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通过网络药理学和分子对接探究安神定志方治疗乳腺癌创伤后应激障碍的临床疗效及作用机制。

Clinical Efficacy and Mechanistic Insights of Anshen Dingzhi Prescription on Breast Cancer-Related PTSD Through Network Pharmacology and Molecular Docking.

机构信息

The First Affiliated Hospital of Anhui University of Chinese Medicine, Hefei, China.

Anhui University of Chinese Medicine, Hefei, China.

出版信息

Integr Cancer Ther. 2024 Jan-Dec;23:15347354241285435. doi: 10.1177/15347354241285435.

DOI:10.1177/15347354241285435
PMID:39344020
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11450869/
Abstract

Anshen Dingzhi prescription (ADP) is a classic prescription of traditional Chinese medicine, which has been used in the treatment of neuropsychiatric diseases. However, its treatment of breast cancer-related post-traumatic stress disorder (BC-PTSD) lacks clinical research evidence and its mechanism is not clear. The present study investigated the efficacy and action mechanism of ADP against BC-PTSD. The results of the clinical trial showed that after 4 weeks of treatment, both groups showed reduced post-traumatic stress disorder checklist-civilian version (PCL-C), Pittsburgh sleep quality index (PSQI), self-rating depression scale (SDS) and self-rating anxiety scale (SAS) scores, and increased functional assessment of cancer therapy-breast (FACT-B) scores. The serum cortisol (CORT), tumor necrosis factor-alpha (TNF-α) and interleukin-1 beta (IL-1β) levels were decreased and brain-derived neurotrophic factor (BDNF) level were increased, and the improvement of serum TNF-α, IL-1β, and BDNF in treatment group was better than that of the control group. The overall treatment efficacy in the treatment group (43.90%) was superior to that in the control group (23.81%), and the overall incidence of adverse effects was lower than that in the control group. The results of network analysis and molecular docking showed that ADP blood components could act on IL1B, TNF, and BDNF. ADP contributes to the treatment of BC-PTSD symptoms, with a mechanism possibly related to its regulatory effect on TNF-α, IL-1β, and BDNF levels.Trial registration: Chinese Clinical Trial Registry, http://www.chictr.org.cn,ChiCTR2300077801.

摘要

安神定志方(ADP)是一种经典的中药方剂,已用于治疗神经精神疾病。然而,其治疗乳腺癌相关创伤后应激障碍(BC-PTSD)缺乏临床研究证据,其机制尚不清楚。本研究探讨了 ADP 治疗 BC-PTSD 的疗效和作用机制。临床试验结果表明,治疗 4 周后,两组 PTSD Checklist-Civilian 版(PCL-C)、匹兹堡睡眠质量指数(PSQI)、抑郁自评量表(SDS)和焦虑自评量表(SAS)评分均降低,功能评估癌症治疗-乳房(FACT-B)评分均升高。血清皮质醇(CORT)、肿瘤坏死因子-α(TNF-α)和白细胞介素-1β(IL-1β)水平降低,脑源性神经营养因子(BDNF)水平升高,治疗组血清 TNF-α、IL-1β和 BDNF 的改善优于对照组。治疗组总有效率(43.90%)优于对照组(23.81%),不良反应总发生率低于对照组。网络分析和分子对接结果表明,ADP 血液成分可作用于 IL1B、TNF 和 BDNF。ADP 有助于治疗 BC-PTSD 症状,其机制可能与其对 TNF-α、IL-1β 和 BDNF 水平的调节作用有关。试验注册:中国临床试验注册中心,http://www.chictr.org.cn,ChiCTR2300077801。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d74f/11450869/8447d710c44b/10.1177_15347354241285435-fig8.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d74f/11450869/9ef1074e2ba7/10.1177_15347354241285435-fig1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d74f/11450869/4fc3ab0f35ef/10.1177_15347354241285435-fig2.jpg
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https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d74f/11450869/28ca5bb57e66/10.1177_15347354241285435-fig5.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d74f/11450869/3701fbe3eec2/10.1177_15347354241285435-fig6.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d74f/11450869/335b1a75d93c/10.1177_15347354241285435-fig7.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d74f/11450869/8447d710c44b/10.1177_15347354241285435-fig8.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d74f/11450869/9ef1074e2ba7/10.1177_15347354241285435-fig1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d74f/11450869/4fc3ab0f35ef/10.1177_15347354241285435-fig2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d74f/11450869/3f5a8064622e/10.1177_15347354241285435-fig3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d74f/11450869/62f9c3e05556/10.1177_15347354241285435-fig4.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d74f/11450869/28ca5bb57e66/10.1177_15347354241285435-fig5.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d74f/11450869/3701fbe3eec2/10.1177_15347354241285435-fig6.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d74f/11450869/335b1a75d93c/10.1177_15347354241285435-fig7.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d74f/11450869/8447d710c44b/10.1177_15347354241285435-fig8.jpg

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