Evidence of insulin-dependent signalling mechanisms produced by Citrus sinensis (L.) Osbeck fruit peel in an insulin resistant diabetic animal model
Citrus sinensis (L.) Osbeck is extensively cultivated worldwide and one of the most consumed fruits in the world. We evaluated the therapeutic properties of the methanol extract from Citrus sinensis fruit peel (CSMe) in high-fat diet-fed streptozotocin-induced insulin-resistant diabetic rats. Body w...
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Veröffentlicht in: | Food and chemical toxicology 2018-06, Vol.116 (Pt B), p.86-99 |
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creator | Sathiyabama, Rajiv Gandhi Rajiv Gandhi, Gopalsamy Denadai, Marina Sridharan, Gurunagarajan Jothi, Gnanasekaran Sasikumar, Ponnusamy Siqueira Quintans, Jullyana de Souza Narain, Narendra Cuevas, Luis Eduardo Coutinho, Henrique Douglas Melo Ramos, Andreza Guedes Barbosa Quintans-Júnior, Lucindo José Gurgel, Ricardo Queiroz |
description | Citrus sinensis (L.) Osbeck is extensively cultivated worldwide and one of the most consumed fruits in the world. We evaluated the therapeutic properties of the methanol extract from Citrus sinensis fruit peel (CSMe) in high-fat diet-fed streptozotocin-induced insulin-resistant diabetic rats. Body weight, food intake, and water consumption were analysed. Biochemical and molecular biologic indices, and the expression of insulin receptor-induced signalling molecules were assessed to identify possible mechanisms. In addition, we conducted histology of pancreatic and adipose tissues. UHPLC-MS/MS analysis showed the presence of 17 dietary phenolics at substantial concentrations. High-fat diet-fed streptozotocin-induced diabetic rats administered CSMe (50 and 100 mg/kg) had reduced fasting blood glucose (56.1% and 55.7%, respectively) and plasma insulin levels (22.9% and 32.7%, respectively) compared with untreated diabetic control rats. CSMe reversed the biochemical abnormalities in diabetic rats, showed cytoprotective activity, and increased the intensity of the positive immunoreactions for insulin in pancreatic islets. CSMe treatment increased the expression of PPARγ in the adipose tissue and signalling molecules GLUT4 and insulin receptor. Our data suggest that CSMe could optimize glucose uptake of adipose tissues through the insulin-dependent signalling cascade mechanism and it should be investigated in the management of individuals with type 2 diabetes mellitus.
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•Citrus sinensis peel methanol extract lowered blood glucose level in diabetic rats.•Citrus sinensis peel contained fine concentrations of phenolic compounds.•Citrus sinensis peel possessed cytoprotective action.•Citrus sinensis peel promoted insulin receptor signalling. |
doi_str_mv | 10.1016/j.fct.2018.03.050 |
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•Citrus sinensis peel methanol extract lowered blood glucose level in diabetic rats.•Citrus sinensis peel contained fine concentrations of phenolic compounds.•Citrus sinensis peel possessed cytoprotective action.•Citrus sinensis peel promoted insulin receptor signalling.