Hosford D A, Crain B J, Cao Z, Bonhaus D W, Friedman A H, Okazaki M M, Nadler J V, McNamara J O
Division of Neurology, Duke University Medical Center, Durham, North Carolina 27710.
J Neurosci. 1991 Feb;11(2):428-34. doi: 10.1523/JNEUROSCI.11-02-00428.1991.
Based on results from the kindling model of epilepsy, we hypothesized that enhanced binding of radioligands to the NMDA receptor and decreased binding to the alpha-amino-3-hydroxy-5-methyl-4- isoxazolepropionate (AMPA)-sensitive quisqualate (ASQ) receptor would be found within epileptic hippocampi of humans with complex partial epilepsy (CPE). To test these hypotheses, we used tissue that was surgically removed from patients with intractable CPE, and control tissue that was obtained at autopsy. We used autoradiographic techniques to measure ASQ receptor binding (with 3H-AMPA as the radioligand) and binding to 2 sites on the NMDA receptor/channel complex: the agonist recognition site (with 3H-glutamate) and the phencyclidine (PCP) binding site that resides within the NMDA channel [with 3H-N-(1-[thienyl]cyclohexyl) piperidine (TCP) in the presence of saturating concentrations of NMDA and glycine]. Measurements of receptor binding were corrected for pathologic alterations in neuronal density. Contrary to our expectations, ASQ receptor binding was significantly increased (100%; p less than 0.02) in the dentate gyrus stratum moleculare in patients with CPE (n = 8), and it was unchanged in other hippocampal regions. In nearby sections from the same specimens, binding was significantly decreased to the agonist recognition site of the NMDA receptor in the stratum oriens of area CA3 (46%; p less than 0.05) and was also decreased to the PCP site in the stratum radiatum and stratum oriens of CA3 (44% and 74%, respectively; p less than 0.05). The increase in ASQ receptor binding may contribute to hyperexcitability in these epileptic patients.(ABSTRACT TRUNCATED AT 250 WORDS)
基于癫痫点燃模型的结果,我们推测在患有复杂部分性癫痫(CPE)的人类癫痫海马体中,放射性配体与N-甲基-D-天冬氨酸(NMDA)受体的结合增强,而与α-氨基-3-羟基-5-甲基-4-异恶唑丙酸(AMPA)敏感的喹啉酸(ASQ)受体的结合减少。为了验证这些假设,我们使用了从难治性CPE患者手术切除的组织,以及尸检获得的对照组织。我们采用放射自显影技术测量ASQ受体结合(以3H-AMPA作为放射性配体)以及与NMDA受体/通道复合物上2个位点的结合:激动剂识别位点(以3H-谷氨酸作为放射性配体)和位于NMDA通道内的苯环利定(PCP)结合位点[在存在饱和浓度的NMDA和甘氨酸的情况下,以3H-N-(1-[噻吩基]环己基)哌啶(TCP)作为放射性配体]。受体结合的测量针对神经元密度的病理改变进行了校正。与我们的预期相反,CPE患者(n = 8)齿状回分子层中的ASQ受体结合显著增加(100%;p < 0.02),而在其他海马区域则无变化。在同一标本的相邻切片中,CA3区 Oriens层中NMDA受体激动剂识别位点的结合显著降低(46%;p < 0.05),CA3区放射层和Oriens层中PCP位点的结合也降低(分别为44%和74%;p < 0.05)。ASQ受体结合的增加可能导致这些癫痫患者的兴奋性过高。(摘要截短于250字)