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Updated: Jan 21, 2026

Induction of Atherosclerotic Plaques Through Activation of Mineralocorticoid Receptors in Apolipoprotein E-deficient Mice
Published on: September 26, 2018
Ghrelin-mediated pathway in Apolipoprotein-E deficient mice: a survival system
Rita Rezzani1,2, Caterina Franco1, Gaia Favero1
1Anatomy and Physiopathology Division, Department of Clinical and Experimental Sciences, University of Brescia Brescia, Italy.
Ghrelin hormone may protect kidneys by influencing the ghrelin/sirtuin 1 (SIRT1)/aquaporin (AQP) pathway in a mouse model of kidney disease and high cholesterol. This suggests ghrelin as a potential therapeutic target for renal injury.
Area of Science:
- Nephrology
- Endocrinology
- Metabolic Diseases
Background:
- Renal diseases disrupt metabolic pathways, leading to dyslipidemia and altered lipoprotein profiles.
- Apolipoprotein-E deficient (ApoE-/-) mice exhibit hypercholesterolemia and renal pathology, serving as a model for kidney injury.
- Ghrelin, a hormone found in the kidney, influences renal function and its levels increase with fasting, potentially interacting with the sirtuin 1 (SIRT1)/p53 pathway.
Purpose of the Study:
- To investigate the ghrelin/sirtuin 1 (SIRT1)/aquaporin (AQP) pathway in ApoE-/- mice.
- To clarify the role of this system in age-related renal diseases with or without comorbidities.
- To explore ghrelin as a potential therapeutic target for renal injury.
Main Methods:
- Utilized apolipoprotein-E deficient (ApoE-/-) mice as a model for hypercholesterolemia and renal pathology.
- Examined the ghrelin/sirtuin 1 (SIRT1)/aquaporin (AQP) pathway, focusing on AQP1 and AQP2.
- Assessed the system's role in aging-related renal diseases.
Main Results:
- The study evaluated the ghrelin/SIRT1/AQP1/AQP2 pathway in ApoE-/- mice.
- Results could highlight the significance of this system in renal diseases associated with aging.
- Findings may support ghrelin as a novel therapeutic target for kidney injury.
Conclusions:
- The ghrelin/SIRT1/AQP system plays a role in renal diseases.
- Ghrelin's interaction with SIRT1 and aquaporins warrants further investigation.
- Ghrelin emerges as a potential therapeutic avenue for mitigating renal injury.
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