The multifaceted role of cytochrome P450-Derived arachidonic acid metabolites in diabetes and diabetic cardiomyopathy / Fadumo Ahmed Isse, Ahmed A. El-Sherbeni, Ayman O. S. El-Kadi

Abstract Understanding lipid metabolism is a critical key to understanding the pathogenesis of Diabetes Mellitus (DM). It is known that 60–90% of DM patients are obese or used to be obese. The incidence of obesity is rising owing to the modern sedentary lifestyle that leads to insulin resistance and increased levels of free fatty acids, predisposing tissues to utilize more lipids with less glucose uptake. However, the exact mechanism is not yet fully elucidated. Diabetic cardiomyopathy seems to be associated with these alterations in lipid metabolism. Arachidonic acid (AA) is an important fatty acid that is metabolized to several bioactive compounds by cyclooxygenases, lipoxygenases, and the more recently discovered, cytochrome P450 (P450) enzymes. P450 metabolizes AA to either epoxy-AA (EETs) or hydroxy-AA (HETEs). Studies showed that EETs could have cardioprotective effects and beneficial effects in reversing abnormalities in glucose and insulin homeostasis. Conversely, HETEs, most importantly 12-HETE and 20-HETE, were found to interfere with normal glucose and insulin homeostasis and thus, might be involved in diabetic cardiomyopathy. In this review, we highlight the role of P450-derived AA metabolites in the context of DM and diabetic cardiomyopathy and their potential use as a target for developing new treatments for DM and diabetic cardiomyopathy.

Medienart:

E-Artikel

Erscheinungsjahr:

2022

Erschienen:

2022

Enthalten in:

Zur Gesamtaufnahme - volume:54

Enthalten in:

Drug metabolism reviews - 54(2022), 2, Seite 141-160

Sprache:

Englisch

Beteiligte Personen:

Isse, Fadumo Ahmed [VerfasserIn]
El-Sherbeni, Ahmed A. [VerfasserIn]
El-Kadi, Ayman O. S. [VerfasserIn]

Links:

FID Access [lizenzpflichtig]

Themen:

Arachidonic acid
Cardiovascular diseases
Cytochrome P450
Diabetes
Diabetic cardiomyopathy

Umfang:

1 Online-Ressource (20 p)

doi:

10.1080/03602532.2022.2051045

funding:

Förderinstitution / Projekttitel:

PPN (Katalog-ID):

KFL011123354