Graduate Institute of Medical Sciences, College of Medicine, Taipei Medical University, Taipei, Taiwan.
Department of Pediatrics, MacKay Children's Hospital, Taipei, Taiwan.
BMC Complement Med Ther. 2022 Mar 21;22(1):81. doi: 10.1186/s12906-022-03562-9.
Convulsive status epilepticus (CSE) prevention is critical for pediatric patients with epilepsy. Immediate intervention before CSE reduce severity. Despite its wide usage as an anticonvulsant, valproic acid (VPA) results in harmful side effects such as dose-dependent hepatotoxicity. Hence, reducing VPA dosage to minimize side effects while maintaining its efficacy is necessary, and transcranial photobiomodulation (tPBM) add-on therapy could facilitate this. We recently demonstrated for the first time that tPBM at a wavelength of 808 nm attenuated CSE in peripubertal rats. However, the effects of VPA with the add-on therapy of tPBM prior to seizures have not yet been explored. This study investigated whether adding tPBM to VPA exerts synergistic effect for CSE prevention in peripubertal rats.
A gallium-aluminum-arsenide laser (wavelength of 808 nm with an exposure duration of 100 s and irradiance of 1.333 W/cm at the target) was applied transcranially 30 min after VPA injection in Sprague Dawley rats. All the rats received 90 mg/kg of pentylenetetrazole (PTZ). Except for the saline (n = 3), tPBM + saline (n = 3), and PTZ group (n = 6), all the rats received a PTZ injection 30 min after VPA injection. The rats received add-on tPBM with PTZ immediately after tPBM. In the VPA + PTZ group, the rats received low-dose (100 mg/kg, n = 6), medium-dose (200 mg/kg, n = 6), and high-dose (400 mg/kg, n = 7) VPA. In the VPA + tPBM + PTZ group, the rats received low (100 mg/kg, n = 5), medium (200 mg/kg, n = 6), and high (400 mg/kg, n = 3) doses of VPA. Seizures were evaluated according to the revised Racine's scale in a non-blinded manner.
Adding tPBM to low-dose VPA reduced the incidence of severe status epilepticus and significantly delayed the latency to stage 2 seizures. However, adding tPBM to high-dose VPA increased the maximum seizure stage, prolonged the duration of stage 4-7 seizures, and shortened the latency to stage 6 seizures.
Adding tPBM to low-dose VPA exerted a synergistic prevention effect on PTZ-induced seizures, whereas adding tPBM to high-dose VPA offset the attenuation effect.
癫痫患儿的惊厥性癫痫持续状态(CSE)预防至关重要。在 CSE 发生前进行即时干预可以降低其严重程度。尽管丙戊酸(VPA)被广泛用作抗惊厥药物,但它会导致肝毒性等剂量依赖性的有害副作用。因此,减少 VPA 剂量以最小化副作用同时保持其疗效是必要的,而经颅光生物调节(tPBM)附加治疗可以促进这一点。我们最近首次证明,808nm 的 tPBM 可减轻青春期前大鼠的 CSE。然而,在癫痫发作前添加 tPBM 对 VPA 的影响尚未得到探索。本研究旨在探讨在青春期前大鼠中,添加 tPBM 是否对 VPA 具有协同预防 CSE 的作用。
在 Sprague Dawley 大鼠中,在 VPA 注射后 30 分钟,使用砷化镓铝激光(波长 808nm,曝光时间 100s,目标处辐照度为 1.333W/cm)进行经颅照射。所有大鼠均接受 90mg/kg 的戊四氮(PTZ)。除生理盐水组(n=3)、tPBM+生理盐水组(n=3)和 PTZ 组(n=6)外,所有大鼠在 VPA 注射后 30 分钟均接受 PTZ 注射。在接受 tPBM 后,大鼠立即接受附加的 tPBM 和 PTZ。在 VPA+PTZ 组中,大鼠接受低剂量(100mg/kg,n=6)、中剂量(200mg/kg,n=6)和高剂量(400mg/kg,n=7)VPA。在 VPA+tPBM+PTZ 组中,大鼠接受低(100mg/kg,n=5)、中(200mg/kg,n=6)和高(400mg/kg,n=3)剂量的 VPA。根据修订后的 Racine 量表,以非盲法评估癫痫发作。
在低剂量 VPA 中添加 tPBM 降低了重度癫痫持续状态的发生率,并显著延迟了 2 级癫痫发作的潜伏期。然而,在高剂量 VPA 中添加 tPBM 增加了最大癫痫发作阶段,延长了 4-7 级癫痫发作的持续时间,并缩短了 6 级癫痫发作的潜伏期。
在低剂量 VPA 中添加 tPBM 对 PTZ 诱导的癫痫发作具有协同预防作用,而在高剂量 VPA 中添加 tPBM 则抵消了这种抑制作用。