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Noradrenaline and its end metabolite 3-methoxy-4-hydroxyphenylglycol inhibit lymphocyte chemotaxis: Role of alpha- and beta-adrenoreceptors

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Abstract

The capacity of noradrenaline (NA) and its end metabolite 3-methoxy-4-hydroxyphenylglycol (MHPG) to modulate the chemotaxis of lymphocytes from a primary immunocompetent organ (thymus) and a secondary one (spleen) was investigated over a range of concentrations from 10−12 M to 10−5 M. Lymphocyte chemotaxis was evaluated in a Boyden chamber. The results indicated that 10−5 M of NA inhibits the chemotaxis of lymphocytes from both the immunocompetent organs studied, and that this effect is blocked by either propranolol (10−6 M) or phentolamine (10−5 M). Similarly, 10−5 M of MHPG induced a decrease in the chemotaxis capacity of the lymphocytes. In conclusion, high physiological concentrations of NA and its end metabolite modulate the mobility of lymphocytes, and the participation of both alpha and beta adrenoreceptors is necessary, showing a new aspect of neuroimmune interactions.

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José García, J., del Carmen Sáez, M., de la Fuente, M. et al. Noradrenaline and its end metabolite 3-methoxy-4-hydroxyphenylglycol inhibit lymphocyte chemotaxis: Role of alpha- and beta-adrenoreceptors. Mol Cell Biochem 254, 305–309 (2003). https://doi.org/10.1023/A:1027349904589

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  • DOI: https://doi.org/10.1023/A:1027349904589

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