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Exploring the Mechanism of Indigo Naturalis in the Treatment of Ulcerative Colitis Based on TLR4/MyD88/NF-κB Signaling Pathway and Gut Microbiota.基于TLR4/MyD88/NF-κB信号通路和肠道微生物群探讨青黛治疗溃疡性结肠炎的机制
Front Pharmacol. 2021 Jul 22;12:674416. doi: 10.3389/fphar.2021.674416. eCollection 2021.
2
Tempol improves redox status in mdx dystrophic diaphragm muscle.替普瑞酮可改善 mdx 营养不良型膈肌无力的氧化还原状态。
Int J Exp Pathol. 2020 Dec;101(6):289-297. doi: 10.1111/iep.12376. Epub 2020 Oct 24.
3
Natural products, PGC-1 , and Duchenne muscular dystrophy.天然产物、过氧化物酶体增殖物激活受体γ共激活因子1α与杜氏肌营养不良症
Acta Pharm Sin B. 2020 May;10(5):734-745. doi: 10.1016/j.apsb.2020.01.001. Epub 2020 Jan 8.
4
Biomarkers for Duchenne muscular dystrophy: myonecrosis, inflammation and oxidative stress.杜氏肌营养不良症的生物标志物:肌坏死、炎症和氧化应激。
Dis Model Mech. 2020 Mar 2;13(2):dmm043638. doi: 10.1242/dmm.043638.
5
Comparison of the anti-colitis activities of Qing Dai/Indigo Naturalis constituents in mice.青黛/靛蓝成分在小鼠中的抗结肠炎活性比较。
J Pharmacol Sci. 2020 Apr;142(4):148-156. doi: 10.1016/j.jphs.2020.01.003. Epub 2020 Jan 22.
6
Coenzyme Q10 supplementation acts as antioxidant on dystrophic muscle cells.辅酶 Q10 补充剂可作为抗氧化剂作用于萎缩性肌肉细胞。
Cell Stress Chaperones. 2019 Nov;24(6):1175-1185. doi: 10.1007/s12192-019-01039-2. Epub 2019 Oct 16.
7
Therapeutic developments for Duchenne muscular dystrophy.杜氏肌营养不良症的治疗进展。
Nat Rev Neurol. 2019 Jul;15(7):373-386. doi: 10.1038/s41582-019-0203-3.
8
Tempol treatment shows phenotype improvement in mdx mice.替普瑞酮治疗可改善 mdx 小鼠的表型。
PLoS One. 2019 Apr 22;14(4):e0215590. doi: 10.1371/journal.pone.0215590. eCollection 2019.
9
Duchenne muscular dystrophy and caregiver burden: a systematic review.杜氏肌营养不良症和照顾者负担:系统评价。
Dev Med Child Neurol. 2018 Oct;60(10):987-996. doi: 10.1111/dmcn.13934. Epub 2018 Jun 14.
10
Dystrophic phenotype improvement in the diaphragm muscle of mdx mice by diacerhein.双醋瑞因改善mdx小鼠膈肌的营养不良表型
PLoS One. 2017 Aug 7;12(8):e0182449. doi: 10.1371/journal.pone.0182449. eCollection 2017.

二吲哚生物碱靛蓝在实验性杜氏肌营养不良症模型中的抗氧化作用及相关信号通路。

Antioxidant effects of bis-indole alkaloid indigo and related signaling pathways in the experimental model of Duchenne muscular dystrophy.

机构信息

Instituto de Biologia, Departamento de Biologia Estrutural e Funcional, Universidade Estadual de Campinas (UNICAMP), Cidade Universitária Zeferino Vaz, Campinas, SP, 13083-862, Brazil.

Faculdade de Ceilândia, Universidade de Brasília (UnB), Brasília, Distrito Federal, 72220-275, Brazil.

出版信息

Cell Stress Chaperones. 2022 Jul;27(4):417-429. doi: 10.1007/s12192-022-01282-0. Epub 2022 Jun 10.

DOI:10.1007/s12192-022-01282-0
PMID:35687225
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC9346048/
Abstract

Indigo is a bis-indolic alkaloid that has antioxidant and anti-inflammatory effects reported in literature and is a promissory compound for treating chronic inflammatory diseases. This fact prompted to investigate the effects of this alkaloid in the experimental model of Duchenne muscular dystrophy. The main aim of this study was to evaluate the potential role of the indigo on oxidative stress and related signaling pathways in primary skeletal muscle cell cultures and in the diaphragm muscle from mdx mice. The MTT and Neutral Red assays showed no indigo dose-dependent toxicities in mdx muscle cells at concentrations analyzed (3.12, 6.25, 12.50, and 25.00 μg/mL). Antioxidant effect of indigo, in mdx muscle cells and diaphragm muscle, was demonstrated by reduction in 4-HNE content, HO levels, DHE reaction, and lipofuscin granules. A significant decrease in the inflammatory process was identified by a reduction on TNF and NF-κB levels, on inflammatory area, and on macrophage infiltration in the dystrophic sample, after indigo treatment. Upregulation of PGC-1α and SIRT1 in dystrophic muscle cells treated with indigo was also observed. These results suggest the potential of indigo as a therapeutic agent for muscular dystrophy, through their action anti-inflammatory, antioxidant, and modulator of SIRT1/PGC-1α pathway.

摘要

靛蓝是一种双吲哚生物碱,有文献报道其具有抗氧化和抗炎作用,是治疗慢性炎症性疾病的有前途的化合物。这一事实促使我们研究这种生物碱在杜氏肌营养不良症实验模型中的作用。本研究的主要目的是评估靛蓝对原代骨骼肌细胞培养物和 mdx 小鼠膈肌中氧化应激和相关信号通路的潜在作用。MTT 和中性红测定显示,在所分析的浓度(3.12、6.25、12.50 和 25.00μg/mL)下,靛蓝对 mdx 肌肉细胞没有剂量依赖性的毒性。靛蓝在 mdx 肌肉细胞和膈肌中的抗氧化作用通过降低 4-HNE 含量、HO 水平、DHE 反应和脂褐素颗粒来证明。在经过靛蓝处理后,在营养不良样本中,TNF 和 NF-κB 水平、炎症面积和巨噬细胞浸润的减少,表明炎症过程发生了显著减少。在接受靛蓝处理的营养不良肌肉细胞中,PGC-1α和 SIRT1 的上调也被观察到。这些结果表明,靛蓝具有作为肌肉疾病治疗剂的潜力,通过其抗炎、抗氧化和 SIRT1/PGC-1α 通路调节剂的作用。