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Skate cartilage extracts containing chondroitin sulfate ameliorates hyperlipidemia-induced inflammation and oxidative stress in high cholesterol diet-fed LDL receptor knockout mice in comparison with shark chondroitin sulfate

BACKGROUND/OBJECTIVES In this study, we investigated the beneficial effects of skate cartilage extracts containing chondroitin sulfate (SCS) on hyperlipidemia-induced inflammation and oxidative stress in high cholesterol diet (HCD)-fed mice in comparison with the effects of shark cartilage-derived c...

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Published in:Nutrition research and practice 2020, 14(3), , pp.175-187
Main Authors: Seol, Bo Gyeong, Kim, Ji Hyun, Woo, Minji, Song, Yeong Ok, Choi, Yung Hyun, Noh, Jeong Sook, Cho, Eun Ju
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description BACKGROUND/OBJECTIVES In this study, we investigated the beneficial effects of skate cartilage extracts containing chondroitin sulfate (SCS) on hyperlipidemia-induced inflammation and oxidative stress in high cholesterol diet (HCD)-fed mice in comparison with the effects of shark cartilage-derived chondroitin sulfate (CS). MATERIALS/METHODS Low-density lipoprotein receptor knockout (LDLR-KO) mice were fed HCD with an oral administration of CS (50 and 100 mg/kg BW/day), SCS (100 and 200 mg/kg BW/day), or water, respectively, for ten weeks. RESULTS The administration of CS or SCS reduced the levels of serum triglyceride (TG), total cholesterol (TC), and LDL cholesterol and elevated the levels of high-density lipoprotein cholesterol, compared with those of the control group (P < 0.05). Furthermore, CS or SCS significantly attenuated inflammation by reducing the serum levels of interleukin (IL)-1β and hepatic protein expression levels of nuclear factor kappa B, inducible nitric oxide synthase, cyclooxygenase-2, and IL-1beta (P < 0.05). In particular, the serum level of tumor necrosis factor-alpha was reduced only in the 100 mg/kg BW/day of SCS-fed group, whereas the IL-6 level was reduced in the 100 and 200 mg/kg BW/day of SCS-fed groups (P < 0.05). In addition, lipid peroxidation and nitric oxide production were attenuated in the livers of the CS and SCS groups mediated by the upregulation of hepatic proteins of antioxidant enzymes, such as superoxide dismutase, catalase, and glutathione peroxidase (P < 0.05). CONCLUSIONS These results suggest that the biological effects of SCS, similar to those of CS, are attributed to improved lipid profiles as well as suppressed inflammation and oxidative stress induced by the intake of HCD.
doi_str_mv 10.4162/nrp.2020.14.3.175
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MATERIALS/METHODS Low-density lipoprotein receptor knockout (LDLR-KO) mice were fed HCD with an oral administration of CS (50 and 100 mg/kg BW/day), SCS (100 and 200 mg/kg BW/day), or water, respectively, for ten weeks. RESULTS The administration of CS or SCS reduced the levels of serum triglyceride (TG), total cholesterol (TC), and LDL cholesterol and elevated the levels of high-density lipoprotein cholesterol, compared with those of the control group (P &lt; 0.05). Furthermore, CS or SCS significantly attenuated inflammation by reducing the serum levels of interleukin (IL)-1β and hepatic protein expression levels of nuclear factor kappa B, inducible nitric oxide synthase, cyclooxygenase-2, and IL-1beta (P &lt; 0.05). In particular, the serum level of tumor necrosis factor-alpha was reduced only in the 100 mg/kg BW/day of SCS-fed group, whereas the IL-6 level was reduced in the 100 and 200 mg/kg BW/day of SCS-fed groups (P &lt; 0.05). In addition, lipid peroxidation and nitric oxide production were attenuated in the livers of the CS and SCS groups mediated by the upregulation of hepatic proteins of antioxidant enzymes, such as superoxide dismutase, catalase, and glutathione peroxidase (P &lt; 0.05). CONCLUSIONS These results suggest that the biological effects of SCS, similar to those of CS, are attributed to improved lipid profiles as well as suppressed inflammation and oxidative stress induced by the intake of HCD.