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1.
Eur J Pharmacol ; 767: 17-23, 2015 Nov 15.
Article in English | MEDLINE | ID: mdl-26420355

ABSTRACT

We aimed at assessing the role of endothelial cell calcium for the endothelial dysfunction of mesenteric resistance arteries of db/db mice (a model of type 2 diabetes) and determine whether treatment with sulfaphenazole, improves endothelial calcium signaling and function. Pressure myography was used to study acetylcholine (ACh) -induced vasodilation. Intracellular calcium ([Ca(2+)]i) transients was measured by confocal laser scanning microscopy and smooth muscle membrane potential with sharp microelectrodes. The impaired dilation to ACh observed in mesenteric resistance arteries from db/db mice was improved by treatment of the mice with sulfaphenazole for 8 weeks. The impaired dilation to ACh was associated with decreased endothelial [Ca(2+)]i and smooth muscle hyperpolarization. Sulfaphenazole applied in vitro improved endothelial mediated dilation of arteries from db/db mice both in the absence and the presence of inhibitors of nitric oxide and cyclooxygenase. Sulfaphenazole also increased the percentage of endothelial cells with ACh induced increases of [Ca(2+)]i. The study shows that impaired endothelial [Ca(2+)]i control can explain the reduced endothelial function in arteries from diabetic mice and that sulfaphenazole treatment improves endothelial [Ca(2+)]i responses to ACh and consequently endothelium-dependent vasodilation. These observations provide mechanistic insight into endothelial dysfunction in diabetes.


Subject(s)
Acetylcholine/pharmacology , Calcium Signaling/drug effects , Diabetes Mellitus, Type 2/metabolism , Endothelial Cells/drug effects , Endothelium, Vascular/drug effects , Mesenteric Arteries/drug effects , Vasodilation/drug effects , Animals , Cyclooxygenase Inhibitors/pharmacology , Cytochrome P-450 Enzyme System/biosynthesis , Cytochrome P450 Family 2 , Diabetes Mellitus, Type 2/genetics , Endothelial Cells/metabolism , Endothelium, Vascular/metabolism , Male , Membrane Potentials/drug effects , Mice , Mice, Mutant Strains , Nitric Oxide/antagonists & inhibitors , Prostaglandin-Endoperoxide Synthases , Sulfaphenazole/pharmacology
2.
Am J Physiol Regul Integr Comp Physiol ; 305(9): R1021-30, 2013 Nov 01.
Article in English | MEDLINE | ID: mdl-24005251

ABSTRACT

The high blood pressure in giraffe leg arteries renders giraffes vulnerable to edema. We investigated in 11 giraffes whether large and small arteries in the legs and the tight fascia protect leg capillaries. Ultrasound imaging of foreleg arteries in anesthetized giraffes and ex vivo examination revealed abrupt thickening of the arterial wall and a reduction of its internal diameter just below the elbow. At and distal to this narrowing, the artery constricted spontaneously and in response to norepinephrine and intravascular pressure recordings revealed a dynamic, viscous pressure drop along the artery. Histology of the isolated median artery confirmed dense sympathetic innervation at the narrowing. Structure and contractility of small arteries from muscular beds in the leg and neck were compared. The arteries from the legs demonstrated an increased media thickness-to-lumen diameter ratio, increased media volume, and increased numbers of smooth muscle cells per segment length and furthermore, they contracted more strongly than arteries from the neck (500 ± 49 vs. 318 ± 43 mmHg; n = 6 legs and neck, respectively). Finally, the transient increase in interstitial fluid pressure following injection of saline was 5.5 ± 1.7 times larger (n = 8) in the leg than in the neck. We conclude that 1) tissue compliance in the legs is low; 2) large arteries of the legs function as resistance arteries; and 3) structural adaptation of small muscle arteries allows them to develop an extraordinary tension. All three findings can contribute to protection of the capillaries in giraffe legs from a high arterial pressure.


Subject(s)
Arterial Pressure , Brachial Artery/physiopathology , Capillaries/physiopathology , Edema/prevention & control , Lower Extremity/blood supply , Ruminants , Tibial Arteries/physiopathology , Adaptation, Physiological , Animals , Brachial Artery/diagnostic imaging , Brachial Artery/pathology , Capillary Permeability , Edema/physiopathology , Hydrostatic Pressure , Male , Tibial Arteries/diagnostic imaging , Tibial Arteries/pathology , Time Factors , Ultrasonography , Vascular Resistance , Vasoconstriction
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