</description><identifier>ISSN: 0278-6915</identifier><identifier>EISSN: 1873-6351</identifier><identifier>DOI: 10.1016/j.fct.2018.03.050</identifier><identifier>PMID: 29614383</identifier><language>eng</language><publisher>England: Elsevier Ltd</publisher><subject>Adipose ; Citrus sinensis ; Diabetes ; Histology ; Insulin receptor ; Pancreatic β-cell</subject><ispartof>Food and chemical toxicology, 2018-06, Vol.116 (Pt B), p.86-99</ispartof><rights>2018 Elsevier Ltd</rights><rights>Copyright © 2018 Elsevier Ltd. All rights reserved.</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c396t-274c8468afc085f2e1c0d03526d9642d34d12cda8f1ff8894cfbee105f7e3fae3</citedby><cites>FETCH-LOGICAL-c396t-274c8468afc085f2e1c0d03526d9642d34d12cda8f1ff8894cfbee105f7e3fae3</cites><orcidid>0000-0001-5241-7463 ; 0000-0001-5155-938X</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktohtml>$$Uhttps://dx.doi.org/10.1016/j.fct.2018.03.050$$EHTML$$P50$$Gelsevier$$H</linktohtml><link.rule.ids>314,780,784,3549,27923,27924,45994</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/29614383$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Sathiyabama, Rajiv Gandhi</creatorcontrib><creatorcontrib>Rajiv Gandhi, Gopalsamy</creatorcontrib><creatorcontrib>Denadai, Marina</creatorcontrib><creatorcontrib>Sridharan, Gurunagarajan</creatorcontrib><creatorcontrib>Jothi, Gnanasekaran</creatorcontrib><creatorcontrib>Sasikumar, Ponnusamy</creatorcontrib><creatorcontrib>Siqueira Quintans, Jullyana de Souza</creatorcontrib><creatorcontrib>Narain, Narendra</creatorcontrib><creatorcontrib>Cuevas, Luis Eduardo</creatorcontrib><creatorcontrib>Coutinho, Henrique Douglas Melo</creatorcontrib><creatorcontrib>Ramos, Andreza Guedes Barbosa</creatorcontrib><creatorcontrib>Quintans-Júnior, Lucindo José</creatorcontrib><creatorcontrib>Gurgel, Ricardo Queiroz</creatorcontrib><title>Evidence of insulin-dependent signalling mechanisms produced by Citrus sinensis (L.) Osbeck fruit peel in an insulin resistant diabetic animal model</title><title>Food and chemical toxicology</title><addtitle>Food Chem Toxicol</addtitle><description>Citrus sinensis (L.) Osbeck is extensively cultivated worldwide and one of the most consumed fruits in the world. We evaluated the therapeutic properties of the methanol extract from Citrus sinensis fruit peel (CSMe) in high-fat diet-fed streptozotocin-induced insulin-resistant diabetic rats. Body weight, food intake, and water consumption were analysed. Biochemical and molecular biologic indices, and the expression of insulin receptor-induced signalling molecules were assessed to identify possible mechanisms. In addition, we conducted histology of pancreatic and adipose tissues. UHPLC-MS/MS analysis showed the presence of 17 dietary phenolics at substantial concentrations. High-fat diet-fed streptozotocin-induced diabetic rats administered CSMe (50 and 100 mg/kg) had reduced fasting blood glucose (56.1% and 55.7%, respectively) and plasma insulin levels (22.9% and 32.7%, respectively) compared with untreated diabetic control rats. CSMe reversed the biochemical abnormalities in diabetic rats, showed cytoprotective activity, and increased the intensity of the positive immunoreactions for insulin in pancreatic islets. CSMe treatment increased the expression of PPARγ in the adipose tissue and signalling molecules GLUT4 and insulin receptor. Our data suggest that CSMe could optimize glucose uptake of adipose tissues through the insulin-dependent signalling cascade mechanism and it should be investigated in the management of individuals with type 2 diabetes mellitus.
