Luteolin improves mitochondrial dynamics and function in ulcerative colitis via the miR-195-5p/Notch signalling pathway

Luteolin (Lut), a plant extract widely found in nature, has demonstrated extensive therapeutic potential across various diseases. In this study, Lut treatment mitigated dextran sulphate sodium (DSS)-induced intestinal mucosal injury in a mouse model of ulcerative colitis (UC), which is associated wi...

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Main Authors: Moxixuan Liu, Yuge Wang, Zhao Liu, Senxia Liu, Qian Yang, Bolin Li
Format: Article
Language:English
Published: Elsevier 2025-01-01
Series:Journal of Functional Foods
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Online Access:http://www.sciencedirect.com/science/article/pii/S1756464624006479
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author Moxixuan Liu
Yuge Wang
Zhao Liu
Senxia Liu
Qian Yang
Bolin Li
author_facet Moxixuan Liu
Yuge Wang
Zhao Liu
Senxia Liu
Qian Yang
Bolin Li
author_sort Moxixuan Liu
collection DOAJ
description Luteolin (Lut), a plant extract widely found in nature, has demonstrated extensive therapeutic potential across various diseases. In this study, Lut treatment mitigated dextran sulphate sodium (DSS)-induced intestinal mucosal injury in a mouse model of ulcerative colitis (UC), which is associated with the activation of the Notch signalling pathway. Notably, colonic tissues exhibited reduced expression of Notch1, Notch2, RBPJ, MAML1, Hes1, Jagged1, and DLL4 following Lut administration. Additionally, our findings corroborate the hypothesis that miR-195-5p plays a critical role as a mediator in the negative feedback regulation of the Notch signalling pathway. In UC mice, inhibition of mitochondrial respiration and decreased energy production were observed, but Lut treatment effectively enhanced the energy metabolism within colon tissues. Moreover, mitochondrial fission was elevated, and fusion was suppressed in the colons of UC mice. Lut administration significantly increased the expression of mitochondrial fusion factors MFN1 and MFN2, reduced the expression of mitochondrial fission factors Fis1 and Crmp1, and markedly improved mitochondrial morphology, change mitochondrial membrane potential. During the entire mice experiment, a dosage of 100 mg/kg/d of Lut demonstrated significant advantages over 50 mg/kg/d of Lut in the treatment of UC. Furthermore, in Caco-2 cells, Lut attenuated LPS-induced activation of the Notch signalling pathway, evidenced by the downregulation of Notch1, MAML1, Hes1, Jagged1, and DLL4. The inhibitory role of miR-195-5p on the Notch signalling pathway was further substantiated by miR-195-5p overexpression in Caco-2 cells. LPS treatment also induced increased mitochondrial fission and decreased fusion in Caco-2 cells, while Lut effectively restored the levels of mitochondrial fusion factors MFN1 and MFN2, lowered the levels of mitochondrial fission factors Fis1 and Crmp1, and improved mitochondrial viability. These results indicate that Lut may exert an inhibitory effect on the Notch signalling pathway via miR-195-5p, while its impact on mitochondrial dynamics and the preservation of mitochondrial morphology and function offers protection against UC-associated colonic damage and LPS-induced injury in Caco-2 cells.
