Ma Q P, Han J S
Department of Physiology, Beijing Medical University, China.
Peptides. 1992 Mar-Apr;13(2):261-5. doi: 10.1016/0196-9781(92)90106-d.
Previous studies from this laboratory suggested that the periaqueductal gray (PAG), nucleus accumbens, and amygdala might take part in a serial, unidirectional mesolimbic loop to play their roles in pain modulation. It has been proposed that morphine injected into one of these nuclei would cause the release of opioid peptides in one nucleus after another. This working hypothesis was examined in the present study by perfusing simultaneously the PAG and the amygdala after microinjection of morphine into the N. accumbens. It was found that microinjection of morphine increased the content of immunoreactive enkephalins (ir-ENK) and immunoreactive beta-endorphin (ir-beta-EP) in the perfusate of the PAG and the amygdala. When the perfusion fluid contained 3 microM of naloxone, the increase of ir-ENK and ir-beta-EP was reduced significantly. These results indicate that the three nuclei were not serially connected in a unidirectional loop.
该实验室之前的研究表明,导水管周围灰质(PAG)、伏隔核和杏仁核可能参与了一个连续的、单向的中脑边缘环路,以在疼痛调节中发挥作用。有人提出,向这些核团之一注射吗啡会导致阿片肽在一个接一个的核团中释放。在本研究中,通过在向伏隔核微量注射吗啡后同时灌注PAG和杏仁核,对这一工作假设进行了检验。结果发现,向伏隔核微量注射吗啡会增加PAG和杏仁核灌流液中免疫反应性脑啡肽(ir-ENK)和免疫反应性β-内啡肽(ir-β-EP)的含量。当灌流液中含有3微摩尔纳洛酮时,ir-ENK和ir-β-EP的增加显著减少。这些结果表明,这三个核团并非以单向环路的形式连续连接。