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靶向慢性前列腺炎中的脑-肠-前列腺轴:机制与治疗方法

Targeting the brain-gut-prostate axis in chronic prostatitis: mechanisms and therapeutics.

作者信息

Song Shiwei, Zhang Chunlei, Zhang Bin, Yin Jinlong, Yu Chang, Wang Xuanrong, Wang Qing, Ma Fulin, Yang Changfeng, Chang Dehui

机构信息

Department of Urology, 940th Hospital of the Joint Logistics Support Force, Lanzhou, China.

First School of Clinical Medicine, Gansu University of Chinese Medicine, Lanzhou, China.

出版信息

Front Endocrinol (Lausanne). 2025 Jul 4;16:1628094. doi: 10.3389/fendo.2025.1628094. eCollection 2025.


DOI:10.3389/fendo.2025.1628094
PMID:40687578
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC12270845/
Abstract

Chronic prostatitis/chronic pelvic pain syndrome (CP/CPPS), a refractory urinary system disorder, is closely associated with dysregulation of the brain-gut-prostate axis. Emerging evidence highlights the pivotal role of gut microbiota dysbiosis and its bidirectional interactions with the neuroimmune system in CP/CPPS pathogenesis. This systematic review integrates perspectives from microbiomics, neuroimmunology, and metabolomics to propose a theoretical framework of the brain-gut-prostate axis and multi-dimensional therapeutic strategies targeting this axis. By transcending conventional localized anti-inflammatory approaches, these strategies aim to address clinical resistance and phenotypic heterogeneity. Mechanistic insights into microbiota-derived metabolites (e.g., short-chain fatty acids, SCFAs), neuroendocrine signaling (e.g., thyrotropin-releasing hormone, TRH), and immune crosstalk (e.g., Th17/Treg imbalance) are explored, alongside innovative therapies such as microbiome modulation, neural interventions, and immune regulation. This holistic paradigm not only provides new mechanistic insights but also offers promising avenues for personalized management and translational research in CP/CPPS, potentially overcoming current therapeutic bottlenecks.

摘要

慢性前列腺炎/慢性盆腔疼痛综合征(CP/CPPS)是一种难治性泌尿系统疾病,与脑-肠-前列腺轴的失调密切相关。新出现的证据强调了肠道微生物群失调及其与神经免疫系统的双向相互作用在CP/CPPS发病机制中的关键作用。本系统综述整合了微生物组学、神经免疫学和代谢组学的观点,提出了脑-肠-前列腺轴的理论框架以及针对该轴的多维治疗策略。通过超越传统的局部抗炎方法,这些策略旨在解决临床耐药性和表型异质性问题。探讨了微生物群衍生代谢物(如短链脂肪酸,SCFAs)、神经内分泌信号(如促甲状腺激素释放激素,TRH)和免疫串扰(如Th17/Treg失衡)的机制,以及微生物群调节、神经干预和免疫调节等创新疗法。这种整体范式不仅提供了新的机制见解,还为CP/CPPS的个性化管理和转化研究提供了有前景的途径,有可能克服当前的治疗瓶颈。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/81e4/12270845/7ce6dd1a44d4/fendo-16-1628094-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/81e4/12270845/7ce6dd1a44d4/fendo-16-1628094-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/81e4/12270845/7ce6dd1a44d4/fendo-16-1628094-g001.jpg

相似文献

[1]
Targeting the brain-gut-prostate axis in chronic prostatitis: mechanisms and therapeutics.

Front Endocrinol (Lausanne). 2025-7-4

[2]
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Mol Biol Rep. 2025-6-21

[3]
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[4]
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[5]
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[6]
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[7]
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[8]
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[9]
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[10]
Gut Microbiota-Targeted Therapeutics for Metabolic Disorders: Mechanistic Insights into the Synergy of Probiotic-Fermented Herbal Bioactives.

Int J Mol Sci. 2025-6-7

本文引用的文献

[1]
The characteristics of brain function alterations in patients with chronic prostatitis/chronic pelvic pain syndrome across varying symptom severities evaluated by NIH-CPSI.

Front Neurosci. 2025-2-26

[2]
Study progress of etiologic mechanisms of chronic prostatitis/chronic pelvic pain syndrome.

Int Immunopharmacol. 2025-2-20

[3]
Probiotics in the Management of Chronic Bacterial Prostatitis Patients: A Randomized, Double-Blind Trial to Evaluate a Possible Link Between Gut Microbiota Restoring and Symptom Relief.

Microorganisms. 2025-1-10

[4]
Inflammatory Prostatitis Plus IBS-D Subtype and Correlation with Immunomodulating Agent Imbalance in Seminal Plasma: Novel Combined Treatment.

Diseases. 2024-10-18

[5]
The role of gut microbiota in prostate inflammation and benign prostatic hyperplasia and its therapeutic implications.

Heliyon. 2024-9-21

[6]
The role of TRPV1 in chronic prostatitis: a review.

Front Pharmacol. 2024-9-19

[7]
NLRP3-mediated IL-1β in regulating the imbalance between Th17 and Treg in experimental autoimmune prostatitis.

Sci Rep. 2024-8-13

[8]
Chronic prostatitis/chronic pelvic pain syndrome induces metabolomic changes in expressed prostatic secretions and plasma.

Asian J Androl. 2025-1-1

[9]
Unraveling CCL20's role by regulating Th17 cell chemotaxis in experimental autoimmune prostatitis.

J Cell Mol Med. 2024-5

[10]
Genetic insights into gut microbiota and risk of prostatitis: a Mendelian randomization study.

Front Microbiol. 2024-4-12

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