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Antidepressant activities and regulative effects on serotonin transporter of Nardostachys jatamansi DC

Nardostachys jatamansi (D.Don) DC. (family Caprifoliaceae, NJ) is well-documented and commonly used in the systems of traditional medicine in China, Tibet, Nepal, Bhutan, India and Japan for curing digestive and neuropsychiatric disorders with a long history of medication. However, the possible acti...

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Published in:Journal of ethnopharmacology 2021-03, Vol.268, p.113601, Article 113601
Main Authors: Li, Ran, Wang, Zhi-Mei, Wang, Yan, Dong, Xueqi, Zhang, Li-Hua, Wang, Tao, Zhu, Yan, Gao, Xiu-Mei, Wu, Hong-Hua, Xu, Yan-Tong
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container_title Journal of ethnopharmacology
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creator Li, Ran
Wang, Zhi-Mei
Wang, Yan
Dong, Xueqi
Zhang, Li-Hua
Wang, Tao
Zhu, Yan
Gao, Xiu-Mei
Wu, Hong-Hua
Xu, Yan-Tong
description Nardostachys jatamansi (D.Don) DC. (family Caprifoliaceae, NJ) is well-documented and commonly used in the systems of traditional medicine in China, Tibet, Nepal, Bhutan, India and Japan for curing digestive and neuropsychiatric disorders with a long history of medication. However, the possible action mechanisms of antidepressant effects of NJ remain unraveled. The aim of this study was to systematically investigate chemical substances of NJ and their effects on serotonin transporter (SERT) in antidepressant activity. Antidepressant effects of total methanol extract of NJ were evaluated by tail suspension test (TST) and open field test (OFT). Then the total extract was analyzed by ultra-high-performance liquid chromatography (UHPLC) method, and its effect on SERT activity was evaluated by high content assay (HCA) to determine half maximal effective concentration (EC50). This total extract was subfractioned into twenty subfractions by preparative high-performance liquid chromatography (p-HPLC) method, and ‘subfraction-SERT activity’ relationship curve was fitted with medians of the retention time of those subfractions and their SERT activity values. Then, the fraction NJFr.01 enriched with SERT enhancers was optimized, prepared and analyzed by UHPLC method. Antidepressant effects of the fraction NJFr.01 were evaluated by TST and OFT. Further, major constituents of the total extract and fraction NJFr.01 were isolated by p-HPLC and identified by extensive nuclear magnetic resonance (NMR) analyses and comparisons with those reported data, and their SERT activities were also evaluated. Finally, antagonistic effects of chlorogenic acid and desoxo-narchinol A against fluoxetine on SERT were evaluated. Results of TST and OFT demonstrated antidepressant effects of toatal extract of NJ. The EC50 of total extract on SERT enhancement was 31.63 μg/mL. The fitted ‘subfraction-SERT activity’ relationship curve revealed that fraction NJFr.01 was enriched with SERT enhancing constituents. Both total extract and fraction NJFr.01 significantly enhanced SERT activity, while the rest fraction NJFr.02 didn't show any SERT activity. Then, antidepressant effects of fraction NJFr.01 were demonstrated by TST and OFT. Further, phytochemistry investigation and UHPLC analyses confirmed the identification of fourteen constituents in the total extract of NJ, including 7-oxonardinoperoxide (1), desoxo-narchinol A (2), kanshone B (3), narchinol B (4), nardosinonediol (5), kanshone A (6),
doi_str_mv 10.1016/j.jep.2020.113601
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(family Caprifoliaceae, NJ) is well-documented and commonly used in the systems of traditional medicine in China, Tibet, Nepal, Bhutan, India and Japan for curing digestive and neuropsychiatric disorders with a long history of medication. However, the possible action mechanisms of antidepressant effects of NJ remain unraveled. The aim of this study was to systematically investigate chemical substances of NJ and their effects on serotonin transporter (SERT) in antidepressant activity. Antidepressant effects of total methanol extract of NJ were evaluated by tail suspension test (TST) and open field test (OFT). Then the total extract was analyzed by ultra-high-performance liquid