Cho J, Kong J Y, Jeong D Y, Lee K D, Lee D U, Kang B S
Department of Pharmacology, College of Medicine, Dongguk University, Kyongju, Kyongbuk, Korea.
Life Sci. 2001 Feb 16;68(13):1567-73. doi: 10.1016/s0024-3205(01)00944-4.
Acori graminei Rhizoma (AGR) is shown to exhibit a number of pharmacological actions including sedation and anticonvulsive action. To further characterize its actions in the CNS, the present study evaluated the effects of essential oils (EO) from AGR on the excitotoxic neuronal cell death induced in primary rat cortical cell cultures. EO inhibited the glutamate-induced excitotoxicity in a concentration-dependent manner, with the IC50 of 0.241 mg/ml. EO exerted more potent neuroprotection against the toxicity induced by NMDA (IC50 = 0.139 mg/ml). In contrast, the AMPA-induced toxicity was not inhibited by EO. Receptor-ligand binding studies were performed to investigate the neuroprotective action mechanism. EO dramatically inhibited the specific bindings of a use-dependent NMDA receptorion channel blocker [3H]MK-801, indicating an NMDA receptor antagonist-like action. However, the bindings of [3H]MDL 105,519, a ligand selective for the glycine binding site of NMDA receptor, were not considerably inhibited. These results demonstrated that EO extracted from AGR exhibited neuroprotective effects on cultured cortical neurons through the blockade of NMDA receptor activity, and that the glycine binding site appeared not to be the major site of action.
石菖蒲根茎(AGR)已被证明具有多种药理作用,包括镇静和抗惊厥作用。为了进一步明确其在中枢神经系统中的作用,本研究评估了石菖蒲根茎挥发油(EO)对原代大鼠皮质细胞培养物中诱导的兴奋性毒性神经元细胞死亡的影响。挥发油以浓度依赖性方式抑制谷氨酸诱导的兴奋性毒性,IC50为0.241mg/ml。挥发油对NMDA诱导的毒性具有更强的神经保护作用(IC50 = 0.139mg/ml)。相比之下,挥发油不抑制AMPA诱导的毒性。进行了受体-配体结合研究以探讨神经保护作用机制。挥发油显著抑制一种使用依赖性NMDA受体离子通道阻滞剂[3H]MK-801的特异性结合,表明具有NMDA受体拮抗剂样作用。然而,[3H]MDL 105,519(一种对NMDA受体甘氨酸结合位点具有选择性的配体)的结合未受到明显抑制。这些结果表明,从石菖蒲根茎中提取的挥发油通过阻断NMDA受体活性对培养的皮质神经元表现出神经保护作用,并且甘氨酸结合位点似乎不是主要作用位点。