Hirami lemon ( var. ) modulates the gut-brain axis in a chronic mild stress-induced depression mouse model
Citrus reticulata var. depressa , commonly known as Hirami lemon, is a native citrus species found in Taiwan and Okinawa islands of Japan. While several Citrus species are known to possess antidepressant activity by modulating the gut microbiota, the antidepressant effect of Hirami lemon and its und...
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Published in | Food & function Vol. 14; no. 16; pp. 7535 - 7549 |
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Main Authors | , , , , |
Format | Journal Article |
Language | English |
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England
Royal Society of Chemistry
14.08.2023
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Abstract | Citrus reticulata
var.
depressa
, commonly known as Hirami lemon, is a native citrus species found in Taiwan and Okinawa islands of Japan. While several
Citrus
species are known to possess antidepressant activity by modulating the gut microbiota, the antidepressant effect of Hirami lemon and its underlying mechanisms have not been thoroughly investigated. In this study, we explored the potential antidepressant efficacy of the fruit extract (CD) and the essential oil (CDE) from Hirami lemon peel using a chronic mild stress (CMS)-induced mouse model and analyzed the association of gut microbiome changes. Our findings revealed that mice subjected to CMS exhibited anxiety- and depression-like behaviors as assessed by elevated plus-maze and forced swimming tests, respectively. Significantly, oral administration of CDE and CD notably reversed CMS-induced depression- and anxiety-like behaviors in CMS-induced mice. Moreover, compared to the non-stressed group, CMS significantly altered the gut microbiome, characterized by highly diverse bacterial communities, reduced Bacteroidetes, and increased Firmicutes. However, oral administration of CDE and CD restored gut microbiota dysbiosis. We also performed a qualitative analysis of CD and CDE using UPLC-MS and GC-MS, respectively. The CD contained 25 compounds, of which 3 were polymethoxy flavones and flavanones. Three major compounds, nobiletin, tangeretin and hesperidin, accounted for 56.88% of the total relative peak area. In contrast, the CDE contained 11 terpenoids, of which 8 were identified as major compounds, with
d
-limonene (45.71%) being the most abundant, followed by γ-terpinene (34.65%), linalool (6.46%),
p
-cymene (2.57%), α-terpineol (2.04%), α-pinene (1.89%), α-terpinolene (1.46%), and β-pinene (1.16%), accounting for 95.94% of the total oil. In conclusion, our study demonstrated the potential of Hirami lemon as a source of natural antidepressant agents for the prevention and treatment of major depressive disorders.
Hirami lemon modulates the gut-brain axis in a chronic mild stress-induced depression mouse model. |
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AbstractList | Citrus reticulata
var.
depressa
, commonly known as Hirami lemon, is a native citrus species found in Taiwan and Okinawa islands of Japan. While several
Citrus
species are known to possess antidepressant activity by modulating the gut microbiota, the antidepressant effect of Hirami lemon and its underlying mechanisms have not been thoroughly investigated. In this study, we explored the potential antidepressant efficacy of the fruit extract (CD) and the essential oil (CDE) from Hirami lemon peel using a chronic mild stress (CMS)-induced mouse model and analyzed the association of gut microbiome changes. Our findings revealed that mice subjected to CMS exhibited anxiety- and depression-like behaviors as assessed by elevated plus-maze and forced swimming tests, respectively. Significantly, oral administration