Antidepressant effects of Peiyuan Jieyu formula in a mouse model of chronic stress in conjunction with lipopolysaccharide-induced depression

犬尿氨酸 尾部悬挂试验 氟西汀 抗抑郁药 肿瘤坏死因子α 内分泌学 医学 内科学 脂多糖 犬尿氨酸途径 吲哚胺2,3-双加氧酶 药理学 巴比妥酸 炎症 慢性应激 腹腔注射 色氨酸 行为绝望测验 血清素 化学 海马体 生物化学 受体 氨基酸 NMDA受体
作者
Qin Tang,Yu Li,Tao Yang,Xiaoxu Fan,Lina Li,Chang Hong-sheng
出处
期刊:Journal of Traditional Chinese Medical Sciences [Elsevier BV]
卷期号:11 (1): 111-119 被引量:5
标识
DOI:10.1016/j.jtcms.2023.12.007
摘要

To explore the mechanism of the Peiyuan Jieyu formula in treating depression by assessing its impact on a lipopolysaccharide-induced (LPS-induced) depression model. We created a mouse model of depression by exposing mice that had previously received chronic stress to intraperitoneal LPS injections. The mice were divided into the following groups: control, model, fluoxetine, Tiansi Yin, Sini powder, and low-, medium-, and high Peiyuan Jieyu formula dose groups. Forced swim and tail suspension tests were used to assess the efficacy of the depression (despair) model, and weight gain rates were also measured. Furthermore, serum levels of various depression and inflammation-associated molecules, including tumor necrosis factor-α (TNF-α), interferon-γ (IFN-γ), tryptophan, 5-hydroxytryptamine, kynurenine (KYN), and kynurenic acid (KA) were assessed. Furthermore, the expression levels of ionic calcium-binding adaptor molecule-1 (IBA-1) and indoleamine 2,3-dioxygenase (IDO) mRNA in hippocampal microglia were measured. The model group displayed greater despair-associated immobility, which was shortened in response to various doses of Peiyuan Jieyu formula. Furthermore, formula administration significantly reduced serum TNF-α levels and hippocampal IDO mRNA expression. The high formula dose also reduced IFN-γ and IBA-1 levels, the latter was also decreased in response to the medium formula dose. However, the low formula dose reduced serum KYN level and KYN/tryptophan (TRP) and KYN/KA ratios. The Peiyuan Jieyu formula holds immense potential in treating depression, potentially inhibiting inflammation and improving TRP-KYN metabolic disorders.
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