanzhou University, LanZhou, Gansu, China.

Rongrong Deng (R)

Lanzhou University, Lanzhou, Gansu, China.
Lanzhou University Second Hospital, Lanzhou University, LanZhou, Gansu, China.

Jianqin Wang (J)

Lanzhou University Second Hospital, Lanzhou University, LanZhou, Gansu, China.

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