Kovács Zsolt, D'Agostino Dominic P, Diamond David M, Ari Csilla
Department of Biology, ELTE Eötvös Loránd University, Savaria University Centre, Szombathely, Hungary.
Laboratory of Metabolic Medicine, Department of Molecular Pharmacology and Physiology, Morsani College of Medicine, University of South Florida, Tampa, FL, United States.
Front Mol Neurosci. 2019 Feb 28;12:45. doi: 10.3389/fnmol.2019.00045. eCollection 2019.
It has been demonstrated previously that exogenous ketone supplements such as ketone ester (KE) decreased absence epileptic activity in a well-studied animal model of human absence epilepsy, Wistar Albino Glaxo/Rijswijk (WAG/Rij) rats. It is known that lipopolysaccharide (LPS)-generated changes in inflammatory processes increase absence epileptic activity, while previous studies show that ketone supplement-evoked ketosis can modulate inflammatory processes. Thus, we investigated in the present study whether administration of exogenous ketone supplements, which were mixed with standard rodent chow (containing 10% KE + 10% ketone salt/KS, % by weight, KEKS) for 10 days, can modulate the LPS-evoked changes in absence epileptic activity in WAG/Rij rats. At first, KEKS food alone was administered and changes in spike-wave discharge (SWD) number, SWD time, discharge frequency within SWDs, blood glucose, and beta-hydroxybutyrate (βHB) levels, as well as body weight and sleep-waking stages were measured. In a separate experiment, intraperitoneal (i.p.) injection of LPS (50 μg/kg) alone and a cyclooxygenase 1 and 2 (COX-1 and COX-2) inhibitor indomethacin (10 mg/kg) alone, as well as combined IP injection of indomethacin with LPS (indomethacin + LPS) were applied in WAG/Rij rats to elucidate their influences on SWD number. In order to determine whether KEKS food can modify the LPS-evoked changes in SWD number, KEKS food in combination with IP LPS (50 μg/kg) (KEKS + LPS), as well as KEKS food with IP indomethacin (10 mg/kg) and LPS (50 μg/kg) (KEKS + indomethacin + LPS) were also administered. We demonstrated that KEKS food significantly increased blood βHB levels and decreased not only the spontaneously generated absence epileptic activity (SWD number), but also the LPS-evoked increase in SWD number in WAG/Rij rats. Our results suggest that administration of exogenous ketone supplements (ketogenic foods) may be a promising therapeutic tool in the treatment of epilepsy.
先前已经证明,外源性酮补充剂,如酮酯(KE),在一种经过充分研究的人类失神癫痫动物模型——Wistar白化Glaxo/Rijswijk(WAG/Rij)大鼠中,可降低失神癫痫活动。已知脂多糖(LPS)引起的炎症过程变化会增加失神癫痫活动,而先前的研究表明,酮补充剂诱发的酮症可调节炎症过程。因此,在本研究中,我们调查了将外源性酮补充剂与标准啮齿动物饲料(含10% KE + 10%酮盐/KS,重量百分比,KEKS)混合10天进行给药,是否能调节WAG/Rij大鼠中LPS诱发的失神癫痫活动变化。首先,单独给予KEKS食物,并测量棘波放电(SWD)次数、SWD时间、SWD内放电频率、血糖、β-羟基丁酸(βHB)水平,以及体重和睡眠-觉醒阶段的变化。在另一个实验中,对WAG/Rij大鼠单独腹腔注射LPS(50 μg/kg)和环氧化酶1和2(COX-1和COX-2)抑制剂吲哚美辛(10 mg/kg),以及将吲哚美辛与LPS联合腹腔注射(吲哚美辛 + LPS),以阐明它们对SWD次数的影响。为了确定KEKS食物是否能改变LPS诱发的SWD次数变化,还给予了KEKS食物与腹腔注射LPS(50 μg/kg)联合使用(KEKS + LPS),以及KEKS食物与腹腔注射吲哚美辛(10 mg/kg)和LPS(50 μg/kg)联合使用(KEKS + 吲哚美辛 + LPS)。我们证明,KEKS食物显著提高了血液βHB水平,不仅降低了自发产生的失神癫痫活动(SWD次数),还降低了WAG/Rij大鼠中LPS诱发的SWD次数增加。我们的结果表明,给予外源性酮补充剂(生酮食物)可能是治疗癫痫的一种有前景的治疗工具。