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      Constitutive nitric oxide synthase-mediated caspase-3 S-nitrosylation in ghrelin protection against Porphyromonas gingivalis-induced salivary gland acinar cell apoptosis.

      Inflammopharmacology
      Amidines, pharmacology, Animals, Apoptosis, drug effects, Ascorbic Acid, Benzylamines, Caspase 3, metabolism, Cells, Cultured, Cysteine, analogs & derivatives, Enzyme Inhibitors, Ghrelin, Inositol Phosphates, Lipopolysaccharides, NG-Nitroarginine Methyl Ester, Nitric Oxide Synthase, antagonists & inhibitors, Nitric Oxide Synthase Type II, Phosphorylation, Porphyromonas gingivalis, chemistry, Protein Kinase Inhibitors, Proto-Oncogene Proteins c-akt, Pyrimidines, Rats, Rats, Inbred Strains, S-Nitrosothiols, Sublingual Gland, cytology, src-Family Kinases

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          Abstract

          Recent advances in identifying the salivary constituents capable of influencing the oral mucosal inflammatory responses have brought to focus the importance of a peptide hormone, ghrelin. Here, we report on the involvement of ghrelin in controlling the apoptotic processes induced in sublingual salivary gland acinar cells by the lipopolysaccharide (LPS) of a periodontopathic bacterium, Porphyromonas gingivalis. We show that the countering effect of ghrelin on the LPS-induced acinar cell apoptosis was associated with the increase in constitutive nitric oxide synthase (cNOS) activity, and the reduction in caspase-3 and inducible nitric oxide synthase (iNOS). The loss in countering effect of ghrelin on the LPS-induced changes in apoptosis and caspase-3 activity was attained with Src kinase inhibitor, PP2, as well as Akt inhibitor, SH-5, and cNOS inhibitor, L-NAME, but not the iNOS inhibitor, 1400W. The effect of ghrelin on the LPS-induced changes in cNOS activity, moreover, was reflected in the increased cNOS phosphorylation that was sensitive to PP2 as well as SH-5. Furthermore, the ghrelin-induced up-regulation in cNOS activity was associated with the increase in caspase-3 S-nitrosylation that was susceptible to the blockage by SH-5 and L-NAME. The findings point to the involvement of ghrelin in Src/Akt kinase-mediated cNOS activation and the apoptogenic signal inhibition through the NO-induced caspase-3 S-nitrosylation.

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