• 文献检索
  • 文档翻译
  • 深度研究
  • 学术资讯
  • Suppr Zotero 插件Zotero 插件
  • 邀请有礼
  • 套餐&价格
  • 历史记录
应用&插件
Suppr Zotero 插件Zotero 插件浏览器插件Mac 客户端Windows 客户端微信小程序
定价
高级版会员购买积分包购买API积分包
服务
文献检索文档翻译深度研究API 文档MCP 服务
关于我们
关于 Suppr公司介绍联系我们用户协议隐私条款
关注我们

Suppr 超能文献

核心技术专利:CN118964589B侵权必究
粤ICP备2023148730 号-1Suppr @ 2026

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验

保元解毒汤通过调节小鼠肌肉线粒体功能减轻癌症恶病质诱导的肌肉萎缩。

Baoyuan Jiedu decoction alleviating cancer cachexia-Induced muscle atrophy by regulating muscle mitochondrial function in mice.

作者信息

Zhang Beiying, Bi Qianyu, Huang Shengqi, Lv Siyuan, Zong Xin, Wang Mengran, Ji Xuming

机构信息

School of Basic Medical Science, Zhejiang Chinese Medical University, Hangzhou, China.

Weifang Nursing Vocational College, Weifang, China.

出版信息

Front Pharmacol. 2022 Aug 19;13:914597. doi: 10.3389/fphar.2022.914597. eCollection 2022.

DOI:10.3389/fphar.2022.914597
PMID:36060011
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC9437209/
Abstract

Cancer cachexia is a complex syndrome that leads to an ongoing loss of skeletal muscle mass in many malignant tumors. Our previous studies have evaluated the effectiveness of Baoyuan Jiedu decoction (BJD) in alleviating cancer-induced muscle atrophy. However, the mechanisms of BJD regulating muscle atrophy could not be fully understood. Therefore, we further investigated the mechanisms of BJD mitigating muscle atrophy both in an mouse model and the Lewis-conditioned medium-induced C2C12 myotube atrophy model. We confirmed the quality of BJD extracts by HPLC. In an study, body weight loss and muscle atrophy were alleviated with BJD treatment. GO analysis suggested that ATP metabolism and mitochondria were involved. The results of the electron microscope show that BJD treatment may have a healing effect on mitochondrial structure. Moreover, ATP content and mitochondrial numbers were improved with BJD treatment. Furthermore, both and , we demonstrated that the BJD treatment could improve mitochondrial function owing to the increased number of mitochondria, balanced dynamic, and regulation of the electron transport chain according to the protein and mRNA expressions. In addition, oxidative stress caused by mitochondrial dysfunction was ameliorated by BJD treatment in mice. Consequently, our study provides proof for BJD treatment alleviating cancer cachexia-induced muscle atrophy by modulating mitochondrial function in mice.

摘要

癌症恶病质是一种复杂的综合征,会导致许多恶性肿瘤患者的骨骼肌质量持续流失。我们之前的研究评估了保元解毒汤(BJD)在减轻癌症引起的肌肉萎缩方面的有效性。然而,BJD调节肌肉萎缩的机制尚未完全明确。因此,我们进一步研究了BJD在小鼠模型和Lewis条件培养基诱导的C2C12肌管萎缩模型中减轻肌肉萎缩的机制。我们通过高效液相色谱法(HPLC)确认了BJD提取物的质量。在一项研究中,BJD治疗减轻了体重减轻和肌肉萎缩。基因本体(GO)分析表明,ATP代谢和线粒体参与其中。电子显微镜结果显示,BJD治疗可能对线粒体结构有修复作用。此外,BJD治疗提高了ATP含量和线粒体数量。此外,在体内和体外,我们都证明,根据蛋白质和mRNA表达情况,BJD治疗可通过增加线粒体数量、平衡动力学以及调节电子传递链来改善线粒体功能。此外,BJD治疗改善了体内小鼠因线粒体功能障碍引起的氧化应激。因此,我们的研究为BJD治疗通过调节体内小鼠的线粒体功能减轻癌症恶病质引起的肌肉萎缩提供了证据。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5d1c/9437209/0dc27dc9a15e/fphar-13-914597-g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5d1c/9437209/0a184fa72a8c/fphar-13-914597-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5d1c/9437209/f694a779bba2/fphar-13-914597-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5d1c/9437209/47d11bf8e896/fphar-13-914597-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5d1c/9437209/14b22ac860a1/fphar-13-914597-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5d1c/9437209/bdc993aa4a2a/fphar-13-914597-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5d1c/9437209/0dc27dc9a15e/fphar-13-914597-g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5d1c/9437209/0a184fa72a8c/fphar-13-914597-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5d1c/9437209/f694a779bba2/fphar-13-914597-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5d1c/9437209/47d11bf8e896/fphar-13-914597-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5d1c/9437209/14b22ac860a1/fphar-13-914597-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5d1c/9437209/bdc993aa4a2a/fphar-13-914597-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5d1c/9437209/0dc27dc9a15e/fphar-13-914597-g006.jpg

