نتایج جستجو برای: vasopressin type 2 receptor

تعداد نتایج: 3791004  

Journal: :American journal of physiology. Heart and circulatory physiology 2003
Pinggang Liu Derek A Misurski Venkat Gopalakrishnan

With the use of fura 2 measurements in multiple and single cells, we examined whether cysteinyl leukotrienes (CysLT) mediate angiotensin II (ANG II)-evoked increases in cytosolic free Ca(2+) concentration ([Ca(2+)](i)) in neonatal rat cardiomyocytes. ANG II-evoked CysLT release peaked at 1 min. The angiotensin type 1 (AT(1)) antagonist losartan, but not the AT(2) antagonist PD-123319, attenuate...

Journal: :Journal of the American Society of Nephrology : JASN 2007
Doyeob Kim Min Wang Qi Cai Heddwen Brooks Gregory R Dressler

Pax transactivation-domain interacting protein (PTIP) is a widely expressed nuclear protein that is essential for early embryonic development. PTIP was first identified on the basis of its interactions with the developmental regulator Pax2 but can also bind to other nuclear transcription factors. The Pax2 protein is essential for development of the renal epithelia and for regulating the respons...

Journal: :Journal of the American Society of Nephrology : JASN 2005
T Mary Fujiwara Daniel G Bichet

The identification, characterization, and mutational analysis of three different genes-the arginine vasopressin gene (AVP), the arginine vasopressin receptor 2 gene (AVPR2), and the vasopressin-sensitive water channel gene (aquaporin 2 [AQP2])-provide the basis for understanding of three different hereditary forms of "pure" diabetes insipidus: Neurohypophyseal diabetes insipidus, X-linked nephr...

Journal: :American journal of physiology. Renal physiology 2004
Hua Lu Tian-Xiao Sun Richard Bouley Karen Blackburn Margaret McLaughlin Dennis Brown

Inhibition of clathrin-mediated endocytosis by expression of a GTPase-deficient dynamin mutant (dynamin-2/K44A) for 16 h results in an accumulation of plasma membrane aquaporin-2 (AQP2) in epithelial cells stably transfected with wild-type AQP2. We now show a similar effect of K44A dynamin in LLC-PK1 cells transfected with an S256 phosphorylation-deficient AQP2 mutant, AQP2(S256A), and in AQP2-...

2004
Lixia Zhao Roberta D. Brinton

Previous research from our laboratory has demonstrated that V1 vasopressin receptor agonist (V1 agonist) induces a complex intracellular Ca 2 -signaling cascade in cortical astrocytes that is initiated by G-protein-coupled V1a vasopressin receptor-mediated cytoplasmic and nuclear Ca 2 rise and converges during activation of the nuclear transcription factor cAMP response element-binding protein ...

Journal: :Journal of Molecular Endocrinology 2002

Journal: :Clinical science 2003
James Walter Ferguson George Therapondos David E Newby Peter Clive Hayes

Vasopressin, or antidiuretic hormone, is a peptide hormone that is released from the posterior pituitary gland in response to changes in blood pressure and plasma osmolality. The main pathophysiological states associated with high plasma vasopressin concentrations are cirrhosis, cardiac failure and syndrome of inappropriate antidiuretic hormone (SIADH) secretion. Pharmacological treatments for ...

Journal: :Journal of pharmacological sciences 2009
Gozoh Tsujimoto Yukio Takano

Arginine vasopressin (AVP) is a cyclic nonapeptide that is centrally synthesized in the hypothalamus. Vasopressin has a plethora of biological effects including not only organ regulation but also behavioral ones, which are mediated by the vasopressin-receptor subtypes V1a (vascular), V1b (pituitary) V2 (renal), and oxytocin receptors. Recently, non-peptide vasopressin receptor–selective agonist...

Journal: :The Journal of pharmacology and experimental therapeutics 2006
Rosemarie Macion-Dazard Nicholas Callahan Zhen Xu Nan Wu Marc Thibonnier Menachem Shoham

Whereas arginine vasopressin binds to its receptor subtypes V(1)R and V(2)R with equal affinity of approximately 2 nM, nonpeptide antagonists interact differently with vasopressin receptor subtypes. The V(2)R antagonist binding site was mapped by site-directed mutagenesis at six selected amino acid positions, K100D, A110W, M120V, L175Y, R202S, and F307I, predicted to be involved in antagonist b...

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