Coreopsis tinctoria Nutt ameliorates high glucose-induced renal fibrosis and inflammation via the TGF-β1/SMADS/AMPK/NF-κB pathways
Abstract Background Coreopsis tinctoria Nutt is an ethnomedicine widely used in Xinjiang, China. It is consumed as a herbal tea by local Uyghur people to treat high blood pressure and diarrhea. Our previous study confirmed that the ethyl acetate extract of Coreopsis tinctoria (AC) had a protective e...
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doaj-ac09c60be0d24d4a89786d4eed0d74c92020-11-25T02:02:23ZengBMCBMC Complementary and Alternative Medicine1472-68822019-01-0119111210.1186/s12906-018-2410-7Coreopsis tinctoria Nutt ameliorates high glucose-induced renal fibrosis and inflammation via the TGF-β1/SMADS/AMPK/NF-κB pathwaysLan Yao0Jie Li1Linlin Li2Xinxia Li3Rui Zhang4Yujie Zhang5Xinmin Mao6College of Traditional Chinese Medicine, Xinjiang Medical UniversityCollege of Traditional Chinese Medicine, Xinjiang Medical UniversityCollege of Basic Medicine, Xinjiang Medical UniversityCenter of Analysis and Test, Xinjiang Medical UniversityCollege of Basic Medicine, Xinjiang Medical UniversityCollege of Traditional Chinese Medicine, Xinjiang Medical UniversityCollege of Traditional Chinese Medicine, Xinjiang Medical UniversityAbstract Background Coreopsis tinctoria Nutt is an ethnomedicine widely used in Xinjiang, China. It is consumed as a herbal tea by local Uyghur people to treat high blood pressure and diarrhea. Our previous study confirmed that the ethyl acetate extract of Coreopsis tinctoria (AC) had a protective effect on diabetic nephropathy (DN) in an in vivo experiment. Here we aim to elucidate the protective mechanism of AC and marein, the main ingredient in Coreopsis tinctoria on renal fibrosis and inflammation in vitro under high glucose (HG) conditions. Methods A HG-induced barrier dysfunction model in rat mesangial cells (HBZY-1) was established. The cells were exposed to AC and marein and/or HG for 24 h. Then, the renal protective effects of AC and marein via transforming growth factor-β1 (TGF-β1)/Smads, AMP-activated kinase protein (AMPK), and nuclear factor kappa beta (NF-κB) signaling were assessed. Results Both AC and marein suppressed rat mesangial cell hyperplasia and significantly attenuated the expression of HG-disrupted fibrotic and inflammatory proteins in HBZY-1 cells. It was also confirmed that AC and marein remarkably attenuated HG-induced renal inflammation and fibrosis by regulating the AMPK, TGF-β1/Smads, and NF-κB signaling pathways. Conclusion These results indicated that AC and marein may delay the progression of DN, at least in part, by suppressing HG-induced renal inflammation and fibrosis. Marein may be one of the bioactive compounds in AC.http://link.springer.com/article/10.1186/s12906-018-2410-7Ethyl acetate extract of Coreopsis tinctoriaAnti-fibrosis and anti-inflammationHigh glucose-treated mesangial cellsMechanism |
collection |
DOAJ |
language |
English |
format |
Article |
sources |
DOAJ |
author |
Lan Yao Jie Li Linlin Li Xinxia Li Rui Zhang Yujie Zhang Xinmin Mao |
spellingShingle |
Lan Yao Jie Li Linlin Li Xinxia Li Rui Zhang Yujie Zhang Xinmin Mao Coreopsis tinctoria Nutt ameliorates high glucose-induced renal fibrosis and inflammation via the TGF-β1/SMADS/AMPK/NF-κB pathways BMC Complementary and Alternative Medicine Ethyl acetate extract of Coreopsis tinctoria Anti-fibrosis and anti-inflammation High glucose-treated mesangial cells Mechanism |
author_facet |
Lan Yao Jie Li Linlin Li Xinxia Li Rui Zhang Yujie Zhang Xinmin Mao |
author_sort |
Lan Yao |
title |
Coreopsis tinctoria Nutt ameliorates high glucose-induced renal fibrosis and inflammation via the TGF-β1/SMADS/AMPK/NF-κB pathways |
title_short |
Coreopsis tinctoria Nutt ameliorates high glucose-induced renal fibrosis and inflammation via the TGF-β1/SMADS/AMPK/NF-κB pathways |
title_full |
Coreopsis tinctoria Nutt ameliorates high glucose-induced renal fibrosis and inflammation via the TGF-β1/SMADS/AMPK/NF-κB pathways |
title_fullStr |
Coreopsis tinctoria Nutt ameliorates high glucose-induced renal fibrosis and inflammation via the TGF-β1/SMADS/AMPK/NF-κB pathways |
title_full_unstemmed |
Coreopsis tinctoria Nutt ameliorates high glucose-induced renal fibrosis and inflammation via the TGF-β1/SMADS/AMPK/NF-κB pathways |
title_sort |
coreopsis tinctoria nutt ameliorates high glucose-induced renal fibrosis and inflammation via the tgf-β1/smads/ampk/nf-κb pathways |
publisher |
BMC |
series |
BMC Complementary and Alternative Medicine |
issn |
1472-6882 |
publishDate |
2019-01-01 |
description |
Abstract Background Coreopsis tinctoria Nutt is an ethnomedicine widely used in Xinjiang, China. It is consumed as a herbal tea by local Uyghur people to treat high blood pressure and diarrhea. Our previous study confirmed that the ethyl acetate extract of Coreopsis tinctoria (AC) had a protective effect on diabetic nephropathy (DN) in an in vivo experiment. Here we aim to elucidate the protective mechanism of AC and marein, the main ingredient in Coreopsis tinctoria on renal fibrosis and inflammation in vitro under high glucose (HG) conditions. Methods A HG-induced barrier dysfunction model in rat mesangial cells (HBZY-1) was established. The cells were exposed to AC and marein and/or HG for 24 h. Then, the renal protective effects of AC and marein via transforming growth factor-β1 (TGF-β1)/Smads, AMP-activated kinase protein (AMPK), and nuclear factor kappa beta (NF-κB) signaling were assessed. Results Both AC and marein suppressed rat mesangial cell hyperplasia and significantly attenuated the expression of HG-disrupted fibrotic and inflammatory proteins in HBZY-1 cells. It was also confirmed that AC and marein remarkably attenuated HG-induced renal inflammation and fibrosis by regulating the AMPK, TGF-β1/Smads, and NF-κB signaling pathways. Conclusion These results indicated that AC and marein may delay the progression of DN, at least in part, by suppressing HG-induced renal inflammation and fibrosis. Marein may be one of the bioactive compounds in AC. |
topic |
Ethyl acetate extract of Coreopsis tinctoria Anti-fibrosis and anti-inflammation High glucose-treated mesangial cells Mechanism |
url |
http://link.springer.com/article/10.1186/s12906-018-2410-7 |
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