Beas-Zárate C, Sánchez-Ruíz M Y, Ureña-Guerrero M E, Feria-Velasco A
C.I.B.O., I.M.S.S., Depto. de Biol. Cel. y Molec., C.U.C.B.A., U. de G., Guadalajara, Jalisco, Mexico.
Neurochem Int. 1998 Sep;33(3):217-32. doi: 10.1016/s0197-0186(98)00002-3.
Monosodium L-glutamate (MSG) causes neuronal lesions in certain brain regions when systemically given to young animals. Also, when glutamate (Glu) builds up in the intersynaptic space, it induces neuroexcitatory and neurocytotoxic effects, events mediated by several Glu receptors. Some of these receptors such as NMDA and AMPA receptors are present in the very earliest developmental stages of the central nervous system and play a major role in neuronal plasticity during synaptogenesis. In this paper, the GABAergic system vulnerability was determined in terms of [3H]-GABA release during postnatal development. [3H]-GABA release on days 14, 21, 30, and 60 days after birth was assessed for the cerebral cortex (CC), hippocampus (Hp) and striatum (S) in rats perinatally treated at days 1, 3, 5, and 7 after birth with MSG. The results show a major decrease in baseline [3H]-GABA release in the CC (30 and 60 days after birth) and the Hp (beginning day 21 after birth) vs the control groups [intact rats and rats given a NaCl solution equimolar to that of MSG (eqNaCl)] while in the S baseline release remained unchanged. Stimulated [3H]-GABA release was decreased in the CC on days 14 and 21 after birth and significantly increased on day 60 after birth vs the controls. In the Hp, a decrease was seen on days 14, 21, and 60 after birth vs the controls while stimulated [3H]-GABA release was decreased in the S vs the controls at all ages studied. No significant differences in stimulated [3H]-GABA release were found between the intact group and the group treated with eqNaCl on days 30 and 60 after birth. Results show that CC, Hp and S GABAergic neurones are a major target for the effect of perinatally given MSG and suggest a possible decrease in the number of Hp GABAergic neurones while these results in CC and S suggest a modified neuronal plasticity. NMDA receptor and calcium involvement are discussed as significant mediators of these events.
给幼龄动物全身注射L-谷氨酸钠(MSG)会导致某些脑区出现神经元损伤。此外,当谷氨酸(Glu)在突触间隙中积累时,会诱导神经兴奋和神经细胞毒性作用,这些作用由几种Glu受体介导。其中一些受体,如NMDA和AMPA受体,在中枢神经系统的最早发育阶段就已存在,并在突触形成过程中的神经元可塑性中起主要作用。在本文中,根据出生后发育过程中[3H]-GABA的释放情况来确定GABA能系统的脆弱性。对出生后第1、3、5和7天经MSG围产期处理的大鼠,在出生后第14、21、30和60天评估其大脑皮层(CC)、海马体(Hp)和纹状体(S)中[3H]-GABA的释放。结果显示,与对照组[完整大鼠和给予与MSG等摩尔的NaCl溶液(eqNaCl)的大鼠]相比,CC(出生后30天和60天)和Hp(出生后第21天开始)的基线[3H]-GABA释放显著减少,而S中的基线释放保持不变。与对照组相比,出生后第14天和21天CC中刺激后的[3H]-GABA释放减少,出生后第60天显著增加。在Hp中,与对照组相比,出生后第14、21和60天出现减少,而在所有研究年龄中,与对照组相比,S中刺激后的[3H]-GABA释放减少。在出生后第30天和60天,完整组和用eqNaCl处理的组之间在刺激后的[3H]-GABA释放方面未发现显著差异。结果表明,CC、Hp和S中的GABA能神经元是围产期给予MSG影响的主要靶点,并提示Hp中GABA能神经元数量可能减少,而CC和S中的这些结果提示神经元可塑性发生改变。讨论了NMDA受体和钙参与这些事件作为重要介质的情况。