Sea Buckthorn and Grape Antioxidant Effects in Hyperlipidemic Rats: Relationship with the Atorvastatin Therapy

Background. Medications to reduce oxidative stress are preventing cellular damage associated with hyperlipidemia. In this regard, statins (e.g., atorvastatin) act primarily by decrease in low-density lipoprotein-c but, in the last decade, hepatotoxicity, associated with liver injuries in the next mo...

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Veröffentlicht in:Evidence-based complementary and alternative medicine 2020, Vol.2020 (2020), p.1-7, Article 1736803
Hauptverfasser: Brezovan, Diana, Hermenean, Anca, Cristina, Romeo Teodor, Muselin, Florin, Dumitrescu, Eugenia, Orășan, Sergiu A., Hulea, Călin I., Moruzi, Răzvan F., Radulov, Isidora, Bordean, Despina M., Mohamed, Erieg A., Herman, Hildegard
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container_issue 2020
container_start_page 1
container_title Evidence-based complementary and alternative medicine
container_volume 2020
creator Brezovan, Diana
Hermenean, Anca
Cristina, Romeo Teodor
Muselin, Florin
Dumitrescu, Eugenia
Orășan, Sergiu A.
Hulea, Călin I.
Moruzi, Răzvan F.
Radulov, Isidora
Bordean, Despina M.
Mohamed, Erieg A.
Herman, Hildegard
description Background. Medications to reduce oxidative stress are preventing cellular damage associated with hyperlipidemia. In this regard, statins (e.g., atorvastatin) act primarily by decrease in low-density lipoprotein-c but, in the last decade, hepatotoxicity, associated with liver injuries in the next months after treatments’ initiation, was reported. In this case, associated phytotherapy can be a solution. Purpose. To investigate the antioxidant potential and response to free radicals, in the case of hyperlipidemic rats treated with atorvastatin. Sea buckthorn (Hippophae rhamnoides) and a grape extract (antioxivita) efficiency in the oxidative stress were investigated, also being ascertained the rats’ organs cytoarchitecture. Methods. Eighty-four hyperlipidemic Wistar rats were divided into seven groups and orally treated as follows: ATS, atorvastatin (20 mg/kg·bw); ATS + Hr, atorvastatin + H. rhamnoides; ATS + Aox, atorvastatin + grape extract; Hr, H. rhamnoides; and Aox, grape extract (both as 100 mg/kg·bw). HFD and Control received high fat diet and normal fodder only. After two and six months, respectively, rats were euthanized and the heart, liver, and kidneys were gathered. The tissue samples were prepared by homogenization of 0.5 g tissue, in ethanol, kept for 48 hours at 4°C–10°C and then filtered, in order to assess organs’ cytoarchitecture and the TAC’s values (by using cupric ion reducing antioxidant capacity (CUPRAC) assay). The test tubes were incubated, at room temperature, for 30 minutes, and then analyzed using a spectrophotometer at 450–650 nm. Results. The statistics (ANOVA) revealed that sea buckthorn diminished notably (p
doi_str_mv 10.1155/2020/1736803
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Medications to reduce oxidative stress are preventing cellular damage associated with hyperlipidemia. In this regard, statins (e.g., atorvastatin) act primarily by decrease in low-density lipoprotein-c but, in the last decade, hepatotoxicity, associated with liver injuries in the next months after treatments’ initiation, was reported. In this case, associated phytotherapy can be a solution. Purpose. To investigate the antioxidant potential and response to free radicals, in the case of hyperlipidemic rats treated with atorvastatin. Sea buckthorn (Hippophae rhamnoides) and a grape extract (antioxivita) efficiency in the oxidative stress were investigated, also being ascertained the rats’ organs cytoarchitecture. Methods. Eighty-four hyperlipidemic Wistar rats were divided into seven groups and orally treated as follows: ATS, atorvastatin (20 mg/kg·bw); ATS + Hr, atorvastatin + H. rhamnoides; ATS + Aox, atorvastatin + grape extract; Hr, H. rhamnoides; and Aox, grape extract (both as 100 mg/kg·bw). HFD and Control received high fat diet and normal fodder only. After two and six months, respectively, rats were euthanized and the heart, liver, and kidneys were gathered. The tissue samples were prepared by homogenization of 0.5 g tissue, in ethanol, kept for 48 hours at 4°C–10°C and