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Sex-specific susceptibility to type 2 diabetes mellitus and preventive effect of linalyl acetate
Biological, psychosocial and lifestyle risk factors interact in the development of type 2 diabetes mellitus (T2DM). To date, the effects of sex, chronic stress (CS) and high-fat diet (HFD) on T2DM and the ability of linalyl acetate (LA) to prevent T2DM have not been determined. This study therefore...
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Published in: | Life sciences (1973) 2020-11, Vol.260, p.118432-8, Article 118432 |
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description | Biological, psychosocial and lifestyle risk factors interact in the development of type 2 diabetes mellitus (T2DM). To date, the effects of sex, chronic stress (CS) and high-fat diet (HFD) on T2DM and the ability of linalyl acetate (LA) to prevent T2DM have not been determined. This study therefore explored the differential effects of CS and HFD on T2DM, as well as the ability of LA to prevent T2DM development, in male and female rats.
T2DM was induced in rats by feeding an HFD and placing them under immobilization stress for 2 h/day for 3 weeks. Low-dose streptozotocin was administered on day 15, and LA was administered for 3 weeks.
Fasting blood sugar (FBS) increased in HFD-fed male, but not female, rats. CS further increased FBS in HFD-fed rats, whereas CS alone did not alter FBS. The homeostatic model assessment-insulin resistance (HOMA-IR) showed results similar to FBS. Serum corticosterone levels markedly increased only in HFD-fed male rats exposed to CS. Pancreas nuclear factor kappa B (NF-κB) levels were higher in HFD-fed male rats exposed to CS than in control rats although there were no sex differences. LA 10 mg/kg significantly reduced FBS, serum insulin, HOMA-IR, and serum corticosterone levels in HFD-fed male rats exposed to CS. LA 10 mg/kg also tended to reduce NF-κB in the pancreas and significantly increased mitochondrial membrane potential (MMP) in the liver.
Male rats are vulnerable to T2DM induced by CS and HFD, and LA can prevent T2DM in these rats not only by reducing insulin resistance and corticosterone levels but by increasing MMP in the liver. |
doi_str_mv | 10.1016/j.lfs.2020.118432 |
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T2DM was induced in rats by feeding an HFD and placing them under immobilization stress for 2 h/day for 3 weeks. Low-dose streptozotocin was administered on day 15, and LA was administered for 3 weeks.
Fasting blood sugar (FBS) increased in HFD-fed male, but not female, rats. CS further increased FBS in HFD-fed rats, whereas CS alone did not alter FBS. The homeostatic model assessment-insulin resistance (HOMA-IR) showed results similar to FBS. Serum corticosterone levels markedly increased only in HFD-fed male rats exposed to CS. Pancreas nuclear factor kappa B (NF-κB) levels were higher in HFD-fed male rats exposed to CS than in control rats although there were no sex differences. LA 10 mg/kg significantly reduced FBS, serum insulin, HOMA-IR, and serum corticosterone levels in HFD-fed male rats exposed to CS. LA 10 mg/kg also tended to reduce NF-κB in the pancreas and significantly increased mitochondrial membrane potential (MMP) in the liver.
Male rats are vulnerable to T2DM induced by CS and HFD, and LA can prevent T2DM in these rats not only by reducing insulin resistance and corticosterone levels but by increasing MMP in the liver.</description><identifier>ISSN: 0024-3205</identifier><identifier>EISSN: 1879-0631</identifier><identifier>DOI: 10.1016/j.lfs.2020.118432</identifier><language>eng</language><publisher>New York: Elsevier Inc</publisher><subject>Acetic acid ; Chronic stress ; Corticosterone ; Diabetes ; Diabetes mellitus ; Diabetes mellitus (non-insulin dependent) ; Exposure ; Gender aspects ; Gender differences ; High fat diet ; Immobilization ; Insulin ; Insulin resistance ; Linalyl acetate ; Liver ; Membrane potential ; Mitochondria ; NF-κB protein ; Pancreas ; Risk analysis ; Risk factors ; Rodents ; Sex ; Sex differences ; Streptozocin ; Type 2 diabetes mellitus</subject><ispartof>Life sciences (1973), 2020-11, Vol.260, p.118432-8, Article 118432</ispartof><rights>2020 Elsevier Inc.</rights><rights>Copyright Elsevier BV Nov 2020</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c424t-1749abf04e56889a0fcd824de5b16dde06c33cbf775dec3b3fa6cdd33cc5114d3</citedby><cites>FETCH-LOGICAL-c424t-1749abf04e56889a0fcd824de5b16dde06c33cbf775dec3b3fa6cdd33cc5114d3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,27924,27925</link.rule.ids></links><search><creatorcontrib>Shin, You Kyoung</creatorcontrib><creatorcontrib>Hsieh, Yu Shan</creatorcontrib><creatorcontrib>Han, A Young</creatorcontrib><creatorcontrib>Kwon, Soonho</creatorcontrib><creatorcontrib>Kang, Purum</creatorcontrib><creatorcontrib>Seol, Geun Hee</creatorcontrib><title>Sex-specific susceptibility to type 2 diabetes mellitus and preventive effect of linalyl acetate</title><title>Life sciences (1973)</title><description>Biological, psychosocial and lifestyle risk factors interact in the development of type 2 diabetes mellitus (T2DM). To date, the effects of sex, chronic stress (CS) and high-fat diet (HFD) on T2DM and the ability of linalyl acetate (LA) to prevent T2DM have not been determined. This study therefore explored the differential effects of CS and HFD on T2DM, as well as the ability of LA to prevent T2DM development, in male and female rats.
