Broekkamp C L, Phillips A G
Pharmacol Biochem Behav. 1979 Sep;11(3):289-95. doi: 10.1016/0091-3057(79)90137-0.
The intracerebral microinjection technique was used to localize sites in the brain where morphine facilitated the self-stimulation rate at hypothalamic electrode sites. Bilateral injections of morphine (2 x 1 microgram) into the ventral tegmental area and substantia nigra produced the strongest enhancement at the shortest latencies. At these sites, bilateral injections of 200 ng of morphine also produced a significant enhancement whereas a dose of 50 ng was below threshold for the rate increasing effect. The enhancement by morphine was effectively antagonized by naloxone (5 mg/kg). When injected bilaterally into the same area, D-Ala2-Met5-enkephalinamide (2 x 1 microgram) also induced a strong enhancement of self-stimulation lasting for 70 minutes. A possible dopaminergic substrate for the opiate induced behavioral stimulation is discussed.
采用脑内微量注射技术来定位脑内吗啡能促进下丘脑电极部位自我刺激率的位点。向腹侧被盖区和黑质双侧注射吗啡(2×1微克)在最短潜伏期产生最强的增强作用。在这些位点,双侧注射200纳克吗啡也产生显著增强作用,而50纳克的剂量低于增加率效应的阈值。吗啡的增强作用可被纳洛酮(5毫克/千克)有效拮抗。当双侧注射到同一区域时,D-丙氨酸2-甲硫氨酸5-脑啡肽酰胺(2×1微克)也诱导自我刺激强烈增强,持续70分钟。本文讨论了阿片类药物诱导行为刺激的一种可能的多巴胺能底物。