Boulat O, Waldmeier P, Maitre L
Research Department, CIBA-GEIGY AG, Basel, Switzerland.
J Neural Transm Gen Sect. 1990;82(3):181-95. doi: 10.1007/BF01272761.
Among the drugs commonly used in the treatment of memory disorders of the elderly, vincamine and hydergine have been shown to moderately increase the firing rate of noradrenergic locus coeruleus (LC) neurons. Since changes in electrical activity of noradrenergic neurons are generally reflected in corresponding alterations of the turnover of this transmitter, the effects of these drugs on the accumulation of 3,4-dihydroxyphenylacetic acid (DOPAC) and dopamine (DA) in the presence and absence of the dopamine-beta-hydroxylase inhibitor, FLA 63, were studied in the LC as well as in two of its projection areas, the hippocampus and the cerebellum. Characterization of this procedure with the alpha 2-adrenoceptor antagonist, idazoxan, the corresponding agonist, clonidine, the alpha 1-adrenoceptor antagonist prazosine, and haloperidol, suggested that--DOPAC changes are more suitable than those of DA or DOPAC/DA ratios in reflecting changes in noradrenaline (NA) turnover, inhibiting DBH is advantageous if NA turnover is to be measured in projection areas, but not in LC, and haloperidol and prazosine, in principle, did not affect NA turnover. Vincamine and hydergine at 10 mg/kg doses, at which they were reported to increase LC firing by 50%, did not induce a change in NA turnover in any of the areas. This, together with the data obtained with haloperidol, suggests that a minimal increase in the firing rate of LC cells (+140%) is required before it could influence the turnover of NA, as measured by DOPAC changes. Thus, the stimulating effect of nootropics on the central noradrenergic system may be more sensitively detected by electrophysiological techniques than by biochemical ones.
在常用于治疗老年人记忆障碍的药物中,长春胺和氢化麦角碱已被证明可适度提高去甲肾上腺素能蓝斑(LC)神经元的放电率。由于去甲肾上腺素能神经元电活动的变化通常反映在该递质周转的相应改变中,因此研究了这些药物在存在和不存在多巴胺-β-羟化酶抑制剂FLA 63的情况下对3,4-二羟基苯乙酸(DOPAC)和多巴胺(DA)在LC及其两个投射区域海马体和小脑中积累的影响。用α2-肾上腺素能受体拮抗剂咪唑克生、相应的激动剂可乐定、α1-肾上腺素能受体拮抗剂哌唑嗪和氟哌啶醇对该程序进行表征表明,——DOPAC变化比DA或DOPAC/DA比值变化更适合反映去甲肾上腺素(NA)周转的变化,若要在投射区域而非LC中测量NA周转,抑制DBH是有利的,并且原则上氟哌啶醇和哌唑嗪不影响NA周转。长春胺和氢化麦角碱以10mg/kg的剂量给药,据报道该剂量可使LC放电增加50%,但在任何区域均未引起NA周转的变化。这与用氟哌啶醇获得的数据一起表明,在通过DOPAC变化测量影响NA周转之前,LC细胞的放电率至少需要增加(+140%)。因此,与生化技术相比,通过电生理技术可能更灵敏地检测到促智药对中枢去甲肾上腺素能系统的刺激作用。