Marshall E F, Milne J, Dodds S M
Department of Psychiatry Research Unit, University of Newcastle upon Tyne, UK.
Neuroreport. 1992 Nov;3(11):1009-12. doi: 10.1097/00001756-199211000-00016.
Head-twitch response and phosphatidylinositol (PIP) hydrolysis in cortex and spinal cord were measured after single or chronic (21 days) administration of paroxetine to normal mice or to mice neonatally treated with 5,7-dihydroxytryptamine, a serotonergic neurotoxin. In normal animals, a down-regulation of 5-HT-receptor numbers after chronic paroxetine was suggested by the attenuation of head-twitch responses compared with a single dose. There was a concomitant decrease in PIP hydrolysis. In DHT-treated animals, although changes in behavioural responses were comparable to those in normals, PIP hydrolysis in cortex and spinal cord after chronic paroxetine increased significantly. These results demonstrate that head-twitch responses and PIP hydrolysis may not be mediated by the same receptor and that the effects of chronic administration of paroxetine depend on the functional state of the serotonergic pathways.
在正常小鼠或新生期用5,7-二羟色胺(一种血清素能神经毒素)处理的小鼠单次或长期(21天)给予帕罗西汀后,测量其头部抽搐反应以及皮质和脊髓中的磷脂酰肌醇(PIP)水解情况。在正常动物中,与单次给药相比,长期给予帕罗西汀后头部抽搐反应减弱,提示5-羟色胺受体数量下调。同时PIP水解减少。在经DHT处理的动物中,虽然行为反应的变化与正常动物相当,但长期给予帕罗西汀后皮质和脊髓中的PIP水解显著增加。这些结果表明,头部抽搐反应和PIP水解可能不是由同一受体介导的,并且长期给予帕罗西汀的作用取决于血清素能通路的功能状态。