Thongwong Putthiwat, Wattanathorn Jintanaporn, Thukham-Mee Wipawee
Department of Physiology and Graduate School (Neuroscience Program), Faculty of Medicine, Khon Kaen University, Khon Kaen 40000, Thailand.
Research Institute for High Human Performance and Health Promotion, Khon Kaen University, Khon Kaen 40000, Thailand.
Nutrients. 2024 Nov 29;16(23):4144. doi: 10.3390/nu16234144.
Despite the increasing importance of the condition of post-stroke cognitive impairment (PSCI), the current therapy efficacy is limited. Since oxidative stress and inflammation are targeted in anti-stroke therapy, we aimed to assess the protective effect against PSI of an orodispersible film loaded with silkworm pupae hydrolysate and a combined extract of holy basil and ginger (JP1), which show antioxidant, and anti-inflammation effects. Male Wistar rats (200-250 g) were administered JP1 at doses of 1, 10, and 100 mg/kg BW 45 min before a 6 h immobilization stress exposure for 14 days. Then, the right middle cerebral artery was permanently occluded (MCAO) and JP1 was continually administered for 21 days after MCAO. Spatial and non-spatial memory and the possible underlying mechanisms were also explored. JP1 improved oxidative stress, inflammation, apoptosis, Erk signaling pathway, cholinergic function, and the growth of and spp. in feces. These results suggest that JP1 improves PSCI, possibly involving the above mechanisms. Furthermore, serum corticosterone also decreased. Our results suggest that JP1 is a potential candidate for combating PSCI following exposure to stroke plus stress. However, a clear understanding of the precise active ingredient and the detailed mechanisms require further investigation.
尽管中风后认知障碍(PSCI)的病情愈发重要,但目前的治疗效果有限。由于氧化应激和炎症是抗中风治疗的靶点,我们旨在评估载有蚕蛹水解物以及圣罗勒和生姜混合提取物(JP1)的口腔崩解膜对PSCI的保护作用,该提取物具有抗氧化和抗炎作用。体重200 - 250克的雄性Wistar大鼠在暴露于6小时固定应激14天前45分钟,分别以1、10和100毫克/千克体重的剂量给予JP1。然后,永久性闭塞右侧大脑中动脉(MCAO),并在MCAO后连续给予JP1 21天。还探究了空间和非空间记忆以及可能的潜在机制。JP1改善了氧化应激、炎症、细胞凋亡、Erk信号通路、胆碱能功能以及粪便中双歧杆菌属和拟杆菌属的生长。这些结果表明JP1改善了PSCI,可能涉及上述机制。此外,血清皮质酮也有所降低。我们的结果表明,JP1是中风加应激后对抗PSCI的潜在候选物。然而,对确切活性成分和详细机制的清晰理解还需要进一步研究。