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1.
Neuroimmunomodulation ; 9(1): 23-33, 2001.
Artículo en Inglés | MEDLINE | ID: mdl-11435749

RESUMEN

OBJECTIVE: Dopamine, a catecholamine neurotransmitter, influences growth and proliferation of lymphocytes. Pharmacological doses of dopamine have been shown to modulate T cell functions significantly, but no information is available on the effect of physiological concentrations of circulating dopamine on CD4+ and CD8+ T cell functions. This information may be of importance since significantly elevated plasma dopamine levels were observed in humans during uncoping stress, and suppression of T cell functions during stress is a well-known phenomenon. However, the mechanism inducing the suppression of T cell functions during stress is not yet clear. In the present investigation, we evaluated the effect of the dopamine level attained in the plasma of individuals with uncoping stress on the proliferation and cytotoxicity of CD4+ and CD8+ T cells in vitro. METHODS: T cell subpopulations were separated by panning. The effect of dopamine on IL-2-induced cell proliferation in vitro was evaluated by [3H]thymidine incorporation and cytotoxicity by 51Cr release, receptors by radioligand binding, cAMP by an assay kit and apoptosis by DNA fragmentation. RESULTS: At these elevated physiological concentrations, dopamine was found to inhibit significantly the proliferation and cytotoxicity of CD4+ and CD8+ T cells in vitro. This dopamine-mediated inhibition of proliferation was more marked on CD8+ T cells than on CD4+ T cells. The underlying mechanism was found to be D1 class of dopamine-receptor-mediated stimulation of intracellular cAMP. CONCLUSION: Results may be of significance to understand the role of peripheral dopamine in human neuroimmune communication in terms of physiological homeostasis in health and disease.


Asunto(s)
Adenina/análogos & derivados , Linfocitos T CD4-Positivos/efectos de los fármacos , Linfocitos T CD8-positivos/efectos de los fármacos , Dopamina/farmacología , Inmunidad Celular/efectos de los fármacos , Neoplasias de la Boca/inmunología , Neuroinmunomodulación/fisiología , Receptores Dopaminérgicos/fisiología , Estrés Psicológico/inmunología , 3',5'-AMP Cíclico Fosfodiesterasas/antagonistas & inhibidores , Adenina/farmacología , Inhibidores de Adenilato Ciclasa , Adulto , Bucladesina/farmacología , Linfocitos T CD4-Positivos/inmunología , Linfocitos T CD4-Positivos/metabolismo , Linfocitos T CD8-positivos/inmunología , Linfocitos T CD8-positivos/metabolismo , División Celular/efectos de los fármacos , Células Cultivadas/efectos de los fármacos , AMP Cíclico/agonistas , AMP Cíclico/fisiología , Citotoxicidad Inmunológica/efectos de los fármacos , Dopamina/administración & dosificación , Relación Dosis-Respuesta a Droga , Inhibidores Enzimáticos/farmacología , Femenino , Humanos , Interferón gamma/metabolismo , Interleucina-2/metabolismo , Activación de Linfocitos/efectos de los fármacos , Masculino , Persona de Mediana Edad , Neoplasias de la Boca/sangre , Neoplasias de la Boca/complicaciones , Neoplasias de la Boca/psicología , Psiconeuroinmunología , Receptores Dopaminérgicos/efectos de los fármacos , Sistemas de Mensajero Secundario/efectos de los fármacos , Estrés Psicológico/sangre , Estrés Psicológico/etiología , Teofilina/farmacología
2.
Neoplasma ; 39(3): 163-5, 1992.
Artículo en Inglés | MEDLINE | ID: mdl-1528321

RESUMEN

Brain catecholamines (CA) were studied in discrete brain areas of benzo(a)pyrene (b(a)p) induced fibrosarcoma bearing mice. Dopamine (DA) and norepinephrine (NE) levels decreased significantly in different brain areas especially in corpus striatum and hypothalamus with the tumor progression, indicating an inverse relationship between brain DA and NE levels and tumor growth. Since impaired hormonal and immunological functions are manifestation of systemic alteration during tumor growth, it appears that during malignant growth an alteration of these brain CA may play an important role in the regulation of systemic alterations.


Asunto(s)
Benzo(a)pireno , Encéfalo/metabolismo , Catecolaminas/metabolismo , Transformación Celular Neoplásica/metabolismo , Fibrosarcoma/metabolismo , Neoplasias Experimentales/metabolismo , Animales , División Celular/fisiología , Transformación Celular Neoplásica/inducido químicamente , Cuerpo Estriado/metabolismo , Dopamina/metabolismo , Epinefrina/metabolismo , Fibrosarcoma/inducido químicamente , Hipotálamo/metabolismo , Masculino , Ratones , Ratones Endogámicos A , Neoplasias Experimentales/inducido químicamente , Norepinefrina/metabolismo
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