Liu Jian, Yang Hui, Zhao Hong-Qing, Li Wei, Liu Zhuo, Wang Yu-Hong
Center for Medical Research and Innovation, the First Hospital of Hunan University of Chinese Medicine Changsha 410007, China.
Hunan Key Laboratory of Traditional Chinese Medicine Prevention and Treatment of Depressive Diseases Changsha 410208, China Science & Technology Innovation Center, Hunan University of Chinese Medicine Changsha 410208, China.
Zhongguo Zhong Yao Za Zhi. 2024 Sep;49(17):4597-4606. doi: 10.19540/j.cnki.cjcmm.20240611.707.
This study aims to reveal the protective effect and mechanism of Zuogui Jiangtang Jieyu Formula on the damage to hippo-campal synaptic microenvironment in rats with diabetes-related depression(DD) via regulating microglia immune receptor molecule-like family member f(CD300f)/Toll-like receptor 4(TLR4) signal. Firstly, the model of DD rats was established by a two-week high-fat diet+STZ injection+chronic mild and unpredictable stress plus isolation for 28 days. The rats were randomly divided into normal group, model group, CD300f blocker(CLM1, 2 μg·kg(-1)) group, CD300f agonist(Fcγ, 5 μg·kg(-1)) group, positive drug(0.18 g·kg(-1) metformin+1.8 mg·kg(-1) fluoxetine) group, and high-dose and low-dose(20.52 and 10.26 g·kg~(-1)) Zuogui Jiangtang Jieyu Formula groups. Depression-like behavior of rats was evaluated by open field and forced swimming experiments. The levels of blood glucose and insulin were detected by biochemical analysis. The levels of tumor necrosis factor α(TNF-α), interleukin-1β(IL-1β), indoleamine 2, 3-dioxygenase(IDO), 5-hydroxytryptamine(5-HT), and dopamine(DA) in the hippocampus were detected by enzyme-linked immunosorbent assay. The changes in the synaptic ultrastructure in hippocampal neurons of rats were observed by transmission electron microscopy. The protein expressions of CD300f, TLR4, synaptophysin(SYN), and postsynaptic density protein 95(PSD-95) in microglial cells of the hippocampus were detected by immunofluorescence and Western blot. The results indicated that compared with that in the normal group, the total movement distance in open field experiments was reduced in the model group, and the immobility time in forced swimming experiments increased, with an elevated insulin level in serum, as well as TNF-α, IL-1β, and IDO levels in the hippocampus. The 5-HT and DA levels in the hippocampus were reduced. In addition, the CD300f expression was down-regulated in microglial cells of the hippocampus, and the TLR4 expression was up-regulated. Moreover, the expression of synapse-related proteins SYN and PSD-95 in hippocampal neurons decreased, and the synaptic ultrastructure of hippocampal neurons was significantly damaged. Compared with the model group, the CD300f blocker and agonist aggravated and alleviated the above abnormal changes, respectively. High-dose and low-dose Zuogui Jiangtang Jieyu Formula could significantly improve the above depression-like beha-vior in rats, inhibit the abnormal increase of TNF-α, IL-1β, and IDO and the decrease of 5-HT and DA, effectively increase the expression of CD300f in microglial cells, and decrease the expression of TLR4. They could up-regulate the protein expression of presyna-ptic membrane SYN and postsynaptic membrane PSD-95 in hippocampal neurons and finally improve the damage to the hippocampal synaptic microenvironment. In conclusion, this research confirmed that Zuogui Jiangtang Jieyu Formula effectively alleviated the depression-like behavior and inhibited inflammatory activation of microglial cells in the hippocampus of rats with DD, and the mechanism might be related to the regulation of CD300f/TLR4 signal to alleviate the damage to hippocampal synaptic microenvironment.
本研究旨在通过调节小胶质细胞免疫受体分子样家族成员f(CD300f)/Toll样受体4(TLR4)信号,揭示左归丸降糖解郁方对糖尿病相关性抑郁(DD)大鼠海马突触微环境损伤的保护作用及机制。首先,通过两周高脂饮食+链脲佐菌素注射+慢性轻度不可预测应激加隔离28天建立DD大鼠模型。将大鼠随机分为正常组、模型组、CD300f阻断剂(CLM1,2μg·kg⁻¹)组、CD300f激动剂(Fcγ,5μg·kg⁻¹)组、阳性药物(0.18g·kg⁻¹二甲双胍+1.8mg·kg⁻¹氟西汀)组以及高剂量和低剂量(20.52和10.26g·kg⁻¹)左归丸降糖解郁方组。通过旷场实验和强迫游泳实验评估大鼠的抑郁样行为。通过生化分析检测血糖和胰岛素水平。采用酶联免疫吸附测定法检测海马中肿瘤坏死因子α(TNF-α)、白细胞介素-1β(IL- β)、吲哚胺2,3-双加氧酶(IDO)、5-羟色胺(5-HT)和多巴胺(DA)的水平。通过透射电子显微镜观察大鼠海马神经元突触超微结构的变化。采用免疫荧光和蛋白质免疫印迹法检测海马小胶质细胞中CD300f、TLR4、突触素(SYN)和突触后致密蛋白95(PSD-95)的蛋白表达。结果表明,与正常组相比,模型组旷场实验中的总移动距离缩短,强迫游泳实验中的不动时间增加,血清胰岛素水平升高,海马中TNF-α、IL-1β和IDO水平升高,海马中5-HT和DA水平降低。此外,海马小胶质细胞中CD300f表达下调,TLR4表达上调。而且,海马神经元中突触相关蛋白SYN和PSD-95的表达降低,海马神经元的突触超微结构明显受损。与模型组相比,CD300f阻断剂和激动剂分别加重和减轻了上述异常变化。高剂量和低剂量左归丸降糖解郁方均可显著改善大鼠上述抑郁样行为,抑制TNF-α、IL-1β和IDO的异常升高以及5-HT和DA的降低,有效增加小胶质细胞中CD300f的表达,降低TLR4的表达。它们可上调海马神经元突触前膜SYN和突触后膜PSD-95的蛋白表达,最终改善海马突触微环境的损伤。综上所述,本研究证实左归丸降糖解郁方有效减轻DD大鼠的抑郁样行为并抑制海马小胶质细胞的炎性激活,其机制可能与调节CD300f/TLR4信号以减轻海马突触微环境损伤有关。