of CDE and CD notably reversed CMS-induced depression- and anxiety-like behaviors in CMS-induced mice. Moreover, compared to the non-stressed group, CMS significantly altered the gut microbiome, characterized by highly diverse bacterial communities, reduced Bacteroidetes, and increased Firmicutes. However, oral administration of CDE and CD restored gut microbiota dysbiosis. We also performed a qualitative analysis of CD and CDE using UPLC-MS and GC-MS, respectively. The CD contained 25 compounds, of which 3 were polymethoxy flavones and flavanones. Three major compounds, nobiletin, tangeretin and hesperidin, accounted for 56.88% of the total relative peak area. In contrast, the CDE contained 11 terpenoids, of which 8 were identified as major compounds, with
d
-limonene (45.71%) being the most abundant, followed by γ-terpinene (34.65%), linalool (6.46%),
p
-cymene (2.57%), α-terpineol (2.04%), α-pinene (1.89%), α-terpinolene (1.46%), and β-pinene (1.16%), accounting for 95.94% of the total oil. In conclusion, our study demonstrated the potential of Hirami lemon as a source of natural antidepressant agents for the prevention and treatment of major depressive disorders. Citrus reticulata var. depressa, commonly known as Hirami lemon, is a native citrus species found in Taiwan and Okinawa islands of Japan. While several Citrus species are known to possess antidepressant activity by modulating the gut microbiota, the antidepressant effect of Hirami lemon and its underlying mechanisms have not been thoroughly investigated. In this study, we explored the potential antidepressant efficacy of the fruit extract (CD) and the essential oil (CDE) from Hirami lemon peel using a chronic mild stress (CMS)-induced mouse model and analyzed the association of gut microbiome changes. Our findings revealed that mice subjected to CMS exhibited anxiety- and depression-like behaviors as assessed by elevated plus-maze and forced swimming tests, respectively. Significantly, oral administration of CDE and CD notably reversed CMS-induced depression- and anxiety-like behaviors in CMS-induced mice. Moreover, compared to the non-stressed group, CMS significantly altered the gut microbiome, characterized by highly diverse bacterial communities, reduced Bacteroidetes, and increased Firmicutes. However, oral administration of CDE and CD restored gut microbiota dysbiosis. We also performed a qualitative analysis of CD and CDE using UPLC-MS and GC-MS, respectively. The CD contained 25 compounds, of which 3 were polymethoxy flavones and flavanones. Three major compounds, nobiletin, tangeretin and hesperidin, accounted for 56.88% of the total relative peak area. In contrast, the CDE contained 11 terpenoids, of which 8 were identified as major compounds, with D-limonene (45.71%) being the most abundant, followed by γ-terpinene (34.65%), linalool (6.46%), p-cymene (2.57%), α-terpineol (2.04%), α-pinene (1.89%), α-terpinolene (1.46%), and β-pinene (1.16%), accounting for 95.94% of the total oil. In conclusion, our study demonstrated the potential of Hirami lemon as a source of natural antidepressant agents for the prevention and treatment of major depressive disorders.Citrus reticulata var. depressa, commonly known as Hirami lemon, is a native citrus species found in Taiwan and Okinawa islands of Japan. While several Citrus species are known to possess antidepressant activity by modulating the gut microbiota, the antidepressant effect of Hirami lemon and its underlying mechanisms have not been thoroughly investigated. In this study, we explored the potential antidepressant efficacy of the fruit extract (CD) and the essential oil (CDE) from Hirami lemon peel using a chronic mild stress (CMS)-induced mouse model and analyzed the association of gut microbiome changes. Our findings