nalorphine and propargylglycine

nalorphine has been researched along with propargylglycine* in 1 studies

Other Studies

1 other study(ies) available for nalorphine and propargylglycine

Article	Year
The hydra GSH receptor. Pharmacological and radioligand binding studies. Comparative biochemistry and physiology. C, Comparative pharmacology and toxicology, 1987, Volume: 87, Issue:2 1. The GSH-induced feeding response of hydra has been studied using pharmacological and biochemical methods. 2. Dopaminergic agonists inhibit the response, whereas dopaminergic blocking agents increase it. Phosphodiesterase inhibitors completely inhibit the feeding response. 3. The specific binding of the competitive inhibitor of feeding response, [3H]glutamate, to hydra cellular fractions has been evaluated, and a strong GSH-sensitive binding has been observed in a nematocyst-rich fraction. 4. After pharmacological reduction of the nematocyst number, both feeding response and glutamate binding are severely reduced. 5. Ca2+ ions must be present for the feeding response to occur, whereas glutamate binding occurs both without Ca2+ and in the presence of EDTA. Topics: Alkynes; Animals; Calcium; Colchicine; Edetic Acid; Glutamates; Glutamic Acid; Glutathione; Glycine; Hydra; Nalorphine; Naloxone; Pargyline; Phosphodiesterase Inhibitors; Receptors, Cell Surface; Receptors, Peptide	1987

Article

Year

The hydra GSH receptor. Pharmacological and radioligand binding studies.

Comparative biochemistry and physiology. C, Comparative pharmacology and toxicology, 1987, Volume: 87, Issue:2

1. The GSH-induced feeding response of hydra has been studied using pharmacological and biochemical methods. 2. Dopaminergic agonists inhibit the response, whereas dopaminergic blocking agents increase it. Phosphodiesterase inhibitors completely inhibit the feeding response. 3. The specific binding of the competitive inhibitor of feeding response, [3H]glutamate, to hydra cellular fractions has been evaluated, and a strong GSH-sensitive binding has been observed in a nematocyst-rich fraction. 4. After pharmacological reduction of the nematocyst number, both feeding response and glutamate binding are severely reduced. 5. Ca2+ ions must be present for the feeding response to occur, whereas glutamate binding occurs both without Ca2+ and in the presence of EDTA.

Topics: Alkynes; Animals; Calcium; Colchicine; Edetic Acid; Glutamates; Glutamic Acid; Glutathione; Glycine; Hydra; Nalorphine; Naloxone; Pargyline; Phosphodiesterase Inhibitors; Receptors, Cell Surface; Receptors, Peptide

1987