Czyrak A, Rogóz Z, Skuza G, Zajaczkowski W, Maj J
Institute of Pharmacology, Polish Academy of Sciences, Kraków.
J Basic Clin Physiol Pharmacol. 1992 Jan-Mar;3(1):1-17. doi: 10.1515/jbcpp.1992.3.1.1.
S-Adenosyl-L-methionine (SAM), main methyl donor, was tested in mice and rats in several models which are predictive of possible antidepressant activity. In the forced swimming test in rats the effect of SAM was compared with that of the tricyclic antidepressant amitriptyline. SAM decreased dose-dependently immobility time in the forced swimming test in mice and rats, these effects being antagonized by haloperidol and prazosin (the latter only in rats). Locomotor or exploratory activity in mice and rats was not increased by SAM. D-Amphetamine-induced locomotor hyper-activity in rats was increased by repeated (14 days, twice daily) treatment with SAM. Behavioural stimulation induced by D-amphetamine or L-dopa (given with benserazide) in mice was not changed by a single dose of SAM. The drug reduced hypothermia induced by apomorphine in mice. Hypothermia induced by reserpine or clonidine in mice was not antagonized. SAM increased the amplitude of the acoustic startle reflex. The above results indicate that the psychopharmacological profile of SAM resembles that of antidepressants in only some tests. The mechanism by which SAM produces its antidepressant effect needs further investigation.
S-腺苷-L-甲硫氨酸(SAM)作为主要的甲基供体,在多种可预测其潜在抗抑郁活性的小鼠和大鼠模型中进行了测试。在大鼠的强迫游泳试验中,将SAM的效果与三环类抗抑郁药阿米替林的效果进行了比较。SAM在小鼠和大鼠的强迫游泳试验中剂量依赖性地减少了不动时间,这些作用被氟哌啶醇和哌唑嗪拮抗(后者仅在大鼠中)。SAM并未增加小鼠和大鼠的运动或探索活动。重复(14天,每日两次)给予SAM可增加大鼠中由D-苯丙胺诱导的运动性多动。单剂量的SAM并未改变小鼠中由D-苯丙胺或左旋多巴(与苄丝肼合用)诱导的行为兴奋。该药物减少了小鼠中由阿扑吗啡诱导的体温过低。SAM并未拮抗小鼠中由利血平或可乐定诱导的体温过低。SAM增加了听觉惊吓反射的幅度。上述结果表明,SAM的精神药理学特征仅在某些测试中类似于抗抑郁药。SAM产生其抗抑郁作用的机制需要进一步研究。