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Effects of Different No-Ozone Cold Plasma Treatment Methods on Mouse Osteoblast Proliferation and Differentiation
: Enhanced osteoblast differentiation may be leveraged to prevent and treat bone-related diseases such as osteoporosis. No-ozone cold plasma (NCP) treatment is a promising and safe strategy to enhance osteoblast differentiation. Therefore, this study aimed to determine the effectiveness of direct an...
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Published in: | Medicina (Kaunas, Lithuania) Lithuania), 2024-08, Vol.60 (8), p.1318 |
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description | : Enhanced osteoblast differentiation may be leveraged to prevent and treat bone-related diseases such as osteoporosis. No-ozone cold plasma (NCP) treatment is a promising and safe strategy to enhance osteoblast differentiation. Therefore, this study aimed to determine the effectiveness of direct and indirect NCP treatment methods on osteoblast differentiation. Mouse osteoblastic cells (MC3T3-E1) were treated with NCP using different methods, i.e., no NCP treatment (NT group; control), direct NCP treatment (DT group), direct NCP treatment followed by media replacement (MC group), and indirect treatment with NCP-treated media only (PAM group).
: The MC3T3-E1 cells were subsequently assessed for cell proliferation, alkaline phosphatase (ALP) activity, calcium deposition, and ALP and osteocalcin mRNA expression using real-time polymerase chain reaction.
: Cell proliferation significantly increased in the NCP-treated groups (DT and PAM; MC and PAM) compared to the NT group after 24 h (
< 0.038) and 48 h (
< 0.000). ALP activity was increased in the DT and PAM groups at 1 week (
< 0.115) and in the DT, MC, and PAM groups at 2 weeks (
< 0.000) compared to the NT group. Calcium deposition was higher in the NCP-treated groups than in NT group at 2 and 3 weeks (
< 0.000). ALP mRNA expression peaked in the MC group at 2 weeks compared to the NP group (
< 0.014). Osteocalcin mRNA expression increased in the MC group at 2 weeks (
< 0.000) and was the highest in the PAM group at 3 weeks (
< 0.000). Thus, the effects of direct (DT and MC) and indirect (PAM) treatment varied, with MC direct treatment showing the most significant impact on osteoblast activity.
: The MC group exhibited enhanced osteoblast differentiation, indicating that direct NCP treatment followed by media replacement is the most effective method for promoting bone formation. |
doi_str_mv | 10.3390/medicina60081318 |
format | article |
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: The MC3T3-E1 cells were subsequently assessed for cell proliferation, alkaline phosphatase (ALP) activity, calcium deposition, and ALP and osteocalcin mRNA expression using real-time polymerase chain reaction.
: Cell proliferation significantly increased in the NCP-treated groups (DT and PAM; MC and PAM) compared to the NT group after 24 h (
< 0.038) and 48 h (
< 0.000). ALP activity was increased in the DT and PAM groups at 1 week (
< 0.115) and in the DT, MC, and PAM groups at 2 weeks (
< 0.000) compared to the NT group. Calcium deposition was higher in the NCP-treated groups than in NT group at 2 and 3 weeks (
< 0.000). ALP mRNA expression peaked in the MC group at 2 weeks compared to the NP group (
< 0.014). Osteocalcin mRNA expression increased in the MC group at 2 weeks (
< 0.000) and was the highest in the PAM group at 3 weeks (
< 0.000). Thus, the effects of direct (DT and MC) and indirect (PAM) treatment varied, with MC direct treatment showing the most significant impact on osteoblast activity.