then filtered, in order to assess organs’ cytoarchitecture and the TAC’s values (by using cupric ion reducing antioxidant capacity (CUPRAC) assay). The test tubes were incubated, at room temperature, for 30 minutes, and then analyzed using a spectrophotometer at 450–650 nm. Results. The statistics (ANOVA) revealed that sea buckthorn diminished notably (p&lt;0.001) the oxidative stress in the heart, liver, and kidney. After six months, the TAC’s reduced levels for the heart were significant (p&lt;0.001) in ATS + Aox. In the case of histology, the liver’s cytoarchitecture in ATS revealed abnormal cytoarchitecture. In ATS + Hr, ATS + Aox, Hr, and Aox, cell regeneration improved in different stages, especially for ATS + Hr and ATS + Aox, in comparison with HFD, which exhibited fat degeneration. Kidney’s cytoarchitecture revealed cellular healing, especially in ATS + Hr and ATS + Aox.</description><identifier>ISSN: 1741-427X</identifier><identifier>EISSN: 1741-4288</identifier><identifier>DOI: 10.1155/2020/1736803</identifier><identifier>PMID: 32655657</identifier><language>eng</language><publisher>Cairo, Egypt: Hindawi Publishing Corporation</publisher><subject>Animals ; Antilipemic agents ; Antioxidants ; Atorvastatin ; Berries ; Cardiovascular disease ; Carotenoids ; Degeneration ; Drug dosages ; Ethanol ; Flavonoids ; Free radicals ; Heart ; Hepatotoxicity ; High fat diet ; Hippophae rhamnoides ; Hyperlipidemia ; Integrative &amp; Complementary Medicine ; Kidneys ; Life Sciences &amp; Biomedicine ; Liver ; Low density lipoproteins ; Medical research ; Metabolism ; Oxidative stress ; Phenols ; Phytotherapy ; Polyphenols ; Science &amp; Technology ; Statins ; Veterinary medicine</subject><ispartof>Evidence-based complementary and alternative medicine, 2020, Vol.2020 (2020), p.1-7, Article 1736803</ispartof><rights>Copyright © 2020 Erieg A. Mohamed et al.</rights><rights>COPYRIGHT 2020 John Wiley &amp; Sons, Inc.</rights><rights>Copyright © 2020 Erieg A. Mohamed et al. This is an open access article distributed under the Creative Commons Attribution License (the “License”), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License. http://creativecommons.org/licenses/by/4.0</rights><rights>Copyright © 2020 Erieg A. Mohamed et al. 2020</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>true</woscitedreferencessubscribed><woscitedreferencescount>3</woscitedreferencescount><woscitedreferencesoriginalsourcerecordid>wos000549966000002</woscitedreferencesoriginalsourcerecordid><citedby>FETCH-LOGICAL-c499t-ff4880062dda9e70b710e8c516f9978816146a6ab1571898e0a13b789d5ce8433</citedby><cites>FETCH-LOGICAL-c499t-ff4880062dda9e70b710e8c516f9978816146a6ab1571898e0a13b789d5ce8433</cites><orcidid>0000-0002-6741-0245 ; 0000-0002-7394-3654 ; 0000-0001-8510-6653 ; 0000-0002-6172-9861 ; 0000-0001-7113-9163 ; 0000-0002-9899-9101 ; 0000-0002-1647-7992 ; 0000-0002-8346-6230 ; 0000-0003-2907-4233 ; 0000-0002-5420-1516 ; 0000-0001-7769-6358</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/PMC7327606/pdf/$$EPDF$$P50$$Gpubmedcentral$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC7327606/$$EHTML$$P50$$Gpubmedcentral$$Hfree_for_read</linktohtml><link.rule.ids>230,315,728,781,785,886,4025,27928,27929,27930,28253,53796,53798</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/32655657$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><contributor>Dias Novaes, Rômulo</contributor><contributor>Rômulo Dias Novaes</contributor><creatorcontrib>Brezovan, Diana</creatorcontrib><creatorcontrib>Hermenean, Anca</creatorcontrib><creatorcontrib>Cristina, Romeo Teodor</creatorcontrib><creatorcontrib>Muselin, Florin</creatorcontrib><creatorcontrib>Dumitrescu, Eugenia</creatorcontrib><creatorcontrib>Orășan, Sergiu A.</creatorcontrib><creatorcontrib>Hulea, Călin I.</creatorcontrib><creatorcontrib>Moruzi, Răzvan F.</creatorcontrib><creatorcontrib>Radulov, Isidora</creatorcontrib><creatorcontrib>Bordean, Despina M.</creatorcontrib><creatorcontrib>Mohamed, Erieg A.