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通过脑内或全身给予单胺氧化酶抑制剂在大鼠中诱导产生的条件性味觉厌恶。

Conditioned taste aversion induced in rats by intracerebral or systemic administration of monoamine oxidase inhibitors.

作者信息

Buresová O, Bures J

出版信息

Psychopharmacology (Berl). 1987;91(2):209-12. doi: 10.1007/BF00217064.

DOI:10.1007/BF00217064
PMID:3107033
Abstract

Conditioned taste aversion (CTA) elicited by systemic or intracerebral application of the monoamine oxidase inhibitors clorgyline (C), pargyline (P) or deprenyl (D) was studied in 402 rats. Water-deprived animals were allowed 15 min access to 0.1% sodium saccharin (CS) followed 10 min later by IP or by intracerebral injection of the drug. In the latter case, the animals were anesthetized 5 min after saccharin drinking with pentobarbital and the drug was stereotaxically injected (1 microliter/min, 1-2 microliters) into the target structure. CTA was assessed in a two-choice retention test performed 2 days later. A geometric progression of three to six dosages applied to groups of rats (n = 10) was employed to establish the effective doses of the drugs which were 4, 20 and 32 mg/kg with IP and 2.5, 10 and 80 micrograms per rat with intracerebral (n. raphé magnus) injections of C, P, and D, respectively. The ratios of intracerebral to systemic dosages eliciting comparable CTA were 1:300 for C, 1:800 for P and 1:100 for D. Injections of 2.5 micrograms C and 10 micrograms P into the mesencephalic reticular formation, medial hypothalamus and cerebral cortex were ineffective, as were injections of 10 micrograms P into the nucleus of the solitary tract and cerebellum. The results indicate that CTA is elicited more efficiently by inhibition of monoamine oxidase A (selectively inhibited by C) than of monoamine oxidase B (selectively inhibited by D).

摘要

在402只大鼠中研究了通过全身或脑内应用单胺氧化酶抑制剂氯吉兰(C)、帕吉林(P)或司来吉兰(D)引发的条件性味觉厌恶(CTA)。将缺水的动物给予15分钟时间饮用0.1%的糖精钠(CS),10分钟后腹腔注射或脑内注射药物。在后一种情况下,在饮用糖精5分钟后用戊巴比妥麻醉动物,并将药物立体定位注射(1微升/分钟,1 - 2微升)到目标结构中。在2天后进行的双选保留试验中评估CTA。对大鼠组(n = 10)应用三到六个剂量的几何级数来确定药物的有效剂量,腹腔注射时分别为4、20和32毫克/千克,脑内(中缝大核)注射C、P和D时分别为每只大鼠2.5、10和80微克。引发可比CTA的脑内与全身剂量之比,C为1:300,P为1:800,D为1:100。向中脑网状结构、下丘脑内侧和大脑皮层注射2.5微克C和10微克P无效,向孤束核和小脑注射10微克P也无效。结果表明,抑制单胺氧化酶A(被C选择性抑制)比抑制单胺氧化酶B(被D选择性抑制)能更有效地引发CTA。

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