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Updated: May 23, 2026

Measurement of Endothelium-Dependent Vasorelaxation in the Mouse Thoracic Aorta Using Tensometric Small Volume Chamber Myography
Published on: August 12, 2022
Endothelium-derived relaxing factor-mediated vasodilation in mouse mesenteric vascular beds
Hiroki Fujiwara1, Yoshihiro Wake, Narumi Hashikawa-Hobara
1Department of Clinical Pharmaceutical Science, Okayama University, 1-1-1 Tsushima-naka, Okayama 700-8530, Japan.
The endothelium in mouse mesenteric arteries regulates vascular tone via prostanoids, endothelium-derived hyperpolarizing factor (EDHF), and nitric oxide. This mechanism differs from that observed in rat mesenteric arteries, highlighting species-specific vascular control.
Area of Science:
- Vascular Biology
- Endothelial Function
- Physiology
Background:
- The endothelium regulates vascular tone, primarily via endothelium-derived hyperpolarizing factor (EDHF) in rats.
- The role of the endothelium in mouse resistance arteries remains less understood.
Purpose of the Study:
- To investigate the mechanisms by which the endothelium in mouse mesenteric arteries regulates vascular tone.
- To compare endothelial regulation in mouse mesenteric arteries with that in rat mesenteric arteries.
Main Methods:
- Isolated mesenteric vascular beds from male C57BL/6 mice were perfused.
- Vascular responses to acetylcholine, A23187, and sodium nitroprusside (SNP) were measured.
- The effects of inhibitors (NOS, cyclooxygenase, K(+)-channel, gap-junction) on vasodilation were assessed.
Main Results:
- Acetylcholine and A23187 induced concentration-dependent vasodilation, abolished by endothelium dysfunction.
- Vasodilation to acetylcholine and A23187 was inhibited by nitric oxide synthase and K(+)-channel inhibitors.
- Prostanoids contributed to A23187-induced vasodilation, while gap-junctions mediated acetylcholine-induced vasodilation.
Conclusions:
- The endothelium in mouse mesenteric arteries regulates vascular tone through a combination of prostanoids, EDHF, and nitric oxide.
- These findings indicate a distinct endothelial regulatory system in mouse mesenteric arteries compared to rats.
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