</creatorcontrib><creatorcontrib>Herman, Hildegard</creatorcontrib><title>Sea Buckthorn and Grape Antioxidant Effects in Hyperlipidemic Rats: Relationship with the Atorvastatin Therapy</title><title>Evidence-based complementary and alternative medicine</title><addtitle>EVID-BASED COMPL ALT</addtitle><addtitle>Evid Based Complement Alternat Med</addtitle><description>Background. Medications to reduce oxidative stress are preventing cellular damage associated with hyperlipidemia. In this regard, statins (e.g., atorvastatin) act primarily by decrease in low-density lipoprotein-c but, in the last decade, hepatotoxicity, associated with liver injuries in the next months after treatments’ initiation, was reported. In this case, associated phytotherapy can be a solution. Purpose. To investigate the antioxidant potential and response to free radicals, in the case of hyperlipidemic rats treated with atorvastatin. Sea buckthorn (Hippophae rhamnoides) and a grape extract (antioxivita) efficiency in the oxidative stress were investigated, also being ascertained the rats’ organs cytoarchitecture. Methods. Eighty-four hyperlipidemic Wistar rats were divided into seven groups and orally treated as follows: ATS, atorvastatin (20 mg/kg·bw); ATS + Hr, atorvastatin + H. rhamnoides; ATS + Aox, atorvastatin + grape extract; Hr, H. rhamnoides; and Aox, grape extract (both as 100 mg/kg·bw). HFD and Control received high fat diet and normal fodder only. After two and six months, respectively, rats were euthanized and the heart, liver, and kidneys were gathered. The tissue samples were prepared by homogenization of 0.5 g tissue, in ethanol, kept for 48 hours at 4°C–10°C and then filtered, in order to assess organs’ cytoarchitecture and the TAC’s values (by using cupric ion reducing antioxidant capacity (CUPRAC) assay). The test tubes were incubated, at room temperature, for 30 minutes, and then analyzed using a spectrophotometer at 450–650 nm. Results. The statistics (ANOVA) revealed that sea buckthorn diminished notably (p&lt;0.001) the oxidative stress in the heart, liver, and kidney. After six months, the TAC’s reduced levels for the heart were significant (p&lt;0.001) in ATS + Aox. In the case of histology, the liver’s cytoarchitecture in ATS revealed abnormal cytoarchitecture. In ATS + Hr, ATS + Aox, Hr, and Aox, cell regeneration improved in different stages, especially for ATS + Hr and ATS + Aox, in comparison with HFD, which exhibited fat degeneration. Kidney’s cytoarchitecture revealed cellular healing, especially in ATS + Hr and ATS + Aox.</description><subject>Animals</subject><subject>Antilipemic agents</subject><subject>Antioxidants</subject><subject>Atorvastatin</subject><subject>Berries</subject><subject>Cardiovascular disease</subject><subject>Carotenoids</subject><subject>Degeneration</subject><subject>Drug dosages</subject><subject>Ethanol</subject><subject>Flavonoids</subject><subject>Free radicals</subject><subject>Heart</subject><subject>Hepatotoxicity</subject><subject>High fat diet</subject><subject>Hippophae rhamnoides</subject><subject>Hyperlipidemia</subject><subject>Integrative &amp; Complementary Medicine</subject><subject>Kidneys</subject><subject>Life Sciences &amp; Biomedicine</subject><subject>Liver</subject><subject>Low density lipoproteins</subject><subject>Medical research</subject><subject>Metabolism</subject><subject>Oxidative stress</subject><subject>Phenols</subject><subject>Phytotherapy</subject><subject>Polyphenols</subject><subject>Science &amp; 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Medical Complete (Alumni)</collection><collection>Nursing &amp; Allied Health Database (Alumni Edition)</collection><collection>Health &amp; Medical Collection (Alumni Edition)</collection><collection>Psychology Database</collection><collection>Research Library</collection><collection>Research Library (Corporate)</collection><collection>Nursing &amp; Allied Health Premium</collection><collection>Access via ProQuest (Open Access)</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>ProQuest One Psychology</collection><collection>ProQuest Central Basic</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>Evidence-based complementary and alternative medicine</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Brezovan, Diana</au><au>Hermenean, Anca</au><au>Cristina, Romeo Teodor</au><au>Muselin, Florin</au><au>Dumitrescu, Eugenia</au><au>Orășan, Sergiu A.</au><au>Hulea, Călin I.</au><au>Moruzi, Răzvan F.</au><au>Radulov, Isidora</au><au>Bordean, Despina M.</au><au>Mohamed, Erieg A.