Kouyoumdjian J C, Ebadi M
J Neurochem. 1981 Jan;36(1):251-7. doi: 10.1111/j.1471-4159.1981.tb02401.x.
The intracerebroventricular injection of pyridoxal phosphate (PLP, 0.125-1.25 mumol/rat) causes epileptic seizures (4 min leads to 1 min) that are preventable or reversible by GABA (1 mumol/rat), by muscimol (0.025 mumol/rat), or by diazepam (1.75 mumol/rat). At the peak of PLP-induced convulsions, the activities of GAD and GABA-T in 14 regions of rat brain remained unaltered, whereas the concentrations of PLP remained elevated. The PLP-induced convulsion was blocked by DABA (10 mumol/rat) but was not altered by beta-alanine (50 mumol/rat). The previous in vitro studies have shown that PLP increases the uptake of [3H]GABA into synaptosomes and inhibits the binding of [3H]GABA to synaptic membranes. These data suggest that PLP-induced convulsion is due to reduced availability of GABA to its recognition sites, rather than to alteration in the activity of GABA metabolizing enzymes, or unavailability of PLP as a coenzyme for GAD and GABA-T. Since the duration of PLP-induced epileptic seizures is short and can be prevented by GABA agonists, PLP may be used as a tool to study the nature of GABA-mediated neuroinhibition and the properties of GABA receptor sites.
脑室内注射磷酸吡哆醛(PLP,0.125 - 1.25 μmol/大鼠)会引发癫痫发作(4分钟发作持续1分钟),而GABA(1 μmol/大鼠)、蝇蕈醇(0.025 μmol/大鼠)或地西泮(1.75 μmol/大鼠)可预防或逆转这种发作。在PLP诱导的惊厥高峰期,大鼠脑14个区域的谷氨酸脱羧酶(GAD)和GABA转氨酶(GABA-T)活性保持不变,而PLP浓度仍升高。DABA(10 μmol/大鼠)可阻断PLP诱导的惊厥,但β-丙氨酸(50 μmol/大鼠)对其无影响。先前的体外研究表明,PLP可增加[³H]GABA进入突触体的摄取,并抑制[³H]GABA与突触膜的结合。这些数据表明,PLP诱导的惊厥是由于GABA与其识别位点的可利用性降低,而非GABA代谢酶活性的改变,也不是PLP作为GAD和GABA-T辅酶的不可利用性。由于PLP诱导的癫痫发作持续时间短且可被GABA激动剂预防,PLP可用作研究GABA介导的神经抑制性质和GABA受体位点特性的工具。