revealed that mice subjected to CMS exhibited anxiety- and depression-like behaviors as assessed by elevated plus-maze and forced swimming tests, respectively. Significantly, oral administration of CDE and CD notably reversed CMS-induced depression- and anxiety-like behaviors in CMS-induced mice. Moreover, compared to the non-stressed group, CMS significantly altered the gut microbiome, characterized by highly diverse bacterial communities, reduced Bacteroidetes, and increased Firmicutes. However, oral administration of CDE and CD restored gut microbiota dysbiosis. We also performed a qualitative analysis of CD and CDE using UPLC-MS and GC-MS, respectively. The CD contained 25 compounds, of which 3 were polymethoxy flavones and flavanones. Three major compounds, nobiletin, tangeretin and hesperidin, accounted for 56.88% of the total relative peak area. In contrast, the CDE contained 11 terpenoids, of which 8 were identified as major compounds, with D-limonene (45.71%) being the most abundant, followed by γ-terpinene (34.65%), linalool (6.46%), p-cymene (2.57%), α-terpineol (2.04%), α-pinene (1.89%), α-terpinolene (1.46%), and β-pinene (1.16%), accounting for 95.94% of the total oil. In conclusion, our study demonstrated the potential of Hirami lemon as a source of natural antidepressant agents for the prevention and treatment of major depressive disorders. var. , commonly known as Hirami lemon, is a native citrus species found in Taiwan and Okinawa islands of Japan. While several species are known to possess antidepressant activity by modulating the gut microbiota, the antidepressant effect of Hirami lemon and its underlying mechanisms have not been thoroughly investigated. In this study, we explored the potential antidepressant efficacy of the fruit extract (CD) and the essential oil (CDE) from Hirami lemon peel using a chronic mild stress (CMS)-induced mouse model and analyzed the association of gut microbiome changes. Our findings revealed that mice subjected to CMS exhibited anxiety- and depression-like behaviors as assessed by elevated plus-maze and forced swimming tests, respectively. Significantly, oral administration of CDE and CD notably reversed CMS-induced depression- and anxiety-like behaviors in CMS-induced mice. Moreover, compared to the non-stressed group, CMS significantly altered the gut microbiome, characterized by highly diverse bacterial communities, reduced Bacteroidetes, and increased Firmicutes. However, oral administration of CDE and CD restored gut microbiota dysbiosis. We also performed a qualitative analysis of CD and CDE using UPLC-MS and GC-MS, respectively. The CD contained 25 compounds, of which 3 were polymethoxy flavones and flavanones. Three major compounds, nobiletin, tangeretin and hesperidin, accounted for 56.88% of the total relative peak area. In contrast, the CDE contained 11 terpenoids, of which 8 were identified as major compounds, with D-limonene (45.71%) being the most abundant, followed by γ-terpinene (34.65%), linalool (6.46%), -cymene (2.57%), α-terpineol (2.04%), α-pinene (1.89%), α-terpinolene (1.46%), and β-pinene (1.16%), accounting for 95.94% of the total oil. In conclusion, our study demonstrated the potential of Hirami lemon as a source of natural antidepressant agents for the prevention and treatment of major depressive disorders. Citrus reticulata var. depressa, commonly known as Hirami lemon, is a native citrus species found in Taiwan and Okinawa islands of Japan. While several Citrus species are known to possess antidepressant activity by modulating the gut microbiota, the antidepressant effect of Hirami lemon and its underlying mechanisms have not been thoroughly investigated. In this study, we explored the potential antidepressant efficacy of the fruit extract (CD) and the essential oil (CDE) from Hirami lemon peel using a chronic mild stress (CMS)-induced mouse model and analyzed the association of gut microbiome changes. Our findings revealed that mice subjected to CMS exhibited anxiety- and depression-like behaviors as assessed by elevated plus-maze and forced swimming tests, respectively. Significantly, oral administration of CDE and CD notably reversed CMS-induced depression- and anxiety-like behaviors in CMS-induced mice. Moreover, compared to the non-stressed group, CMS significantly altered the gut microbiome, characterized by highly diverse bacterial communities, reduced Bacteroidetes, and increased Firmicutes. However, oral administration of CDE and CD restored gut microbiota dysbiosis. We also performed a qualitative analysis of CD and CDE using UPLC-MS and GC-MS, respectively. The CD contained 25 compounds, of which 3 were polymethoxy flavones and flavanones. Three major compounds, nobiletin, tangeretin and hesperidin, accounted for 56.88% of the total relative peak area. In contrast, the CDE contained 11 terpenoids, of which 8 were identified as major compounds, with d-limonene (45.71%) being the most abundant, followed by γ-terpinene (34.65%), linalool (6.46%), p-cymene (2.57%), α-terpineol (2.04%), α-pinene (1.89%), α-terpinolene (1.46%), and β-pinene (1.16%), accounting for 95.94% of the total oil. In conclusion, our study demonstrated the potential of Hirami lemon as a source of natural antidepressant agents for the prevention and treatment of major depressive disorders. Citrus reticulata var. depressa , commonly known as Hirami lemon, is a native citrus species found in Taiwan and Okinawa islands of Japan. While several Citrus species are known to possess antidepressant activity by modulating the gut microbiota, the antidepressant effect of Hirami lemon and its underlying mechanisms have not been thoroughly investigated. In this study, we explored the potential antidepressant efficacy of the fruit extract (CD) and the essential oil (CDE) from Hirami lemon peel using a chronic mild stress (CMS)-induced mouse model and analyzed the association of gut microbiome changes. Our findings revealed that mice subjected to CMS exhibited anxiety- and depression-like behaviors as assessed by elevated plus-maze and forced swimming tests, respectively. Significantly, oral administration of CDE and CD notably reversed CMS-induced depression- and anxiety-like behaviors in CMS-induced mice. Moreover, compared to the non-stressed group, CMS significantly altered the gut microbiome, characterized by highly diverse bacterial communities, reduced Bacteroidetes, and increased Firmicutes. However, oral administration of CDE and CD restored gut microbiota dysbiosis. We also performed a qualitative analysis of CD and CDE using UPLC-MS and GC-MS, respectively. The CD contained 25 compounds, of which 3 were polymethoxy flavones and flavanones. Three major compounds, nobiletin, tangeretin and hesperidin, accounted for 56.88% of the total relative peak area. In contrast, the CDE contained 11 terpenoids, of which 8 were identified as major compounds, with d -limonene (45.71%) being the most abundant, followed by γ-terpinene (34.65%), linalool (6.46%), p -cymene (2.57%), α-terpineol (2.04%), α-pinene (1.89%), α-terpinolene (1.46%), and β-pinene (1.16%), accounting for 95.94% of the total oil. In conclusion, our study demonstrated the potential of Hirami lemon as a source of natural antidepressant agents for the prevention and treatment of major depressive disorders. Hirami lemon modulates the gut-brain axis in a chronic mild stress-induced depression mouse model. |
Author | Wang, Sheng-Yang Wu, Pei-Chen Tsai, Po-Heng Li, Hui-Ru Senthil Kumar, K. J |
