Abstract | AIMS:
Humanin (HN) is an endogenous mitochondrial-derived cytoprotective peptide that has shown protective effects against atherosclerosis and is expressed in human vessels. However, its effects on the progression of kidney disease are unknown. We hypothesized that HN would protect the kidney in the early phase of atherogenesis. MAIN METHODS: Forty-eight mice were studied in four groups (n=12 each). Twenty-four ApoE deficient mice were fed a 16-week high- cholesterol diet supplemented with saline or HN (4mg/kg/day, intraperitoneal). C57BL/6 mice were fed a normal diet supplemented with saline or HN. Microvascular architecture was assessed with micro-CT and vascular wall remodeling by alpha-SMA staining. The effects of HN on angiogenesis, inflammation, apoptosis and fibrosis were evaluated in the kidney tissue by Western blotting and histology. KEY FINDINGS: SIGNIFICANCE: HN attenuates renal microvascular remodeling, inflammation and apoptosis in the early stage of kidney disease in hypercholesterolemic ApoE(-/-) mice. HN may serve as a novel therapeutic target to mitigate kidney damage in early atherosclerosis.
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Authors | Xin Zhang, Victor H Urbieta-Caceres, Alfonso Eirin, Caitlin C Bell, John A Crane, Hui Tang, Kyra L Jordan, Yun-Kyu Oh, Xiang-Yang Zhu, Michael J Korsmo, Adi R Bachar, Pinchas Cohen, Amir Lerman, Lilach O Lerman |
Journal | Life sciences
(Life Sci)
Vol. 91
Issue 5-6
Pg. 199-206
(Sep 04 2012)
ISSN: 1879-0631 [Electronic] Netherlands |
PMID | 22820173
(Publication Type: Journal Article, Research Support, Non-U.S. Gov't)
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Copyright | Copyright © 2012 Elsevier Inc. All rights reserved. |
Chemical References |
- Apolipoproteins E
- Intracellular Signaling Peptides and Proteins
- humanin
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Topics |
- Animals
- Apolipoproteins E
(genetics)
- Apoptosis
(drug effects)
- Atherosclerosis
(drug therapy, physiopathology)
- Blotting, Western
- Disease Progression
- Female
- Hypercholesterolemia
(drug therapy, physiopathology)
- Inflammation
(drug therapy, physiopathology)
- Intracellular Signaling Peptides and Proteins
(metabolism, physiology)
- Kidney
(blood supply, drug effects, metabolism)
- Kidney Diseases
(drug therapy, etiology)
- Mice
- Mice, Inbred C57BL
- Mice, Knockout
- Microvessels
(drug effects)
- Neovascularization, Pathologic
(drug therapy)
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