Elsevier

Immunopharmacology

Volume 16, Issue 3, November–December 1988, Pages 125-137

Opposite effects of the catecholamines dopamine and norepinephrine on murine polyclonal B-cell activation

https://doi.org/10.1016/0162-3109(88)90001-XGet rights and content

Abstract

The effects of dopamine (DA) and norepinephrine (NE) on polyclonal B-cell activation induced in vitro by lipopolysaccharide (LPS) and on cyclic AMP response in BALB/c mouse lymphocytes were investigated. DA at non-cytotoxic concentrations (5 × 10−5 M and 10−4 M) inhibited, but NE (5 × 10−6 M to 5 × 10−5 M) enhanced LPS-stimulated proliferation and Ig synthesis by lymphocytes from spleen, mesenteric lymph nodes and Peyer's patches. Depletion of adherent cells and T lymphocytes did not prevent the respective effects of DA and NE, and the drug effects were reproduced on nude (nu+nu+)spleen cell proliferation and differentiation stimulated by LPS. The inhibitory effect of DA persisted even if the drug was added as late as 48 h after the mitogen. In contrast, NE was no longer stimulatory if added 2 h later than LPS. The effect of DA was blocked neither by DA1 or DA2 dopaminergic antagonists (SCH 23390 and sulpiride respectively), nor by α-or β-adrenoceptor antagonists (phentolamine and propranolol respectively). Enhancement by NE was antagonized by propranolol, but not by phentolamine. Both DA and NE raised the level of cyclic AMP in unfractionated spleen cells as well as in B-enriched spleen cells but DA was less potent than NE. Pre-incubation of spleen lymphocytes with LPS for 1–24 h did not alter their cyclic AMP response to NE but it prevented the loss of sensitivity to DA after 4 or 24 h of in vitro incubation. The lysosomotropic agent chloroquine induced suppression of LPS-stimulated proliferation and Ig production with a dose-response profile similar to that of DA. Altogether, these results indicate that the catecholamines can exert opposite effects on polyclonal B-cell activation by acting directly on B lymphocytes.

References (35)

  • S Axelsson et al.

    In vitro uptake of L-dopa and catecholamines into the epidermal Langerhans cell

    Acta Dermatovener

    (1978)
  • MA Bach

    Differences in cyclic AMP changes after stimulation by prostaglandins and isoproterenol in lymphocyte subpopulations

    J Clin Invest

    (1975)
  • RG Coffey et al.

    Neurotransmitters, hormones, and cyclic nucleotides in lymphocyte regulation

  • C Corbel et al.

    Requirement for macrophages or for macrophage- or T cell-derived factors in the mitogenic stimulation of murine B lymphocytes by lipopolysaccharides

    Eur J Immunol

    (1983)
  • MM Dale et al.

    A comparison of dimaprit, nordimaprit, methylamine and chloroquine as inhibitors of mitogen-induced lymphocyte activation

    Br J Pharmac

    (1984)
  • H Das et al.

    Molecular mechanism of mitogen action: processing of receptor induced by epidermal growth factor

  • AL DeFranco et al.

    B-lymphocyte signal traduction in response to anti-immunoglobulin and bacterial lipopolysaccharide

    Immunol Rev

    (1987)
  • Cited by (44)

    • Neuronal regulation of B-cell immunity: Anticipatory immune posturing?

      2022, Neuron
      Citation Excerpt :

      In vitro studies of lymphocyte responses to NE and various agonists or antagonists of adrenergic receptors lead to several important observations. First, β2AR stimulation may enhance or inhibit B cell activation and antibody production in vitro, depending on activation states of B cells and other signals they receive (Sanders and Munson, 1984; Kouassi et al., 1988; Holteδ et al., 1988; Gilbert and Hoffmann, 1985). Second, stimulation of βAR, β2AR in particular, inhibits T cell proliferation (Bourne and Melmon, 1971; Bartik et al., 1994; Bauman et al., 1994; Johnson et al., 1981) and modulates cytokine production by T cells (Ramer-Quinn et al., 1997; Sanders et al., 1997; Swanson et al., 2001).

    • B-cell response to seasonal influenza vaccine in mice is amenable to pharmacological modulation through β-adrenoceptor

      2022, Life Sciences
      Citation Excerpt :

      In the same vein are findings indicating that administration of a β2-agonist alone to asthmatics increases the serum level of IgG, but did not affect the serum level of any other Ig isotype [34]. Noradrenaline was also found to exert stimulatory effect on LPS-stimulated Ig synthesis in vitro when added 2 h before LPS, but not when added after LPS [35], suggesting modulatory action of noradrenaline on B-cells at early stages of the antibody response. It was shown that whatever the source of lymphoid cells (spleen, lymph nodes or Peyer's patches) stimulatory influence of noradrenaline on Ig synthesis always paralleled its enhancing effect on B-cell proliferative response [35].

    • Effect of repeated administration of lipopolysaccharide on inflammatory and stress markers in saliva of growing pigs

      2014, Veterinary Journal
      Citation Excerpt :

      An increase in salivary IgA has been reported in pigs as a response to acute stress during restraint (Muneta et al., 2010) and in response to cumulative multitasking stress in humans (Wetherell et al., 2004). Furthermore, studies performed in laboratory rodents have shown that catecholamines can enhance LPS-stimulated proliferation and immunoglobulin synthesis by B lymphocytes (Kouassi et al., 1988), including IgA (Li et al., 1990). Thus an increase in salivary IgA is not only associated with activation of the adaptive immune system, but can also occur non-specifically in response to stress.

    • Sympathetic modulation of immunity: Relevance to disease

      2008, Cellular Immunology
      Citation Excerpt :

      CTL clonal studies indicate that rises in intracellular cAMP can inhibit the TCR-dependent release of granules [219], which may explain β2-AR-mediated inhibition of cytotoxic T cell activity. β2-AR stimulation has been reported to enhance [220] or inhibit LPS-induced B cell proliferation [195,220] and anti-IgG antibody production [166,220]. Similarly, in vitro Th cell-dependent antibody production increases [220,221] or decreases [13,222–225] following β-AR stimulation.

    • The immunopotentiator effects of nefopam

      2007, International Immunopharmacology
    • Innervation of lymphoid organs: Clinical implications

      2006, Clinical Neuroscience Research
    View all citing articles on Scopus
    View full text