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1 cause of its lack of agonist activity at the vasopressin V2 receptor.
2  and beta2-adrenergic receptors, but not the vasopressin (V2) receptor.
3 iven fluid secretion (PDE3), and response to vasopressin V2 receptor activation (both).
4  than the mixed vasopressin type 1a receptor/vasopressin V2 receptor agonist arginine vasopressin bec
5  treatment of selepressin with the selective vasopressin V2 receptor agonist desmopressin were simila
6  This study sought to examine the effects of vasopressin V2 receptor antagonism with tolvaptan on the
7 d effects were blocked by treatment with the vasopressin V2 receptor antagonist SR121463B, but not by
8  mice before and after administration of the vasopressin V2 receptor antagonist tolvaptan.
9 aptan (OPC-41061), a novel, oral, nonpeptide vasopressin V2-receptor antagonist in patients with chro
10 he effect of long-term administration of the vasopressin V2-receptor antagonist tolvaptan (30 mg/day)
11 atinine clearance, >/=60 ml per minute), the vasopressin V2-receptor antagonist tolvaptan slowed the
12    Tolvaptan, an oral, nonpeptide, selective vasopressin V2-receptor antagonist, shows promise in thi
13 ypervolemic hyponatremia, tolvaptan, an oral vasopressin V2-receptor antagonist, was effective in inc
14 inhibition of renal intracellular cAMP using vasopressin V2 receptor antagonists, and somatostatin an
15                        Vaptans acting on the vasopressin V2 receptors (aquaretics) have attracted att
16 isease caused most often by mutations in the vasopressin V2 receptor (AVPR2).
17       One group of nephrotic rats received a vasopressin V2 receptor blocker (V2X) from 4 to 16 wk af
18                                 Tolvaptan, a vasopressin V2 receptor blocker, shows promise for manag
19          The data support roles for multiple vasopressin V2-receptor-dependent signaling pathways in
20                     Functional engagement of vasopressin V2 receptors is reported to produce rises in
21                             We conclude that vasopressin V2 receptors mediate the antidiuretic effect
22 eamino-(8-D-arginine)-vasopressin (dDAVP), a vasopressin V2 receptor-selective agonist, for 7 d into
23 unctional, shortened, "diabetic" form of the vasopressin V2 receptor that is the product of incomplet
24 asopressin (AVP) affects kidney function via vasopressin V2 receptors that are linked to activation o
25 II type 1A receptor, neurotensin receptor 1, vasopressin V2 receptor, thyrotropin-releasing hormone r
26   After agonist-induced internalization, the vasopressin V2 receptor (V2R) does not recycle to the pl
27             The seven-transmembrane-spanning vasopressin V2 receptor (V2R) is a Gs-coupled receptor t
28  to recycle and resensitize rapidly, and the vasopressin V2 receptor (V2R), known to recycle and rese
29                                 OPC-31260, a vasopressin V2 receptor (VPV2) antagonist, was shown to
30                                          The vasopressin V2 receptor (VPV2R) antagonist OPC31260 has
31 ous to the human disorders to test whether a vasopressin V2 receptor (VPV2R) antagonist, OPC31260, wo
32  beta2-adrenergic, angiotensin II type 1 and vasopressin V2 receptors was altered by the beta-arresti
33 -7 cells, we found that angiotensin AT1a and vasopressin V2 receptors, which form stable receptor-bet

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