通过抑制炎症和防止海马损伤,吸入 H2/O2(66.7 %/33.3 %)可减轻糖尿病并发抑郁症小鼠的抑郁样行为。

Huaju Fan, Yanhua Shi, Haiqiang Liu, Xiaofei Zuo, Yanmei Yang, Hao Yin, Yanyan Li, Xianghui Wang, Li Liu, Fengjiao Wang, Huifang Han, Qianying Wu, Nana Yang, Yaohui Tang, Guohua Lu
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引用次数: 0

摘要

糖尿病并发抑郁症(DD)是一种常见的心身疾病。它以严重的认知障碍为特征,致残率和死亡率都很高。虽然有常规的治疗方案,但这些方案在控制糖尿病并发抑郁症方面的疗效仍然有限。分子氢(H2)是一种选择性羟自由基清除剂,在治疗各种系统性疾病方面已显示出治疗潜力。本研究旨在探讨氢对 DD 的治疗效果。通过腹腔注射链脲佐菌素(STZ,150 毫克/千克)和脂多糖(LPS,0.5 毫克/千克),建立了 DD 小鼠模型。诱导DD后,对小鼠进行为期7天的H2/O2(66.7%/33.3%)吸入治疗。通过标准行为测试进行行为评估,并使用酶联免疫吸附试验(ELISA)检测外周血血清和海马组织中的炎症细胞因子水平。此外,还对海马进行了磁共振成像(MRI)扫描和免疫荧光染色,以评估海马结构的完整性。结果表明,吸入 H2/O2(66.7 %/33.3 %)能明显改善 DD 小鼠的抑郁行为和症状,逆转海马体积缩小,降低外周血血清和海马组织中的炎性细胞因子水平,并抑制海马中 A1 星形胶质细胞的活化。我们的研究表明,H2/O2(66.7%/33.3%)吸入疗法可为 DD 及其相关症状提供一种前景广阔的治疗策略。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Inhalation of H2/O2 (66.7 %/33.3 %) mitigates depression-like behaviors in diabetes mellitus complicated with depression mice via suppressing inflammation and preventing hippocampal damage.

Diabetes mellitus complicated with depression (DD) is a prevalent psychosomatic disorder. It is characterized by severe cognitive impairment, and associated with high rates of disability and mortality. Although conventional treatment options are available, the efficacy of these regimens in managing DD remains limited. Molecular hydrogen (H2), a selective hydroxyl radical scavenger, has shown therapeutic potential in the treatment of various systemic diseases. This study aims to investigate the therapeutic effects of H2 on DD. A DD mouse model was established through intraperitoneal injection of streptozotocin (STZ, 150 mg/kg) and lipopolysaccharide (LPS, 0.5 mg/kg). Following the induction of DD, the mice were treated with H2/O2 (66.7 %/33.3 %)inhalation for 7 days. Behavioral assessments were conducted by standard behavioral tests, and the levels of inflammatory cytokines in peripheral blood serum and hippocampal tissue were measured using enzyme-linked immunosorbent assay (ELISA). Furthermore, magnetic resonance imaging (MRI) scans and immunofluorescence staining of the hippocampus were performed to evaluate hippocampal structural integrity. The results demonstrated that inhalation of H2/O2 (66.7 %/33.3 %) significantly ameliorated depressive behaviors and symptoms in DD mice, reversed hippocampal volume reduction, decreased inflammatory cytokine levels in peripheral blood serum and hippocampal tissue, and inhibited the activation of A1 astrocytes in the hippocampus. Our study suggests that H2/O2 (66.7 %/33.3 %) inhalation therapy may offer a promising treatment strategy for DD and its associated symptoms.

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