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•Citrus sinensis peel methanol extract lowered blood glucose level in diabetic rats.•Citrus sinensis peel contained fine concentrations of phenolic compounds.•Citrus sinensis peel possessed cytoprotective action.•Citrus sinensis peel promoted insulin receptor signalling.</description><subject>Adipose</subject><subject>Citrus sinensis</subject><subject>Diabetes</subject><subject>Histology</subject><subject>Insulin receptor</subject><subject>Pancreatic β-cell</subject><issn>0278-6915</issn><issn>1873-6351</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2018</creationdate><recordtype>article</recordtype><recordid>eNp9kcFu3CAQhlHVqtkkfYBeKo7pwc4ANsbqqVqlTaWVcmnOCMOQsrXxFuxIeY88cFlt0mNPSMM3_zB8hHxkUDNg8npfe7vUHJiqQdTQwhuyYaoTlRQte0s2wDtVyZ61Z-Q85z0AdKyT78kZ7yVrhBIb8nzzGBxGi3T2NMS8jiFWDg8YS3WhOTxEM5baA53Q_jIx5CnTQ5rdatHR4Yluw5LWXMCIMYdMr3b1Z3qXB7S_qU9rWOgBcSzR1MTXATRhQRdTBrhgBlyCLbdhMiOdZofjJXnnzZjxw8t5Qe6_3fzc3la7u-8_tl93lRW9XCreNVY1UhlvQbWeI7PgQLRcul423InGMW6dUZ55r1TfWD8gMmh9h8IbFBfk6pRbFvqzYl70FLLFcTQR5zVrDpx1QgjoC8pOqE1zzgm9PqTy4PSkGeijDL3XRYY-ytAgdJFRej69xK_DhO5fx-vvF-DLCcCy5GPApLMNRxkuJCxhbg7_if8LSBydIQ</recordid><startdate>20180601</startdate><enddate>20180601</enddate><creator>Sathiyabama, Rajiv Gandhi</creator><creator>Rajiv Gandhi, Gopalsamy</creator><creator>Denadai, Marina</creator><creator>Sridharan, Gurunagarajan</creator><creator>Jothi, Gnanasekaran</creator><creator>Sasikumar, Ponnusamy</creator><creator>Siqueira Quintans, Jullyana de Souza</creator><creator>Narain, Narendra</creator><creator>Cuevas, Luis Eduardo</creator><creator>Coutinho, Henrique Douglas Melo</creator><creator>Ramos, Andreza Guedes Barbosa</creator><creator>Quintans-Júnior, Lucindo José</creator><creator>Gurgel, Ricardo Queiroz</creator><general>Elsevier Ltd</general><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7X8</scope><orcidid>https://orcid.org/0000-0001-5241-7463</orcidid><orcidid>https://orcid.org/0000-0001-5155-938X</orcidid></search><sort><creationdate>20180601</creationdate><title>Evidence of insulin-dependent signalling mechanisms produced by Citrus sinensis (L.) Osbeck fruit peel in an insulin resistant diabetic animal model</title><author>Sathiyabama, Rajiv Gandhi ; Rajiv Gandhi, Gopalsamy ; Denadai, Marina ; Sridharan, Gurunagarajan ; Jothi, Gnanasekaran ; Sasikumar, Ponnusamy ; Siqueira Quintans, Jullyana de Souza ; Narain, Narendra ; Cuevas, Luis Eduardo ; Coutinho, Henrique Douglas Melo ; Ramos, Andreza Guedes Barbosa ; Quintans-Júnior, Lucindo José ; Gurgel, Ricardo Queiroz</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c396t-274c8468afc085f2e1c0d03526d9642d34d12cda8f1ff8894cfbee105f7e3fae3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2018</creationdate><topic>Adipose</topic><topic>Citrus sinensis</topic><topic>Diabetes</topic><topic>Histology</topic><topic>Insulin receptor</topic><topic>Pancreatic β-cell</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Sathiyabama, Rajiv Gandhi</creatorcontrib><creatorcontrib>Rajiv Gandhi, Gopalsamy</creatorcontrib><creatorcontrib>Denadai, Marina</creatorcontrib><creatorcontrib>Sridharan, Gurunagarajan</creatorcontrib><creatorcontrib>Jothi, Gnanasekaran</creatorcontrib><creatorcontrib>Sasikumar, Ponnusamy</creatorcontrib><creatorcontrib>Siqueira Quintans, Jullyana de Souza</creatorcontrib><creatorcontrib>Narain, Narendra</creatorcontrib><creatorcontrib>Cuevas, Luis Eduardo</creatorcontrib><creatorcontrib>Coutinho, Henrique Douglas Melo</creatorcontrib><creatorcontrib>Ramos, Andreza Guedes