Mutual modulation between norepinephrine and nitric oxide in haemocytes during the mollusc immune response

Sci Rep. 2014 Nov 7:4:6963. doi: 10.1038/srep06963.

Abstract

Nitric oxide (NO) is one of the most important immune molecules in innate immunity of invertebrates, and it can be regulated by norepinephrine in ascidian haemocytes. In the present study, the mutual modulation and underlying mechanism between norepinephrine and NO were explored in haemocytes of the scallop Chlamys farreri. After lipopolysaccharide stimulation, NO production increased to a significant level at 24 h, and norepinephrine concentration rose to remarkable levels at 3 h and 12~48 h. A significant decrease of NO production was observed in the haemocytes concomitantly stimulated with lipopolysaccharide and α-adrenoceptor agonist, while a dramatic increase of NO production was observed in the haemocytes incubated with lipopolysaccharide and β-adrenoceptor agonist. Meanwhile, the concentration of cyclic adenosine monophosphate (cAMP) decreased significantly in the haemocytes treated by lipopolysaccharide and α/β-adrenoceptor agonist, while the content of Ca(2+) was elevated in those triggered by lipopolysaccharide and β-adrenoceptor agonist. When the haemocytes was incubated with NO donor, norepinephrine concentration was significantly enhanced during 1~24 h. Collectively, these results suggested that norepinephrine exerted varied effects on NO production at different immune stages via a novel α/β-adrenoceptor-cAMP/Ca(2+) regulatory pattern, and NO might have a feedback effect on the synthesis of norepinephrine in the scallop haemocytes.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adrenergic alpha-Agonists / pharmacology
  • Adrenergic alpha-Antagonists / pharmacology
  • Adrenergic beta-Agonists / pharmacology
  • Adrenergic beta-Antagonists / pharmacology
  • Animals
  • Calcium / metabolism
  • Cyclic AMP / metabolism
  • Hemocytes / cytology
  • Hemocytes / drug effects
  • Hemocytes / immunology*
  • Hemocytes / metabolism
  • Immunity, Innate
  • Isoproterenol / pharmacology
  • Lipopolysaccharides / pharmacology
  • Nitric Oxide / immunology
  • Nitric Oxide / metabolism*
  • Nitric Oxide Donors / pharmacology
  • Nitroprusside / pharmacology
  • Norepinephrine / immunology
  • Norepinephrine / metabolism*
  • Pectinidae
  • Phenylephrine / pharmacology
  • Prazosin / pharmacology
  • Primary Cell Culture
  • Propranolol / pharmacology
  • Receptors, Adrenergic, alpha / immunology
  • Receptors, Adrenergic, alpha / metabolism*
  • Receptors, Adrenergic, beta / immunology
  • Receptors, Adrenergic, beta / metabolism*

Substances

  • Adrenergic alpha-Agonists
  • Adrenergic alpha-Antagonists
  • Adrenergic beta-Agonists
  • Adrenergic beta-Antagonists
  • Lipopolysaccharides
  • Nitric Oxide Donors
  • Receptors, Adrenergic, alpha
  • Receptors, Adrenergic, beta
  • Nitroprusside
  • Phenylephrine
  • Nitric Oxide
  • Propranolol
  • Cyclic AMP
  • Isoproterenol
  • Calcium
  • Norepinephrine
  • Prazosin