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              <text>&lt;a href="http://doi.org/10.1016/s0014-2999(98)00700-6" target="_blank" rel="noreferrer noopener"&gt;http://doi.org/10.1016/s0014-2999(98)00700-6&lt;/a&gt;</text>
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              <text>207–216</text>
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              <text>2</text>
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              <text>361</text>
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                <text>Sex differences in extracellular and intracellular calcium-mediated vascular reactivity to vasopressin in rat aorta.</text>
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                <text>European journal of pharmacology</text>
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                <text>1998</text>
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                <text>1998-11</text>
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                <text>*Sex Characteristics; 1; 3-Pyridinecarboxylic acid; 4-dihydro-2; 6-dimethyl-5-nitro-4-(2-(trifluoromethyl)phenyl)-; Animals; Aorta/drug effects/*metabolism; Calcium Channel Agonists/*pharmacology; Calcium Channel Blockers/*pharmacology; Calcium/*metabolism; Diltiazem/pharmacology; Dose-Response Relationship; Drug; Female; In Vitro Techniques; Male; Methyl ester/pharmacology; Potassium Chloride/pharmacology; Rats; Simvastatin/pharmacology; Sprague-Dawley; Vasoconstriction/*drug effects; Vasopressins/*metabolism</text>
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                <text>Eatman D; Stallone J N; Rutecki G W; Whittier F C</text>
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                <text>In rat thoracic aorta, contractile responses to arginine vasopressin are two-fold higher in females than in males. To determine the roles of extracellular and intracellular Ca2+ in this sexual dimorphism in vascular function, vascular reactivity and Ca2+ channel function were examined in thoracic aortae of male and female rats. In the presence of diltiazem (10 microM), maximal contraction to vasopressin was reduced to a greater extent in male (65+/-2%) than in female aortae (38+/-1%). Maximal contractile responses to KCl and Bay K 8644 were similar in male and female aortae. Sensitivity to KCI was slightly but significantly higher in male than in female aorta; in contrast, sensitivity to Bay K 8644 was nearly three-fold higher in males than in females. Removal of the endothelium enhanced sensitivity to KCl similarly in male and female aortae. In the presence of simvastatin (60 microM; an inhibitor of intracellular Ca2+ release), reactivity to vasopressin was reduced substantially in female (42+/-1%) but unaltered in male aortae. Removal of the endothelium enhanced the inhibitory effect of simvastatin in both female (73+/-2%) and male aortae (41+/-2%). These findings demonstrate that male aortae depend more upon extracellular Ca2+ influx, whereas female aortae depend more upon intracellular Ca2+ release for vasopressin-induced contraction.</text>
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                <text>&lt;a href="http://doi.org/10.1016/s0014-2999(98)00700-6" target="_blank" rel="noreferrer noopener"&gt;10.1016/s0014-2999(98)00700-6&lt;/a&gt;</text>
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        <name>*Sex Characteristics</name>
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        <name>3-Pyridinecarboxylic acid</name>
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        <name>6-dimethyl-5-nitro-4-(2-(trifluoromethyl)phenyl)-</name>
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        <name>NEOMED College of Medicine</name>
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        <name>Potassium Chloride/pharmacology</name>
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