chromatography (UHPLC) method, and its effect on SERT activity was evaluated by high content assay (HCA) to determine half maximal effective concentration (EC50). This total extract was subfractioned into twenty subfractions by preparative high-performance liquid chromatography (p-HPLC) method, and ‘subfraction-SERT activity’ relationship curve was fitted with medians of the retention time of those subfractions and their SERT activity values. Then, the fraction NJFr.01 enriched with SERT enhancers was optimized, prepared and analyzed by UHPLC method. Antidepressant effects of the fraction NJFr.01 were evaluated by TST and OFT. Further, major constituents of the total extract and fraction NJFr.01 were isolated by p-HPLC and identified by extensive nuclear magnetic resonance (NMR) analyses and comparisons with those reported data, and their SERT activities were also evaluated. Finally, antagonistic effects of chlorogenic acid and desoxo-narchinol A against fluoxetine on SERT were evaluated. Results of TST and OFT demonstrated antidepressant effects of toatal extract of NJ. The EC50 of total extract on SERT enhancement was 31.63 μg/mL. The fitted ‘subfraction-SERT activity’ relationship curve revealed that fraction NJFr.01 was enriched with SERT enhancing constituents. Both total extract and fraction NJFr.01 significantly enhanced SERT activity, while the rest fraction NJFr.02 didn't show any SERT activity. Then, antidepressant effects of fraction NJFr.01 were demonstrated by TST and OFT. Further, phytochemistry investigation and UHPLC analyses confirmed the identification of fourteen constituents in the total extract of NJ, including 7-oxonardinoperoxide (1), desoxo-narchinol A (2), kanshone B (3), narchinol B (4), nardosinonediol (5), kanshone A (6), 1-hydroxylaristolone (7), debilon (8), nardosinone (9), kanshone H (10), 1,8,9,10-tetradehydroaristolan-2-one (11), (−)-aristolone (12), 1(10)-aristolene-2-one (13) and jatamol A (14), and seven constituents in the fraction NJFr.01, including chlorogenic acid (15), 8α-dihydrogeniposide (16), 7-deoxy-8-epi-loganic acid (17), adoxosidic acid (18), 8-epi-loganic acid (19), 8α-6,7-dihydroapodantheroside acetate (20) and 6″-acetylpatrinalloside (21). Their structures were established by NMR analyses and comparisons with those reported data. HCA results of these constituents demonstrated the major components of fraction NJFr.01 enhanced SERT activity. Antagonistic results showed that chlorogenic acid and desoxo-narchinol A reversed inhibition effect of fluoxetine on SERT activity. This study first systematically expatiated the roles of SERT activity in antidepressant effects of NJ, including total methanol extract and the water-soluble fraction NJFr.01 enriched with SERT enhancing constituents. This is the first report of natural SERT enhancing extract and fractions with antidepressant potential in NJ. Both total extract and fraction NJFr.01 of N. jatamansi possess antidepressant potentials.SERT Enhancers and inhibitors were co-existed in N. jatamansi.Antagonistic effects were observed between SERT enhancers of N. jatamansi and fluoxetine on SERT.Serotonin transporters play important roles in antidepressant effects of Nardostachys jatamansi DC. [Display omitted]</description><identifier>ISSN: 0378-8741</identifier><identifier>EISSN: 1872-7573</identifier><identifier>DOI: 10.1016/j.jep.2020.113601</identifier><identifier>PMID: 33220358</identifier><language>eng</language><publisher>Ireland: Elsevier B.V</publisher><subject>Animals ; Antidepressant ; Antidepressive Agents - isolation &amp; purification ; Antidepressive Agents - pharmacology ; Antidepressive Agents - therapeutic use ; Caprifoliaceae ; Depression - drug therapy ; Depression - metabolism ; Depression - psychology ; Dose-Response Relationship, Drug ; Drugs, Chinese Herbal - isolation &amp; purification ; Drugs, Chinese Herbal - pharmacology ; Drugs, Chinese Herbal - therapeutic use ; Hindlimb Suspension - adverse effects ; Hindlimb Suspension - physiology ; Hindlimb Suspension - psychology ; Locomotion - drug effects ; Locomotion - physiology ; Male ; Mice ; Mice, Inbred ICR ; Nardostachys ; Nardostachys jatamansi ; Serotonin Plasma Membrane Transport Proteins - metabolism ; Serotonin transporter</subject><ispartof>Journal of ethnopharmacology, 2021-03, Vol.268, p.113601, Article 113601</ispartof><rights>2020 Elsevier B.V.