相似文献

1
Baoyuan Jiedu decoction alleviating cancer cachexia-Induced muscle atrophy by regulating muscle mitochondrial function in mice.保元解毒汤通过调节小鼠肌肉线粒体功能减轻癌症恶病质诱导的肌肉萎缩。
Front Pharmacol. 2022 Aug 19;13:914597. doi: 10.3389/fphar.2022.914597. eCollection 2022.
2
Baoyuan Jiedu Decoction Alleviates Cancer-Induced Myotube Atrophy by Regulating Mitochondrial Dynamics Through p38 MAPK/PGC-1α Signaling Pathway.保元解毒汤通过p38丝裂原活化蛋白激酶/过氧化物酶体增殖物激活受体γ共激活因子-1α信号通路调节线粒体动力学,减轻癌症诱导的肌管萎缩。
Front Oncol. 2020 Sep 30;10:523577. doi: 10.3389/fonc.2020.523577. eCollection 2020.
3
Chinese Herbal Medicine Baoyuan Jiedu Decoction Inhibited Muscle Atrophy of Cancer Cachexia through Atrogin-l and MuRF-1.中药保元解毒汤通过Atrogin-1和MuRF-1抑制癌症恶病质的肌肉萎缩。
Evid Based Complement Alternat Med. 2017;2017:6268378. doi: 10.1155/2017/6268378. Epub 2017 Feb 14.
4
Alantolactone ameliorates cancer cachexia-associated muscle atrophy mainly by inhibiting the STAT3 signaling pathway.冬凌草甲素主要通过抑制 STAT3 信号通路改善癌症恶病质相关的肌肉萎缩。
Phytomedicine. 2022 Jan;95:153858. doi: 10.1016/j.phymed.2021.153858. Epub 2021 Nov 15.
5
Modified Sijunzi decoction can alleviate cisplatin-induced toxicity and prolong the survival time of cachectic mice by recovering muscle atrophy.加味四君子汤可通过恢复肌肉萎缩来减轻顺铂引起的毒性并延长恶病质小鼠的存活时间。
J Ethnopharmacol. 2019 Apr 6;233:47-55. doi: 10.1016/j.jep.2018.12.035. Epub 2018 Dec 24.
6
IL-6 regulation on skeletal muscle mitochondrial remodeling during cancer cachexia in the ApcMin/+ mouse.白细胞介素-6 对 ApcMin/+ 小鼠癌症恶病质骨骼肌线粒体重构的调节作用。
Skelet Muscle. 2012 Jul 6;2:14. doi: 10.1186/2044-5040-2-14.
7
Phosphorylation of Dynamin-Related Protein 1 (DRP1) Regulates Mitochondrial Dynamics and Skeletal Muscle Wasting in Cancer Cachexia.动力相关蛋白1(DRP1)的磷酸化调节癌症恶病质中的线粒体动力学和骨骼肌萎缩。
Front Cell Dev Biol. 2021 Aug 5;9:673618. doi: 10.3389/fcell.2021.673618. eCollection 2021.
8
Repeated eccentric contractions positively regulate muscle oxidative metabolism and protein synthesis during cancer cachexia in mice.重复进行离心收缩可正向调节小鼠癌症恶病质期间的肌肉氧化代谢和蛋白质合成。
J Appl Physiol (1985). 2020 Jun 1;128(6):1666-1676. doi: 10.1152/japplphysiol.00908.2019. Epub 2020 May 14.
9
IL-17A contributes to skeletal muscle atrophy in lung cancer-induced cachexia via JAK2/STAT3 pathway.IL-17A 通过 JAK2/STAT3 通路促进肺癌恶病质所致骨骼肌萎缩。
Am J Physiol Cell Physiol. 2022 May 1;322(5):C814-C824. doi: 10.1152/ajpcell.00463.2021. Epub 2022 Mar 23.
10
IMB0901 inhibits muscle atrophy induced by cancer cachexia through MSTN signaling pathway.IMB0901 通过 MSTN 信号通路抑制癌性恶病质引起的肌肉萎缩。
Skelet Muscle. 2019 Mar 28;9(1):8. doi: 10.1186/s13395-019-0193-2.

