Abstract
1. In rat thoracic aortae, contractions induced by methoxamine were inhibited by chloroethylclonidine, whereas oxymetazoline-induced contractions, which were more dependent on Ca(2+)-entry, were insensitive to chloroethylclonidine. 2. Aminophylline inhibited the contractions and 45Ca(2+)-uptake induced by both methoxamine and oxymetazoline. However, oxymetazoline-induced contractions were more sensitive to inhibition by aminophylline and D600. 3. Thus, the partial selectivity of aminophylline for the chloroethylclonidine-resistant, highly dependent on extracellular Ca2+, oxymetazoline-mediated responses may be explained by a preferential inhibition of agonist-induced Ca2+ entry as compared to inhibition of other transduction pathways.
MeSH terms
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Adrenergic alpha-Agonists / pharmacology
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Adrenergic alpha-Antagonists / pharmacology*
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Aminophylline / pharmacology*
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Animals
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Aorta, Thoracic / drug effects*
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Aorta, Thoracic / metabolism
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Calcium / metabolism
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Calcium Radioisotopes
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Clonidine / analogs & derivatives*
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Clonidine / pharmacology
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Female
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Gallopamil / pharmacology
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In Vitro Techniques
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Male
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Methoxamine / antagonists & inhibitors
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Methoxamine / pharmacology
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Muscle Contraction / drug effects
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Muscle, Smooth, Vascular / drug effects*
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Muscle, Smooth, Vascular / metabolism
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Oxymetazoline / antagonists & inhibitors
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Oxymetazoline / pharmacology
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Rats
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Rats, Sprague-Dawley
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Receptors, Adrenergic, alpha / drug effects*
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Receptors, Adrenergic, alpha / metabolism
Substances
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Adrenergic alpha-Agonists
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Adrenergic alpha-Antagonists
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Calcium Radioisotopes
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Receptors, Adrenergic, alpha
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Aminophylline
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Gallopamil
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chlorethylclonidine
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Oxymetazoline
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Methoxamine
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Clonidine
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Calcium