Mitigation and mechanism of low dose linoleic acid on depression caused by disorder of gut microbiome
Depression is a widely prevalent mental disorder, and nutritional interventions play an increasingly important role in its treatment. In this paper, effects of linoleic acid (LA) on depressive behavior in mice induced by gut microbiome disorders were investigated. Fifty C57BL/6J male mice were rando...
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Published in | Nutritional neuroscience Vol. 28; no. 2; pp. 245 - 262 |
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Language | English |
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01.02.2025
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Abstract | Depression is a widely prevalent mental disorder, and nutritional interventions play an increasingly important role in its treatment. In this paper, effects of linoleic acid (LA) on depressive behavior in mice induced by gut microbiome disorders were investigated.
Fifty C57BL/6J male mice were randomly separated into five groups, control group (CK), ceftriaxone sodium group (CRO), low-dose linoleic acid group (LLA, 1 g/kg), medium-dose linoleic acid group (MLA, 2 g/kg), and high-dose linoleic acid group (HLA, 5 g/kg). In the LLA, MLA, and HLA groups, mice were treated with ceftriaxone sodium (CRO) to induce depressive behaviors, followed by LA administration. Behavioral tests were used to evaluate depressive behavior. High-throughput sequencing and Hematoxylin-eosin (H&E) staining in gut microenvironment were carried out. ELISA kits were used to measure brain inflammatory factors, and 5-hydroxy-tryptamine (5-HT). Gas chromatography and western blot were used to determine fatty acids compositions and the enzymes expression involved in lipid metabolism in brain respectively.
The results showed that 10 weeks CRO treatment contribute to depressive behavior, gut microbiome disturbance, and serotonin system disturbance. LLA and MLA improved the depressive-like behavior, and significantly increased the levels of 5-HT1A, 5-HTT and 5-HT in the hippocampus. LLA was found to improve the diversity of gut microbiome and alleviate colon tissue damage. Meantime, LLA increased the content of linoleic acid, improved the expression of FADS2 and COX-2, increased IL-10 levels, and decreased IL-6 levels in the brain.
LA alleviated depressive behavior in mice by improving the gut microenvironment, regulate fatty acid metabolism, and modulate inflammation. |
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AbstractList | Depression is a widely prevalent mental disorder, and nutritional interventions play an increasingly important role in its treatment. In this paper, effects of linoleic acid (LA) on depressive behavior in mice induced by gut microbiome disorders were investigated.OBJECTIVESDepression is a widely prevalent mental disorder, and nutritional interventions play an increasingly important role in its treatment. In this paper, effects of linoleic acid (LA) on depressive behavior in mice induced by gut microbiome disorders were investigated.Fifty C57BL/6J male mice were randomly separated into five groups, control group (CK), ceftriaxone sodium group (CRO), low-dose linoleic acid group (LLA, 1 g/kg), medium-dose linoleic acid group (MLA, 2 g/kg), and high-dose linoleic acid group (HLA, 5 g/kg). In the LLA, MLA, and HLA groups, mice were treated with ceftriaxone sodium (CRO) to induce depressive behaviors, followed by LA administration. Behavioral tests were used to evaluate depressive behavior. High-throughput sequencing and Hematoxylin-eosin (H&E) staining in gut microenvironment were carried out. ELISA kits were used to measure brain inflammatory factors, and 5-hydroxy-tryptamine (5-HT). Gas chromatography and western blot were used to determine fatty acids compositions and the enzymes expression involved in lipid metabolism in brain respectively.METHODSFifty C57BL/6J male mice were randomly separated into five groups, control group (CK), ceftriaxone sodium group (CRO), low-dose linoleic acid group (LLA, 1 g/kg), medium-dose linoleic acid group (MLA, 2 g/kg), and high-dose linoleic acid group (HLA, 5 g/kg). In the LLA, MLA, and HLA groups, mice were treated with ceftriaxone sodium (CRO) to induce depressive behaviors, followed by LA administration. Behavioral tests were used to evaluate depressive behavior. High-throughput sequencing and Hematoxylin-eosin (H&E) staining in gut microenvironment were carried out. ELISA