Artery Research

Volume 20, Issue C, December 2017, Pages 56 - 56

4.2 SEX-DEPENDENT EFFECTS OF PERIVASCULAR ADIPOSE TISSUE ON VASCULAR FUNCTION

Authors
Christian Delles, Sarah McNeilly, Sheon Mary, Adam Sheikh, Heather Small
University of Glasgow, UK
Available Online 6 December 2017.
DOI
10.1016/j.artres.2017.10.040How to use a DOI?
Abstract

Background: Premenopausal women are relatively protected against hypertension compared to males. Estrogen levels have been identified as a potential underlying cause, but the pathophysiological mechanisms remain incompletely understood. We hypothesised that sex-dependent effects of perivascular adipose tissue PVAT mediate altered vascular function in hypertension.

Methods: The effect of PVAT was investigated on resistance vessels of 16 week old male and female stroke-prone spontaneously hypertensive rats (SHRSP).

Results: Wire-myography was used on 3rd-order mesenteric vessels (maximum contraction: male +PVAT 113.3 ± 1.1 vs. female +PVAT 91.4 ± 11.36 %). Noradrenaline mediated vasoconstriction was increased in SHRSP males compared to females. KATP channel-mediated vasorelaxation by cromakalim was impaired in males compared to females (maximum relaxation: male +PVAT 46.9 ± 3.9 % vs. female +PVAT 97.3 ± 2.7 %) A cross-over study assessing function of male PVAT on female vessels and vice versa confirmed the reduced KATP mediated vasorelaxation induced by male PVAT (maximum relaxation: female +PVATfemale 90.6 ± 1.4 % vs. female +PVATmale 65.8 ± 3.5 %). An adipokine array with subsequent western blot validation identified resistin as a potential modifier of vascular reactivity. Resistin was increased by approximately 2-fold in SHRSP male PVAT. Male and female vessels pretreated with resistin (40 ng/ml) showed no difference in response to noradrenaline. However, vasorelaxation in response to cromakalim was significantly impaired in resistin treated female vessels, similar to levels observed in male vessels (maximum relaxation: female +PVAT 97.3 ± 0.9 % vs. female +PVAT +resistin 36.8 ± 2.3 %).

Conclusion: We identified a novel role for resistin in sex-dependent PVAT mediated vascular function in hypertension through a KATP channel mediated mechanism.

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Journal
Artery Research
Volume-Issue
20 - C
Pages
56 - 56
Publication Date
2017/12/06
ISSN (Online)
1876-4401
ISSN (Print)
1872-9312
DOI
10.1016/j.artres.2017.10.040How to use a DOI?
Open Access
This is an open access article distributed under the CC BY-NC license.

Cite this article

TY  - JOUR
AU  - Christian Delles
AU  - Sarah McNeilly
AU  - Sheon Mary
AU  - Adam Sheikh
AU  - Heather Small
PY  - 2017
DA  - 2017/12/06
TI  - 4.2 SEX-DEPENDENT EFFECTS OF PERIVASCULAR ADIPOSE TISSUE ON VASCULAR FUNCTION
JO  - Artery Research
SP  - 56
EP  - 56
VL  - 20
IS  - C
SN  - 1876-4401
UR  - https://doi.org/10.1016/j.artres.2017.10.040
DO  - 10.1016/j.artres.2017.10.040
ID  - Delles2017
ER  -