Barbosa</creatorcontrib><creatorcontrib>Quintans-Júnior, Lucindo José</creatorcontrib><creatorcontrib>Gurgel, Ricardo Queiroz</creatorcontrib><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><jtitle>Food and chemical toxicology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Sathiyabama, Rajiv Gandhi</au><au>Rajiv Gandhi, Gopalsamy</au><au>Denadai, Marina</au><au>Sridharan, Gurunagarajan</au><au>Jothi, Gnanasekaran</au><au>Sasikumar, Ponnusamy</au><au>Siqueira Quintans, Jullyana de Souza</au><au>Narain, Narendra</au><au>Cuevas, Luis Eduardo</au><au>Coutinho, Henrique Douglas Melo</au><au>Ramos, Andreza Guedes Barbosa</au><au>Quintans-Júnior, Lucindo José</au><au>Gurgel, Ricardo Queiroz</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Evidence of insulin-dependent signalling mechanisms produced by Citrus sinensis (L.) Osbeck fruit peel in an insulin resistant diabetic animal model</atitle><jtitle>Food and chemical toxicology</jtitle><addtitle>Food Chem Toxicol</addtitle><date>2018-06-01</date><risdate>2018</risdate><volume>116</volume><issue>Pt B</issue><spage>86</spage><epage>99</epage><pages>86-99</pages><issn>0278-6915</issn><eissn>1873-6351</eissn><abstract>Citrus sinensis (L.) Osbeck is extensively cultivated worldwide and one of the most consumed fruits in the world. We evaluated the therapeutic properties of the methanol extract from Citrus sinensis fruit peel (CSMe) in high-fat diet-fed streptozotocin-induced insulin-resistant diabetic rats. Body weight, food intake, and water consumption were analysed. Biochemical and molecular biologic indices, and the expression of insulin receptor-induced signalling molecules were assessed to identify possible mechanisms. In addition, we conducted histology of pancreatic and adipose tissues. UHPLC-MS/MS analysis showed the presence of 17 dietary phenolics at substantial concentrations. High-fat diet-fed streptozotocin-induced diabetic rats administered CSMe (50 and 100 mg/kg) had reduced fasting blood glucose (56.1% and 55.7%, respectively) and plasma insulin levels (22.9% and 32.7%, respectively) compared with untreated diabetic control rats. CSMe reversed the biochemical abnormalities in diabetic rats, showed cytoprotective activity, and increased the intensity of the positive immunoreactions for insulin in pancreatic islets. CSMe treatment increased the expression of PPARγ in the adipose tissue and signalling molecules GLUT4 and insulin receptor. Our data suggest that CSMe could optimize glucose uptake of adipose tissues through the insulin-dependent signalling cascade mechanism and it should be investigated in the management of individuals with type 2 diabetes mellitus.
[Display omitted]
•Citrus sinensis peel methanol extract lowered blood glucose level in diabetic rats.•Citrus sinensis peel contained fine concentrations of phenolic compounds.•Citrus sinensis peel possessed cytoprotective action.•Citrus sinensis peel promoted insulin receptor signalling.</abstract><cop>England</cop><pub>Elsevier Ltd</pub><pmid>29614383</pmid><doi>10.1016/j.fct.2018.03.050</doi><tpages>14</tpages><orcidid>https://orcid.org/0000-0001-5241-7463</orcidid><orcidid>https://orcid.org/0000-0001-5155-938X</orcidid><oa>free_for_read</oa></addata></record> |
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subjects | Adipose Citrus sinensis Diabetes Histology Insulin receptor Pancreatic β-cell |
title | Evidence of insulin-dependent signalling mechanisms produced by Citrus sinensis (L.) Osbeck fruit peel in an insulin resistant diabetic animal model |
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