kits were used to measure brain inflammatory factors, and 5-hydroxy-tryptamine (5-HT). Gas chromatography and western blot were used to determine fatty acids compositions and the enzymes expression involved in lipid metabolism in brain respectively.The results showed that 10 weeks CRO treatment contribute to depressive behavior, gut microbiome disturbance, and serotonin system disturbance. LLA and MLA improved the depressive-like behavior, and significantly increased the levels of 5-HT1A, 5-HTT and 5-HT in the hippocampus. LLA was found to improve the diversity of gut microbiome and alleviate colon tissue damage. Meantime, LLA increased the content of linoleic acid, improved the expression of FADS2 and COX-2, increased IL-10 levels, and decreased IL-6 levels in the brain.RESULTSThe results showed that 10 weeks CRO treatment contribute to depressive behavior, gut microbiome disturbance, and serotonin system disturbance. LLA and MLA improved the depressive-like behavior, and significantly increased the levels of 5-HT1A, 5-HTT and 5-HT in the hippocampus. LLA was found to improve the diversity of gut microbiome and alleviate colon tissue damage. Meantime, LLA increased the content of linoleic acid, improved the expression of FADS2 and COX-2, increased IL-10 levels, and decreased IL-6 levels in the brain.LA alleviated depressive behavior in mice by improving the gut microenvironment, regulate fatty acid metabolism, and modulate inflammation.DISCUSSIONLA alleviated depressive behavior in mice by improving the gut microenvironment, regulate fatty acid metabolism, and modulate inflammation. Depression is a widely prevalent mental disorder, and nutritional interventions play an increasingly important role in its treatment. In this paper, effects of linoleic acid (LA) on depressive behavior in mice induced by gut microbiome disorders were investigated. Fifty C57BL/6J male mice were randomly separated into five groups, control group (CK), ceftriaxone sodium group (CRO), low-dose linoleic acid group (LLA, 1 g/kg), medium-dose linoleic acid group (MLA, 2 g/kg), and high-dose linoleic acid group (HLA, 5 g/kg). In the LLA, MLA, and HLA groups, mice were treated with ceftriaxone sodium (CRO) to induce depressive behaviors, followed by LA administration. Behavioral tests were used to evaluate depressive behavior. High-throughput sequencing and Hematoxylin-eosin (H&E) staining in gut microenvironment were carried out. ELISA kits were used to measure brain inflammatory factors, and 5-hydroxy-tryptamine (5-HT). Gas chromatography and western blot were used to determine fatty acids compositions and the enzymes expression involved in lipid metabolism in brain respectively. The results showed that 10 weeks CRO treatment contribute to depressive behavior, gut microbiome disturbance, and serotonin system disturbance. LLA and MLA improved the depressive-like behavior, and significantly increased the levels of 5-HT1A, 5-HTT and 5-HT in the hippocampus. LLA was found to improve the diversity of gut microbiome and alleviate colon tissue damage. Meantime, LLA increased the content of linoleic acid, improved the expression of FADS2 and COX-2, increased IL-10 levels, and decreased IL-6 levels in the brain. LA alleviated depressive behavior in mice by improving the gut microenvironment, regulate fatty acid metabolism, and modulate inflammation. |
Author | Lou, Maoshan Song, Yinan Yu, Haining Shen, Shengrong |
Author_xml | – sequence: 1 givenname: Haining surname: Yu fullname: Yu, Haining organization: College of Pharmaceutical Science, Zhejiang University of Technology, Hangzhou, People’s Republic of China – sequence: 2 givenname: Yinan surname: Song fullname: Song, Yinan organization: College of Pharmaceutical Science, Zhejiang University of Technology, Hangzhou, People’s Republic of China – sequence: 3 givenname: Maoshan surname: Lou fullname: Lou, Maoshan organization: College of Pharmaceutical Science, Zhejiang University of Technology, Hangzhou, People’s Republic of China – sequence: 4 givenname: Shengrong surname: Shen fullname: Shen, Shengrong organization: Department of Nutrition, Zhejiang University, Hangzhou, People’s Republic of China |
