Supported synthesis of adenosine nucleotides and derivatives on a benzene‐centred tripodal soluble support

Author(s):  
Lucie Appy ◽  
Suzanne Peyrottes ◽  
Béatrice Roy
ChemBioChem ◽  
2003 ◽  
Vol 4 (2-3) ◽  
pp. 162-170 ◽  
Author(s):  
Daniel Geißler ◽  
Wolfgang Kresse ◽  
Burkhard Wiesner ◽  
Jürgen Bendig ◽  
Helmut Kettenmann ◽  
...  

1968 ◽  
Vol 22 (2) ◽  
pp. 355-357 ◽  
Author(s):  
Chien-Ho Chiu-Lin

1996 ◽  
Vol 270 (2) ◽  
pp. G246-G252 ◽  
Author(s):  
R. S. Chari ◽  
S. M. Schutz ◽  
J. E. Haebig ◽  
G. H. Shimokura ◽  
P. B. Cotton ◽  
...  

Activation of purinergic receptors by ATP stimulates Cl- efflux in biliary epithelial cells. To determine whether purinergic agonists are present under physiological conditions, we have assayed mammalian bile for nucleotides and assessed whether hepatoma and cholangiocarcinoma cell lines are capable of nucleotide release. Bile samples were collected from human, rat, and pig donors and assayed for nucleotide concentrations by luminometry. ATP, ADP, and AMP were present in bile from each species, and the average total nucleotide concentration in human bile was 5.21 +/- 0.91 microM (n = 16). In an in vitro model of HTC rat hepatoma cells or Mz-ChA-1 cholangiocarcinoma cells on a superfused column, nucleotides were present in the effluent from each cell type. Addition of alpha, beta-methyleneadenosine 5'-diphosphate (50 microM) to inhibit 5'-nucleotidase activity increased AMP concentrations two- to threefold. Exposure to forskolin (100 microM) or ionomycin (2 microM) stimulated nucleotide release from cholangiocarcinoma but not hepatoma cells. These studies indicate that adenosine nucleotides are present in bile in concentrations sufficient to activate purinergic receptors. Purinergic receptor activation by local nucleotide release might constitute an autocrine and/or paracrine mechanism for modulation of biliary secretion.


Author(s):  
H. Schmid-Schönbein ◽  
I. Rohling-Winkel ◽  
P. Blasberg ◽  
E. Jüngling ◽  
A. Wehmeyer ◽  
...  

ADP stemning from red blood has been shown to “activate platelets” producing shape change, as well as aggregation and release. However, the mode of release of ADP from intact RBC has never been established. Contrary to popular misconceptions, high shear stresses (τ) prevail during natural hemostatic plug formationin arteries and arterioles. Therefore, we tested ADP-release from RBC subjected for 5-100 msec in tube flow (τ-0-200N/m2) during passage through a hollow fiber (0 400 μm, L = 20 cm) with semipermeable walls (AMICON R). Samples from the fluid layer near the wall were ultrafiltered through it and became accessible for chemical analysis. Concentrations of K+, adenosine nucleotides (HPLC), and Hb (In the supernatant) before and after shear exposure were measured. At T > 50 N/m2T K+, adenosine nue Ieotides, and hemoglobin concentrations rose in the supernatant. Only K+ was higher in the u1 trafiltrate than in the latter, whereas total concentration of adenosine nucleotides were not different and hemoglobin did not permeate. There was no difference between the relative molar concentration of total adenosine nucleotides of hemoglobin, i.e. the nucleotides and hemoglobin content of 10-4 and 10-3 of all RBC were liberated. In the ultrafiltrate (ADP) > 2 χ 10-7 M/L, sufficient to activate platelets in the presence of Ca++.


2019 ◽  
Vol 130 ◽  
pp. 125-138 ◽  
Author(s):  
Karine Minari ◽  
Érika Chang de Azevedo ◽  
Vanessa Thomaz Rodrigues Kiraly ◽  
Fernanda Aparecida Heleno Batista ◽  
Fábio Rogério de Moraes ◽  
...  

2001 ◽  
Vol 276 (19) ◽  
pp. 16379-16390 ◽  
Author(s):  
Lynda A. Sellers ◽  
Joseph Simon ◽  
Tina S. Lundahl ◽  
Diane J. Cousens ◽  
Patrick P. A. Humphrey ◽  
...  

1982 ◽  
Vol 14 (05) ◽  
pp. 233-236 ◽  
Author(s):  
L. Scionti ◽  
A. Puxeddu ◽  
G. Calabrese ◽  
C. Gatteschi ◽  
M. De Angelis ◽  
...  

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