: The MC group exhibited enhanced osteoblast differentiation, indicating that direct NCP treatment followed by media replacement is the most effective method for promoting bone formation.]]></description><identifier>ISSN: 1648-9144</identifier><identifier>ISSN: 1010-660X</identifier><identifier>EISSN: 1648-9144</identifier><identifier>DOI: 10.3390/medicina60081318</identifier><identifier>PMID: 39202599</identifier><language>eng</language><publisher>Switzerland: MDPI AG</publisher><subject>Air pollution ; alkaline phosphatase ; Alkaline Phosphatase - analysis ; Alkaline Phosphatase - metabolism ; Animals ; Bones ; Cell Differentiation - drug effects ; Cell Proliferation - drug effects ; Cold ; Density ; Gases ; Medical equipment ; Medical research ; Methods ; Mice ; mouse osteoblast ; Nitrogen dioxide ; no-ozone cold plasma ; osteoblast differentiation ; Osteoblasts - drug effects ; osteocalcin ; Osteocalcin - analysis ; Osteoporosis ; Ozone - pharmacology ; Ozone - therapeutic use ; Plasma ; Plasma Gases - pharmacology ; Plasma Gases - therapeutic use ; Plasma physics ; Process controls ; Proteins</subject><ispartof>Medicina (Kaunas, Lithuania), 2024-08, Vol.60 (8), p.1318</ispartof><rights>COPYRIGHT 2024 MDPI AG</rights><rights>2024 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/). Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License.</rights><rights>2024 by the authors. 2024</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.proquest.com/docview/3098085277/fulltextPDF?pq-origsite=primo$$EPDF$$P50$$Gproquest$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://www.proquest.com/docview/3098085277?pq-origsite=primo$$EHTML$$P50$$Gproquest$$Hfree_for_read</linktohtml><link.rule.ids>230,314,727,780,784,885,25751,27922,27923,37010,37011,44588,53789,53791,74896</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/39202599$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Choi, Byul-Bo Ra</creatorcontrib><creatorcontrib>Park, Sang-Rye</creatorcontrib><creatorcontrib>Kim, Gyoo-Cheon</creatorcontrib><title>Effects of Different No-Ozone Cold Plasma Treatment Methods on Mouse Osteoblast Proliferation and Differentiation</title><title>Medicina (Kaunas, Lithuania)</title><addtitle>Medicina (Kaunas)</addtitle><description><![CDATA[: Enhanced osteoblast differentiation may be leveraged to prevent and treat bone-related diseases such as osteoporosis. No-ozone cold plasma (NCP) treatment is a promising and safe strategy to enhance osteoblast differentiation. Therefore, this study aimed to determine the effectiveness of direct and indirect NCP treatment methods on osteoblast differentiation. Mouse osteoblastic cells (MC3T3-E1) were treated with NCP using different methods, i.e., no NCP treatment (NT group; control), direct NCP treatment (DT group), direct NCP treatment followed by media replacement (MC group), and indirect treatment with NCP-treated media only (PAM group).
: The MC3T3-E1 cells were subsequently assessed for cell proliferation, alkaline phosphatase (ALP) activity, calcium deposition, and ALP and osteocalcin mRNA expression using real-time polymerase chain reaction.
: Cell proliferation significantly increased in the NCP-treated groups (DT and PAM; MC and PAM) compared to the NT group after 24 h (
< 0.038) and 48 h (
< 0.000). ALP activity was increased in the DT and PAM groups at 1 week (
< 0.115) and in the DT, MC, and PAM groups at 2 weeks (
< 0.000) compared to the NT group. Calcium deposition was higher in the NCP-treated groups than in NT group at 2 and 3 weeks (
< 0.000). ALP mRNA expression peaked in the MC group at 2 weeks compared to the NP group (
< 0.014). Osteocalcin mRNA expression increased in the MC group at 2 weeks (
< 0.000) and was the highest in the PAM group at 3 weeks (
< 0.000). Thus, the effects of direct (DT and MC) and indirect (PAM) treatment varied, with MC direct treatment showing the most significant impact on osteoblast activity.
