ALTERED PATTERNS OF CATECHOLAMINERGIC FIBERS IN FOCAL CORTICAL DYSPLASIA IN 2 PATIENTS WITH PARTIAL SEIZURES

被引:20
|
作者
TROTTIER, S
EVRARD, B
BIRABEN, A
CHAUVEL, P
机构
[1] CHR PONTCHAILLOU,INSERM,CJF 90 12,F-35000 RENNES,FRANCE
[2] CHR PONTCHAILLOU,NEUROL CLIN,F-35000 RENNES,FRANCE
关键词
PARTIAL SEIZURES; FOCAL CORTICAL DYSPLASIA; CATECHOLAMINERGIC AFFERENTS; CYTOARCHITECTONIC TECHNIQUES; IMMUNOHISTOCHEMICAL TECHNIQUES;
D O I
10.1016/0920-1211(94)90026-4
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
We present the histologic study of two patients who underwent cerebral cortex resection for partial seizures linked with cortical dysplasia. The distinction of areas of seizure origin from areas of seizure propagation was made according to stereoelectroencephalographic criteria. Samples of epileptogenic tissue were studied by using cytoarchitectonic and immunohistochemical stainings. We mapped the catecholaminergic afferents by employing antisera directed against tyrosine hydroxylase and dopamine-beta-hydroxylase enzymes. The epileptic activity was correlated with the underlying patterns of cytoarchitectonic' and immunohistochemical changes. The neuropathological features were focal and consisted of large neurons dispersed through all but the first cortical layer (associated in one case to giant glial cells), of variable disturbance of lamination, of neuronal ectopia in the white matter and of moderate proliferation of small glial cells. Areas of seizure onset coincided with that of dysplastic zones. Both laminar distribution and density of catecholaminergic fibers were altered in the dysplastic cortices (area of seizure onset) and there was an increase in the density of tyrosine hydroxylase-immunoreactive fibers in the surrounding areas of seizure propagation. Our results indicate that these developmental epileptogenic lesions were associated with abnormal neuronal circuitry. They provide evidence at the structural level of the increase in tyrosine hydroxylase activity previously reported in spiking areas of human epileptogenic cerebral cortex and they suggest that catecholamines may contribute toward limiting seizure activity propagation.
引用
收藏
页码:161 / 179
页数:19
相关论文
共 50 条
  • [1] Evidence for altered synaptic inhibition in patients with focal cortical dysplasia
    Calcagnotto, ME
    Paredes, MF
    Tihan, T
    Barbaro, NM
    Baraban, SC
    EPILEPSIA, 2005, 46 : 9 - 9
  • [2] EATING SEIZURES ASSOCIATED WITH FOCAL CORTICAL DYSPLASIA
    VERDU, A
    RUIZFALCO, ML
    BRAIN & DEVELOPMENT, 1991, 13 (05): : 352 - 354
  • [3] Gene therapy for seizures in focal cortical dysplasia
    Kiani, Lisa
    NATURE REVIEWS NEUROLOGY, 2024, 20 (02) : 63 - 63
  • [4] Gene therapy for seizures in focal cortical dysplasia
    Lisa Kiani
    Nature Reviews Neurology, 2024, 20 : 63 - 63
  • [5] Utility of ictal SPECT in patients with partial seizures and cortical dysplasia
    Raja, S
    Chandra, S
    Sosa, VN
    Saha, GB
    Wyllie, E
    Prakesh, K
    Morris, MN
    Go, RT
    EUROPEAN JOURNAL OF NUCLEAR MEDICINE, 1999, 26 (09): : 1130 - 1130
  • [6] Population pharmacokinetics of everolimus in patients with seizures associated with focal cortical dysplasia
    Park, Jinha
    Kim, Se Hee
    Hahn, Jongsung
    Kang, Hoon-Chul
    Lee, Sang-Guk
    Kim, Heung Dong
    Chang, Min Jung
    FRONTIERS IN PHARMACOLOGY, 2023, 14
  • [7] THE EXTRACELLULAR MATRIX AND ALTERED DIFFUSION IN FOCAL CORTICAL DYSPLASIA
    Homola, A.
    Vargova, L.
    Cicanic, M.
    Zamecnik, J.
    Marusic, P.
    Krsek, P.
    Sykova, E.
    GLIA, 2011, 59 : S106 - S106
  • [8] Gelastic seizures in a child with focal cortical dysplasia of the cingulate gyrus
    McConachie, NS
    King, MD
    NEURORADIOLOGY, 1997, 39 (01) : 44 - 45
  • [9] Gelastic seizures in a child with focal cortical dysplasia of the cingulate gyrus
    N. S. McConachie
    M. D. King
    Neuroradiology, 1997, 39 : 44 - 45
  • [10] Expression Patterns of TRPC1 in Cortical Lesions from Patients with Focal Cortical Dysplasia
    Zang, Zhenle
    Li, Song
    Zhang, Wei
    Chen, Xin
    Zheng, Dahai
    Shu, Haifeng
    Guo, Wei
    Zhao, Bangyun
    Shen, Kaifeng
    Wei, YuJia
    Zheng, Xin
    Liu, Shiyong
    Yang, Hui
    JOURNAL OF MOLECULAR NEUROSCIENCE, 2015, 57 (02) : 265 - 272