Miura Akihiko, Yamanashi Takehiko, Kajitani Naofumi, Fukuda Saki, Tsunetomi Kyohei, Matsuo Ryoichi, Nishiguchi Tsuyoshi, Pu Shenghong, Nakada Yumeto, Shirayama Yukihiko, Watanabe Ken, Kaneko Koichi, Iwata Masaaki
Division of Neuropsychiatry, Department of Brain and Neurosciences, School of Medicine, Faculty of Medicine, Tottori University, Yonago 683-8503, Japan.
Division of Clinical Laboratory, Tottori University Hospital, Yonago 683-8504, Japan.
Yonago Acta Med. 2025 Jan 23;68(1):58-67. doi: 10.33160/yam.2025.02.007. eCollection 2025 Feb.
Inflammation is believed to contribute to the pathophysiology of depression, with increased levels of inflammatory cytokines, such as interleukin-1β (IL-1β), observed in patients. Depression is also common in individuals with chronic inflammatory diseases. IL-1β disrupts synaptic transmission and reduces neurogenesis in the hippocampus, playing a crucial role in depression development. Our prior research found that stress activates microglia in the brain to produce IL-1β via the nucleotide-binding oligomerization domain-like receptor family pyrin domain containing 3 (NLRP3) inflammasome. Additionally, β-hydroxybutyrate (BHB), an endogenous ketone body, alleviates stress-induced depression by inhibiting NLRP3 activation and IL-1β production. However, BHB's poor bioavailability limits its effectiveness. Medium-chain triglycerides (MCTs) can increase blood BHB levels, making them a potential treatment for stress-induced depression.
We tested MCT in two animal models: social defeat (SD) in mice and chronic unpredictable stress (CUS) in rats. MCT was orally administered to both groups to assess blood BHB levels. Behavioral tests, including the forced swim test (FST), were performed, and brain tissue was analyzed for IL-1β levels and spine density.
MCT administration increased blood BHB levels 7-11 times within 1 hour. In the SD model, MCT significantly reduced immobility time in the FST, suggesting antidepressant effects. While the CUS model showed no significant change, a trend toward reduced immobility time was observed. MCT treatment also reduced stress-induced IL-1β levels in the rat hippocampus, although spine density remained unchanged.
MCT appears to alleviate stress-induced depression-like behaviors, likely through the suppression of IL-1β in the hippocampus. Owing to its ease of oral administration, MCT may offer a practical treatment for stress-related depression.
炎症被认为与抑郁症的病理生理过程有关,在患者体内观察到炎症细胞因子水平升高,如白细胞介素-1β(IL-1β)。抑郁症在患有慢性炎症性疾病的个体中也很常见。IL-1β会破坏突触传递并减少海马体中的神经发生,在抑郁症的发展中起关键作用。我们之前的研究发现,应激会激活大脑中的小胶质细胞,通过含3个吡啉结构域的核苷酸结合寡聚化结构域样受体家族(NLRP3)炎性小体产生IL-1β。此外,β-羟基丁酸(BHB)作为一种内源性酮体,通过抑制NLRP3激活和IL-1β产生来减轻应激诱导的抑郁症。然而,BHB较差的生物利用度限制了其有效性。中链甘油三酯(MCT)可以提高血液中BHB的水平,使其成为应激诱导抑郁症的一种潜在治疗方法。
我们在两种动物模型中测试了MCT:小鼠的社会挫败(SD)模型和大鼠的慢性不可预测应激(CUS)模型。两组均口服MCT以评估血液中BHB的水平。进行了行为测试,包括强迫游泳试验(FST),并分析脑组织中的IL-1β水平和脊柱密度。
服用MCT后1小时内,血液中BHB水平升高了7至11倍。在SD模型中,MCT显著减少了FST中的不动时间,表明具有抗抑郁作用。虽然CUS模型没有显著变化,但观察到不动时间有减少的趋势。MCT治疗还降低了大鼠海马体中应激诱导的IL-1β水平,尽管脊柱密度保持不变。
MCT似乎可以减轻应激诱导的类似抑郁的行为,可能是通过抑制海马体中的IL-1β实现的。由于其易于口服给药,MCT可能为与应激相关的抑郁症提供一种实用的治疗方法。