Enteral siRNA delivery technique for therapeutic gene silencing in the liver via the lymphatic route
An efficient targeting delivery technology is needed for functional oligonucleotides to exert their potential effect on the target gene without an adverse effect in vivo . Development of enteral delivery systems for nucleic acids is a major challenge because of their large molecular size and instabi...
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creator | Murakami, Masahiro Nishina, Kazutaka Watanabe, Chie Yoshida-Tanaka, Kie Piao, Wenying Kuwahara, Hiroya Horikiri, Yuji Miyata, Kanjiro Nishiyama, Nobuhiro Kataoka, Kazunori Yoshida, Masayuki Mizusawa, Hidehiro Yokota, Takanori |
description | An efficient targeting delivery technology is needed for functional oligonucleotides to exert their potential effect on the target gene without an adverse effect
in vivo
. Development of enteral delivery systems for nucleic acids is a major challenge because of their large molecular size and instability. Here, we describe a new enteral delivery technique that enables small interfering RNA (siRNA) selectively delivered to the liver to silence its target
Apolipoprotein B
gene expression. A nuclease-resistant synthetic siRNA was conjugated with α-tochopherol and administered as lipid nanoparticle to the large intestine of the mice in a postprandial state. The selective transport into the liver, effective gene silence and consequently significant reduction in serum low density lipoprotein-cholesterol level, were demonstrated. The chylomicron-mediated pathway via the lymphatic route was suggested as major mechanism. This unique approach may provide a basis for developing oral and rectal delivery systems for nucleic acids targeting liver. |
doi_str_mv | 10.1038/srep17035 |
format | Article |
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in vivo
. Development of enteral delivery systems for nucleic acids is a major challenge because of their large molecular size and instability. Here, we describe a new enteral delivery technique that enables small interfering RNA (siRNA) selectively delivered to the liver to silence its target
Apolipoprotein B
gene expression. A nuclease-resistant synthetic siRNA was conjugated with α-tochopherol and administered as lipid nanoparticle to the large intestine of the mice in a postprandial state. The selective transport into the liver, effective gene silence and consequently significant reduction in serum low density lipoprotein-cholesterol level, were demonstrated. The chylomicron-mediated pathway via the lymphatic route was suggested as major mechanism. This unique approach may provide a basis for developing oral and rectal delivery systems for nucleic acids targeting liver.</description><identifier>ISSN: 2045-2322</identifier><identifier>EISSN: 2045-2322</identifier><identifier>DOI: 10.1038/srep17035</identifier><identifier>PMID: 26593819</identifier><language>eng</language><publisher>London: Nature Publishing Group UK</publisher><subject>13/89 ; 14/19 ; 631/154/152 ; 631/154/309/2144 ; 64/60 ; Administration, Rectal ; alpha-Tocopherol - administration & dosage ; alpha-Tocopherol - chemistry ; alpha-Tocopherol - metabolism ; Animals ; Apolipoprotein B ; Apolipoproteins B - antagonists & inhibitors ; Apolipoproteins B - genetics ; Apolipoproteins B - metabolism ; Biological Transport ; Cholesterol ; Chylomicrons - blood ; Drug Delivery Systems - methods ; Gene expression ; Gene Silencing ; Humanities and Social Sciences ; Jejunum - drug effects ; Jejunum - metabolism ; Large intestine ; Lipoproteins, LDL - blood ; Liver ; Liver - drug effects ; Liver - metabolism ; Low density lipoprotein ; Lymphatic Vessels - physiology ; Mice ; Mice, Inbred C57BL ; Mice, Inbred ICR ; multidisciplinary ; Nanoparticles ; Nanoparticles - administration & dosage ; Nanoparticles - chemistry ; Nanoparticles - metabolism ; Nuclease ; Nucleic acids ; Oligonucleotides ; Organophosphorus Compounds - administration & dosage ; Organophosphorus Compounds - chemistry ; Organophosphorus Compounds - metabolism ; Postprandial Period - physiology ; Rectum ; RNA, Small Interfering - administration & dosage ; RNA, Small Interfering - genetics ; RNA, Small Interfering - metabolism ; Science ; siRNA</subject><ispartof>Scientific reports, 2015-11, Vol.5 (1), p.17035, Article 17035</ispartof><rights>The Author(s) 2015</rights><rights>Copyright Nature Publishing Group Nov 2015</rights><rights>Copyright © 2015, Macmillan Publishers Limited 2015 Macmillan Publishers Limited</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c548t-ce96fb3bc7e6476528dd8615376cb6a0475265882dcd77eb124987c2b46c4943</citedby><cites>FETCH-LOGICAL-c548t-ce96fb3bc7e6476528dd8615376cb6a0475265882dcd77eb124987c2b46c4943</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC4655470/pdf/$$EPDF$$P50$$Gpubmedcentral$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC4655470/$$EHTML$$P50$$Gpubmedcentral$$Hfree_for_read</linktohtml><link.rule.ids>230,314,723,776,780,860,881,27901,27902,41096,42165,51551,53766,53768</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/26593819$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Murakami, Masahiro</creatorcontrib><creatorcontrib>Nishina, Kazutaka</creatorcontrib><creatorcontrib>Watanabe, Chie</creatorcontrib><creatorcontrib>Yoshida-Tanaka, Kie</creatorcontrib><creatorcontrib>Piao, Wenying</creatorcontrib><creatorcontrib>Kuwahara, Hiroya</creatorcontrib><creatorcontrib>Horikiri, Yuji</creatorcontrib><creatorcontrib>Miyata, Kanjiro</creatorcontrib><creatorcontrib>Nishiyama, Nobuhiro</creatorcontrib><creatorcontrib>Kataoka, Kazunori</creatorcontrib><creatorcontrib>Yoshida, Masayuki</creatorcontrib><creatorcontrib>Mizusawa, Hidehiro</creatorcontrib><creatorcontrib>Yokota, Takanori</creatorcontrib><title>Enteral siRNA delivery technique for therapeutic gene silencing in the liver via the lymphatic route</title><title>Scientific reports</title><addtitle>Sci Rep</addtitle><addtitle>Sci Rep</addtitle><description>An efficient targeting delivery technology is needed for functional oligonucleotides to exert their potential effect on the target gene without an adverse effect
in vivo
. Development of enteral delivery systems for nucleic acids is a major challenge because of their large molecular size and instability. Here, we describe a new enteral delivery technique that enables small interfering RNA (siRNA) selectively delivered to the liver to silence its target
Apolipoprotein B
gene expression. A nuclease-resistant synthetic siRNA was conjugated with α-tochopherol and administered as lipid nanoparticle to the large intestine of the mice in a postprandial state. The selective transport into the liver, effective gene silence and consequently significant reduction in serum low density lipoprotein-cholesterol level, were demonstrated. The chylomicron-mediated pathway via the lymphatic route was suggested as major mechanism. This unique approach may provide a basis for developing oral and rectal delivery systems for nucleic acids targeting liver.</description><subject>13/89</subject><subject>14/19</subject><subject>631/154/152</subject><subject>631/154/309/2144</subject><subject>64/60</subject><subject>Administration, Rectal</subject><subject>alpha-Tocopherol - administration & dosage</subject><subject>alpha-Tocopherol - chemistry</subject><subject>alpha-Tocopherol - metabolism</subject><subject>Animals</subject><subject>Apolipoprotein B</subject><subject>Apolipoproteins B - antagonists & inhibitors</subject><subject>Apolipoproteins B - genetics</subject><subject>Apolipoproteins B - metabolism</subject><subject>Biological Transport</subject><subject>Cholesterol</subject><subject>Chylomicrons - blood</subject><subject>Drug Delivery Systems - methods</subject><subject>Gene expression</subject><subject>Gene Silencing</subject><subject>Humanities and Social Sciences</subject><subject>Jejunum - drug effects</subject><subject>Jejunum - metabolism</subject><subject>Large intestine</subject><subject>Lipoproteins, LDL - blood</subject><subject>Liver</subject><subject>Liver - drug effects</subject><subject>Liver - metabolism</subject><subject>Low density lipoprotein</subject><subject>Lymphatic Vessels - physiology</subject><subject>Mice</subject><subject>Mice, Inbred C57BL</subject><subject>Mice, Inbred ICR</subject><subject>multidisciplinary</subject><subject>Nanoparticles</subject><subject>Nanoparticles - administration & dosage</subject><subject>Nanoparticles - chemistry</subject><subject>Nanoparticles - metabolism</subject><subject>Nuclease</subject><subject>Nucleic acids</subject><subject>Oligonucleotides</subject><subject>Organophosphorus Compounds - administration & dosage</subject><subject>Organophosphorus Compounds - chemistry</subject><subject>Organophosphorus Compounds - metabolism</subject><subject>Postprandial Period - physiology</subject><subject>Rectum</subject><subject>RNA, Small Interfering - administration & dosage</subject><subject>RNA, Small Interfering - 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administration & dosage</topic><topic>alpha-Tocopherol - chemistry</topic><topic>alpha-Tocopherol - metabolism</topic><topic>Animals</topic><topic>Apolipoprotein B</topic><topic>Apolipoproteins B - antagonists & inhibitors</topic><topic>Apolipoproteins B - genetics</topic><topic>Apolipoproteins B - metabolism</topic><topic>Biological Transport</topic><topic>Cholesterol</topic><topic>Chylomicrons - blood</topic><topic>Drug Delivery Systems - methods</topic><topic>Gene expression</topic><topic>Gene Silencing</topic><topic>Humanities and Social Sciences</topic><topic>Jejunum - drug effects</topic><topic>Jejunum - metabolism</topic><topic>Large intestine</topic><topic>Lipoproteins, LDL - blood</topic><topic>Liver</topic><topic>Liver - drug effects</topic><topic>Liver - metabolism</topic><topic>Low density lipoprotein</topic><topic>Lymphatic Vessels - physiology</topic><topic>Mice</topic><topic>Mice, Inbred C57BL</topic><topic>Mice, Inbred ICR</topic><topic>multidisciplinary</topic><topic>Nanoparticles</topic><topic>Nanoparticles - administration & dosage</topic><topic>Nanoparticles - chemistry</topic><topic>Nanoparticles - metabolism</topic><topic>Nuclease</topic><topic>Nucleic acids</topic><topic>Oligonucleotides</topic><topic>Organophosphorus Compounds - administration & dosage</topic><topic>Organophosphorus Compounds - chemistry</topic><topic>Organophosphorus Compounds - metabolism</topic><topic>Postprandial Period - physiology</topic><topic>Rectum</topic><topic>RNA, Small Interfering - administration & dosage</topic><topic>RNA, Small Interfering - genetics</topic><topic>RNA, Small Interfering - metabolism</topic><topic>Science</topic><topic>siRNA</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Murakami, Masahiro</creatorcontrib><creatorcontrib>Nishina, Kazutaka</creatorcontrib><creatorcontrib>Watanabe, Chie</creatorcontrib><creatorcontrib>Yoshida-Tanaka, Kie</creatorcontrib><creatorcontrib>Piao, Wenying</creatorcontrib><creatorcontrib>Kuwahara, Hiroya</creatorcontrib><creatorcontrib>Horikiri, Yuji</creatorcontrib><creatorcontrib>Miyata, Kanjiro</creatorcontrib><creatorcontrib>Nishiyama, Nobuhiro</creatorcontrib><creatorcontrib>Kataoka, Kazunori</creatorcontrib><creatorcontrib>Yoshida, Masayuki</creatorcontrib><creatorcontrib>Mizusawa, Hidehiro</creatorcontrib><creatorcontrib>Yokota, Takanori</creatorcontrib><collection>Springer Nature OA/Free Journals</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>ProQuest Central (Corporate)</collection><collection>Health & Medical Collection</collection><collection>ProQuest Central (purchase pre-March 2016)</collection><collection>Biology Database (Alumni Edition)</collection><collection>Medical Database (Alumni Edition)</collection><collection>Science Database (Alumni Edition)</collection><collection>ProQuest SciTech Collection</collection><collection>ProQuest Natural Science Collection</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 Edition)</collection><collection>ProQuest One Sustainability</collection><collection>ProQuest Central UK/Ireland</collection><collection>ProQuest Central Essentials</collection><collection>Biological Science Collection</collection><collection>ProQuest Central</collection><collection>Natural Science Collection</collection><collection>ProQuest One Community College</collection><collection>ProQuest Central Korea</collection><collection>Health Research Premium Collection</collection><collection>Health Research Premium Collection (Alumni)</collection><collection>ProQuest Central Student</collection><collection>SciTech Premium