T2DM was induced in rats by feeding an HFD and placing them under immobilization stress for 2 h/day for 3 weeks. Low-dose streptozotocin was administered on day 15, and LA was administered for 3 weeks.
Fasting blood sugar (FBS) increased in HFD-fed male, but not female, rats. CS further increased FBS in HFD-fed rats, whereas CS alone did not alter FBS. The homeostatic model assessment-insulin resistance (HOMA-IR) showed results similar to FBS. Serum corticosterone levels markedly increased only in HFD-fed male rats exposed to CS. Pancreas nuclear factor kappa B (NF-κB) levels were higher in HFD-fed male rats exposed to CS than in control rats although there were no sex differences. LA 10 mg/kg significantly reduced FBS, serum insulin, HOMA-IR, and serum corticosterone levels in HFD-fed male rats exposed to CS. LA 10 mg/kg also tended to reduce NF-κB in the pancreas and significantly increased mitochondrial membrane potential (MMP) in the liver.
Male rats are vulnerable to T2DM induced by CS and HFD, and LA can prevent T2DM in these rats not only by reducing insulin resistance and corticosterone levels but by increasing MMP in the liver.</description><subject>Acetic acid</subject><subject>Chronic stress</subject><subject>Corticosterone</subject><subject>Diabetes</subject><subject>Diabetes mellitus</subject><subject>Diabetes mellitus (non-insulin dependent)</subject><subject>Exposure</subject><subject>Gender aspects</subject><subject>Gender differences</subject><subject>High fat diet</subject><subject>Immobilization</subject><subject>Insulin</subject><subject>Insulin resistance</subject><subject>Linalyl acetate</subject><subject>Liver</subject><subject>Membrane potential</subject><subject>Mitochondria</subject><subject>NF-κB protein</subject><subject>Pancreas</subject><subject>Risk analysis</subject><subject>Risk factors</subject><subject>Rodents</subject><subject>Sex</subject><subject>Sex differences</subject><subject>Streptozocin</subject><subject>Type 2 diabetes mellitus</subject><issn>0024-3205</issn><issn>1879-0631</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2020</creationdate><recordtype>article</recordtype><recordid>eNp9kMtKAzEUhoMoWC8P4C7gxs3UXGemuJLiDQou1HXMJCeQks6MSabYtzelrly4OuTk-0P-D6ErSuaU0Pp2PQ8uzRlh5UxbwdkRmtG2WVSk5vQYzQhhouKMyFN0ltKaECJlw2fo8w2-qzSC8c4bnKZkYMy-88HnHc4DzrsRMMPW6w4yJLyBUK6mhHVv8RhhC332W8DgHJiMB4eD73XYBawNZJ3hAp04HRJc_s5z9PH48L58rlavTy_L-1VlBBO5oo1Y6M4RAbJu24UmztiWCQuyo7W1QGrDuelc00gLhnfc6dpYW3ZGUiosP0c3h3fHOHxNkLLa-FImBN3DMCXFhBC8KfFFQa__oOthiuXXe6qWDSWSykLRA2XikFIEp8boNzruFCVq71ytVXGu9s7VwXnJ3B0yUJpuPUSVjIfegPWx6FF28P-kfwB8_oqt</recordid><startdate>20201101</startdate><enddate>20201101</enddate><creator>Shin, You Kyoung</creator><creator>Hsieh, Yu Shan</creator><creator>Han, A Young</creator><creator>Kwon, Soonho</creator><creator>Kang, Purum</creator><creator>Seol, Geun Hee</creator><general>Elsevier Inc</general><general>Elsevier BV</general><scope>AAYXX</scope><scope>CITATION</scope><scope>7QP</scope><scope>7QR</scope><scope>7TK</scope><scope>7U7</scope><scope>7U9</scope><scope>8FD</scope><scope>C1K</scope><scope>FR3</scope><scope>H94</scope><scope>P64</scope><scope>RC3</scope><scope>7X8</scope></search><sort><creationdate>20201101</creationdate><title>Sex-specific susceptibility to type 2 diabetes mellitus and preventive effect of linalyl acetate</title><author>Shin, You Kyoung ; Hsieh, Yu Shan ; Han, A Young ; Kwon, Soonho ; Kang, Purum ; Seol, Geun Hee</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c424t-1749abf04e56889a0fcd824de5b16dde06c33cbf775dec3b3fa6cdd33cc5114d3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2020</creationdate><topic>Acetic acid</topic><topic>Chronic stress</topic><topic>Corticosterone</topic><topic>Diabetes</topic><topic>Diabetes mellitus</topic><topic>Diabetes mellitus (non-insulin dependent)</topic><topic>Exposure</topic><topic>Gender aspects</topic><topic>Gender differences</topic><topic>High fat diet</topic><topic>Immobilization</topic><topic>Insulin</topic><topic>Insulin resistance</topic><topic>Linalyl acetate</topic><topic>Liver</topic><topic>Membrane potential</topic><topic>Mitochondria</topic><topic>NF-κB