Senik Mohd Harizal, Abu Izuddin Fahmy, Fadhullah Widad
Department of Neurosciences, School of Medical Sciences, Universiti Sains Malaysia, Kelantan, Malaysia.
School of Life Sciences, Medical School, Queen's Medical Centre, University of Nottingham, Nottingham, United Kingdom.
Malays J Med Sci. 2021 Feb;28(1):15-26. doi: 10.21315/mjms2021.28.1.3. Epub 2021 Feb 24.
Kainic acid (KA)-induced seizures may be a valuable tool in the assessment of anti-epileptic drug efficacy in complex partial seizures. This study investigated the effects of KA on ATP-sensitive K (K) channels opening probability (NPo), which plays a crucial role in neuronal activities.
For the optimisation and validation protocol, β-cells were plated onto 35 mm plastic petri dishes and maintained in RPMI-1640 media supplemented with 10 mM glucose, 10% FCS and 25 mM of N-2-hydroxyethylpiperazine-N-ethanesulfonic acid (HEPES). The treatment effects of 10 mM glucose and 30 μM fluoxetine on K channels NPo of β-cells were assessed via cell-attached patch-clamp recordings. For hippocampus cell experiments, hippocampi were harvested from day 17 of maternal Lister-hooded rat foetus, and then transferred to a Ca and Mg-free HEPES-buffered Hank's salt solution (HHSS). The dissociated cells were cultured and plated onto a 25 mm round cover glasses coated with poly-d-lysine (0.1 mg/mL) in a petri dish. The K channels NPo of hippocampus cells when perfused with 1 mM and 10 mM of KA were determined.
NPo of β-cells showed significant decreasing patterns ( < 0.001) when treated with 10 mM glucose 0.048 (0.027) as well as 30 μM fluoxetine 0.190 (0.141) as compared to basal counterpart. In hippocampus cell experiment, a significant increase ( < 0.001) in mean NPo 2.148 (0.175) of neurons when applied with 1 mM of KA as compared to basal was observed.
The two concentrations of KA used in the study exerted contrasting effects toward the mean of NPo. It is hypothesised that KA at lower concentration (1 mM) opens more K channels, leading to hyperpolarisation of the neurons, which may prevent neuronal hyper excitability. No effect was shown in 10 mM KA treatment, suggesting that only lower than 10 mM KA produced significant changes in K channels. This implies further validation of KA concentration to be used in the future.
海藻酸(KA)诱导的癫痫发作可能是评估抗癫痫药物对复杂部分性癫痫疗效的一种有价值的工具。本研究调查了KA对ATP敏感性钾(K)通道开放概率(NPo)的影响,该通道在神经元活动中起关键作用。
为了优化和验证实验方案,将β细胞接种到35mm塑料培养皿中,置于补充有10mM葡萄糖、10%胎牛血清和25mM N-2-羟乙基哌嗪-N-乙磺酸(HEPES)的RPMI-1640培养基中培养。通过细胞贴附式膜片钳记录评估10mM葡萄糖和30μM氟西汀对β细胞K通道NPo的治疗效果。对于海马细胞实验,从孕17天的利斯特戴帽大鼠胎儿中取出海马,然后转移到无钙和镁的HEPES缓冲汉克斯盐溶液(HHSS)中。将解离的细胞培养并接种到培养皿中涂有聚-d-赖氨酸(0.1mg/mL)的25mm圆形盖玻片上。测定灌注1mM和10mM KA时海马细胞的K通道NPo。
与基础状态相比,用10mM葡萄糖(0.048,0.027)和30μM氟西汀(0.190,0.141)处理时,β细胞的NPo呈现显著下降趋势(<0.001)。在海马细胞实验中,与基础状态相比,应用1mM KA时神经元的平均NPo(2.148,0.175)显著增加(<0.001)。
本研究中使用的两种浓度的KA对NPo的平均值产生了相反的影响。据推测,较低浓度(1mM)的KA会打开更多的K通道,导致神经元超极化,这可能会阻止神经元过度兴奋。10mM KA处理未显示出效果,表明只有低于10mM的KA才会使K通道产生显著变化。这意味着未来需要进一步验证KA的使用浓度。