A-18-Famide and F-8-Famide, endogenous mammalian equivalents of the molluscan neuropeptide FMRFamide (Phe-Met-Arg-Phe-NH2), inhibit colonic bead expulsion time in mice
- 1 July 1989
- Vol. 10 (4) , 873-875
- https://doi.org/10.1016/0196-9781(89)90127-7
Abstract
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This publication has 14 references indexed in Scilit:
- Supraspinal FMRFamide antagonizes morphine-induced horizontal, but not vertical, locomotor activityPeptides, 1989
- The action of FMRFamide (Phe-Met-Arg-Phe-NH2) and related peptides on mammalsPeptides, 1988
- The effect of Phe-Met-Arg-Phe-NH2 (FMRFamide) on morphine-induced inhibition of colonic propulsive motility in miceNeuroscience Letters, 1987
- Calcium channel blockers inhibit the antagonistic effects of PheMetArgPhe-amide (FMRFamide) on morphine- and stress-induced analgesia in miceBrain Research, 1987
- C57BL/6J-bg J (beige) mice: Differential sensitivity in the tail flick test to centrally administered MU- and delta-opioid receptor agonistsLife Sciences, 1987
- Interactions of Tyr-MIF-1 at opiate receptor sitesPharmacology Biochemistry and Behavior, 1986
- Low affinity inhibition of opioid receptor binding by FMRFamideNeuropeptides, 1986
- FMRFamide, a putative endogenous opiate antagonist: Evidence from suppression of defeat-induced analgesia and feeding in miceNeuropeptides, 1985
- Inhibitory Influences of FMRFamide on Morphine- and Deprivation-Induced FeedingNeuroendocrinology, 1985
- Structure of a Molluscan Cardioexcitatory NeuropeptideScience, 1977