Collection</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>ProQuest Biological Science Collection</collection><collection>Health & Medical Collection (Alumni Edition)</collection><collection>Medical Database</collection><collection>Science Database</collection><collection>Biological Science Database</collection><collection>Publicly Available Content Database</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 Basic</collection><collection>MEDLINE - Academic</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>Scientific reports</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Murakami, Masahiro</au><au>Nishina, Kazutaka</au><au>Watanabe, Chie</au><au>Yoshida-Tanaka, Kie</au><au>Piao, Wenying</au><au>Kuwahara, Hiroya</au><au>Horikiri, Yuji</au><au>Miyata, Kanjiro</au><au>Nishiyama, Nobuhiro</au><au>Kataoka, Kazunori</au><au>Yoshida, Masayuki</au><au>Mizusawa, Hidehiro</au><au>Yokota, Takanori</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Enteral siRNA delivery technique for therapeutic gene silencing in the liver via the lymphatic route</atitle><jtitle>Scientific reports</jtitle><stitle>Sci Rep</stitle><addtitle>Sci Rep</addtitle><date>2015-11-23</date><risdate>2015</risdate><volume>5</volume><issue>1</issue><spage>17035</spage><pages>17035-</pages><artnum>17035</artnum><issn>2045-2322</issn><eissn>2045-2322</eissn><abstract>An efficient targeting delivery technology is needed for functional oligonucleotides to exert their potential effect on the target gene without an adverse effect
in vivo
. Development of enteral delivery systems for nucleic acids is a major challenge because of their large molecular size and instability. Here, we describe a new enteral delivery technique that enables small interfering RNA (siRNA) selectively delivered to the liver to silence its target
Apolipoprotein B
gene expression. A nuclease-resistant synthetic siRNA was conjugated with α-tochopherol and administered as lipid nanoparticle to the large intestine of the mice in a postprandial state. The selective transport into the liver, effective gene silence and consequently significant reduction in serum low density lipoprotein-cholesterol level, were demonstrated. The chylomicron-mediated pathway via the lymphatic route was suggested as major mechanism. This unique approach may provide a basis for developing oral and rectal delivery systems for nucleic acids targeting liver.</abstract><cop>London</cop><pub>Nature Publishing Group UK</pub><pmid>26593819</pmid><doi>10.1038/srep17035</doi><oa>free_for_read</oa></addata></record> |
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source | Nature Open Access; MEDLINE; DOAJ Directory of Open Access Journals; Elektronische Zeitschriftenbibliothek - Frei zugängliche E-Journals; PubMed Central; Alma/SFX Local Collection; Springer Nature OA/Free Journals; Free Full-Text Journals in Chemistry |
subjects | 13/89 14/19 631/154/152 631/154/309/2144 64/60 Administration, Rectal alpha-Tocopherol - administration & dosage alpha-Tocopherol - chemistry alpha-Tocopherol - metabolism Animals Apolipoprotein B Apolipoproteins B - antagonists & inhibitors Apolipoproteins B - genetics Apolipoproteins B - metabolism Biological Transport Cholesterol Chylomicrons - blood Drug Delivery Systems - methods Gene expression Gene Silencing Humanities and Social Sciences Jejunum - drug effects Jejunum - metabolism Large intestine Lipoproteins, LDL - blood Liver Liver - drug effects Liver - metabolism Low density lipoprotein Lymphatic Vessels - physiology Mice Mice, Inbred C57BL Mice, Inbred ICR multidisciplinary Nanoparticles Nanoparticles - administration & dosage Nanoparticles - chemistry Nanoparticles - metabolism Nuclease Nucleic acids Oligonucleotides Organophosphorus Compounds - administration & dosage Organophosphorus Compounds - chemistry Organophosphorus Compounds - metabolism Postprandial Period - physiology Rectum RNA, Small Interfering - administration & dosage RNA, Small Interfering - genetics RNA, Small Interfering - metabolism Science siRNA |
title | Enteral siRNA delivery technique for therapeutic gene silencing in the liver via the lymphatic route |
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