</rights><rights>Copyright © 2020 Elsevier B.V. All rights reserved.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c353t-ff33f776c842746c9990f5cb40a49e22846e9071259ce9e25d9eeee83fa810b43</citedby><cites>FETCH-LOGICAL-c353t-ff33f776c842746c9990f5cb40a49e22846e9071259ce9e25d9eeee83fa810b43</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,27924,27925</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/33220358$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Li, Ran</creatorcontrib><creatorcontrib>Wang, Zhi-Mei</creatorcontrib><creatorcontrib>Wang, Yan</creatorcontrib><creatorcontrib>Dong, Xueqi</creatorcontrib><creatorcontrib>Zhang, Li-Hua</creatorcontrib><creatorcontrib>Wang, Tao</creatorcontrib><creatorcontrib>Zhu, Yan</creatorcontrib><creatorcontrib>Gao, Xiu-Mei</creatorcontrib><creatorcontrib>Wu, Hong-Hua</creatorcontrib><creatorcontrib>Xu, Yan-Tong</creatorcontrib><title>Antidepressant activities and regulative effects on serotonin transporter of Nardostachys jatamansi DC</title><title>Journal of ethnopharmacology</title><addtitle>J Ethnopharmacol</addtitle><description>Nardostachys jatamansi (D.Don) DC. (family Caprifoliaceae, NJ) is well-documented and commonly used in the systems of traditional medicine in China, Tibet, Nepal, Bhutan, India and Japan for curing digestive and neuropsychiatric disorders with a long history of medication. However, the possible action mechanisms of antidepressant effects of NJ remain unraveled. The aim of this study was to systematically investigate chemical substances of NJ and their effects on serotonin transporter (SERT) in antidepressant activity. Antidepressant effects of total methanol extract of NJ were evaluated by tail suspension test (TST) and open field test (OFT). Then the total extract was analyzed by ultra-high-performance liquid chromatography (UHPLC) method, and its effect on SERT activity was evaluated by high content assay (HCA) to determine half maximal effective concentration (EC50). This total extract was subfractioned into twenty subfractions by preparative high-performance liquid chromatography (p-HPLC) method, and ‘subfraction-SERT activity’ relationship curve was fitted with medians of the retention time of those subfractions and their SERT activity values. Then, the fraction NJFr.01 enriched with SERT enhancers was optimized, prepared and analyzed by UHPLC method. Antidepressant effects of the fraction NJFr.01 were evaluated by TST and OFT. Further, major constituents of the total extract and fraction NJFr.01 were isolated by p-HPLC and identified by extensive nuclear magnetic resonance (NMR) analyses and comparisons with those reported data, and their SERT activities were also evaluated. Finally, antagonistic effects of chlorogenic acid and desoxo-narchinol A against fluoxetine on SERT were evaluated. Results of TST and OFT demonstrated antidepressant effects of toatal extract of NJ. The EC50 of total extract on SERT enhancement was 31.63 μg/mL. The fitted ‘subfraction-SERT activity’ relationship curve revealed that fraction NJFr.01 was enriched with SERT enhancing constituents. Both total extract and fraction NJFr.01 significantly enhanced SERT activity, while the rest fraction NJFr.02 didn't show any SERT activity. Then, antidepressant effects of fraction NJFr.01 were demonstrated by TST and OFT. Further, phytochemistry investigation and UHPLC analyses confirmed the identification of fourteen constituents in the total extract of NJ, including 7-oxonardinoperoxide (1), desoxo-narchinol A (2), kanshone B (3), narchinol B (4), nardosinonediol (5), kanshone A (6), 1-hydroxylaristolone (7), debilon (8), nardosinone (9), kanshone H (10), 1,8,9,10-tetradehydroaristolan-2-one (11), (−)-aristolone (12), 1(10)-aristolene-2-one (13) and jatamol A (14), and seven constituents in the fraction NJFr.01, including chlorogenic acid (15), 8α-dihydrogeniposide (16), 7-deoxy-8-epi-loganic acid (17), adoxosidic acid (18), 8-epi-loganic acid (19), 8α-6,7-dihydroapodantheroside acetate (20) and 6″-acetylpatrinalloside (21). Their structures were established by NMR analyses and comparisons with those reported data. HCA results of these constituents demonstrated the major components