AuthorAffiliation | Academy of Circle Economy National Chung Hsing University Bachelor Program of Biotechnology Special Crop and Metabolome Discipline Cluster Ph.D. Program in Microbial Genomics Academia Sinica Department of Forestry Agricultural Biotechnology Research Center |
AuthorAffiliation_xml | – sequence: 0 name: Academia Sinica – sequence: 0 name: National Chung Hsing University – sequence: 0 name: Special Crop and Metabolome Discipline Cluster – sequence: 0 name: Ph.D. Program in Microbial Genomics – sequence: 0 name: Academy of Circle Economy – sequence: 0 name: Bachelor Program of Biotechnology – sequence: 0 name: Department of Forestry – sequence: 0 name: Agricultural Biotechnology Research Center |
Author_xml | – sequence: 1 givenname: Po-Heng surname: Tsai fullname: Tsai, Po-Heng – sequence: 2 givenname: Pei-Chen surname: Wu fullname: Wu, Pei-Chen – sequence: 3 givenname: Hui-Ru surname: Li fullname: Li, Hui-Ru – sequence: 4 givenname: K. J surname: Senthil Kumar fullname: Senthil Kumar, K. J – sequence: 5 givenname: Sheng-Yang surname: Wang fullname: Wang, Sheng-Yang |
BackLink | https://www.ncbi.nlm.nih.gov/pubmed/37526032$$D View this record in MEDLINE/PubMed |
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Cites_doi | 10.1097/FBP.0000000000000321 10.3390/antiox11020239 10.3389/fnbeh.2018.00241 10.1515/dmpt-2021-0125 10.3389/fnins.2021.640648 10.3945/ajcn.114.088518 10.1023/A:1010904214482 10.1093/bioinformatics/btr507 10.1016/S1353-8020(01)00043-8 10.3390/nu11071464 10.1186/s13065-015-0145-9 10.1021/jf000227d 10.1186/s12992-020-00589-w 10.1093/bioinformatics/btr381 10.1016/j.bbi.2013.12.015 10.1111/j.1467-789X.2006.00195.x 10.1002/fsn3.1566 10.1002/ffj.3197 10.1016/j.jenvman.2020.111832 10.1038/s41392-022-00974-4 10.1128/AEM.01541-09 10.1111/jfbc.14164 10.3390/foods11091299 10.3389/fnbeh.2018.00266 10.1016/j.physbeh.2010.10.008 10.1093/ajcn/79.5.727 10.1021/jacs.8b11414 10.1002/mnfr.201200606 10.1016/j.physbeh.2004.01.013 10.1038/nmeth.f.303 10.1139/cjpp-2014-0281 10.1177/2515690X20957225 10.3748/wjg.v27.i39.6715 10.1016/j.biopsych.2013.05.001 10.3390/nu14102111 10.1097/00001756-200112040-00053 10.1016/j.foodchem.2012.02.054 10.3389/fmicb.2019.02407 10.1038/srep43859 10.3390/ijms21239277 10.3390/ijms19071966 10.1016/j.tins.2013.01.005 10.14806/ej.17.1.200 10.1016/j.neuropharm.2015.10.034 10.1016/j.tins.2016.09.002 10.1101/gr.112730.110 10.37871/jbres1560 10.1021/acs.jafc.8b02462 10.1093/bioinformatics/btu170 10.1016/j.lfs.2015.02.021 10.3389/fpsyt.2020.00541 10.1016/j.psyneuen.2015.10.001 10.1038/ismej.2011.41 10.4014/jmb.1709.09027 10.1080/0972060X.2021.1978869 10.3390/metabo12010050 10.1038/s41430-021-00991-6 10.1016/j.ynstr.2016.08.002 10.1016/j.bbi.2010.10.023 10.1038/ismej.2012.8 10.1093/nar/gkm864 10.2174/1871527316666170328113309 |
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References | Manach (D3FO01301D/cit40/1) 2004; 79 Teigiserova (D3FO01301D/cit12/1) 2021; 280 Tanaka (D3FO01301D/cit20/1) 1926; 2 Datla (D3FO01301D/cit16/1) 2001; 12 Magoč (D3FO01301D/cit30/1) 2011; 27 Ducottet (D3FO01301D/cit25/1) 2004; 81 El-Marasy (D3FO01301D/cit60/1) 2014; 92 Pruesse (D3FO01301D/cit33/1) 2007; 35 Lin (D3FO01301D/cit21/1) 2006; 8 Gosselin (D3FO01301D/cit44/1) 2017; 28 Bolger (D3FO01301D/cit28/1) 2014; 30 Ishola (D3FO01301D/cit50/1) 2022; 37 Vijay (D3FO01301D/cit4/1) 2022; 76 Sun (D3FO01301D/cit24/1) 2018; 66 Haaz (D3FO01301D/cit41/1) 2006; 7 Guzmán-Gutiérrez (D3FO01301D/cit56/1) 2015; 128 Dinan (D3FO01301D/cit7/1) 2013; 74 Wang (D3FO01301D/cit51/1) 2019; 141 Braidy (D3FO01301D/cit17/1) 2017; 16 Kean (D3FO01301D/cit15/1) 2015; 101 Lau (D3FO01301D/cit22/1) 2021; 24 Edgar (D3FO01301D/cit31/1) 2011; 27 Serrano-Dueñas (D3FO01301D/cit43/1) 2002; 8 Marin (D3FO01301D/cit23/1) 2017; 7 Bailey (D3FO01301D/cit67/1) 2011; 25 Kim (D3FO01301D/cit38/1) 2017; 27 Youssef (D3FO01301D/cit49/1) 2022; 46 Saini (D3FO01301D/cit13/1) 2022; 11 Li (D3FO01301D/cit36/1) 2018; 12 Bharwani (D3FO01301D/cit68/1) 2016; 63 Ortega (D3FO01301D/cit65/1) 2022; 12 Willis (D3FO01301D/cit37/1) 2019; 10 Monteiro (D3FO01301D/cit19/1) 2022; 11 Willner (D3FO01301D/cit42/1) 2017; 6 Caporaso (D3FO01301D/cit35/1) 2010; 7 Jurek (D3FO01301D/cit9/1) 2022; 3 Aprotosoaie (D3FO01301D/cit55/1) 2014; 29 Salari (D3FO01301D/cit1/1) 2020; 16 Choi (D3FO01301D/cit52/1) 2000; 48 Pferschy-Wenzig (D3FO01301D/cit11/1) 2022; 14 Harada (D3FO01301D/cit54/1) 2018; 12 Peterson (D3FO01301D/cit10/1) 2020; 25 Caporaso (D3FO01301D/cit27/1) 2012; 6 Silva Brum (D3FO01301D/cit57/1) 2001; 26 Wang (D3FO01301D/cit6/1) 2014; 38 Dosoky (D3FO01301D/cit18/1) 2018; 19 Barandouzi (D3FO01301D/cit66/1) 2020; 11 Lv (D3FO01301D/cit14/1) 2015; 9 Li (D3FO01301D/cit45/1) 2021; 76 Shinomiya (D3FO01301D/cit47/1) 2012; 66 Herlemann (D3FO01301D/cit26/1) 2011; 5 Seo (D3FO01301D/cit46/1) 2020; 21 Haas (D3FO01301D/cit32/1) 2011; 21 Schloss (D3FO01301D/cit34/1) 2009; 75 Stevens (D3FO01301D/cit39/1) 2019; 11 Hou (D3FO01301D/cit3/1) 2022; 7 Foster (D3FO01301D/cit5/1) 2013; 36 Iannitti (D3FO01301D/cit61/1) 2020; 8 Lai (D3FO01301D/cit62/1) 2013; 57 Martin (D3FO01301D/cit29/1) 2011; 17 Yi (D3FO01301D/cit58/1) 2011; 102 Sarkar (D3FO01301D/cit8/1) 2016; 39 Björkholm (D3FO01301D/cit48/1) 2016; 102 Öztürk (D3FO01301D/cit53/1) 2012; 134 Baldi (D3FO01301D/cit63/1) 2021; 27 Lai (D3FO01301D/cit59/1) 2016; 35 Pontifex (D3FO01301D/cit64/1) 2021; 15 |
References_xml | – volume: 28 start-page: 466 year: 2017 ident: D3FO01301D/cit44/1 publication-title: Behav. Pharmacol. doi: 10.1097/FBP.0000000000000321 – volume: 11 start-page: 239 year: 2022 ident: D3FO01301D/cit13/1 publication-title: Antioxidants doi: 10.3390/antiox11020239 – volume: 12 start-page: 241 year: 2018 ident: D3FO01301D/cit54/1 publication-title: Front. Behav. Neurosci. doi: 10.3389/fnbeh.2018.00241 – volume: 8 start-page: 1 year: 2006 ident: D3FO01301D/cit21/1 publication-title: Seed Nursery – volume: 37 start-page: 277 year: 2022 ident: D3FO01301D/cit50/1 publication-title: Drug Metab. Pers. Ther. doi: 10.1515/dmpt-2021-0125 – volume: 15 start-page: 640648 year: 2021 ident: D3FO01301D/cit64/1 publication-title: Front. Neurosci. doi: 10.3389/fnins.2021.640648 – volume: 101 start-page: 506 year: 2015 ident: D3FO01301D/cit15/1 publication-title: Am. J. Clin. Nutr. doi: 10.3945/ajcn.114.088518 – volume: 26 start-page: 191 year: 2001 ident: D3FO01301D/cit57/1 publication-title: Neurochem. Res. doi: 10.1023/A:1010904214482 – volume: 27 start-page: 2957 year: 2011 ident: D3FO01301D/cit30/1 publication-title: Bioinformatics doi: 10.1093/bioinformatics/btr507 – volume: 8 start-page: 325 year: 2002 ident: D3FO01301D/cit43/1 publication-title: Parkinsonism Relat. Disord. doi: 10.1016/S1353-8020(01)00043-8 – volume: 11 start-page: 1464 year: 2019 ident: D3FO01301D/cit39/1 publication-title: Nutrients doi: 10.3390/nu11071464 – volume: 9 start-page: 68 year: 2015 ident: D3FO01301D/cit14/1 publication-title: Chem. Cent. J. doi: 10.1186/s13065-015-0145-9 – volume: 48 start-page: 4156 year: 2000 ident: D3FO01301D/cit52/1 publication-title: J. Agric. Food Chem. doi: 10.1021/jf000227d – volume: 16 start-page: 57 year: 2020 ident: D3FO01301D/cit1/1 publication-title: Global Health doi: 10.1186/s12992-020-00589-w – volume: 27 start-page: 2194 year: 2011 ident: D3FO01301D/cit31/1 publication-title: Bioinformatics doi: 10.1093/bioinformatics/btr381 – volume: 35 start-page: 1154 year: 2016 ident: D3FO01301D/cit59/1 publication-title: Lat. Am. J. Pharm. – volume: 38 start-page: 1 year: 2014 ident: D3FO01301D/cit6/1 publication-title: Brain, Behav., Immun. doi: 10.1016/j.bbi.2013.12.015 – volume: 7 start-page: 79 year: 2006 ident: D3FO01301D/cit41/1 publication-title: Obes. Rev. doi: 10.1111/j.1467-789X.2006.00195.x – volume: 8 start-page: 3173 year: 2020 ident: D3FO01301D/cit61/1 publication-title: Food Sci. Nutr. doi: 10.1002/fsn3.1566 – volume: 29 start-page: 193 year: 2014 ident: D3FO01301D/cit55/1 publication-title: Flavour Fragrance J. doi: 10.1002/ffj.3197 – volume: 280 start-page: 111832 year: 2021 ident: D3FO01301D/cit12/1 publication-title: J. Environ. Manage. doi: 10.1016/j.jenvman.2020.111832 – volume: 7 start-page: 135 year: 2022 ident: D3FO01301D/cit3/1 publication-title: Signal Transduction Targeted Ther. doi: 10.1038/s41392-022-00974-4 – volume: 75 start-page: 7537 year: 2009 ident: D3FO01301D/cit34/1 publication-title: Appl. Environ. Microbiol. doi: 10.1128/AEM.01541-09 – volume: 46 start-page: e14164 year: 2022 ident: D3FO01301D/cit49/1 publication-title: J. Food Biochem. doi: 10.1111/jfbc.14164 – volume: 11 start-page: 1299 year: 2022 ident: D3FO01301D/cit19/1 publication-title: Foods doi: 10.3390/foods11091299 – volume: 12 start-page: 266 year: 2018 ident: D3FO01301D/cit36/1 publication-title: Front. Behav. Neurosci. doi: 10.3389/fnbeh.2018.00266 – volume: 102 start-page: 1 year: 2011 ident: D3FO01301D/cit58/1 publication-title: Physiol. Behav. doi: 10.1016/j.physbeh.2010.10.008 – volume: 79 start-page: 727 year: 2004 ident: D3FO01301D/cit40/1 publication-title: Am. J. Clin. Nutr. doi: 10.1093/ajcn/79.5.727 – volume: 66 start-page: 111 year: 2012 ident: D3FO01301D/cit47/1 publication-title: Acta Med. Okayama – volume: 141 start-page: 2061 year: 2019 ident: D3FO01301D/cit51/1 publication-title: J. Am. Chem. Soc. doi: 10.1021/jacs.8b11414 – volume: 57 start-page: 551 year: 2013 ident: D3FO01301D/cit62/1 publication-title: Mol. Nutr. Food Res. doi: 10.1002/mnfr.201200606 – volume: 76 start-page: 249 year: 2021 ident: D3FO01301D/cit45/1 publication-title: Pharmazie – volume: 81 start-page: 417 year: 2004 ident: D3FO01301D/cit25/1 publication-title: Physiol. Behav. doi: 10.1016/j.physbeh.2004.01.013 – volume: 7 start-page: 335 year: 2010 ident: D3FO01301D/cit35/1 publication-title: Nat. Methods doi: 10.1038/nmeth.f.303 – volume: 92 start-page: 945 year: 2014 ident: D3FO01301D/cit60/1 publication-title: Can. J. Physiol. Pharmacol. doi: 10.1139/cjpp-2014-0281 – volume: 25 start-page: 1 year: 2020 ident: D3FO01301D/cit10/1 publication-title: J. Evidence-Based Integr. Med. doi: 10.1177/2515690X20957225 – volume: 27 start-page: 6715 year: 2021 ident: D3FO01301D/cit63/1 publication-title: World J. Gastroenterol. doi: 10.3748/wjg.v27.i39.6715 – volume: 74 start-page: 720 year: 2013 ident: D3FO01301D/cit7/1 publication-title: Biol. Psychiatry doi: 10.1016/j.biopsych.2013.05.001 – volume: 14 start-page: 2111 year: 2022 ident: D3FO01301D/cit11/1 publication-title: Nutrients doi: 10.3390/nu14102111 – volume: 12 start-page: 3871 year: 2001 ident: D3FO01301D/cit16/1 publication-title: NeuroReport doi: 10.1097/00001756-200112040-00053 – volume: 134 start-page: 48 year: 2012 ident: D3FO01301D/cit53/1 publication-title: Food Chem. doi: 10.1016/j.foodchem.2012.02.054 – volume: 10 start-page: 2407 year: 2019 ident: D3FO01301D/cit37/1 publication-title: Front. Microbiol. doi: 10.3389/fmicb.2019.02407 – volume: 7 start-page: 43859 year: 2017 ident: D3FO01301D/cit23/1 publication-title: Sci. Rep. doi: 10.1038/srep43859 – volume: 21 start-page: 9277 year: 2020 ident: D3FO01301D/cit46/1 publication-title: Int. J. Mol. Sci. doi: 10.3390/ijms21239277 – volume: 19 start-page: 1966 year: 2018 ident: D3FO01301D/cit18/1 publication-title: Int. J. Mol. Sci. doi: 10.3390/ijms19071966 – volume: 36 start-page: 305 year: 2013 ident: D3FO01301D/cit5/1 publication-title: Trends Neurosci. doi: 10.1016/j.tins.2013.01.005 – volume: 17 start-page: 10 year: 2011 ident: D3FO01301D/cit29/1 publication-title: EMBnet J. doi: 10.14806/ej.17.1.200 – volume: 102 start-page: 72 