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Effects of Salviae Miltiorrhizae Radix Hot Aqueous Extract on Nitric Oxide and Prostaglandin E(2) Production and on 1,1-diphenyl-2-picryl hydrazyl Radical Scavenging in Macrophages

OBJECTIVES: The objective of this study is to investigate the effects of Salviae Miltiorrhizae Radix hot aqueous extract on nitric oxide (NO) and prostaglandin E(2) (PGE(2) ) production and on 1,1-diphenyl-2-picryl hydrazyl (DPPH) free-radical scavenging in macrophages. METHODS: Salviae Miltiorrhiza...

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Autores principales: Yeo, In Ho, Lee, Cham Kyul, Lee, Eun Yong
Formato: Online Artículo Texto
Lenguaje:English
Publicado: KOREAN PHARMACOPUNCTURE INSTITUTE 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4331987/
https://www.ncbi.nlm.nih.gov/pubmed/25780684
http://dx.doi.org/10.3831/KPI.2014.17.001
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author Yeo, In Ho
Lee, Cham Kyul
Lee, Eun Yong
author_facet Yeo, In Ho
Lee, Cham Kyul
Lee, Eun Yong
author_sort Yeo, In Ho
collection PubMed
description OBJECTIVES: The objective of this study is to investigate the effects of Salviae Miltiorrhizae Radix hot aqueous extract on nitric oxide (NO) and prostaglandin E(2) (PGE(2) ) production and on 1,1-diphenyl-2-picryl hydrazyl (DPPH) free-radical scavenging in macrophages. METHODS: Salviae Miltiorrhizae Radix(300 g) was heated at 100℃ with distilled water (2 L) for 4 hours. The extract was filtered and concentrated to 100 mL by using a rotary evaporator, was frozen at -80℃, and was then freeze-dried by using a freezing-drying system. The RAW 264.7 macrophage was subcultured by using 10-㎍/mL lipopolysaccharide (LPS). In order to evaluate cytotoxicity, we performed (3-(4,5-dimrthylthiazol-2-yl)-2,5-diphenyltetrazolium bromide) (MTT) assays and measured the cell viability. The NO production was measured by using Griess assays, and the PGE(2) production was measured by using enzyme immunoassays. The antioxidant activity, the DPPH free-radical scavenging capability, was measured by using the DPPH method. RESULTS: Cell viability with the 1-, 5-, 25-, 125- and 625-㎍/mL Salviae Miltiorrhizae Radix hot aqueous extract was not significantly decreased compared to the cell viability without the extract. When 125 and 625 ㎍/mL of Salviae Miltiorrhizae Radix hot aqueous extract were used, NO production in LPS-stimulated RAW 264.7 macrophages was significantly inhibited compared to that in the control group. When 25, 125, and 625 ㎍/mL of Salviae Miltiorrhizae Radix hot aqueous extract were used, PGE(2) production in LPS-stimulated RAW 264.7 macrophages was significantly inhibited compared to that in the control group. The 125- and 625-㎍/mL Salviae Miltiorrhizae Radix hot aqueous extracts had high DPPH free-radical scavenging capabilities in RAW 264.7 macrophages. CONCLUSION: This study indicates that Salviae Miltiorrhizae Radix hot aqueous extract suppresses NO and PGE(2) production and improves DPPH free-radical scavenging capability. Thus, it seems that Salviae Miltiorrhizae Radix hot aqueous extract may have an anti-inflammation effect and antioxidant activity.
