Danlou Tablet Activates Autophagy of Vascular Adventitial Fibroblasts Through PI3K/Akt/mTOR to Protect Cells From Damage Caused by Atherosclerosis

Danlou tablet (DLT), a commercial Chinese patent medicine, has been widely used to treat cardiovascular diseases for many years. Atherosclerosis (AS) is the leading cause of cardiovascular disease. Increasing evidence indicates that autophagy plays a vital role in the development of AS. Here we inve...

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Main Authors: Li Wang (Author), Tong Wu (Author), Chunying Si (Author), He Wang (Author), Ke Yue (Author), Shasha Shang (Author), Xiaohui Li (Author), Yushan Chen (Author), Huaimin Guan (Author)
Format: Book
Published: Frontiers Media S.A., 2021-11-01T00:00:00Z.
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100 1 0 |a Li Wang  |e author 
700 1 0 |a Tong Wu  |e author 
700 1 0 |a Chunying Si  |e author 
700 1 0 |a He Wang  |e author 
700 1 0 |a Ke Yue  |e author 
700 1 0 |a Shasha Shang  |e author 
700 1 0 |a Xiaohui Li  |e author 
700 1 0 |a Yushan Chen  |e author 
700 1 0 |a Huaimin Guan  |e author 
245 0 0 |a Danlou Tablet Activates Autophagy of Vascular Adventitial Fibroblasts Through PI3K/Akt/mTOR to Protect Cells From Damage Caused by Atherosclerosis 
260 |b Frontiers Media S.A.,   |c 2021-11-01T00:00:00Z. 
500 |a 1663-9812 
500 |a 10.3389/fphar.2021.730525 
520 |a Danlou tablet (DLT), a commercial Chinese patent medicine, has been widely used to treat cardiovascular diseases for many years. Atherosclerosis (AS) is the leading cause of cardiovascular disease. Increasing evidence indicates that autophagy plays a vital role in the development of AS. Here we investigated whether DLT could activate autophagy to improve AS and further clarified its underlying mechanisms. In an ApoE−/− mice model, the results of Oil red O, Masson's trichrome, and H&E staining techniques showed that DLT significantly inhibited lipid accumulation and fibrosis formation in atherosclerotic plaque tissue. DLT also inhibited serum triglyceride, cholesterol, and low-density lipoprotein levels and suppressed serum levels of inflammatory factors interleukin-6 and tumor necrosis factor-α in ApoE−/− mice. Moreover, DLT suppressed proliferation, migration, and invasion of human vascular adventitial fibroblasts (HVAFs) by inhibiting the PI3K/Akt/mTOR pathway. In addition, western blot analysis showed that Danlou tablet treatment decreased the expression of p62 and increased Beclin 1 and LC3 I -to-LC3 II ratios in HVAFs. The role of autophagy in treating atherosclerosis by DLT is confirmed by 3-methyladenine (autophagy inhibitor) and rapamycin (autophagy activator) in HVAFs. In summary, DLT activated PI3K/Akt/mTOR-mediated autophagy of vascular adventitial fibroblasts to protect cells from damage caused by atherosclerosis. 
546 |a EN 
690 |a atherosclerosis 
690 |a danlou tablet 
690 |a autophagy 
690 |a PI3K/AKT/mTOR 
690 |a Chinese patent medicine 
690 |a Therapeutics. Pharmacology 
690 |a RM1-950 
655 7 |a article  |2 local 
786 0 |n Frontiers in Pharmacology, Vol 12 (2021) 
787 0 |n https://www.frontiersin.org/articles/10.3389/fphar.2021.730525/full 
787 0 |n https://doaj.org/toc/1663-9812 
856 4 1 |u https://doaj.org/article/bf6afad25e8449d7a812bff9b5448a7f  |z Connect to this object online.