Table 1

Oxo-M inhibition of agonist-stimulated cAMP accumulation

AgonistFold Stimulation1-aTotal Inhibition1-bInhibition of Agonist-Simulated1-b
Control+1 μM Oxo-M
% %
Forskolin (10 μM)14.93  ± 3.144.79  ± 1.0467.1  ± 3.0670
Isoproterenol (1 μM)2.51  ± 0.251.59  ± 0.0832.8  ± 4.5738
PGE1 (10 μM)2.27  ± 0.151.66  ± 0.0826.5  ± 2.3720
PGE2(10 μM)2.28  ± 0.281.56  ± 0.0729.4  ± 6.8529
Dopamine (10 μM)1.42  ± 0.200.96  ± 0.0729.9  ± 5.2426
Cicaprost (0.8 μM)2.45  ± 0.252.03  ± 0.2317.0  ± 3.085
PGI2(10 μM)1.52  ± 0.121.35  ± 0.2112.4  ± 7.1201-c
5-HT (10 μM)1.43  ± 0.200.98  ± 0.0925.0  ± 3.0623
5-MT (10 μM)1.25  ± 0.050.92  ± 0.1126.5  ± 7.9901-c
Dimaprit (10 μM)1.32  ± 0.121.04  ± 0.1721.7  ± 6.9201-c
VIP (10 μM)1.33  ± 0.160.85  ± 0.0633.0  ± 9.0639
SKF-38393 (10 μM)1.08  ± 0.050.86  ± 0.03
2-Chloroadenosine (10 μM)1.09  ± 0.070.92  ± 0.03
CGS-21680 (10 μM)1.12  ± 0.030.81  ± 0.05
PGD2 1-d (10 μM)1.08  ± 0.061.00  ± 0.07
Secretin (10 μM)0.93  ± 0.030.93  ± 0.01
Vasopressin (10 μM)0.97  ± 00.97  ± 0.01
  • 1-a Fold stimulation over basal, mean ± S.E.M. of 3 to 12 experiments.

  • 1-b Inhibition expressed only for agents that elicited significant stimulation.

  • 1-c Negative percent effect.

  • 1-d PGD2, prostaglandin D2.