引用本文的文献

1
A comprehensive review of animal models for cancer cachexia: Implications for translational research.癌症恶病质动物模型的全面综述:对转化研究的启示
Genes Dis. 2023 Sep 13;11(6):101080. doi: 10.1016/j.gendis.2023.101080. eCollection 2024 Nov.

本文引用的文献

1
UBE2L3, a Partner of MuRF1/TRIM63, Is Involved in the Degradation of Myofibrillar Actin and Myosin.UBE2L3 是 MuRF1/TRIM63 的伴侣,参与肌球蛋白细丝和肌球蛋白的降解。
Cells. 2021 Aug 3;10(8):1974. doi: 10.3390/cells10081974.
2
Cancer-Mediated Muscle Cachexia: Etiology and Clinical Management.癌症介导的肌肉恶病质:病因学与临床管理
Trends Endocrinol Metab. 2021 Jun;32(6):382-402. doi: 10.1016/j.tem.2021.03.007. Epub 2021 Apr 19.
3
Zi Shen Decoction Inhibits Growth and Metastasis of Lung Cancer via Regulating the AKT/GSK-3/-Catenin Pathway.
滋肾汤通过调控AKT/GSK-3/β-连环蛋白信号通路抑制肺癌的生长和转移。
Oxid Med Cell Longev. 2021 Mar 9;2021:6685282. doi: 10.1155/2021/6685282. eCollection 2021.
4
Mitophagy in tumorigenesis and metastasis.肿瘤发生和转移中的自噬。
Cell Mol Life Sci. 2021 Apr;78(8):3817-3851. doi: 10.1007/s00018-021-03774-1. Epub 2021 Feb 13.
5
Uncoupling proteins in the mitochondrial defense against oxidative stress.线粒体对抗氧化应激的解偶联蛋白。
Prog Retin Eye Res. 2021 Jul;83:100941. doi: 10.1016/j.preteyeres.2021.100941. Epub 2021 Jan 8.
6
Baoyuan Jiedu Decoction Alleviates Cancer-Induced Myotube Atrophy by Regulating Mitochondrial Dynamics Through p38 MAPK/PGC-1α Signaling Pathway.保元解毒汤通过p38丝裂原活化蛋白激酶/过氧化物酶体增殖物激活受体γ共激活因子-1α信号通路调节线粒体动力学,减轻癌症诱导的肌管萎缩。
Front Oncol. 2020 Sep 30;10:523577. doi: 10.3389/fonc.2020.523577. eCollection 2020.
7
Advances in cancer cachexia: Intersection between affected organs, mediators, and pharmacological interventions.癌症恶病质的研究进展:受影响器官、介质和药物干预的交叉点。
Biochim Biophys Acta Rev Cancer. 2020 Apr;1873(2):188359. doi: 10.1016/j.bbcan.2020.188359. Epub 2020 Mar 25.
8
Promising models for cancer-induced cachexia drug discovery.有前景的癌症恶病质药物发现模型。
Expert Opin Drug Discov. 2020 May;15(5):627-637. doi: 10.1080/17460441.2020.1724954. Epub 2020 Feb 13.
9
Modified Bu-zhong-yi-qi decoction synergies with 5 fluorouracile to inhibits gastric cancer progress via PD-1/PD- L1-dependent T cell immunization.补中益气汤协同 5-氟尿嘧啶通过 PD-1/PD-L1 依赖的 T 细胞免疫抑制胃癌进展。
Pharmacol Res. 2020 Feb;152:104623. doi: 10.1016/j.phrs.2019.104623. Epub 2019 Dec 30.
10
Chlorogenic acid effectively treats cancers through induction of cancer cell differentiation.绿原酸通过诱导癌细胞分化有效地治疗癌症。
Theranostics. 2019 Sep 19;9(23):6745-6763. doi: 10.7150/thno.34674. eCollection 2019.