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. 2000 Dec 19;97(26):14692–14696. doi: 10.1073/pnas.97.26.14692

Table 1.

Pharmacology of opioid receptor subtype for 130 pS channel activation

Drugs tested Cells tested Cells with channel (%)
Endomorphin-1 (0.5 μM) 51 25 (49)
Endomorphin-1 (0.5 μM) + CTOP (0.1 μM) 42 3 (7)*
Endomorphin-1 (0.5 μM) + ICI-174864 (0.5 μM) 20 10 (50)
Endomorphin-1 (0.5 μM) + nor-binaltorphimine (0.1 μM) 21 10 (48)
DPDPEV (1 μM) 16 1 (6)
U-50,488 (5 μM) 19 0 (0)

CTOP, d-phe-cys-tyr-d-trp-orn-thr-pen-thr-NH2; DPDPE, [d-pen2, d-pen5]-enkephalin. Pen, penicillamine; Orn, ornithine. 

*

P < 0.001 vs. endomorphin-1 alone.