Homocellular Conduction Along Endothelium and Smooth Muscle of Arterioles in Hamster Cheek Pouch
| Autor: | Stephane Budel, Steven S. Segal, Iain S. Bartlett |
|---|---|
| Rok vydání: | 2003 |
| Předmět: |
Male
Endothelium Physiology Vasodilator Agents Bradykinin Vasodilation Nitric Oxide Nitroarginine Muscle Smooth Vascular Potassium Chloride Microcirculation Phenylephrine chemistry.chemical_compound Cheek pouch Arteriole Cricetinae medicine.artery medicine Animals Vasoconstrictor Agents Enzyme Inhibitors Serum Albumin Mesocricetus Chemistry Dextrans Anatomy Acetylcholine Arterioles Cheek medicine.anatomical_structure Vasoconstriction Biophysics Cattle Endothelium Vascular Sodium nitroprusside Nitric Oxide Synthase medicine.symptom Cardiology and Cardiovascular Medicine Fluorescein-5-isothiocyanate medicine.drug |
| Zdroj: | Circulation Research. 93:61-68 |
| ISSN: | 1524-4571 0009-7330 |
| DOI: | 10.1161/01.res.0000080318.81205.fd |
| Popis: | We investigated roles for homocellular (endothelium or smooth muscle) and heterocellular (myoendothelial) conduction pathways along hamster cheek pouch arterioles in vivo (n=64; diameter, 33+/-1 microm). Endothelium-dependent and -independent vasoactive agents were delivered from micropipettes (0.5 or 1 second pulse) onto an arteriole while observing diameter changes at defined distances along the vessel. Acetylcholine (ACh) produced maximal diameter (63+/-1 microm) locally and vasodilation conducted rapidly ( approximately 10 microm response at 2 mm,1 second). Responses to bradykinin (BK) were similar, whereas sodium nitroprusside produced maximal dilation locally without conduction. KCl evoked biphasic conduction of vasoconstriction and vasodilation, whereas phenylephrine (PE) produced conducted vasoconstriction. Disrupting the integrity of endothelium as a conduction pathway using focal light-dye treatment (LDT) abolished conducted vasodilation to BK and to KCl but not to ACh. Disruption of smooth muscle integrity with LDT abolished conducted vasoconstriction with no effect on conducted vasodilation. After LDT of respective cell layers at sites 1 mm apart, vasodilation to ACh conducted past disrupted smooth muscle or disrupted endothelium, but not beyond both sites in series. The loss of conduction after selective LDT indicates a lack of effective myoendothelial coupling along the arteriolar wall. During NO synthase inhibition (L-NA, 100 micromol/L), conducted vasodilation was abolished to BK and to KCl yet remained intact to ACh. However, after LDT of smooth muscle, L-NA inhibited conduction to ACh by 60%. Thus, conduction of vasodilation entails a wave of NO release along arteriolar endothelium that is masked when smooth muscle provides a parallel conduction pathway. |
| Databáze: | OpenAIRE |
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