protein</topic><topic>Pancreas</topic><topic>Risk analysis</topic><topic>Risk factors</topic><topic>Rodents</topic><topic>Sex</topic><topic>Sex differences</topic><topic>Streptozocin</topic><topic>Type 2 diabetes mellitus</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Shin, You Kyoung</creatorcontrib><creatorcontrib>Hsieh, Yu Shan</creatorcontrib><creatorcontrib>Han, A Young</creatorcontrib><creatorcontrib>Kwon, Soonho</creatorcontrib><creatorcontrib>Kang, Purum</creatorcontrib><creatorcontrib>Seol, Geun Hee</creatorcontrib><collection>CrossRef</collection><collection>Calcium & Calcified Tissue Abstracts</collection><collection>Chemoreception Abstracts</collection><collection>Neurosciences Abstracts</collection><collection>Toxicology Abstracts</collection><collection>Virology and AIDS Abstracts</collection><collection>Technology Research Database</collection><collection>Environmental Sciences and Pollution Management</collection><collection>Engineering Research Database</collection><collection>AIDS and Cancer Research Abstracts</collection><collection>Biotechnology and BioEngineering Abstracts</collection><collection>Genetics Abstracts</collection><collection>MEDLINE - Academic</collection><jtitle>Life sciences (1973)</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Shin, You Kyoung</au><au>Hsieh, Yu Shan</au><au>Han, A Young</au><au>Kwon, Soonho</au><au>Kang, Purum</au><au>Seol, Geun Hee</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Sex-specific susceptibility to type 2 diabetes mellitus and preventive effect of linalyl acetate</atitle><jtitle>Life sciences (1973)</jtitle><date>2020-11-01</date><risdate>2020</risdate><volume>260</volume><spage>118432</spage><epage>8</epage><pages>118432-8</pages><artnum>118432</artnum><issn>0024-3205</issn><eissn>1879-0631</eissn><abstract>Biological, psychosocial and lifestyle risk factors interact in the development of type 2 diabetes mellitus (T2DM). To date, the effects of sex, chronic stress (CS) and high-fat diet (HFD) on T2DM and the ability of linalyl acetate (LA) to prevent T2DM have not been determined. This study therefore explored the differential effects of CS and HFD on T2DM, as well as the ability of LA to prevent T2DM development, in male and female rats.
T2DM was induced in rats by feeding an HFD and placing them under immobilization stress for 2 h/day for 3 weeks. Low-dose streptozotocin was administered on day 15, and LA was administered for 3 weeks.
Fasting blood sugar (FBS) increased in HFD-fed male, but not female, rats. CS further increased FBS in HFD-fed rats, whereas CS alone did not alter FBS. The homeostatic model assessment-insulin resistance (HOMA-IR) showed results similar to FBS. Serum corticosterone levels markedly increased only in HFD-fed male rats exposed to CS. Pancreas nuclear factor kappa B (NF-κB) levels were higher in HFD-fed male rats exposed to CS than in control rats although there were no sex differences. LA 10 mg/kg significantly reduced FBS, serum insulin, HOMA-IR, and serum corticosterone levels in HFD-fed male rats exposed to CS. LA 10 mg/kg also tended to reduce NF-κB in the pancreas and significantly increased mitochondrial membrane potential (MMP) in the liver.
Male rats are vulnerable to T2DM induced by CS and HFD, and LA can prevent T2DM in these rats not only by reducing insulin resistance and corticosterone levels but by increasing MMP in the liver.</abstract><cop>New York</cop><pub>Elsevier Inc</pub><doi>10.1016/j.lfs.2020.118432</doi><tpages>8</tpages></addata></record> |
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subjects | Acetic acid Chronic stress Corticosterone Diabetes Diabetes mellitus Diabetes mellitus (non-insulin dependent) Exposure Gender aspects Gender differences High fat diet Immobilization Insulin Insulin resistance Linalyl acetate Liver Membrane potential Mitochondria NF-κB protein Pancreas Risk analysis Risk factors Rodents Sex Sex differences Streptozocin Type 2 diabetes mellitus |
title | Sex-specific susceptibility to type 2 diabetes mellitus and preventive effect of linalyl acetate |
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