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publisher Elsevier
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spelling doaj-art-d15f91d1805a41cab0fba0c97d0aa2f12025-01-12T05:24:46ZengElsevierJournal of Functional Foods1756-46462025-01-01124106644Luteolin improves mitochondrial dynamics and function in ulcerative colitis via the miR-195-5p/Notch signalling pathwayMoxixuan Liu0Yuge Wang1Zhao Liu2Senxia Liu3Qian Yang4Bolin Li5Hebei University of Chinese Medicine (Hebei, Chinese), ChinaHebei University of Chinese Medicine (Hebei, Chinese), ChinaHebei Province Hospital of Chinese Medicine (Hebei, Chinese), ChinaHebei University of Chinese Medicine (Hebei, Chinese), ChinaHebei Province Hospital of Chinese Medicine (Hebei, Chinese), China; Corresponding authors.Hebei Province Hospital of Chinese Medicine (Hebei, Chinese), China; Corresponding authors.Luteolin (Lut), a plant extract widely found in nature, has demonstrated extensive therapeutic potential across various diseases. In this study, Lut treatment mitigated dextran sulphate sodium (DSS)-induced intestinal mucosal injury in a mouse model of ulcerative colitis (UC), which is associated with the activation of the Notch signalling pathway. Notably, colonic tissues exhibited reduced expression of Notch1, Notch2, RBPJ, MAML1, Hes1, Jagged1, and DLL4 following Lut administration. Additionally, our findings corroborate the hypothesis that miR-195-5p plays a critical role as a mediator in the negative feedback regulation of the Notch signalling pathway. In UC mice, inhibition of mitochondrial respiration and decreased energy production were observed, but Lut treatment effectively enhanced the energy metabolism within colon tissues. Moreover, mitochondrial fission was elevated, and fusion was suppressed in the colons of UC mice. Lut administration significantly increased the expression of mitochondrial fusion factors MFN1 and MFN2, reduced the expression of mitochondrial fission factors Fis1 and Crmp1, and markedly improved mitochondrial morphology, change mitochondrial membrane potential. During the entire mice experiment, a dosage of 100 mg/kg/d of Lut demonstrated significant advantages over 50 mg/kg/d of Lut in the treatment of UC. Furthermore, in Caco-2 cells, Lut attenuated LPS-induced activation of the Notch signalling pathway, evidenced by the downregulation of Notch1, MAML1, Hes1, Jagged1, and DLL4. The inhibitory role of miR-195-5p on the Notch signalling pathway was further substantiated by miR-195-5p overexpression in Caco-2 cells. LPS treatment also induced increased mitochondrial fission and decreased fusion in Caco-2 cells, while Lut effectively restored the levels of mitochondrial fusion factors MFN1 and MFN2, lowered the levels of mitochondrial fission factors Fis1 and Crmp1, and improved mitochondrial viability. These results indicate that Lut may exert an inhibitory effect on the Notch signalling pathway via miR-195-5p, while its impact on mitochondrial dynamics and the preservation of mitochondrial morphology and function offers protection against UC-associated colonic damage and LPS-induced injury in Caco-2 cells.http://www.sciencedirect.com/science/article/pii/S1756464624006479LuteolinUlcerative colitisCaco-2 cellsNotchMitochondrial dynamics
spellingShingle Moxixuan Liu
Yuge Wang
Zhao Liu
Senxia Liu
Qian Yang
Bolin Li
Luteolin improves mitochondrial dynamics and function in ulcerative colitis via the miR-195-5p/Notch signalling pathway
Journal of Functional Foods
Luteolin
Ulcerative colitis
Caco-2 cells
Notch
Mitochondrial dynamics
title Luteolin improves mitochondrial dynamics and function in ulcerative colitis via the miR-195-5p/Notch signalling pathway
title_full Luteolin improves mitochondrial dynamics and function in ulcerative colitis via the miR-195-5p/Notch signalling pathway
title_fullStr Luteolin improves mitochondrial dynamics and function in ulcerative colitis via the miR-195-5p/Notch signalling pathway
title_full_unstemmed Luteolin improves mitochondrial dynamics and function in ulcerative colitis via the miR-195-5p/Notch signalling pathway
title_short Luteolin improves mitochondrial dynamics and function in ulcerative colitis via the miR-195-5p/Notch signalling pathway
title_sort luteolin improves mitochondrial dynamics and function in ulcerative colitis via the mir 195 5p notch signalling pathway
topic Luteolin
Ulcerative colitis
Caco-2 cells
Notch
Mitochondrial dynamics
url http://www.sciencedirect.com/science/article/pii/S1756464624006479
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