Augmented central nitric oxide production inhibits vasopressin release during hemorrhage in acute alcohol-intoxicated rodents

American Journal of Physiology - Regulatory Integrative and Comparative Physiology

Volumn 301, Issue 5, 2011, Pages

  Whitaker, Annie M ^a   Sulzer, Jesse K ^a   Molina, Patricia E ^a  

^a LOUISIANA STATE UNIVERSITY SCHOOL OF MEDICINE   (United States)

Author keywords

Ethanol; Hypovolemia; L NAME; Mean arterial blood pressure; Osmolality

Indexed keywords

ALCOHOL; ARGIPRESSIN; GLUCOSE; N(G) NITROARGININE METHYL ESTER; NITRIC OXIDE; SODIUM CHLORIDE;

ALCOHOL INTOXICATION; ANIMAL EXPERIMENT; ANIMAL MODEL; ARTICLE; CONTROLLED STUDY; HEMODYNAMICS; HEMORRHAGIC SHOCK; HYPEROSMOLALITY; MALE; NONHUMAN; PARAVENTRICULAR THALAMIC NUCLEUS; PLASMA OSMOLALITY; PRIORITY JOURNAL; RAT; REGULATORY MECHANISM; SUPRAOPTIC NUCLEUS; VASOPRESSIN RELEASE;

ALCOHOLIC INTOXICATION; ANIMALS; ARGININE VASOPRESSIN; BLOOD PRESSURE; BLOOD VOLUME; DISEASE MODELS, ANIMAL; DOWN-REGULATION; ENZYME INHIBITORS; HEMORRHAGE; MALE; NG-NITROARGININE METHYL ESTER; NITRIC OXIDE; NITRIC OXIDE SYNTHASE; OSMOLAR CONCENTRATION; PARAVENTRICULAR HYPOTHALAMIC NUCLEUS; RATS; RATS, SPRAGUE-DAWLEY; SIGNAL TRANSDUCTION; SUPRAOPTIC NUCLEUS; TIME FACTORS; UP-REGULATION;

EID: 80155143217     PISSN: 03636119     EISSN: 15221490     Source Type: Journal    
DOI: 10.1152/ajpregu.00035.2011     Document Type: Article

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