</au><au>Herman, Hildegard</au><au>Dias Novaes, Rômulo</au><au>Rômulo Dias Novaes</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Sea Buckthorn and Grape Antioxidant Effects in Hyperlipidemic Rats: Relationship with the Atorvastatin Therapy</atitle><jtitle>Evidence-based complementary and alternative medicine</jtitle><stitle>EVID-BASED COMPL ALT</stitle><addtitle>Evid Based Complement Alternat Med</addtitle><date>2020</date><risdate>2020</risdate><volume>2020</volume><issue>2020</issue><spage>1</spage><epage>7</epage><pages>1-7</pages><artnum>1736803</artnum><issn>1741-427X</issn><eissn>1741-4288</eissn><abstract>Background. Medications to reduce oxidative stress are preventing cellular damage associated with hyperlipidemia. In this regard, statins (e.g., atorvastatin) act primarily by decrease in low-density lipoprotein-c but, in the last decade, hepatotoxicity, associated with liver injuries in the next months after treatments’ initiation, was reported. In this case, associated phytotherapy can be a solution. Purpose. To investigate the antioxidant potential and response to free radicals, in the case of hyperlipidemic rats treated with atorvastatin. Sea buckthorn (Hippophae rhamnoides) and a grape extract (antioxivita) efficiency in the oxidative stress were investigated, also being ascertained the rats’ organs cytoarchitecture. Methods. Eighty-four hyperlipidemic Wistar rats were divided into seven groups and orally treated as follows: ATS, atorvastatin (20 mg/kg·bw); ATS + Hr, atorvastatin + H. rhamnoides; ATS + Aox, atorvastatin + grape extract; Hr, H. rhamnoides; and Aox, grape extract (both as 100 mg/kg·bw). HFD and Control received high fat diet and normal fodder only. After two and six months, respectively, rats were euthanized and the heart, liver, and kidneys were gathered. The tissue samples were prepared by homogenization of 0.5 g tissue, in ethanol, kept for 48 hours at 4°C–10°C and then filtered, in order to assess organs’ cytoarchitecture and the TAC’s values (by using cupric ion reducing antioxidant capacity (CUPRAC) assay). The test tubes were incubated, at room temperature, for 30 minutes, and then analyzed using a spectrophotometer at 450–650 nm. Results. The statistics (ANOVA) revealed that sea buckthorn diminished notably (p&lt;0.001) the oxidative stress in the heart, liver, and kidney. After six months, the TAC’s reduced levels for the heart were significant (p&lt;0.001) in ATS + Aox. In the case of histology, the liver’s cytoarchitecture in ATS revealed abnormal cytoarchitecture. In ATS + Hr, ATS + Aox, Hr, and Aox, cell regeneration improved in different stages, especially for ATS + Hr and ATS + Aox, in comparison with HFD, which exhibited fat degeneration. Kidney’s cytoarchitecture revealed cellular healing, especially in ATS + Hr and ATS + Aox.</abstract><cop>Cairo, Egypt</cop><pub>Hindawi Publishing Corporation</pub><pmid>32655657</pmid><doi>10.1155/2020/1736803</doi><tpages>7</tpages><orcidid>https://orcid.org/0000-0002-6741-0245</orcidid><orcidid>https://orcid.org/0000-0002-7394-3654</orcidid><orcidid>https://orcid.org/0000-0001-8510-6653</orcidid><orcidid>https://orcid.org/0000-0002-6172-9861</orcidid><orcidid>https://orcid.org/0000-0001-7113-9163</orcidid><orcidid>https://orcid.org/0000-0002-9899-9101</orcidid><orcidid>https://orcid.org/0000-0002-1647-7992</orcidid><orcidid>https://orcid.org/0000-0002-8346-6230</orcidid><orcidid>https://orcid.org/0000-0003-2907-4233</orcidid><orcidid>https://orcid.org/0000-0002-5420-1516</orcidid><orcidid>https://orcid.org/0000-0001-7769-6358</orcidid><oa>free_for_read</oa></addata></record>
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subjects Animals
Antilipemic agents
Antioxidants
Atorvastatin
Berries
Cardiovascular disease
Carotenoids
Degeneration
Drug dosages
Ethanol
Flavonoids
Free radicals
Heart
Hepatotoxicity
High fat diet
Hippophae rhamnoides
Hyperlipidemia
Integrative & Complementary Medicine
Kidneys
Life Sciences & Biomedicine
Liver
Low density lipoproteins
Medical research
Metabolism
Oxidative stress
Phenols
Phytotherapy
Polyphenols
Science & Technology
Statins
Veterinary medicine
title Sea Buckthorn and Grape Antioxidant Effects in Hyperlipidemic Rats: Relationship with the Atorvastatin Therapy
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