Ahlskog J E, Randall P K, Hernandez L, Hoebel B G
Psychopharmacology (Berl). 1984;82(1-2):118-21. doi: 10.1007/BF00426393.
Rats were made hyperphagic by 6-hydroxydopamine (6-OHDA) injected bilaterally into the ventral midbrain; then they were restricted to a 6 h/day feeding schedule and tested for appetite suppression with amphetamine and fenfluramine in randomized order. Amphetamine anorexia was diminished while fenfluramine anorexia was enhanced (both P less than 0.001). The opposite effect on fenfluramine anorexia shows that the effect of 6-OHDA on amphetamine anorexia was not due to hyperphagia masking the anorexia. Norepinephrine in the forebrain was 90% depleted, but DA and serotonin levels were within 9% of normal. These results demonstrate a new way to dissociate amphetamine and fenfluramine anorexia, as others have done with lateral hypothalamic lesions or DA depletion. The 6-OHDA injections, which were of a type that cause hyperphagia, apparently destroyed a substrate for amphetamine anorexia and also facilitated a substrate for fenfluramine anorexia.
通过双侧向腹侧中脑注射6-羟基多巴胺(6-OHDA)使大鼠食欲亢进;然后将它们限制在每天6小时的进食时间表内,并以随机顺序用苯丙胺和芬氟拉明测试食欲抑制情况。苯丙胺所致的厌食症减轻,而芬氟拉明所致的厌食症增强(两者P均小于0.001)。对芬氟拉明所致厌食症的相反作用表明,6-OHDA对苯丙胺所致厌食症的影响并非由于食欲亢进掩盖了厌食症。前脑中去甲肾上腺素耗竭了90%,但多巴胺和血清素水平在正常水平的9%以内。这些结果证明了一种区分苯丙胺和芬氟拉明所致厌食症的新方法,就像其他人通过下丘脑外侧损伤或多巴胺耗竭所做的那样。导致食欲亢进的6-OHDA注射显然破坏了苯丙胺所致厌食症的一个底物,同时也促进了芬氟拉明所致厌食症的一个底物。