of fraction NJFr.01 enhanced SERT activity. Antagonistic results showed that chlorogenic acid and desoxo-narchinol A reversed inhibition effect of fluoxetine on SERT activity. This study first systematically expatiated the roles of SERT activity in antidepressant effects of NJ, including total methanol extract and the water-soluble fraction NJFr.01 enriched with SERT enhancing constituents. This is the first report of natural SERT enhancing extract and fractions with antidepressant potential in NJ. Both total extract and fraction NJFr.01 of N. jatamansi possess antidepressant potentials.SERT Enhancers and inhibitors were co-existed in N. jatamansi.Antagonistic effects were observed between SERT enhancers of N. jatamansi and fluoxetine on SERT.Serotonin transporters play important roles in antidepressant effects of Nardostachys jatamansi DC. [Display omitted]</description><subject>Animals</subject><subject>Antidepressant</subject><subject>Antidepressive Agents - isolation &amp; purification</subject><subject>Antidepressive Agents - pharmacology</subject><subject>Antidepressive Agents - therapeutic use</subject><subject>Caprifoliaceae</subject><subject>Depression - drug therapy</subject><subject>Depression - metabolism</subject><subject>Depression - psychology</subject><subject>Dose-Response Relationship, Drug</subject><subject>Drugs, Chinese Herbal - isolation &amp; purification</subject><subject>Drugs, Chinese Herbal - pharmacology</subject><subject>Drugs, Chinese Herbal - therapeutic use</subject><subject>Hindlimb Suspension - adverse effects</subject><subject>Hindlimb Suspension - physiology</subject><subject>Hindlimb Suspension - psychology</subject><subject>Locomotion - drug effects</subject><subject>Locomotion - physiology</subject><subject>Male</subject><subject>Mice</subject><subject>Mice, Inbred ICR</subject><subject>Nardostachys</subject><subject>Nardostachys jatamansi</subject><subject>Serotonin Plasma Membrane Transport Proteins - metabolism</subject><subject>Serotonin transporter</subject><issn>0378-8741</issn><issn>1872-7573</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2021</creationdate><recordtype>article</recordtype><recordid>eNp9kMtOwzAQRS0EoqXwAWyQfyDFr8SJWFXlKVWwgbXlOmNw1MaR7Vbq3-MqwJLZjOZxr2YOQteUzCmh1W0372CYM8JyTXlF6Ama0lqyQpaSn6Ip4bIuainoBF3E2BFCJBXkHE04Z4zwsp4iu-iTa2EIEKPuE9Ymub1LDiLWfYsDfO42OrcAg7VgUsS-xxGCT753PU5B93HwIUHA3uJXHVofkzZfh4g7nfQ2jx2-X16iM6s3Ea5-8gx9PD68L5-L1dvTy3KxKgwveSqs5dxKWZlaMCkq0zQNsaVZC6JFA4zVooImP8HKxkBulG0DOWpudU3JWvAZoqOvCT7GAFYNwW11OChK1JGZ6lRmpo7M1Mgsa25GzbBbb6H9U_xCygt34wLky_cOgorGQW-gdSEjUa13_9h_A9oDflE</recordid><startdate>20210325</startdate><enddate>20210325</enddate><creator>Li, Ran</creator><creator>Wang, Zhi-Mei</creator><creator>Wang, Yan</creator><creator>Dong, Xueqi</creator><creator>Zhang, Li-Hua</creator><creator>Wang, Tao</creator><creator>Zhu, Yan</creator><creator>Gao, Xiu-Mei</creator><creator>Wu, Hong-Hua</creator><creator>Xu, Yan-Tong</creator><general>Elsevier B.V</general><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope></search><sort><creationdate>20210325</creationdate><title>Antidepressant activities and regulative effects on serotonin transporter of Nardostachys jatamansi DC</title><author>Li, Ran ; 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(family Caprifoliaceae, NJ) is well-documented and commonly used in the systems of traditional medicine in China, Tibet, Nepal, Bhutan, India and Japan for curing digestive and neuropsychiatric disorders with a long history of medication. However, the possible action mechanisms of antidepressant effects of NJ remain unraveled. The aim of this study was to systematically investigate chemical substances of NJ and their effects on serotonin transporter (SERT) in antidepressant activity. Antidepressant effects of total methanol extract of NJ were evaluated by tail suspension test (TST) and open field test (OFT). Then the total extract was analyzed by ultra-high-performance liquid chromatography (UHPLC) method, and its effect on SERT activity was evaluated by high content assay (HCA) to determine half maximal effective concentration (EC50). This total extract was subfractioned into twenty subfractions by preparative high-performance liquid chromatography (p-HPLC) method, and ‘subfraction-SERT