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1.
Front Endocrinol (Lausanne) ; 15: 1336402, 2024.
Artículo en Inglés | MEDLINE | ID: mdl-38742197

RESUMEN

Diabetic kidney disease (DKD), a significant complication associated with diabetes mellitus, presents limited treatment options. The progression of DKD is marked by substantial lipid disturbances, including alterations in triglycerides, cholesterol, sphingolipids, phospholipids, lipid droplets, and bile acids (BAs). Altered lipid metabolism serves as a crucial pathogenic mechanism in DKD, potentially intertwined with cellular ferroptosis, lipophagy, lipid metabolism reprogramming, and immune modulation of gut microbiota (thus impacting the liver-kidney axis). The elucidation of these mechanisms opens new potential therapeutic pathways for DKD management. This research explores the link between lipid metabolism disruptions and DKD onset.


Asunto(s)
Nefropatías Diabéticas , Metabolismo de los Lípidos , Humanos , Nefropatías Diabéticas/metabolismo , Animales , Trastornos del Metabolismo de los Lípidos/metabolismo , Trastornos del Metabolismo de los Lípidos/complicaciones , Microbioma Gastrointestinal
2.
J Diabetes Res ; 2023: 8871677, 2023.
Artículo en Inglés | MEDLINE | ID: mdl-38094870

RESUMEN

Diabetic kidney disease (DKD) is a prevailing complication arising from diabetes mellitus. Unfortunately, there are no trustworthy and efficacious treatment modalities currently available. In recent times, compelling evidence has emerged regarding the intricate correlation between the kidney and the gut microbiota, which is considered the largest immune organ within the human physique. Various investigations have demonstrated that the perturbation of the gut microbiota and its associated metabolites potentially underlie the etiology and progression of DKD. This phenomenon may transpire through perturbation of both the innate and the adaptive immunity, leading to a burdensome allostatic load on the body and ultimately culminating in the development of DKD. Within this literature review, we aim to delve into the intricate interplay between the gut microbiota, its metabolites, and the immune system in the context of DKD. Furthermore, we strive to explore and elucidate potential chemical interventions that could hold promise for the treatment of DKD, thereby offering invaluable insights and directions for future research endeavors.


Asunto(s)
Alostasis , Diabetes Mellitus , Nefropatías Diabéticas , Microbioma Gastrointestinal , Humanos , Riñón , Inmunidad Adaptativa
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