: The MC group exhibited enhanced osteoblast differentiation, indicating that direct NCP treatment followed by media replacement is the most effective method for promoting bone formation.]]></description><subject>Air pollution</subject><subject>alkaline phosphatase</subject><subject>Alkaline Phosphatase - analysis</subject><subject>Alkaline Phosphatase - metabolism</subject><subject>Animals</subject><subject>Bones</subject><subject>Cell Differentiation - drug effects</subject><subject>Cell Proliferation - drug effects</subject><subject>Cold</subject><subject>Density</subject><subject>Gases</subject><subject>Medical equipment</subject><subject>Medical research</subject><subject>Methods</subject><subject>Mice</subject><subject>mouse osteoblast</subject><subject>Nitrogen dioxide</subject><subject>no-ozone cold plasma</subject><subject>osteoblast differentiation</subject><subject>Osteoblasts - drug effects</subject><subject>osteocalcin</subject><subject>Osteocalcin - analysis</subject><subject>Osteoporosis</subject><subject>Ozone - pharmacology</subject><subject>Ozone - therapeutic use</subject><subject>Plasma</subject><subject>Plasma Gases - pharmacology</subject><subject>Plasma Gases - therapeutic use</subject><subject>Plasma physics</subject><subject>Process controls</subject><subject>Proteins</subject><issn>1648-9144</issn><issn>1010-660X</issn><issn>1648-9144</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2024</creationdate><recordtype>article</recordtype><sourceid>PIMPY</sourceid><sourceid>DOA</sourceid><recordid>eNptkk1v1DAQhiMEoqVw54QiceGSMv6IY59QtbRQqWV7KGfLsSdbr5K4dbKV4Nd3ti20i5APHs2883g-XBTvGRwKYeDzgCH6ODoFoJlg-kWxz5TUlWFSvnxm7xVvpmkNIHjd8NfFnjAceG3MfnFz3HXo56lMXfk1kp1xnMsfqVr-TiOWi9SH8qJ30-DKy4xuHrbhc5yvUqCcsTxPmwnL5TRjakk2lxc59ZEwbo4UdmN4wsZ739viVef6Cd893gfFz5Pjy8X36mz57XRxdFYFCTBXgUoMtfYhSImGGzDogWEtgyeLKQYieK07YRQjn8LWAIDnHYcGuObioDh94Ibk1vY6x8HlXza5aO8dKa-sy3P0PVrtRM2NEag4l0YJrVntQaFQWLeGtcT68sC63rQ0c0_NZNfvQHcjY7yyq3RrGRO14o0gwqdHQk43G5xmO8TJY9-7EWmEVoAxjaH9bAv_-I90nTZ5pFltVRp0zZvmSbVy1EEcu0QP-y3UHmlopJAStqrD_6joBByipw13kfw7CR-ed_q3xT8_RtwBD2HCMg</recordid><startdate>20240801</startdate><enddate>20240801</enddate><creator>Choi, Byul-Bo Ra</creator><creator>Park, Sang-Rye</creator><creator>Kim, Gyoo-Cheon</creator><general>MDPI AG</general><general>MDPI</general><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>3V.</scope><scope>7X7</scope><scope>7XB</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>ABUWG</scope><scope>AFKRA</scope><scope>AZQEC</scope><scope>BENPR</scope><scope>CCPQU</scope><scope>DWQXO</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>K9.</scope><scope>M0S</scope><scope>PIMPY</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>PRINS</scope><scope>7X8</scope><scope>5PM</scope><scope>DOA</scope></search><sort><creationdate>20240801</creationdate><title>Effects of Different No-Ozone Cold Plasma Treatment Methods on Mouse Osteoblast Proliferation and Differentiation</title><author>Choi, Byul-Bo Ra ; Park, Sang-Rye ; Kim, Gyoo-Cheon</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-d400t-d920d58cdd44e92909ec01e54dc9ec16103dc88f39614dc6eb9000c2f20702823</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2024</creationdate><topic>Air pollution</topic><topic>alkaline phosphatase</topic><topic>Alkaline Phosphatase - analysis</topic><topic>Alkaline Phosphatase - metabolism</topic><topic>Animals</topic><topic>Bones</topic><topic>Cell Differentiation - drug effects</topic><topic>Cell Proliferation - drug effects</topic><topic>Cold</topic><topic>Density</topic><topic>Gases</topic><topic>Medical equipment</topic><topic>Medical research</topic><topic>Methods</topic><topic>Mice</topic><topic>mouse osteoblast</topic><topic>Nitrogen dioxide</topic><topic>no-ozone cold plasma</topic><topic>osteoblast differentiation</topic><topic>Osteoblasts - drug effects</topic><topic>osteocalcin</topic><topic>Osteocalcin - analysis</topic><topic>Osteoporosis</topic><topic>Ozone - pharmacology</topic><topic>Ozone - therapeutic use</topic><topic>Plasma</topic><topic>Plasma Gases - pharmacology</topic><topic>Plasma Gases - therapeutic use</topic><topic>Plasma physics</topic><topic>Process controls</topic><topic>Proteins</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Choi, Byul-Bo Ra</creatorcontrib><creatorcontrib>Park, Sang-Rye</creatorcontrib><creatorcontrib>Kim, Gyoo-Cheon</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>ProQuest Central (Corporate)</collection><collection>ProQuest_Health & Medical Collection</collection><collection>ProQuest Central (purchase pre-March 2016)</collection><collection>Hospital