نتایج جستجو برای: vasopressin type 2 receptor

تعداد نتایج: 3791004  

Journal: :Biochimica et biophysica acta. Molecular cell research 2021

The G protein-coupled receptor (GPCR) dimer interface plays an important role in the formation and stabilization of dimer. Therefore, identifying potential receptor-receptor is part studying GPCRs. Various strategies have been employed to study GPCR explore its functional significance, but experimental methods lack robustness calculations are laborious. Herein, we report a combined optimized ca...

Journal: :American journal of physiology. Gastrointestinal and liver physiology 2010
Laurent Ferrier Claudine Serradeil-Le Gal Anke M Schulte Valentina Vasina Eric Gaultier Silke Schroedel Maria Grazia Ursino Gilles Chaumaz Marc Pascal Fabrizio De Ponti Lionel Bueno

Vasopressin and its receptors modulate several gut functions, but their role in intestinal inflammation is unknown. Our aims were to determine 1) the localization of V1b receptors in human and rodent colon, 2) the role of vasopressin and V1b receptors in experimental colitis using two approaches: V1b⁻(/)⁻ mice and a selective V1b receptor antagonist, SSR149415, and 3) the mechanisms involved. V...

Journal: :Proceedings of the National Academy of Sciences of the United States of America 1990
W Lutz M Sanders J Salisbury R Kumar

To determine whether receptor-mediated endocytosis occurs in vasopressin-responsive cells, we developed a model system using synthetic fluorescent-labeled vasopressin analogs and A10 (smooth muscle) and LLC-PK1 (kidney epithelial) cells in culture; these cell lines express V1 and V2 vasopressin cell surface receptor types, respectively. We used epifluorescence microscopy to examine the binding,...

1998
William G. North Michael J. Fay Kenneth A. Longo Jiniin Du

Vasopressin is one of several small neuropeptides that are reported to be autocrine growth factors for small cell carcinoma of the lung (SCCL). It has been assumed that this peptide exercises its ntitogenic influences through the Vasopressin V,., receptor, and we have previously demon strated that this receptor is expressed by classical and variant SCCL. Activation of the vasopressin Vla recept...

Journal: :American journal of physiology. Renal physiology 2005
Richard Bouley Nuria Pastor-Soler Ori Cohen Margaret McLaughlin Sylvie Breton Dennis Brown

Vasopressin-stimulated insertion of the aquaporin 2 (AQP2) water channel into the plasma membrane of kidney collecting duct principal cells is a key event in the urinary concentrating mechanism. The paradigm for vasopressin-receptor signaling involves cAMP-mediated protein kinase A activation, which results in the functionally critical phosphorylation of AQP2 on amino acid serine 256. We previo...

1999
YOSHIHIKO SATO HIROYUKI HANAI ATSUHIRO NOGAKI KOKI HIRASAWA EIZO KANEKO HISAYOSHI HAYASHI YUICHI SUZUKI Hiroyuki Hanai Atsuhiro Nogaki Koki Hirasawa Eizo Kaneko Hisayoshi Hayashi

Sato, Yoshihiko, Hiroyuki Hanai, Atsuhiro Nogaki, Koki Hirasawa, Eizo Kaneko, Hisayoshi Hayashi, and Yuichi Suzuki. Role of the vasopressin V1 receptor in regulating the epithelial functions of the guinea pig distal colon. Am. J. Physiol. 277 (Gastrointest. Liver Physiol. 40): G819–G828, 1999.—Vasopressin has a wide spectrum of biological action. In this study, the role of vasopressin in regula...

Journal: :Nephrology Dialysis Transplantation 2023

Abstract Background and Aims Poly(ADP-ribosy)lation (PARylation), which is mediated by poly(ADP-ribose) polymerases (PARPs), catalyzes the transfer of ADP-ribose from NAD+ molecules to acceptor proteins, regulates diverse cellular processes. Since PARP1 gene-deficient mice revealed an increase in urine volume, we aimed examine role PARP1, most abundant type protein PARPs family, vasopressin-med...

2008
L. M. Shewey D. M. Dorsa

Specific binding sites for3H-arginineQasopressin (AVP) have been characterized in rat septal membranes. Scatchard analyses revealed a single class of high-affinity binding sites having an equilibrium dissociation constant of 1.7 f 0.3 nM and total binding capacity of 22.6 k 4.2 fmol/mg protein. Binding displacement studies with peptide analogs of AVP indicate that this binding site is similar t...

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