Laboratory of Stress Medicine, Faculty of Psychology and Mental Health, Second Military Medical University, 800 Xiangyin Road, Shanghai, China.
Department of Psychiatry, Faculty of Psychology and Mental Health, Second Military Medical University, 800 Xiangyin Road, Shanghai, China.
J Neuroinflammation. 2017 Oct 30;14(1):210. doi: 10.1186/s12974-017-0985-4.
Abundant reports indicated that depression was often comorbid with type 2 diabetes and even metabolic syndrome. Considering they might share common biological origins, it was tentatively attributed to the chronic cytokine-mediated inflammatory response which was induced by dysregulation of HPA axis and overactivation of innate immunity. However, the exact mechanisms remain obscure. Herein, we mainly focused on the function of the NLRP3 inflammasome to investigate this issue.
Male C57BL/6 mice were subjected to 12 weeks of chronic unpredictable mild stress (CUMS), some of which were injected with glyburide or fluoxetine. After CUMS procedure, behavioral and metabolic tests were carried out. In order to evaluate the systemic inflammation associated with inflammasome activation, IL-1β and inflammasome components in hippocampi and pancreases, as well as corticosterone and IL-1β in serum were detected separately. Moreover, immunostaining was performed to assess morphologic characteristics of pancreases.
In the present study, we found that 12 weeks' chronic stress resulted in depressive-like behavior comorbid with insulin resistance. Furthermore, antidiabetic drug glyburide, an inhibitor of the NLRP3 inflammasome, was discovered to be effective in preventing the experimental comorbidity. In brief, it improved behavioral performance, ameliorated insulin intolerance as well as insulin signaling in the hippocampus possibly through inhibiting NLRP3 inflammasome activation by suppressing the expression of TXNIP.
All these evidence supported our hypothesis that chronic stress led to comorbidity of depressive-like behavior and insulin resistance via long-term mild inflammation. More importantly, based on the beneficial effects of blocking the activation of the NLRP3 inflammasome, we provided a potential therapeutic target for clinical comorbidity and a new strategy for management of both diabetes and depression.
大量报道表明,抑郁常与 2 型糖尿病甚至代谢综合征并发。鉴于它们可能具有共同的生物学起源,人们推测这是由于 HPA 轴失调和固有免疫过度激活引起的慢性细胞因子介导的炎症反应所致。然而,确切的机制仍不清楚。在此,我们主要关注 NLRP3 炎性小体的功能来探讨这个问题。
雄性 C57BL/6 小鼠接受 12 周的慢性不可预测轻度应激(CUMS),其中一些注射了格列本脲或氟西汀。CUMS 程序后,进行行为和代谢测试。为了评估与炎性小体激活相关的全身炎症,分别检测海马和胰腺中的 IL-1β 和炎性小体成分,以及血清中的皮质酮和 IL-1β。此外,进行免疫染色以评估胰腺的形态特征。
在本研究中,我们发现 12 周的慢性应激导致伴有胰岛素抵抗的抑郁样行为。此外,发现抗糖尿病药物格列本脲,即 NLRP3 炎性小体的抑制剂,可有效预防实验性合并症。简而言之,它通过抑制 TXNIP 来改善行为表现,改善海马中的胰岛素不耐受和胰岛素信号,从而改善行为表现。
所有这些证据都支持我们的假设,即慢性应激通过长期轻度炎症导致抑郁样行为和胰岛素抵抗的合并症。更重要的是,基于阻断 NLRP3 炎性小体激活的有益效果,我们为临床合并症提供了一个潜在的治疗靶点,并为糖尿病和抑郁症的管理提供了一个新策略。