Premium Collection</collection><collection>Hospital Premium Collection (Alumni Edition)</collection><collection>ProQuest Central (Alumni) (purchase pre-March 2016)</collection><collection>ProQuest Central (Alumni)</collection><collection>ProQuest Central</collection><collection>ProQuest Central Essentials</collection><collection>AUTh Library subscriptions: ProQuest Central</collection><collection>ProQuest One Community College</collection><collection>ProQuest Central</collection><collection>Health Research Premium Collection</collection><collection>Health Research Premium Collection (Alumni)</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>Health & Medical Collection (Alumni Edition)</collection><collection>Publicly Available Content (ProQuest)</collection><collection>ProQuest One Academic Eastern Edition (DO NOT USE)</collection><collection>ProQuest One Academic</collection><collection>ProQuest One Academic UKI Edition</collection><collection>ProQuest Central China</collection><collection>MEDLINE - Academic</collection><collection>PubMed Central (Full Participant titles)</collection><collection>Directory of Open Access Journals</collection><jtitle>Medicina (Kaunas, Lithuania)</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Choi, Byul-Bo Ra</au><au>Park, Sang-Rye</au><au>Kim, Gyoo-Cheon</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Effects of Different No-Ozone Cold Plasma Treatment Methods on Mouse Osteoblast Proliferation and Differentiation</atitle><jtitle>Medicina (Kaunas, Lithuania)</jtitle><addtitle>Medicina (Kaunas)</addtitle><date>2024-08-01</date><risdate>2024</risdate><volume>60</volume><issue>8</issue><spage>1318</spage><pages>1318-</pages><issn>1648-9144</issn><issn>1010-660X</issn><eissn>1648-9144</eissn><abstract><![CDATA[: Enhanced osteoblast differentiation may be leveraged to prevent and treat bone-related diseases such as osteoporosis. No-ozone cold plasma (NCP) treatment is a promising and safe strategy to enhance osteoblast differentiation. Therefore, this study aimed to determine the effectiveness of direct and indirect NCP treatment methods on osteoblast differentiation. Mouse osteoblastic cells (MC3T3-E1) were treated with NCP using different methods, i.e., no NCP treatment (NT group; control), direct NCP treatment (DT group), direct NCP treatment followed by media replacement (MC group), and indirect treatment with NCP-treated media only (PAM group).
: The MC3T3-E1 cells were subsequently assessed for cell proliferation, alkaline phosphatase (ALP) activity, calcium deposition, and ALP and osteocalcin mRNA expression using real-time polymerase chain reaction.
: Cell proliferation significantly increased in the NCP-treated groups (DT and PAM; MC and PAM) compared to the NT group after 24 h (
< 0.038) and 48 h (
< 0.000). ALP activity was increased in the DT and PAM groups at 1 week (
< 0.115) and in the DT, MC, and PAM groups at 2 weeks (
< 0.000) compared to the NT group. Calcium deposition was higher in the NCP-treated groups than in NT group at 2 and 3 weeks (
< 0.000). ALP mRNA expression peaked in the MC group at 2 weeks compared to the NP group (
< 0.014). Osteocalcin mRNA expression increased in the MC group at 2 weeks (
< 0.000) and was the highest in the PAM group at 3 weeks (
< 0.000). Thus, the effects of direct (DT and MC) and indirect (PAM) treatment varied, with MC direct treatment showing the most significant impact on osteoblast activity.
: The MC group exhibited enhanced osteoblast differentiation, indicating that direct NCP treatment followed by media replacement is the most effective method for promoting bone formation.]]></abstract><cop>Switzerland</cop><pub>MDPI AG</pub><pmid>39202599</pmid><doi>10.3390/medicina60081318</doi><oa>free_for_read</oa></addata></record> |
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subjects | Air pollution alkaline phosphatase Alkaline Phosphatase - analysis Alkaline Phosphatase - metabolism Animals Bones Cell Differentiation - drug effects Cell Proliferation - drug effects Cold Density Gases Medical equipment Medical research Methods Mice mouse osteoblast Nitrogen dioxide no-ozone cold plasma osteoblast differentiation Osteoblasts - drug effects osteocalcin Osteocalcin - analysis Osteoporosis Ozone - pharmacology Ozone - therapeutic use Plasma Plasma Gases - pharmacology Plasma Gases - therapeutic use Plasma physics Process controls Proteins |
title | Effects of Different No-Ozone Cold Plasma Treatment Methods on Mouse Osteoblast Proliferation and Differentiation |
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