The increase of phospholipase C activity induced by orotic acid is unrelated to lipid peroxidation.

Liver phospholipase-C (PL-C) activity proved to be promptly modified in rats fed with an orotic acid (OA) supplemented diet; an increased of PL-C basal activity was demonstrated after 2 days of diet. In the present work the possible involvement of lipid peroxidation was investigated, since 4-hydroxynonenal (HNE) and 4-hydroxyoctenal (HOE), two end-products of lipid peroxidation, have been shown to induce a strong stimulation of hepatic PL-C. Membrane-bound PL-C activity was evaluated together with the rate of TBArs production by liver homogenates obtained from rats fed with a diet containing 1% OA for 2 and 5 days. PL-C activity was measured by following the rate of formation of Ins-P3 from labelled PtdIns-P2 added to isolated liver membranes. TBArs production was unchanged in the livers of rats fed the OA diet, while basal and GTPgammaS-stimulated PL-C activity increased; furthermore PL-C stimulation by bombesin was deeply impaired by OA.

Early changes of liver phospholipase C activity in rats fed an orotic acid supplemented diet.

In this study of the effect of an orotic-acid (O.A.) diet on the activity of membrane-bound phosphoinositide-specific phospholipase C (PL-C) of rat liver, its enzymatic activity was evaluated in vitro on membranes obtained from the hepatic tissue of male Wistar rats fed a diet containing 1% O.A. for 2 and 5 days and from control rats. The rate of breakdown of labelled phosphatidylinositol-4,5-bisphosphate (Ptdins-P2) added to the isolated membranes was measured both in the absence and in the presence of guanosine-5'-O-thiotriphosphate (GTP gamma S). The enzyme stimulation by bombesin was also analysed. PL-C activity proved to be deeply and early modified by O.A. The basal activity was increased 2 days after feeding on the O.A.-supplemented diet, but the difference from control rats was no more significant after 5 days of this diet. The most interesting changes concerned the response to bombesin; the hormone failed to induce any stimulation of PL-C in O.A.-treated rats after either 2 or 5 days of diet, whereas it nearly doubled Ptdins-P2 breakdown in the liver membranes from control rats. The lack of any stimulation of the phospholipase C by bombesin in O.A.-treated rats indicates a deep impairment of this signal transmission system; its possible causes and consequences are discussed.

Activation of phosphoinositide-specific phospholipase C of rat neutrophils by the chemotactic aldehydes 4-hydroxy-2,3-trans-nonenal and 4-hydroxy-2,3-trans-octenal.

A comparison has been made between the effects of 4-hydroxy-2,3-trans-nonenal (HNE) and 4-hydroxy-2,3-trans-octenal (HOE), two lipid peroxidation products, on the basal and GTPgammaS-stimulated activities of phosphoinositide-specific phospholipase C (PL-C) of rat polymorphonuclear leukocytes. PL-C activity was determined in vitro by measuring the hydrolysis of [3H] phosphatidylinositol-4,5-bis- phosphate (PtdIns-P2) added as exogenous substrate to neutrophil plasma membranes. PL-C was activated by concentrations of HNE ranging from 10(-8) to 10(-6) M both in the presence and in the absence of 2 x 10(-5) M GTPgammaS; HOE stimulated the enzymatic activity between 10(-11) and 10(-8) M; maximal stimulation was given by 10(-11) M HOE plus GTPgammaS. The aldehyde concentrations able to accelerate PtdIns-P2 breakdown displayed a good correspondence with those which have been reported to stimulate the oriented migration of rat neutrophils. Pretreatment of neutrophils with pertussis toxin prevented the stimulation of PL-C by 10(-11) M HOE and by HOE plus GTPgammaS. Our results suggest that the chemotactic action of HNE and HOE might depend on the activation of PL-C; furthermore a regulatory G protein appears to be involved in the acceleration of PtdIns-P2 turnover by HOE.

Effect of 4-hydroxy-2,3-trans-nonenal and related aldehydes on phospholipase C activity of rat neutrophils.

Our work has evaluated the effects of certain lipid peroxidation products, i.e. 4-hydroxy-2,3-trans-nonenal (HNE), 4-hydroxy-2,3-trans-octenal (HOE), 2-trans-nonenal and nonanal, on phosphoinositide-specific phospholipase C (PL-C). The enzymatic activity has been determined in vitro by measuring the hydrolysis of labelled phosphatidylinositol-4,5-bisphosphate added to plasma membranes isolated from rat neutrophils. Concentrations of HNE between 10(-8) and 10(-6) M, and concentrations of HOE ranging from 10(-11) to 10(-8) M, were able to activate PL-C. Neither 2-trans-nonenal nor nonanal induced any change of PL-C activity. HNE, HOE and 2-nonenal, but not nonanal, have been shown to possess chemotactic properties towards rat neutrophils. The good correlation between the concentrations of HNE and HOE active on PL-C and those able to stimulate cell migration suggests that their chemotactic activity might be mediated by the activation of PL-C, as in the case of most chemoattractants. On the contrary, this mechanism of action cannot be applied to 2-nonenal, an aldehyde much more hydrophobic than HNE or HOE; its chemotactic activity might be the consequence of some perturbation of the lipidic environment of the cell membrane where it dissolves easily.

