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日期:2024-07-17
1. Prog Brain Res. 2002;139:197-210. Nonpeptide vasopressin receptor antagonists: development of selective and orally active V1a, V2 and V1b receptor ligands. Serradeil-Le Gal C, Wagnon J, Valette G, Garcia G, Pascal M, Maffrand JP, Le Fur G. The involvem...
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日期:2024-07-19
A vasopressin receptor antagonist (VRA) is an agent which interferes with action at the vasopressin receptors. Most commonly VRAs are used in the treatment of hyponatremia, especially in patients with congestive heart failure, liver cirrhosis or SIADH.[1]...
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日期:2024-07-19
References: Hiroyama M, Wang S, Aoyagi T, Oikawa R, Sanbe A, Takeo S, Tanoue A: Vasopressin promotes cardiomyocyte hypertrophy via the vasopressin V1A receptor in neonatal mice. Eur J Pharmacol. 2007 Mar 22;559(2-3):89-97. Epub 2006 Dec 29. Pubmed ......
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日期:2024-07-20
Tolvaptan for Hyponatremia n engl j med 355;20 www.nejm.org november 16, 2006 2103 244 Patients underwent screening 205 Met inclusion criteria 102 Assigned to tolvaptan 15 mg daily 103 Assigned to placebo 15 mg daily Increased to 30 mg or 60 mg, if ......
Hyponatremia in Cirrhosis and End-Stage Liver Disease: Treatment with the Vasopressin V2-Receptor An
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日期:2024-07-21
Title Hyponatremia in Cirrhosis and End-Stage Liver Disease: Treatment with the Vasopressin V 2-Receptor Antagonist Tolvaptan Journal Digestive Diseases and Sciences Volume 57, Issue 11 , pp 2774-2785 Cover Date 2012-11-01 DOI 10.1007/s10620-012-2276-3...
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日期:2024-07-19
References: Verbalis JG, Goldsmith SR, Greenberg A, et al. Diagnosis, evaluation, and treatment of hyponatremia: expert panel recommendations. Am J Med. 2013;126(10 Suppl 1):S1-S4. Knoers NVAM. Hyperactive vasopressin receptors and disturbed water ......
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日期:2024-07-19
15 Aug 2001 ... Activation of the vasopressin V2 receptor, mainly present in renal collecting ducts
, leads to an increase in intracellular cAMP by stimulating ......
Neuropsychopharmacology - Effects of Buprenorphine Maintenance Dose on [mu]-Opioid Receptor Availabi
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日期:2024-07-17
Top of page INTRODUCTION Buprenorphine (BUP) is a high-affinity, -opioid receptor (OR) partial agonist and -opioid antagonist (Cowan et al, 1977; Heel et al, 1979; Lewis et al, 1983). BUP's OR actions offer agonist substitution (thereby reducing drug use,...