Effects of morphine and naloxone on proliferation of lymphocytes in vitro
Abstract
AIM:
To study the effects of morphine on different lymphocytes and the influence of naloxone.
METHODS:
The proliferation rates of unmature, resting, and activated T-lymphocytes and B-lymphocytes were determined under various concentrations of morphine with or without naloxone in vitro.
RESULTS:
Morphine 1 x 10(-10)-1 x 10(-6) mol L-1 enhanced concanavalin A (Con A)-induced splenic T-cell proliferation, and 1 mumol L-1 enhanced lipopolysaccharide (LPS)-induced splenic B-cell proliferation. Naloxone, which per se enhanced the T-cell proliferation, blocked the enhancing effects of morphine. Morphine (1 x 10(-10)-1 x 10(-5) mol L-1) had no influence on the proliferation of resting splenocytes and Con A-induced thymus cells. Morphine 1 mmol L-1 inhibited the proliferation of resting, LPS-induced splenocytes, and Con A-induced splenic and thymus cells. These inhibiting effects were not blocked by naloxone (50 mumol L-1).
CONCLUSION:
Stimulating effect of morphine on activated T- and B-cells were mediated by opioid receptors and different opioid receptors existed during the differentiation and activation of lymphocytes. The inhibitory effects of morphine (1 mmol L-1) were not mediated by opioid receptors.
Keywords:
To study the effects of morphine on different lymphocytes and the influence of naloxone.
METHODS:
The proliferation rates of unmature, resting, and activated T-lymphocytes and B-lymphocytes were determined under various concentrations of morphine with or without naloxone in vitro.
RESULTS:
Morphine 1 x 10(-10)-1 x 10(-6) mol L-1 enhanced concanavalin A (Con A)-induced splenic T-cell proliferation, and 1 mumol L-1 enhanced lipopolysaccharide (LPS)-induced splenic B-cell proliferation. Naloxone, which per se enhanced the T-cell proliferation, blocked the enhancing effects of morphine. Morphine (1 x 10(-10)-1 x 10(-5) mol L-1) had no influence on the proliferation of resting splenocytes and Con A-induced thymus cells. Morphine 1 mmol L-1 inhibited the proliferation of resting, LPS-induced splenocytes, and Con A-induced splenic and thymus cells. These inhibiting effects were not blocked by naloxone (50 mumol L-1).
CONCLUSION:
Stimulating effect of morphine on activated T- and B-cells were mediated by opioid receptors and different opioid receptors existed during the differentiation and activation of lymphocytes. The inhibitory effects of morphine (1 mmol L-1) were not mediated by opioid receptors.