scholarly journals A synthetic peptide derivative that is a cholecystokinin receptor antagonist.

1987 ◽  
Vol 262 (15) ◽  
pp. 7226-7231 ◽  
Author(s):  
M F Lignon ◽  
M C Galas ◽  
M Rodriguez ◽  
J Laur ◽  
A Aumelas ◽  
...  
1992 ◽  
Vol 102 (5) ◽  
pp. 1742-1751 ◽  
Author(s):  
Per Cantor ◽  
Poul Erik Mortensen ◽  
John Myhre ◽  
Ida Gjorup ◽  
Helge Worning ◽  
...  

1989 ◽  
Vol 96 (4) ◽  
pp. 1158-1164 ◽  
Author(s):  
Guido Adler ◽  
Max Reinshagen ◽  
Irmtraut Koop ◽  
Burkhard Göke ◽  
Anton Schafmayer ◽  
...  

Pancreas ◽  
2014 ◽  
Vol 43 (7) ◽  
pp. 1050-1059 ◽  
Author(s):  
Jill P. Smith ◽  
Timothy K. Cooper ◽  
Christopher O. McGovern ◽  
Evan L. Gilius ◽  
Qing Zhong ◽  
...  

1993 ◽  
Vol 85 (3) ◽  
pp. 277-280 ◽  
Author(s):  
R. J. Lieverse ◽  
J. B. M. J. Jansen ◽  
A. A. M. Masclee ◽  
C. B. H. W. Lamers

1. A double-blind study was undertaken to determine whether the infusion of bombesin inhibits the intake of a carbohydrate-rich meal, consumed 15 min after a 300 ml banana shake, in nine lean healthy subjects and whether the possible inhibition of food intake by bombesin is mediated by cholecystokinin. 2. The amount of food eaten during infusion of bombesin (267 ±60 g) and bombesin combined with the cholecystokinin-receptor antagonist loxiglumide (269±39g) was slightly (P = 0.09) less than during saline infusion (384 ± 40 g). In addition, preprandial feelings of hunger were significantly less during infusion of both bombesin and bombesin combined with loxiglumide. 3. In conclusion, infusion of bombesin tends to inhibit the intake of a carbohydrate-rich meal after a preload by a cholecystokinin-independent mechanism.


1989 ◽  
Vol 257 (1) ◽  
pp. H107-H112
Author(s):  
R. E. Crowell ◽  
D. E. Van Epps ◽  
W. P. Reed

The chemoattractant formyl-methionine-leucine-phenylalanine (FMLP) has recently been shown to possess spasmogenic properties in smooth muscle preparations from various organs. In this study we have investigated the actions of this peptide on isolated rabbit pulmonary artery (PA) ring segments. FMLP stimulated concentration-dependent constriction of PA at resting tension. However, in PA that had been preconstricted by norepinephrine, FMLP stimulated concentration-dependent relaxation. FMLP-stimulated PA constriction was inhibited by earlier exposure to indomethacin or to furegrelate, a thromboxane synthetase inhibitor, but not by earlier exposure to the H1 histamine receptor antagonist pyrilamine. FMLP-stimulated relaxation of PA was totally abolished by indomethacin but not by furegrelate or pyrilamine. Disruption of the endothelium in PA preparations decreased both the constriction and relaxation response to the peptide, suggesting that these cells were involved in these responses. These results indicate that the chemotactic factor FMLP can elicit constriction or relaxation of isolated PA, depending on the underlying active PA tension. In addition, both constriction and relaxation are dependent on cyclooxygenase products and intact endothelium.


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