Endomorphin 1 and 2, the endogenous ligands for the μ receptor, decrease cardiac output and total peripheral resistance in the rat
Champion, H. C.; Zadina, J. E.; Kastin, A. J.; Kadowitz, P. J. Endomorphin 1 and 2, the endogenous ligands for the μ receptor, decrease cardiac output and total peripheral resistance in the rat. Peptides. 18:1393-1397; 1997.
Endomorphin 1.; 2, the endogenous μ-opioid agonists, have novel hypotensive activity in the rabbit
Champion, H. C.; Zadina, J. E.; Kastin, A. J.; Hackler L.; Ge, L-J.; Kadowitz, P. J. Endomorphin 1.; 2, the endogenous μ-opioid agonists, have novel hypotensive activity in the rabbit. Biochem. Biophys. Res. Commun. 235:567-570; 1997.
Endomorphin 1 and 2, the endogenous μ-opioid agonists, possess hypotensive activity in the rat
Czapla, M. A.; Champion, H. C.; Zadina, J. E.; Kastin, A. J.; Hackler, L.; Ge, L-J.; Kadowitz, P. J. Endomorphin 1 and 2, the endogenous μ-opioid agonists, possess hypotensive activity in the rat. Life Sci. 62:PL175-PL179; 1998.
Role of endogenous opioids in central cardiovascular regulation and dysregulation
Herz, A.; Akil, H.; Simon, E. J., eds. Berlin: Springer-Verlag
Faden, A. I. Role of endogenous opioids in central cardiovascular regulation and dysregulation. In: Herz, A.; Akil, H.; Simon, E. J., eds. Handbook of experimental pharmacology. Berlin: Springer-Verlag; 1993:191-204.
Isolation of relatively large amounts of endomorphin-1 and endomorphin-2 from human brain cortex
Hackler, L.; Zadina, J. E.; Ge, L-J.; Kastin, A. J. Isolation of relatively large amounts of endomorphin-1 and endomorphin-2 from human brain cortex. Peptides. 18:1635-1638; 1997.
The cardiovascular actions of morphine and the endogenous opioid peptides
Johnson, M. W.; Mitch, W. E.; Wilcox, C. S. The cardiovascular actions of morphine and the endogenous opioid peptides. Prog. Cardiovasc. Dis. 27:435-450; 1985.
A potent and selective endogenous agonist for the mu-opiate receptor
Zadina, J. E.; Hackler, L.; Ge, L-J.; Kastin, A. J. A potent and selective endogenous agonist for the mu-opiate receptor. Nature (London). 386:499-502; 1997.