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Cites_doi | 10.1126/sciadv.aba8555 10.1677/joe.1.05910 10.1093/nutrit/nuaa025 10.3389/fimmu.2020.594150 10.1016/j.jad.2020.12.143 10.1016/S0140-6736(17)32802-7 10.1039/C8FO02423E 10.1016/j.cell.2015.02.047 10.2165/11595900-000000000-00000 10.1016/j.fct.2021.112699 10.1016/j.nut.2004.07.007 10.3390/nu11092232 10.1002/mnfr.202001004 10.1016/S0924-9338(02)00655-7 10.15430/JCP.2014.19.1.31 10.1017/S0007114520004973 10.3390/ijms24054567 10.1002/ana.23944 10.1016/j.jad.2011.09.007 10.3390/ijms21051769 10.1016/j.psychres.2019.01.100 10.1038/s41588-021-00991-z 10.3945/an.113.003772 10.1001/jama.2009.1943 10.1053/j.gastro.2012.05.007 10.3390/nu13030952 10.1371/journal.pone.0243668 10.3389/fcimb.2020.00258 10.1097/PSY.0b013e3180313a45 10.1186/1743-7075-8-36 10.1089/jmf.2014.7000 10.3945/ajcn.113.069880 10.3389/fnut.2022.841282 10.1111/ejn.14720 10.1016/j.ejphar.2015.03.096 10.3945/an.114.006940 10.1186/s12888-021-03550-2 10.1038/s41564-018-0337-x 10.1046/j.1365-2249.2003.02288.x 10.1016/j.cpr.2020.101943 10.1016/j.bbi.2015.03.016 10.1002/jnr.24476 10.3390/ijms23063204 10.1016/j.pnpbp.2021.110266 10.1080/19490976.2020.1747329 10.1017/S0029665116000732 |
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Keywords | gut microbiome ceftriaxone sodium inflammation lipid metabolism linoleic acid Depression arachidonic acid metabolism serotonin system |
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References_xml | – ident: e_1_3_6_39_1 doi: 10.1126/sciadv.aba8555 – ident: e_1_3_6_33_1 doi: 10.1677/joe.1.05910 – ident: e_1_3_6_12_1 doi: 10.1093/nutrit/nuaa025 – ident: e_1_3_6_20_1 doi: 10.3389/fimmu.2020.594150 – ident: e_1_3_6_38_1 doi: 10.1016/j.jad.2020.12.143 – ident: e_1_3_6_9_1 doi: 10.1016/S0140-6736(17)32802-7 – ident: e_1_3_6_19_1 doi: 10.1039/C8FO02423E – ident: e_1_3_6_35_1 doi: 10.1016/j.cell.2015.02.047 – ident: e_1_3_6_30_1 doi: 10.2165/11595900-000000000-00000 – ident: e_1_3_6_7_1 doi: 10.1016/j.fct.2021.112699 – ident: e_1_3_6_34_1 doi: 10.1016/j.nut.2004.07.007 – ident: e_1_3_6_16_1 doi: 10.3390/nu11092232 – ident: e_1_3_6_43_1 doi: 10.1002/mnfr.202001004 – ident: e_1_3_6_29_1 doi: 10.1016/S0924-9338(02)00655-7 – ident: e_1_3_6_48_1 doi: 10.15430/JCP.2014.19.1.31 – ident: e_1_3_6_22_1 doi: 10.1017/S0007114520004973 – ident: e_1_3_6_45_1 doi: 10.3390/ijms24054567 – ident: e_1_3_6_14_1 doi: 10.1002/ana.23944 – ident: e_1_3_6_23_1 doi: 10.1016/j.jad.2011.09.007 – volume: 155 start-page: 15 issue: 2 year: 2016 ident: e_1_3_6_46_1 article-title: Desaturases of fatty acids (FADS) and their physiological and clinical implication publication-title: Cas Lek Cesk – ident: e_1_3_6_15_1 doi: 10.3390/ijms21051769 – ident: e_1_3_6_31_1 doi: 10.1016/j.psychres.2019.01.100 – ident: e_1_3_6_41_1 doi: 10.1038/s41588-021-00991-z – ident: e_1_3_6_44_1 doi: 10.3945/an.113.003772 – ident: e_1_3_6_10_1 doi: 10.1001/jama.2009.1943 – ident: e_1_3_6_36_1 doi: 10.1053/j.gastro.2012.05.007 – ident: e_1_3_6_17_1 doi: 10.3390/nu13030952 – ident: e_1_3_6_27_1 doi: 10.1371/journal.pone.0243668 – ident: e_1_3_6_6_1 doi: 10.3389/fcimb.2020.00258 – ident: e_1_3_6_32_1 doi: 10.1097/PSY.0b013e3180313a45 – ident: e_1_3_6_25_1 doi: 10.1186/1743-7075-8-36 – ident: e_1_3_6_4_1 doi: 10.1089/jmf.2014.7000 – ident: e_1_3_6_13_1 doi: 10.3945/ajcn.113.069880 – ident: e_1_3_6_24_1 doi: 10.3389/fnut.2022.841282 – ident: e_1_3_6_2_1 doi: 10.1111/ejn.14720 – ident: e_1_3_6_18_1 doi: 10.1016/j.ejphar.2015.03.096 – ident: e_1_3_6_42_1 doi: 10.3945/an.114.006940 – ident: e_1_3_6_5_1 doi: 10.1186/s12888-021-03550-2 – ident: e_1_3_6_40_1 doi: 10.1038/s41564-018-0337-x – ident: e_1_3_6_26_1 doi: 10.1046/j.1365-2249.2003.02288.x – ident: e_1_3_6_28_1 doi: 10.1016/j.cpr.2020.101943 – ident: e_1_3_6_37_1 doi: 10.1016/j.bbi.2015.03.016 – ident: e_1_3_6_8_1 doi: 10.1002/jnr.24476 – ident: e_1_3_6_21_1 doi: 10.3390/ijms23063204 – ident: e_1_3_6_11_1 doi: 10.1016/j.pnpbp.2021.110266 – ident: e_1_3_6_3_1 doi: 10.1080/19490976.2020.1747329 – ident: e_1_3_6_47_1 doi: 10.1017/S0029665116000732 |
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Snippet | Depression is a widely prevalent mental disorder, and nutritional interventions play an increasingly important role in its treatment. In this paper, effects of... |
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SubjectTerms | Animals Behavior, Animal - drug effects Brain - drug effects Brain - metabolism Depression - drug therapy Depression - etiology Depression - microbiology Gastrointestinal Microbiome - drug effects Linoleic Acid - administration & dosage Linoleic Acid - pharmacology Male Mice Mice, Inbred C57BL |
Title | Mitigation and mechanism of low dose linoleic acid on depression caused by disorder of gut microbiome |
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