Scheinin H, MacDonald E, Scheinin M
Eur J Pharmacol. 1986 Sep 23;129(1-2):113-21. doi: 10.1016/0014-2999(86)90342-0.
The changes of free 3-methoxy-4-hydroxyphenylglycol (MHPG) in cerebrospinal fluid (CSF) were compared with the corresponding alterations of free and conjugated MHPG in rat brain tissue after various pharmacological treatments modifying noradrenergic neurotransmission. In addition, the effects of the drug treatments on the concentration of noradrenaline (NA) in brain were determined. alpha-Methyl-p-tyrosine (an inhibitor of tyrosine hydroxylase) induced decreases in free and conjugated MHPG in CSF and brain; the free species appeared to decline more rapidly. Reserpine caused similar biphasic changes in free MHPG in CSF and brain but the rapid and transient initial increase in MHPG-SO4 was very weak. Pargyline (monoamine oxidase inhibitor) induced a sharp decline in the concentration of free MHPG in brain and CSF while MHPG-SO4 in brain definitely decreased more slowly. Relatively similar time courses were seen for all three MHPG parameters after administration of MPV-1248 (alpha 2-antagonist) and clonidine (alpha 2-agonist) i.e., increases and decreases, respectively. The present results support the validity of monitoring drug-induced acute changes in central turnover of NA by repeated measurements of free MHPG levels in rat cisternal CSF.
在进行各种改变去甲肾上腺素能神经传递的药物治疗后,比较了脑脊液(CSF)中游离3-甲氧基-4-羟基苯乙二醇(MHPG)的变化与大鼠脑组织中游离和结合型MHPG的相应改变。此外,还测定了药物治疗对脑中去甲肾上腺素(NA)浓度的影响。α-甲基对酪氨酸(酪氨酸羟化酶抑制剂)导致脑脊液和脑中游离和结合型MHPG减少;游离型似乎下降得更快。利血平使脑脊液和脑中游离MHPG发生类似的双相变化,但MHPG-SO4最初的快速短暂升高非常微弱。帕吉林(单胺氧化酶抑制剂)导致脑和脑脊液中游离MHPG浓度急剧下降,而脑中的MHPG-SO4下降肯定更缓慢。给予MPV-1248(α2拮抗剂)和可乐定(α2激动剂)后,所有三个MHPG参数的时间进程相对相似,即分别升高和降低。目前的结果支持通过重复测量大鼠脑池脑脊液中游离MHPG水平来监测药物诱导的脑中NA中枢周转率急性变化的有效性。