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spelling pubmed-43319872015-03-16 Effects of Salviae Miltiorrhizae Radix Hot Aqueous Extract on Nitric Oxide and Prostaglandin E(2) Production and on 1,1-diphenyl-2-picryl hydrazyl Radical Scavenging in Macrophages Yeo, In Ho Lee, Cham Kyul Lee, Eun Yong J Pharmacopuncture Original Article OBJECTIVES: The objective of this study is to investigate the effects of Salviae Miltiorrhizae Radix hot aqueous extract on nitric oxide (NO) and prostaglandin E(2) (PGE(2) ) production and on 1,1-diphenyl-2-picryl hydrazyl (DPPH) free-radical scavenging in macrophages. METHODS: Salviae Miltiorrhizae Radix(300 g) was heated at 100℃ with distilled water (2 L) for 4 hours. The extract was filtered and concentrated to 100 mL by using a rotary evaporator, was frozen at -80℃, and was then freeze-dried by using a freezing-drying system. The RAW 264.7 macrophage was subcultured by using 10-㎍/mL lipopolysaccharide (LPS). In order to evaluate cytotoxicity, we performed (3-(4,5-dimrthylthiazol-2-yl)-2,5-diphenyltetrazolium bromide) (MTT) assays and measured the cell viability. The NO production was measured by using Griess assays, and the PGE(2) production was measured by using enzyme immunoassays. The antioxidant activity, the DPPH free-radical scavenging capability, was measured by using the DPPH method. RESULTS: Cell viability with the 1-, 5-, 25-, 125- and 625-㎍/mL Salviae Miltiorrhizae Radix hot aqueous extract was not significantly decreased compared to the cell viability without the extract. When 125 and 625 ㎍/mL of Salviae Miltiorrhizae Radix hot aqueous extract were used, NO production in LPS-stimulated RAW 264.7 macrophages was significantly inhibited compared to that in the control group. When 25, 125, and 625 ㎍/mL of Salviae Miltiorrhizae Radix hot aqueous extract were used, PGE(2) production in LPS-stimulated RAW 264.7 macrophages was significantly inhibited compared to that in the control group. The 125- and 625-㎍/mL Salviae Miltiorrhizae Radix hot aqueous extracts had high DPPH free-radical scavenging capabilities in RAW 264.7 macrophages. CONCLUSION: This study indicates that Salviae Miltiorrhizae Radix hot aqueous extract suppresses NO and PGE(2) production and improves DPPH free-radical scavenging capability. Thus, it seems that Salviae Miltiorrhizae Radix hot aqueous extract may have an anti-inflammation effect and antioxidant activity. KOREAN PHARMACOPUNCTURE INSTITUTE 2014-03 /pmc/articles/PMC4331987/ /pubmed/25780684 http://dx.doi.org/10.3831/KPI.2014.17.001 Text en Copyright ©2014, KOREAN PHARMACOPUNCTURE INSTITUTE http://creativecommons.org/licenses/by-nc/3.0/ This is an Open-Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/3.0/) which permits unrestricted noncommercial use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Original Article
Yeo, In Ho
Lee, Cham Kyul
Lee, Eun Yong
Effects of Salviae Miltiorrhizae Radix Hot Aqueous Extract on Nitric Oxide and Prostaglandin E(2) Production and on 1,1-diphenyl-2-picryl hydrazyl Radical Scavenging in Macrophages
title Effects of Salviae Miltiorrhizae Radix Hot Aqueous Extract on Nitric Oxide and Prostaglandin E(2) Production and on 1,1-diphenyl-2-picryl hydrazyl Radical Scavenging in Macrophages
title_full Effects of Salviae Miltiorrhizae Radix Hot Aqueous Extract on Nitric Oxide and Prostaglandin E(2) Production and on 1,1-diphenyl-2-picryl hydrazyl Radical Scavenging in Macrophages
title_fullStr Effects of Salviae Miltiorrhizae Radix Hot Aqueous Extract on Nitric Oxide and Prostaglandin E(2) Production and on 1,1-diphenyl-2-picryl hydrazyl Radical Scavenging in Macrophages
title_full_unstemmed Effects of Salviae Miltiorrhizae Radix Hot Aqueous Extract on Nitric Oxide and Prostaglandin E(2) Production and on 1,1-diphenyl-2-picryl hydrazyl Radical Scavenging in Macrophages
title_short Effects of Salviae Miltiorrhizae Radix Hot Aqueous Extract on Nitric Oxide and Prostaglandin E(2) Production and on 1,1-diphenyl-2-picryl hydrazyl Radical Scavenging in Macrophages
title_sort effects of salviae miltiorrhizae radix hot aqueous extract on nitric oxide and prostaglandin e(2) production and on 1,1-diphenyl-2-picryl hydrazyl radical scavenging in macrophages
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4331987/
https://www.ncbi.nlm.nih.gov/pubmed/25780684
http://dx.doi.org/10.3831/KPI.2014.17.001
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