activity’ relationship curve was fitted with medians of the retention time of those subfractions and their SERT activity values. Then, the fraction NJFr.01 enriched with SERT enhancers was optimized, prepared and analyzed by UHPLC method. Antidepressant effects of the fraction NJFr.01 were evaluated by TST and OFT. Further, major constituents of the total extract and fraction NJFr.01 were isolated by p-HPLC and identified by extensive nuclear magnetic resonance (NMR) analyses and comparisons with those reported data, and their SERT activities were also evaluated. Finally, antagonistic effects of chlorogenic acid and desoxo-narchinol A against fluoxetine on SERT were evaluated. Results of TST and OFT demonstrated antidepressant effects of toatal extract of NJ. The EC50 of total extract on SERT enhancement was 31.63 μg/mL. The fitted ‘subfraction-SERT activity’ relationship curve revealed that fraction NJFr.01 was enriched with SERT enhancing constituents. Both total extract and fraction NJFr.01 significantly enhanced SERT activity, while the rest fraction NJFr.02 didn't show any SERT activity. Then, antidepressant effects of fraction NJFr.01 were demonstrated by TST and OFT. Further, phytochemistry investigation and UHPLC analyses confirmed the identification of fourteen constituents in the total extract of NJ, including 7-oxonardinoperoxide (1), desoxo-narchinol A (2), kanshone B (3), narchinol B (4), nardosinonediol (5), kanshone A (6), 1-hydroxylaristolone (7), debilon (8), nardosinone (9), kanshone H (10), 1,8,9,10-tetradehydroaristolan-2-one (11), (−)-aristolone (12), 1(10)-aristolene-2-one (13) and jatamol A (14), and seven constituents in the fraction NJFr.01, including chlorogenic acid (15), 8α-dihydrogeniposide (16), 7-deoxy-8-epi-loganic acid (17), adoxosidic acid (18), 8-epi-loganic acid (19), 8α-6,7-dihydroapodantheroside acetate (20) and 6″-acetylpatrinalloside (21). Their structures were established by NMR analyses and comparisons with those reported data. HCA results of these constituents demonstrated the major components of fraction NJFr.01 enhanced SERT activity. Antagonistic results showed that chlorogenic acid and desoxo-narchinol A reversed inhibition effect of fluoxetine on SERT activity. This study first systematically expatiated the roles of SERT activity in antidepressant effects of NJ, including total methanol extract and the water-soluble fraction NJFr.01 enriched with SERT enhancing constituents. This is the first report of natural SERT enhancing extract and fractions with antidepressant potential in NJ. Both total extract and fraction NJFr.01 of N. jatamansi possess antidepressant potentials.SERT Enhancers and inhibitors were co-existed in N. jatamansi.Antagonistic effects were observed between SERT enhancers of N. jatamansi and fluoxetine on SERT.Serotonin transporters play important roles in antidepressant effects of Nardostachys jatamansi DC. [Display omitted]</abstract><cop>Ireland</cop><pub>Elsevier B.V</pub><pmid>33220358</pmid><doi>10.1016/j.jep.2020.113601</doi></addata></record>
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identifier ISSN: 0378-8741
ispartof Journal of ethnopharmacology, 2021-03, Vol.268, p.113601, Article 113601
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1872-7573
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recordid cdi_crossref_primary_10_1016_j_jep_2020_113601
source ScienceDirect Freedom Collection
subjects Animals
Antidepressant
Antidepressive Agents - isolation & purification
Antidepressive Agents - pharmacology
Antidepressive Agents - therapeutic use
Caprifoliaceae
Depression - drug therapy
Depression - metabolism
Depression - psychology
Dose-Response Relationship, Drug
Drugs, Chinese Herbal - isolation & purification
Drugs, Chinese Herbal - pharmacology
Drugs, Chinese Herbal - therapeutic use
Hindlimb Suspension - adverse effects
Hindlimb Suspension - physiology
Hindlimb Suspension - psychology
Locomotion - drug effects
Locomotion - physiology
Male
Mice
Mice, Inbred ICR
Nardostachys
Nardostachys jatamansi
Serotonin Plasma Membrane Transport Proteins - metabolism
Serotonin transporter
title Antidepressant activities and regulative effects on serotonin transporter of Nardostachys jatamansi DC
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