The Codonopsis pilosula water extract improves testicular inflammatory aging in D-galactose induced aging mice by modulating the CLEC7A/inflammasome pathway

IF 5.4 2区 医学 Q1 CHEMISTRY, MEDICINAL Journal of ethnopharmacology Pub Date : 2025-03-18 DOI:10.1016/j.jep.2025.119645
Jing Wang , Xuechan Li , Caihong Li , Lijun Liu , Zhenjuan Wang , Juan Feng
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Abstract

Aim of the study

Aging-induced testicular inflammation impairs male fertility. The purpose of this study was to investigate the effectiveness and mechanism of C. pilosula water extract (CPWE) in preventing testicular inflammation in D-galactose-induced aging mice.

Materials and methods

The “The Plant List” database (www.theplantlist.org) provided verified plant taxonomy. D-galactose was intraperitoneally injected to induce an aging mice model, with high, medium, and low dosages of CPWE used as pharmacological interventions. The concentrations of superoxide dismutase (SOD), malondialdehyde (MDA), testosterone and in mouse serum or testicle samples after CPWE treatment were quantified using biochemical method. Hematoxylin and eosin (HE) staining was employed to assess the morphological features of testicular tissues, whereas immunohistochemical (IHC) analysis and enzyme-linked immunosorbent assay (ELISA) were conducted to evaluate the presence and levels of inflammatory cytokines interleukin-6 (IL-6) and interleukin-1β (IL-1β) within testicular samples of mice. Differentially expressed genes were identified using transcriptome sequencing; the genes and pathways regulated by CPWE, as well as immune cell infiltration, were examined using bioinformatics analysis. The expression of target gene and pathway-related protein was confirmed using real-time quantitative PCR and Western blotting.

Results

Treatment with CPWE alleviated the pathological alterations in the testicular tissues of aged mice, increased the concentrations of SOD and testosterone in the serum, and decreased the levels of MDA, IL-6 and IL-1β in the testes. The expression of C-C motif chemokine ligand 21a (Ccl21a) and C-C motif chemokine ligand 27b (Ccl27b) genes was downregulated after treatment with CPWE. The protein levels associated with the C-type lectin domain family 7, member A (CLEC7A)/inflammasome signaling pathway, including IL-1β, Caspase 8 (CASP8), and nuclear factor-kappa B (NF-κB), were found to be downregulated after treatment with CPWE. T cells, B cells, and macrophages showed a strong association with aging and the modulatory effects of CPWE.

Conclusions

The results indicate that CPWE regulates the CLEC7A/inflammasome pathway, thereby inhibiting inflammasomes activation and reducing the expressions of proinflammatory cytokines such as IL-6 and IL-1β, as well as chemokines such as Ccl21a and Ccl27b, providing substantial protection against age-related testicular inflammatory injury.

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党参水提取物通过调节CLEC7A/炎性小体通路改善d -半乳糖诱导的衰老小鼠睾丸炎症老化。
研究目的:衰老引起的睾丸炎症损害男性生育能力。本研究旨在探讨党参水提物(CPWE)对d -半乳糖致衰老小鼠睾丸炎症的预防作用及其机制。材料和方法:“The Plant List”数据库(www.theplantlist.org)提供了经过验证的植物分类。通过腹腔注射d -半乳糖诱导衰老小鼠模型,采用高、中、低剂量CPWE作为药理干预。采用生化法定量测定CPWE处理后小鼠血清或睾丸样品中超氧化物歧化酶(SOD)、丙二醛(MDA)、睾酮浓度。采用苏木精和伊红(HE)染色评价睾丸组织形态学特征,免疫组化(IHC)和酶联免疫吸附法(ELISA)评价小鼠睾丸组织中炎症因子白介素-6 (IL-6)和白细胞介素-1β (IL-1β)的存在和水平。利用转录组测序鉴定差异表达基因;利用生物信息学方法研究CPWE调控的基因和通路以及免疫细胞浸润情况。采用实时定量PCR和Western blotting检测靶基因和通路相关蛋白的表达。结果:CPWE可减轻老龄小鼠睾丸组织的病理改变,提高血清中SOD和睾酮的浓度,降低睾丸组织中MDA、IL-6和IL-1β的水平。CPWE处理后,C-C基序趋化因子配体21a (Ccl21a)和C-C基序趋化因子配体27b (Ccl27b)基因表达下调。与c型凝集素结构域家族7、成员A (CLEC7A)/炎性体信号通路相关的蛋白水平,包括IL-1β、Caspase 8 (CASP8)和核因子κB (NF-κB),在CPWE治疗后被发现下调。T细胞、B细胞和巨噬细胞与衰老和CPWE的调节作用密切相关。结论:CPWE通过调控CLEC7A/炎性小体通路,抑制炎性小体活化,降低IL-6、IL-1β等促炎因子及Ccl21a、Ccl27b等趋化因子的表达,对年龄相关性睾丸炎性损伤具有实质性保护作用。
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来源期刊
Journal of ethnopharmacology
Journal of ethnopharmacology 医学-全科医学与补充医学
CiteScore
10.30
自引率
5.60%
发文量
967
审稿时长
77 days
期刊介绍: The Journal of Ethnopharmacology is dedicated to the exchange of information and understandings about people''s use of plants, fungi, animals, microorganisms and minerals and their biological and pharmacological effects based on the principles established through international conventions. Early people confronted with illness and disease, discovered a wealth of useful therapeutic agents in the plant and animal kingdoms. The empirical knowledge of these medicinal substances and their toxic potential was passed on by oral tradition and sometimes recorded in herbals and other texts on materia medica. Many valuable drugs of today (e.g., atropine, ephedrine, tubocurarine, digoxin, reserpine) came into use through the study of indigenous remedies. Chemists continue to use plant-derived drugs (e.g., morphine, taxol, physostigmine, quinidine, emetine) as prototypes in their attempts to develop more effective and less toxic medicinals.
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