State Key Laboratory of Developmental Biology of Freshwater Fish, Protein Chemistry Laboratory, College of Life Sciences, Hunan Normal University, Changsha, Hunan, China.
Front Immunol. 2023 May 15;14:1171351. doi: 10.3389/fimmu.2023.1171351. eCollection 2023.
Depression has a high incidence and seriously endangers human health. Accumulated evidence indicates that targeting neuroinflammation is a potential avenue for neuroprotection and thus depression prevention. Herein, the effects of latroeggtoxin-VI (LETX-VI), a bioactive protein from the eggs of spider , on lipopolysaccharide (LPS)-induced inflammation and depression were systematically investigated using RAW264.7 macrophages and depression mouse model. Pretreatment with LETX-VI suppressed LPS-evoked NF-κB signaling pathway activation, inhibited LPS-induced over-production of NO, iNOS, IL-6 and TNF-α; at the same time LETX-VI mitigated the inhibitory effect of LPS on the expression of anti-inflammatory factors such as Arg-1, thereby suppressing oxidative stress and excessive inflammation. Culture of PC12 cells with the conditioned medium of RAW264.7 cells pretreated with LETX-VI demonstrated the neuroprotective effect of LETX-VI due to its anti-inflammation effect. In the LPS-induced depression mouse model, pretreatment with LETX-VI improved the LPS-induced depression-like behaviors, inhibited the activation of microglia and astrocytes, prevented the down-regulation of Nurr1 expression and alleviated the LPS-caused adverse changes in the brain tissues. Taken together, these and findings provide powerful insights into the anti-inflammation-based neuroprotective and antidepressant mechanisms of LETX-VI, which is helpful to deeply reveal the biological effects and potential applications of LETX-VI.
抑郁症的发病率很高,严重危害人类健康。大量证据表明,针对神经炎症是神经保护和预防抑郁症的潜在途径。本文系统研究了蜘蛛卵源生物活性蛋白 latroeggtoxin-VI(LETX-VI)对脂多糖(LPS)诱导的炎症和抑郁的作用,采用 RAW264.7 巨噬细胞和抑郁小鼠模型进行了研究。LETX-VI 预处理抑制了 LPS 诱导的 NF-κB 信号通路激活,抑制了 LPS 诱导的 NO、iNOS、IL-6 和 TNF-α的过度产生;同时,LETX-VI 减轻了 LPS 对抗炎因子如 Arg-1 表达的抑制作用,从而抑制了氧化应激和过度炎症。用 LETX-VI 预处理的 RAW264.7 细胞条件培养基培养 PC12 细胞,证明了 LETX-VI 的神经保护作用,这是由于其抗炎作用。在 LPS 诱导的抑郁小鼠模型中,LETX-VI 预处理改善了 LPS 诱导的抑郁样行为,抑制了小胶质细胞和星形胶质细胞的激活,防止了 Nurr1 表达的下调,并缓解了 LPS 引起的脑组织不良变化。总之,这些发现为 LETX-VI 的基于抗炎的神经保护和抗抑郁机制提供了有力的见解,有助于深入揭示 LETX-VI 的生物学效应和潜在应用。