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G F Draetta

Publications and source records attributed to G F Draetta.

22 records · Page 2Linked to original sources

Do porins inhibit the macrophage phagocyting activity by stimulating the adenylate cyclase?

Porins interact with macrophage membranes and inhibit their phagocyting activity. We have tested the porin effect on a biologically relevant membrane-bound enzymic activity, the adenylate cyclase system, which appears to be stimulated both in the presence of Mn2+ and Mg2+ or Mg2+ + Gpp(NH)p. Moreover, for mice macrophages incubated in the presence of porins, there is an increase in the intracellular cAMP content after 5 min of incubation, with a maximum after 15 min of incubation. The results shown suggest that the porin effects on the adenylate cyclase can represent the molecular basis of the porin-dependent inhibition of the macrophages phagocytosis. Our point of view, which proposes a cAMP role in inhibiting the phagocyting activity in macrophages, is supported also by the results of the experiments carried out in the presence of both dibutyryl-cAMP or aminophylline. The phagocyting activity is inhibited in all cases and independently of the bacteria to be phagocyted.

Adenylyl Cyclases↗

The effects of lidocaine and procainamide on the sarcolemmal membrane high affinity cyclic AMP phosphodiesterase of rat myocardium.

The incubation of rat myocardial sarcolemmal membranes with 10(-4)M lidocaine or procainamide results in a decreased fluorescence polarization of the extrinsic probes (diphenylhexatriene and 12-anthroylstearate) and in the stimulation of the membrane-bound high affinity cyclic AMP phosphodiesterase activity (PDE). Lidocaine or procainamide do not contrast, but facilitate the aminophylline inhibitory action on the PDE activity, without modifying the basic molecular mechanism of the inhibitory action. The amplitudes of the effects described are inversely correlated to the temperature, being greater at the lower tested temperature (25 degrees greater than 30 degrees greater than 37 degrees C).

3',5'-Cyclic-AMP Phosphodiesterases↗

Relationship between the fluidity of the membrane lipids and the activity of the membrane-bound proteins: the effects of lidocaine on the adenylate cyclase activity of rat myocardium.

The lidocaine effects on the basal adenylate cyclase activity of the studied membranes depend on the substrate concentration: the drug has an inhibiting effect on non-saturating ATP concentrations, but displays a stimulating effect on the saturating ones. In the presence of maximally stimulating NaF concentrations, lidocaine further stimulates the adenylate cyclase activity through all the ATP concentrations used. In the presence of ATP saturating concentrations, the adenylate cyclase activity stimulated by various Gpp(NH)p concentrations, is inhibited in the presence of lidocaine as well as the enzymic activity stimulated by several l-isoproterenol concentrations in the presence of a fixed Gpp(NH)p concentration.

Adenylyl Cyclases↗