</description><identifier>ISSN: 1976-1457</identifier><identifier>EISSN: 2005-6168</identifier><identifier>DOI: 10.4162/nrp.2020.14.3.175</identifier><identifier>PMID: 32528626</identifier><language>eng</language><publisher>Seoul: 한국영양학회</publisher><subject>Antioxidants ; Cartilage ; Catalase ; Cholesterol ; Chondroitin sulfate ; Cyclooxygenase-2 ; Glutathione peroxidase ; High cholesterol diet ; Hyperlipidemia ; IL-1β ; Inflammation ; Interleukin 1 ; Interleukin 6 ; Lipid peroxidation ; Liver ; Low density lipoprotein ; Low density lipoprotein receptors ; Nitric oxide ; Nitric-oxide synthase ; Oral administration ; Original Research ; Oxidative stress ; Receptor density ; Serum levels ; Superoxide dismutase ; Tumor necrosis factor-α ; 생활과학</subject><ispartof>Nutrition Research and Practice, 2020, 14(3), , pp.175-187</ispartof><rights>Copyright Korean Nutrition Society Jun 2020</rights><rights>2020 The Korean Nutrition Society and the Korean Society of Community Nutrition 2020 The Korean Nutrition Society and the Korean Society of Community Nutrition</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c468t-623a9f6370f71f972c328a4e425f6e458429dc233ab1c504a5062e48ccd9f0973</citedby><cites>FETCH-LOGICAL-c468t-623a9f6370f71f972c328a4e425f6e458429dc233ab1c504a5062e48ccd9f0973</cites><orcidid>0000-0001-6617-2129 ; 0000-0002-4987-7802 ; 0000-0002-2969-6270 ; 0000-0003-4282-3219 ; 0000-0002-2770-2075 ; 0000-0002-1454-3124 ; 0000-0003-4243-2349</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC7263899/pdf/$$EPDF$$P50$$Gpubmedcentral$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC7263899/$$EHTML$$P50$$Gpubmedcentral$$Hfree_for_read</linktohtml><link.rule.ids>230,314,727,780,784,885,27924,27925,53791,53793</link.rule.ids><backlink>$$Uhttps://www.kci.go.kr/kciportal/ci/sereArticleSearch/ciSereArtiView.kci?sereArticleSearchBean.artiId=ART002592305$$DAccess content in National Research Foundation of Korea (NRF)$$Hfree_for_read</backlink></links><search><creatorcontrib>Seol, Bo Gyeong</creatorcontrib><creatorcontrib>Kim, Ji Hyun</creatorcontrib><creatorcontrib>Woo, Minji</creatorcontrib><creatorcontrib>Song, Yeong Ok</creatorcontrib><creatorcontrib>Choi, Yung Hyun</creatorcontrib><creatorcontrib>Noh, Jeong Sook</creatorcontrib><creatorcontrib>Cho, Eun Ju</creatorcontrib><title>Skate cartilage extracts containing chondroitin sulfate ameliorates hyperlipidemia-induced inflammation and oxidative stress in high cholesterol diet-fed LDL receptor knockout mice in comparison with shark chondroitin sulfate</title><title>Nutrition research and practice</title><description>BACKGROUND/OBJECTIVES In this study, we investigated the beneficial effects of skate cartilage extracts containing chondroitin sulfate (SCS) on hyperlipidemia-induced inflammation and oxidative stress in high cholesterol diet (HCD)-fed mice in comparison with the effects of shark cartilage-derived chondroitin sulfate (CS). MATERIALS/METHODS Low-density lipoprotein receptor knockout (LDLR-KO) mice were fed HCD with an oral administration of CS (50 and 100 mg/kg BW/day), SCS (100 and 200 mg/kg BW/day), or water, respectively, for ten weeks. RESULTS The administration of CS or SCS reduced the levels of serum triglyceride (TG), total cholesterol (TC), and LDL cholesterol and elevated the levels of high-density lipoprotein cholesterol, compared with those of the control group (P &lt; 0.05). Furthermore, CS or SCS significantly attenuated inflammation by reducing the serum levels of interleukin (IL)-1β and hepatic protein expression levels of nuclear factor kappa B, inducible nitric oxide synthase, cyclooxygenase-2, and IL-1beta (P &lt; 0.05). In particular, the serum level of tumor necrosis factor-alpha was reduced only in the 100 mg/kg BW/day of SCS-fed group, whereas the IL-6 level was reduced in the 100 and 200 mg/kg BW/day of SCS-fed groups (P &lt; 0.05). 