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Effects of nonpeptide vasopressin V2 antagonist tolvaptan in rats with heart failure.

Effects of nonpeptide vasopressin V2 antagonist tolvaptan in rats with heart failure. Research Abstract Details 

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  • Effects of nonpeptide vasopressin V2 antagonist tolvaptan in rats with heart failure. Abstract Text:

    punniyakoti t veeraveeduPunniyakoti T Veeraveedu,kenichi watanabeKenichi Watanabe,meilei maMeilei Ma,suresh s palaniyandiSuresh S Palaniyandi,ken'ichi yamaguchiKen'ichi Yamaguchi,kenji suzukiKenji Suzuki,makoto kodamaMakoto Kodama,yoshifusa aizawaYoshifusa Aizawa,punniyakoti t veeraveeduPunniyakoti T Veeraveedu,kenichi watanabeKenichi Watanabe,meilei maMeilei Ma,suresh s palaniyandiSuresh S Palaniyandi,ken'ichi yamaguchiKen'ichi Yamaguchi,kenji suzukiKenji Suzuki,makoto kodamaMakoto Kodama,yoshifusa aizawaYoshifusa Aizawa,

    Similar to other neurohormones that are activated in chronic heart failure (CHF), circulating arginine vasopressin (AVP) is elevated in patients with CHF. The precise role of AVP in the pathophysiology of cardiovascular disease is controversial. AVP is a peptide hormone that contributes to water retention and vasoconstriction in CHF through effects on V(2) and V(1a) receptors, respectively. In the present study, the effect of V(2) receptor (V(2)R) blockade using tolvaptan was assessed in a rat model of myosin-induced experimental autoimmune myocarditis. CHF was elicited in Lewis rats by immunization with porcine cardiac myosin, and 28 days after immunization rats were treated for 28 days with oral tolvaptan (3 or 10mg/(kg day)) or vehicle. CHF was characterized by left ventricular remodeling and impaired systolic and diastolic function. Chronic V(2)R blockade increased urine volume and urinary AVP excretion and decreased urine osmolality but had no natriuretic effect, and as a result caused increases in plasma osmolality and sodium. High doses of tolvaptan markedly elevated electrolyte-free water clearance. V(2)R blockade did not activate the renin-angiotensin system, not influence cardiac remodeling, cardiac function, or survival. The upregulation of aquaporin 2 protein in the kidney of CHF rats was inhibited by the administration of V(2)R antagonist. These results suggest that in a rat model of CHF, AVP plays a major role in water retention through the renal V(2)R.

    Effects of nonpeptide vasopressin V2 antagonist tolvaptan in rats with heart failure. Publishing Authors By Initials

    pt veeraveeduPT Veeraveedu,k watanabeK Watanabe,m maM Ma,ss palaniyandiSS Palaniyandi,k yamaguchiK Yamaguchi,k suzukiK Suzuki,m kodamaM Kodama,y aizawaY Aizawa,pt veeraveeduPT Veeraveedu,k watanabeK Watanabe,m maM Ma,ss palaniyandiSS Palaniyandi,k yamaguchiK Yamaguchi,k suzukiK Suzuki,m kodamaM Kodama,y aizawaY Aizawa,

    For similar abstracts research abstracts see: abstracts research

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    Effects of nonpeptide vasopressin V2 antagonist tolvaptan in rats with heart failure. Journal Published:

    PUBLICATION TYPE: Research Support, Non-U.S. Gov

    Journal: Biochemical pharmacology

    VOLUME: 74

    Page Numbers: 1466-75

    Journal Abbreviation: Biochem. Pharmacol.

    ISSN: 0006-2952

    DAY: 22

    MONTH: 07

    YEAR: 2007

    Effects of nonpeptide vasopressin V2 antagonist tolvaptan in rats with heart failure. Information

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    LANGUAGE: eng

    NlmUniqueID: 101032

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    Grant and Affiliation Information for Effects of nonpeptide vasopressin V2 antagonist tolvaptan in rats with heart failure.

    AFFILIATION: Department of Clinical Pharmacology, Faculty of Pharmaceutical Sciences, Niigata University of Pharmacy and Applied Life Sciences, 265-1 Higashizima, Niigata city 956-8603, Japan.

    Country: England

    England Research PublicationEngland Research Publication

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    MEDLINETA: Biochem Pharmacol

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