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Medicinas Complementárias
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1.
Eur J Pain ; 16(2): 204-16, 2012 Feb.
Artículo en Inglés | MEDLINE | ID: mdl-22323373

RESUMEN

We have recently demonstrated that gonadal steroid hormones decrease formalin-induced temporomandibular joint nociception in rats. Given that the attenuation of inflammation is a potential mechanism underlying this antinociceptive effect, we evaluated the effect of gonadal steroid hormones on formalin-induced temporomandibular joint inflammation. Plasma extravasation, a major sign of acute inflammation, and neutrophil migration, an important event related to tissue injury, were evaluated. Formalin induced significantly lower temporomandibular joint plasma extravasation and neutrophil migration in proestrus females than in males and in diestrus females. Since estradiol serum level is high in proestrus females and low in diestrus females and in males, these findings suggest that the high physiological level of estradiol decreases temporomandibular joint inflammation. Estradiol but not progesterone administration in ovariectomized females significantly decreased formalin-induced plasma extravasation and neutrophil migration, an effect that was blocked by the estrogen receptor antagonist ICI 182780. Plasma extravasation and neutrophil migration were not affected by orchiectomy, but testosterone or estradiol administration in orchidectomized males significantly decreased them. The androgen receptor antagonist flutamide blocked the anti-inflammatory effect of testosterone while ICI 182780 blocked that of estradiol in males. Previous intravenous administration of a nonspecific selectin inhibitor significantly decreased formalin-induced temporomandibular joint nociception and neutrophil migration in males, revealing a potent and positive correlation between temporomandibular joint nociception and inflammation. Taken together, these findings demonstrate a pronounced anti-inflammatory effect of estradiol and testosterone in the temporomandibular joint region and suggest that this effect may mediate, at least in part, the antinociceptive effect of these hormones.


Asunto(s)
Antiinflamatorios no Esteroideos/farmacología , Artritis/tratamiento farmacológico , Artritis/patología , Hormonas Esteroides Gonadales/farmacología , Trastornos de la Articulación Temporomandibular/tratamiento farmacológico , Trastornos de la Articulación Temporomandibular/patología , Animales , Antiinflamatorios no Esteroideos/uso terapéutico , Artritis/metabolismo , Modelos Animales de Enfermedad , Femenino , Hormonas Esteroides Gonadales/uso terapéutico , Masculino , Ratas , Ratas Wistar , Trastornos de la Articulación Temporomandibular/metabolismo , Resultado del Tratamiento
2.
Brain Res ; 913(1): 90-4, 2001 Sep 14.
Artículo en Inglés | MEDLINE | ID: mdl-11532252

RESUMEN

The injection of the small-fibre excitant and inflammatory irritant mustard oil (MO) into the temporomandibular joint (TMJ) region of rats evokes a sustained and reversible increase in electromyographic (EMG) activity of jaw muscles. The 'rekindling' of this nociceptive reflex by intrathecal (i.t.) administration of the opiate antagonist naloxone and mu but not delta and kappa selective opioid antagonist, suggests that it may be modulated by endogenous opioid inhibitory mechanisms.


Asunto(s)
Músculos Masticadores/efectos de los fármacos , Contracción Muscular/efectos de los fármacos , Inhibición Neural/efectos de los fármacos , Nociceptores/efectos de los fármacos , Receptores Opioides mu/antagonistas & inhibidores , Reflejo/efectos de los fármacos , Articulación Temporomandibular/efectos de los fármacos , Núcleo Caudal del Trigémino/efectos de los fármacos , Animales , Relación Dosis-Respuesta a Droga , Electromiografía , Inflamación/inducido químicamente , Inflamación/metabolismo , Inflamación/fisiopatología , Masculino , Músculos Masticadores/inervación , Músculos Masticadores/fisiología , Contracción Muscular/fisiología , Planta de la Mostaza , Antagonistas de Narcóticos/farmacología , Inhibición Neural/fisiología , Neuronas/citología , Neuronas/efectos de los fármacos , Neuronas/metabolismo , Nociceptores/citología , Nociceptores/metabolismo , Dolor/inducido químicamente , Dolor/metabolismo , Dolor/fisiopatología , Extractos Vegetales/farmacología , Aceites de Plantas , Ratas , Ratas Sprague-Dawley , Receptores Opioides mu/metabolismo , Reflejo/fisiología , Articulación Temporomandibular/inervación , Articulación Temporomandibular/metabolismo , Núcleo Caudal del Trigémino/citología , Núcleo Caudal del Trigémino/metabolismo
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