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Updated: Jun 9, 2026

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Mesenteric Artery Contraction and Relaxation Studies Using Automated Wire Myography
Published on: September 22, 2011
Ghrelin signaling in human mesenteric arteries
D Z Dimitrova1, S D Dimitrov, I Iliev
1Institute of Biophysics, Bulgarian Academy of Sciences, Sofia, Bulgaria.
Summary
Ghrelin enhances human mesenteric artery contraction via a novel pathway involving Src kinase, MEK, and thromboxane A2. This study identifies new mediators in the ghrelin signaling pathway.
Area of Science:
- Vascular Physiology
- Molecular Signaling
- Gastrointestinal Hormones
Background:
- Ghrelin is known to influence vascular tone.
- The precise signaling mechanisms of ghrelin in human mesenteric arteries remain incompletely understood.
Purpose of the Study:
- To elucidate the novel signaling pathway and mediators involved in ghrelin-induced contraction of human mesenteric arteries.
Main Methods:
- Isometric wire myography was used to measure arterial contractile force.
- Whole-cell patch clamp electrophysiology was performed on isolated smooth muscle cells.
- Pharmacological inhibitors and specific receptor antagonists were employed to dissect the signaling cascade.
Main Results:
- Ghrelin (100 nmol) abolished outward potassium currents via iberiotoxin-sensitive calcium-activated potassium channels.
- Ghrelin dose-dependently increased mesenteric artery contraction.
- This effect was mediated by Src kinase, mitogen-activated protein kinase kinase (MEK), cyclooxygenase 1, and a T prostanoid receptor agonist, likely thromboxane A2.
Conclusions:
- Ghrelin stimulates contraction in human mesenteric arteries through a novel signaling pathway.
- Key components of this pathway include Src kinase, MEK, cyclooxygenase 1, and thromboxane A2.
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