year: 2016 ident: D3FO01301D/cit48/1 publication-title: Neuropharmacology doi: 10.1016/j.neuropharm.2015.10.034 – volume: 2 start-page: 51 year: 1926 ident: D3FO01301D/cit20/1 publication-title: J. Fac. Agric., Kyushu Univ. – volume: 39 start-page: 763 year: 2016 ident: D3FO01301D/cit8/1 publication-title: Trends Neurosci. doi: 10.1016/j.tins.2016.09.002 – volume: 21 start-page: 494 year: 2011 ident: D3FO01301D/cit32/1 publication-title: Genome Res. doi: 10.1101/gr.112730.110 – volume: 3 start-page: 1093 year: 2022 ident: D3FO01301D/cit9/1 publication-title: J. Biomed. Res. Environ. Sci. doi: 10.37871/jbres1560 – volume: 66 start-page: 8415 year: 2018 ident: D3FO01301D/cit24/1 publication-title: J. Agric. Food Chem. doi: 10.1021/acs.jafc.8b02462 – volume: 30 start-page: 2114 year: 2014 ident: D3FO01301D/cit28/1 publication-title: Bioinformatics doi: 10.1093/bioinformatics/btu170 – volume: 128 start-page: 24 year: 2015 ident: D3FO01301D/cit56/1 publication-title: Life Sci. doi: 10.1016/j.lfs.2015.02.021 – volume: 11 start-page: 541 year: 2020 ident: D3FO01301D/cit66/1 publication-title: Front. Psychiatry doi: 10.3389/fpsyt.2020.00541 – volume: 63 start-page: 217 year: 2016 ident: D3FO01301D/cit68/1 publication-title: Psychoneuroendocrinology doi: 10.1016/j.psyneuen.2015.10.001 – volume: 5 start-page: 1571 year: 2011 ident: D3FO01301D/cit26/1 publication-title: ISME J. doi: 10.1038/ismej.2011.41 – volume: 27 start-page: 2089 year: 2017 ident: D3FO01301D/cit38/1 publication-title: J. Microbiol. Biotechnol. doi: 10.4014/jmb.1709.09027 – volume: 24 start-page: 1200 year: 2021 ident: D3FO01301D/cit22/1 publication-title: J. Essent.Oil Bear. Plants doi: 10.1080/0972060X.2021.1978869 – volume: 12 start-page: 50 year: 2022 ident: D3FO01301D/cit65/1 publication-title: Metabolites doi: 10.3390/metabo12010050 – volume: 76 start-page: 489 year: 2022 ident: D3FO01301D/cit4/1 publication-title: Eur. J. Clin. Nutr. doi: 10.1038/s41430-021-00991-6 – volume: 6 start-page: 78 year: 2017 ident: D3FO01301D/cit42/1 publication-title: Neurobiol. Stress doi: 10.1016/j.ynstr.2016.08.002 – volume: 25 start-page: 397 year: 2011 ident: D3FO01301D/cit67/1 publication-title: Brain, Behav., Immun. doi: 10.1016/j.bbi.2010.10.023 – volume: 6 start-page: 1621 year: 2012 ident: D3FO01301D/cit27/1 publication-title: ISME J. doi: 10.1038/ismej.2012.8 – volume: 35 start-page: 7188 year: 2007 ident: D3FO01301D/cit33/1 publication-title: Nucleic Acids Res. doi: 10.1093/nar/gkm864 – volume: 16 start-page: 387 year: 2017 ident: D3FO01301D/cit17/1 publication-title: CNS Neurol. Disord.: Drug Targets doi: 10.2174/1871527316666170328113309 |
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Snippet | Citrus reticulata
var.
depressa
, commonly known as Hirami lemon, is a native citrus species found in Taiwan and Okinawa islands of Japan. While several
Citrus... var. , commonly known as Hirami lemon, is a native citrus species found in Taiwan and Okinawa islands of Japan. While several species are known to possess... Citrus reticulata var. depressa, commonly known as Hirami lemon, is a native citrus species found in Taiwan and Okinawa islands of Japan. While several Citrus... |
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SubjectTerms | Antidepressants Anxiety Citrus depressa Citrus fruits Citrus reticulata Dysbacteriosis Essential oils Flavones Fruits Hesperidin Indigenous species Intestinal microflora Lemons Limonene Linalool Mental depression Mental disorders Microbiomes Microbiota Microorganisms Oral administration p-Cymene Qualitative analysis Tangeretin Terpenes Terpinene Terpineol Terpinolene α-Pinene |
Title | Hirami lemon ( var. ) modulates the gut-brain axis in a chronic mild stress-induced depression mouse model |
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