CostaTJ_ERaOE_Supplementary (AJP-Heart & Circ)

We have revealed for the first time that overexpression of adipose tissue estrogen receptor α (ERα<sup>OE</sup>) amplifies the anti-contractile effect of mesenteric PVAT via the biosynthesis of NADPH oxidase 4 (NOX4)-derived hydrogen peroxide (H<sub>2</sub>O<sub>2</sub>), and this overexpression is protective against HFD-induced PVAT dysfunction. Collectively, these data demonstrate an important mechanism by which ERα signaling is vasculoprotective in the context of PVAT.

Publication Details

Journal
Figshare
Published
2025-01-01
DOI
https://doi.org/10.6084/m9.figshare.28296770.v2
Primary Topic
Neutrophil, Myeloperoxidase and Oxidative Mechanisms
Type
article
Field-Weighted Citation Impact
0.00
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CostaTJ_ERaOE_Supplementary (AJP-Heart & Circ)

Figshare
Neutrophil, Myeloperoxidase and Oxidative Mechanisms
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CostaTJ_ERaOE_Supplementary (AJP-Heart & Circ)

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Abstract

We have revealed for the first time that overexpression of adipose tissue estrogen receptor α (ERα<sup>OE</sup>) amplifies the anti-contractile effect of mesenteric PVAT via the biosynthesis of NADPH oxidase 4 (NOX4)-derived hydrogen peroxide (H<sub>2</sub>O<sub>2</sub>), and this overexpression is protective against HFD-induced PVAT dysfunction. Collectively, these data demonstrate an important mechanism by which ERα signaling is vasculoprotective in the context of PVAT.

Figshare
Openalex Percentile: Top 52%
Neutrophil, Myeloperoxidase and Oxidative Mechanisms
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CostaTJ_ERaOE_Supplementary (AJP-Heart &amp; Circ) · Figshare (2025) | TGRS Research Map | TGRS