Cyclic GMP formation induced by muscarinic receptors is mediated by nitric oxide synthesis in rat cortical primary cultures

Anna F. Castoldi, Luigi Manzo, Lucio G. Costa

Research output: Contribution to journalArticlepeer-review

Abstract

In rat primary cortical cultures, carbachol caused a time- and concentration-dependent increase in guanosine cyclic 3′,5′-monophosphate (cGMP) levels, which was antagonized by the muscarinic antagonist atropine. Glutamate and sodium nitroprusside also caused large increases in cGMP levels, as previously reported. Two nitric oxide (NO) synthase inhibitors, l-NG-nitroarginine and l-NG-monomethylarginine, were tested for their ability to inihibit the carbachol- and the glutamate-induced cGMP formation. The cGMP response to carbachol was decreased by both compounds in a dose-dependent fashion. The effect of l-NG-nitroarginine was competitively reversed by addition of an excess of l-arginine. Similarly, the stimulatory effect of glutamate on cGMP levels was antagonized by l-NG-nitroarginine and l-NG-monomethylarginine. Hemoglobin, a scavenger of NO, also blocked the carbachol-stimulated cGMP production. These results indicate that muscarinic receptor-stimulated cGMP formation in rat cerebral cortex is mediated by NO.

Original languageEnglish
Pages (from-to)57-61
Number of pages5
JournalBrain Research
Volume610
Issue number1
DOIs
Publication statusPublished - Apr 30 1993

Keywords

  • Carbachol
  • Cortical cell culture
  • Cyclic GMP
  • Muscarinic receptor
  • Nitric oxide
  • Nitric oxide synthase inhibitor

ASJC Scopus subject areas

  • Developmental Biology
  • Molecular Biology
  • Clinical Neurology
  • Neuroscience(all)

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