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The mechanisms underlying tolerance and dependence arising from chronicopioid exposure are poorly understood. However, the development of neuroblastomaand neurohybrid cell cultures has provided a simplified model for the study ofopioid receptor adaptation. Using neuroblastoma NG108-15 cells, we have disco-vered that the up-regulation of σ-opioid receptor sites induced by opioid anta-gonists, naltrexone, naloxone and ICI 174864 is preceded by a transient loss ofreceptor sites. This receptor down-regulation was time- and temperature-
The mechanisms underlying tolerance and dependence arising from chronic opioid exposure are poorly understood. However, the development of neuroblastoma and neurohybrid cell cultures has provided a simplified model for the study of opioid receptor adaptation. Using neuroblastoma NG108-15 cells, we have disco-vered that the up -regulation of σ-opioid receptor sites induced by opioid anta-gonists, naltrexone, naloxone and ICI 174864 is preceded by a transient loss of receptor sites. This receptor down-regulation was time- and temperature-