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Calcified Tissue Abstracts</collection><collection>MEDLINE - Academic</collection><collection>PubMed Central (Full Participant titles)</collection><collection>Korean Citation Index</collection><jtitle>Nutrition research and practice</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Seol, Bo Gyeong</au><au>Kim, Ji Hyun</au><au>Woo, Minji</au><au>Song, Yeong Ok</au><au>Choi, Yung Hyun</au><au>Noh, Jeong Sook</au><au>Cho, Eun Ju</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Skate cartilage extracts containing chondroitin sulfate ameliorates hyperlipidemia-induced inflammation and oxidative stress in high cholesterol diet-fed LDL receptor knockout mice in comparison with shark chondroitin sulfate</atitle><jtitle>Nutrition research and practice</jtitle><date>2020-06-01</date><risdate>2020</risdate><volume>14</volume><issue>3</issue><spage>175</spage><epage>187</epage><pages>175-187</pages><issn>1976-1457</issn><eissn>2005-6168</eissn><abstract>BACKGROUND/OBJECTIVES In this study, we investigated the beneficial effects of skate cartilage extracts containing chondroitin sulfate (SCS) on hyperlipidemia-induced inflammation and oxidative stress in high cholesterol diet (HCD)-fed mice in comparison with the effects of shark cartilage-derived chondroitin sulfate (CS). MATERIALS/METHODS Low-density lipoprotein receptor knockout (LDLR-KO) mice were fed HCD with an oral administration of CS (50 and 100 mg/kg BW/day), SCS (100 and 200 mg/kg BW/day), or water, respectively, for ten weeks. RESULTS The administration of CS or SCS reduced the levels of serum triglyceride (TG), total cholesterol (TC), and LDL cholesterol and elevated the levels of high-density lipoprotein cholesterol, compared with those of the control group (P &lt; 0.05). Furthermore, CS or SCS significantly attenuated inflammation by reducing the serum levels of interleukin (IL)-1β and hepatic protein expression levels of nuclear factor kappa B, inducible nitric oxide synthase, cyclooxygenase-2, and IL-1beta (P &lt; 0.05). In particular, the serum level of tumor necrosis factor-alpha was reduced only in the 100 mg/kg BW/day of SCS-fed group, whereas the IL-6 level was reduced in the 100 and 200 mg/kg BW/day of SCS-fed groups (P &lt; 0.05). In addition, lipid peroxidation and nitric oxide production were attenuated in the livers of the CS and SCS groups mediated by the upregulation of hepatic proteins of antioxidant enzymes, such as superoxide dismutase, catalase, and glutathione peroxidase (P &lt; 0.05). CONCLUSIONS These results suggest that the biological effects of SCS, similar to those of CS, are attributed to improved lipid profiles as well as suppressed inflammation and oxidative stress induced by the intake of HCD.</abstract><cop>Seoul</cop><pub>한국영양학회</pub><pmid>32528626</pmid><doi>10.4162/nrp.2020.14.3.175</doi><tpages>13</tpages><orcidid>https://orcid.org/0000-0001-6617-2129</orcidid><orcidid>https://orcid.org/0000-0002-4987-7802</orcidid><orcidid>https://orcid.org/0000-0002-2969-6270</orcidid><orcidid>https://orcid.org/0000-0003-4282-3219</orcidid><orcidid>https://orcid.org/0000-0002-2770-2075</orcidid><orcidid>https://orcid.org/0000-0002-1454-3124</orcidid><orcidid>https://orcid.org/0000-0003-4243-2349</orcidid><oa>free_for_read</oa></addata></record>
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identifier ISSN: 1976-1457
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subjects Antioxidants
Cartilage
Catalase
Cholesterol
Chondroitin sulfate
Cyclooxygenase-2
Glutathione peroxidase
High cholesterol diet
Hyperlipidemia
IL-1β
Inflammation
Interleukin 1
Interleukin 6
Lipid peroxidation
Liver
Low density lipoprotein
Low density lipoprotein receptors
Nitric oxide
Nitric-oxide synthase
Oral administration
Original Research
Oxidative stress
Receptor density
Serum levels
Superoxide dismutase
Tumor necrosis factor-α
생활과학
title Skate cartilage extracts containing chondroitin sulfate ameliorates hyperlipidemia-induced inflammation and oxidative stress in high cholesterol diet-fed LDL receptor knockout mice in comparison with shark chondroitin sulfate
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