Experimental studies on the mechanism of action of 4-hydroxy-2,3-trans-nonenal, a lipid peroxidation product displaying chemotactic activity toward rat neutrophils.

The effects of 4-hydroxy-2,3-trans-nonenal (HNE) and nonanal on the activity of phosphoinositide-specific phospholipase C of rat neutrophils have been studied in parallel with their action on neutrophil oriented migration. Concentrations of HNE ranging from 10(-7) to 10(-5) M significantly stimulated the oriented migration of rat polymorphonuclear leukocytes. HNE stimulated both the basal and GTP gamma S-induced phospholipase C activity when used at concentrations between 10(-8) and 10(-6) M. Nonanal was devoid both of chemotactic activity and of any action on phospholipase C activity. The effect of GTP gamma S on the stimulation of phospholipase C induced by HNE was higher when the lowest dose of the aldehyde was used; the finding of an additive effect between 10(-8) M HNE and 2 x 10(-5) M GTP gamma S suggests that the two compounds may share a final common pathway of action. These results suggest that the chemotactic activity of HNE might be mediated, like that of other more well-known chemoattractants, by the stimulation of phosphoinositide-specific phospholipase C.

Influence of 4-hydroxynonenal on bombesin-induced stimulation of phospholipase C activity in rat liver.

The influence of 4-hydroxynonenal (HNE) on bombesin-induced PIP2-phospholipase C activity (PL-C) was studied in vitro on isolated liver membranes. Both bombesin and HNE stimulated the enzymatic activity at micromolar concentrations and their effect was enhanced by the nucleotide GTPgammaS. An additive synergism was observed with 1 microM bombesin and 0.1 microM HNE. When GTPgammaS was added to the reaction mixture, the degree of PL-C stimulation in the presence of both compounds was not different from the activity value induced by bombesin alone. Since such micromolar amounts of HNE can be actually found in normal liver cells, these results support the hypothesis of a physiological importance of lipid peroxidation in the regulation of phospholipase-C activity.

Effect of 4-hydroxylalkenals on hepatic phosphatidylinositol-4,5-bisphosphate-phospholipase C.

The effects of some 4-hydroxyalkenals, carbonylic products of lipid peroxidation, on hepatic phosphatidylinositol-4,5-bisphosphate (PIP2)-phospholipase C (PL-C) activity were investigated. The enzymatic activity was assayed in vitro by measuring the hydrolysis of [3H]PIP2 added as exogenous substrate to liver membranes. 4-Hydroxyhexenal (HEE), 4-hydroxyoctenal (HOE) and 4-hydroxynonenal (HNE) were able to stimulate both the basal and the GTPgammaS induced PL-C activity, whereas 4-hydroxyundecenal was inactive. HOE was the most active compound, being able to accelerate PIP2 breakdown at concentrations between 10(-12) and 10(-6) M, while in the case of HEE the effective doses ranged from 10(-11) to 10(-7) M and from 10(-9) to 10(-6) M in the case of HNE. 4-Hydroxynonenal was able to increase also bombesin stimulated PL-C activity. As these aldehydes accelerated PIP2 breakdown at doses which can be actually reached in tissues, the effects shown in vitro are likely to occur in vivo.

[Influence of reduced glutathione on changes in the activity of phospholipase C induced by 4-hydroxynonenal]. / Influenza del glutatione ridotto sulle modificazioni dell'attività della fosfolipasi C indotte dal 4-idrossinonenale.

4-Hydroxynonenal (HNE) is a major end-product of lipid peroxidation. 1 mM HNE inhibits the activity of liver phospholipase C (PL-C) and this effect is prevented by 1 mM GSH; on the contrary GSH is unable to counteract the stimulation of PL-C induced by a low concentration of HNE (100 nM). Other hydroxyalkenals are able to stimulate PL-C at low doses (micromolar or less), the most effective being 4-hydroxyoctenal which acts at picomolar doses. The lack of a correlation between the chain length of the aldehydes used and the degree of PL-C stimulation seems to exclude the possibility that their effect could be due to an aspecific solvent action toward the phosphatidylinositol-4,5-diphosphate used as substrate for the enzymatic assay.