Department of Cell and Molecular Biology, "Iuliu Haţieganu" University of Medicine and Pharmacy, Cluj-Napoca, Romania.
Cell Mol Neurobiol. 2011 Jul;31(5):701-14. doi: 10.1007/s10571-011-9667-4. Epub 2011 Feb 26.
The aim of this study is to evaluate the bioelectrical and structural-functional changes in frontal cortex after the bee venom (BV) experimental treatments simulating both an acute envenomation and a subchronic BV therapy. Wistar rats were subcutaneously injected once with three different BV doses: 700 μg/kg (T(1) group), 2100 μg/kg (T(3) group), and 62 mg/kg (sublethal dose-in T(SL) group), and repeated for 30 days with the lowest dose (700 μg/kg-in T(S) group). BV effects were assessed by electrophysiological, histological, histochemical, and ultrastructural methods. Single BV doses produced discharges of negative and biphasic sharp waves, and epileptiform spike-wave complexes. The increasing frequency of these elements suggested a dose-dependent neuronal hyperexcitation or irritation. As compared to the lower doses, the sublethal dose was responsible for a pronounced toxic effect, confirmed by ultrastructural data in both neurons and glial cells that underwent extensive, irreversible changes, triggering the cellular death. Subchronic BV treatment in T(S) group resulted in a slower frequency and increased amplitude of cortical activity suggesting neuronal loss. However, neurons were still stimulated by the last BV dose. Structural-functional data showed a reduced cellular density in frontal cortex of animals in this group, while the remaining neurons displayed both specific (stimulation of neuronal activity) and unspecific modifications (moderate alterations to necrotic phenomena). Molecular mechanisms involved in BV interactions with the nervous tissue are also discussed. We consider all these data very important for clinicians who manage patients with multiple bee stings, or who intend to set an appropriate BV therapy.
本研究旨在评估蜜蜂毒液(BV)实验处理后额叶皮层的生物电和结构功能变化,模拟急性毒液中毒和亚慢性 BV 治疗。Wistar 大鼠单次皮下注射三种不同剂量的 BV:700μg/kg(T(1)组)、2100μg/kg(T(3)组)和 62mg/kg(亚致死剂量-T(SL)组),并以最低剂量(700μg/kg-T(S)组)重复 30 天。BV 效应通过电生理、组织学、组织化学和超微结构方法进行评估。单次 BV 剂量产生负相和双相锐波以及癫痫样棘波复合波放电。这些元素的频率增加表明神经元超兴奋或刺激呈剂量依赖性。与较低剂量相比,亚致死剂量导致明显的毒性作用,这在神经元和神经胶质细胞的超微结构数据中得到证实,这些细胞经历了广泛的、不可逆转的变化,引发细胞死亡。T(S)组的亚慢性 BV 治疗导致皮质活动的频率较慢且幅度增加,表明神经元丢失。然而,神经元仍被最后一次 BV 剂量刺激。结构功能数据显示,该组动物额叶皮层的细胞密度降低,而剩余的神经元表现出特异性(刺激神经元活性)和非特异性改变(中度改变到坏死现象)。还讨论了 BV 与神经组织相互作用涉及的分子机制。我们认为所有这些数据对管理多发性蜜蜂蜇伤患者或打算设定适当的 BV 治疗的临床医生非常重要。