Heym J, Gladfelter W E
Brain Res Bull. 1982 Feb;8(2):131-7. doi: 10.1016/0361-9230(82)90039-9.
Uptake of tritiated serotonin by synaptosomes prepared from rat lateral hypothalamus was examined. Uptake of serotonin into lateral hypothalamic synaptosomes occurred by both saturable and non-saturable processes. The saturable process was a high affinity transport with kinetic parameters that agree closely with those previously reported for serotonin uptake into synaptosomes prepared from other brain regions. Fluoxetine, a selective inhibitor of uptake into serotonergic neurons, was a potent inhibitor of serotonin uptake into lateral hypothalamic synaptosomes. Desipramine and benztropine, noradrenergic and dopaminergic uptake inhibitors respectively, were much less effective. Damage to the ascending serotonergic system, by either electrolytic lesion of the dorsal or median raphe nucleus, or by 5,7 dihydroxytryptamine injections into the midbrain serotonergic pathways, significantly reduced the uptake of serotonin by lateral hypothalamic synaptosomes. Taken together, these data provide further evidence for a serotonergic terminal field within the lateral hypothalamus.
对从大鼠外侧下丘脑制备的突触体摄取氚标记血清素的情况进行了检测。血清素摄取到外侧下丘脑突触体的过程包括可饱和和不可饱和两种机制。可饱和机制是一种高亲和力转运,其动力学参数与先前报道的血清素摄取到从其他脑区制备的突触体中的参数非常一致。氟西汀是一种摄取到血清素能神经元的选择性抑制剂,是血清素摄取到外侧下丘脑突触体的强效抑制剂。地昔帕明和苯海索分别是去甲肾上腺素能和多巴胺能摄取抑制剂,效果则要差得多。通过对背侧或中缝核进行电解损伤,或通过向中脑血清素能通路注射5,7-二羟基色胺来损伤上行血清素能系统,可显著降低外侧下丘脑突触体对血清素的摄取。综上所述,这些数据为外侧下丘脑内存在血清素能终末场提供了进一步的证据。