Substance P analogues act as broad-spectrum neuropeptide antagonists

1998 ◽  
Vol 5 (2-3) ◽  
pp. 199-204
Author(s):  
Michael J. Seckl ◽  
Enrique Rozengurt
2000 ◽  
Vol 118 (4) ◽  
pp. A310-A311
Author(s):  
Shuping V. Wu ◽  
Moon Yang ◽  
John H. Walsh ◽  
Enrique Rozengurt

FEBS Letters ◽  
1999 ◽  
Vol 451 (3) ◽  
pp. 231-234 ◽  
Author(s):  
María Teresa Pastor ◽  
Antonio Diez ◽  
Enrique Pérez-Payá ◽  
Concepción Abad

1993 ◽  
Vol 242 (1) ◽  
pp. 47-52 ◽  
Author(s):  
Tsukasa Sakurada ◽  
Kazushige Katsumata ◽  
Yoichi Manome ◽  
Koichi Tan-No ◽  
Shinobu Sakurada ◽  
...  

Peptides ◽  
1988 ◽  
Vol 9 (3) ◽  
pp. 651-660 ◽  
Author(s):  
M. Randic ◽  
S. Jeftinija ◽  
L. Urban ◽  
C. Raspantini ◽  
K. Folkers

1986 ◽  
Vol 65 (12) ◽  
pp. 1427-1431 ◽  
Author(s):  
E. Bobyock ◽  
E.J. Barbieri ◽  
W.S. Chernick

The intra-arterial infusion of substance P produced dose-related responses of both parotid and submandibular salivary secretion in anesthetized rats. The substance P-induced secretion in both glands was inhibited by the substance P analogues [D-Arg 1, D-Trp7,9, Leu11 ]-substance P and [D-Arg1, D-Pro2, D-Trp7,9, Leu11 ]-substance P, but not by [D-Pro2 , D-Trp7,9]-substance P. The profiles of protein and calcium levels obtained with substance P-induced salivary secretion for both glands were similar to those produced by acetylcholine stimulation and were not altered by the substance P analogues.


1985 ◽  
Vol 110 (1) ◽  
pp. 63-69 ◽  
Author(s):  
Réjean Couture ◽  
Kiran Yashpal ◽  
James L. Henry ◽  
Emanuel Escher ◽  
Domenico Regoli

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