Amelioration of fructose-induced hepatic lipid accumulation by vitamin D 3 supplementation and high-intensity interval training in male Sprague‒Dawley rats
Intrahepatic lipid accumulation (IHL), a hallmark of metabolic disorders, is closely associated with de novo lipogenesis (DNL). Notably, fructose feeding increased the DNL. Lifestyle modifications resulting from dietary changes and increased physical activity/exercise can decrease the IHL content. W...
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description | Intrahepatic lipid accumulation (IHL), a hallmark of metabolic disorders, is closely associated with de novo lipogenesis (DNL). Notably, fructose feeding increased the DNL. Lifestyle modifications resulting from dietary changes and increased physical activity/exercise can decrease the IHL content. We examined the effects of vitamin D
supplementation (VDS), high-intensity interval training (HIIT), and their combination on the transcription factors and enzymes of the DNL pathway in male Sprague‒Dawley rats fed a high-fructose diet (HFrD).
Forty male rats were assigned to 5 groups (n = 8): CS (the control group had a standard diet); CF (the control group had HFrD (10% (w/v) fructose solution in tap water)); and FT (HFrD + HIIT: 10 bouts of 4 min of high-intensity running, corresponding to 85-90% of the maximal speed with 2 min active rest periods of 50% maximal speed, 5 days per week); FD (HFrD + intervention of intraperitoneal injection of 10000 IU/kg/week VDS); FTD (HFrD + HIIT + VDS) that were maintained for 12 weeks. ELISA, the GOD-POD assay, folch, western blotting, and oil red O staining were used to determine insulin, fasting blood glucose (FBG), hepatic triglyceride (TG) and cholesterol levels; SREBP1c, ChREBP-β, ACC1, FASN, p-ACC1, AMPK, p-AMPK, and PKA protein expression; and IHL content, respectively.
Both HIIT and VDS led to significant increases in the levels of PKA, AMPK, p-AMPK, and p-ACC1, as well as significant decreases in the levels of SREBP1c, ChREBP-β, ACC1, FASN, insulin, FBG, liver TG, liver cholesterol, and IHL. HIIT exhibited superior efficacy over VDS in reducing ChREBP-β, ACC1, insulin, FBG, liver TG and cholesterol, as well as increasing p-ACC1 and PKA. Notably, the combined intervention of HIIT and VDS yielded the most substantial improvements across all the parameters.
HFrD causes IHL accumulation and the onset of diabetes, whereas VDS and HIIT, along with their combined effects, prevent the consequences of HFrD. |
doi_str_mv | 10.1186/s12944-024-02347-y |
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supplementation (VDS), high-intensity interval training (HIIT), and their combination on the transcription factors and enzymes of the DNL pathway in male Sprague‒Dawley rats fed a high-fructose diet (HFrD).
Forty male rats were assigned to 5 groups (n = 8): CS (the control group had a standard diet); CF (the control group had HFrD (10% (w/v) fructose solution in tap water)); and FT (HFrD + HIIT: 10 bouts of 4 min of high-intensity running, corresponding to 85-90% of the maximal speed with 2 min active rest periods of 50% maximal speed, 5 days per week); FD (HFrD + intervention of intraperitoneal injection of 10000 IU/kg/week VDS); FTD (HFrD + HIIT + VDS) that were maintained for 12 weeks. ELISA, the GOD-POD assay, folch, western blotting, and oil red O staining were used to determine insulin, fasting blood glucose (FBG), hepatic triglyceride (TG) and cholesterol levels; SREBP1c, ChREBP-β, ACC1, FASN, p-ACC1, AMPK, p-AMPK, and PKA protein expression; and IHL content, respectively.
Both HIIT and VDS led to significant increases in the levels of PKA, AMPK, p-AMPK, and p-ACC1, as well as significant decreases in the levels of SREBP1c, ChREBP-β, ACC1, FASN, insulin, FBG, liver TG, liver cholesterol, and IHL. HIIT exhibited superior efficacy over VDS in reducing ChREBP-β, ACC1, insulin, FBG, liver TG and cholesterol, as well as increasing p-ACC1 and PKA. Notably, the combined intervention of HIIT and VDS yielded the most substantial improvements across all the parameters.
HFrD causes IHL accumulation and the onset of diabetes, whereas VDS and HIIT, along with their combined effects, prevent the consequences of HFrD.</description><identifier>EISSN: 1476-511X</identifier><identifier>DOI: 10.1186/s12944-024-02347-y</identifier><identifier>PMID: 39501326</identifier><language>eng</language><publisher>England</publisher><subject>AMP-Activated Protein Kinases - metabolism ; Animals ; Basic Helix-Loop-Helix Leucine Zipper Transcription Factors - metabolism ; Cholecalciferol - pharmacology ; Dietary Supplements ; Fructose ; High-Intensity Interval Training ; Lipid Metabolism - drug effects ; Lipogenesis - drug effects ; Liver - drug effects ; Liver - metabolism ; Male ; Physical Conditioning, Animal ; Rats ; Rats, Sprague-Dawley ; Sterol Regulatory Element Binding Protein 1 - genetics ; Sterol Regulatory Element Binding Protein 1 - metabolism ; Triglycerides - metabolism</subject><ispartof>Lipids in health and disease, 2024-11, Vol.23 (1), p.362</ispartof><rights>2024. The Author(s).</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,776,780,860,27901,27902</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/39501326$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Shokri, Behnaz</creatorcontrib><creatorcontrib>Mohebbi, Hamid</creatorcontrib><creatorcontrib>Mehrabani, Javad</creatorcontrib><title>Amelioration of fructose-induced hepatic lipid accumulation by vitamin D 3 supplementation and high-intensity interval training in male Sprague‒Dawley rats</title><title>Lipids in health and disease</title><addtitle>Lipids Health Dis</addtitle><description>Intrahepatic lipid accumulation (IHL), a hallmark of metabolic disorders, is closely associated with de novo lipogenesis (DNL). Notably, fructose feeding increased the DNL. Lifestyle modifications resulting from dietary changes and increased physical activity/exercise can decrease the IHL content. We examined the effects of vitamin D
supplementation (VDS), high-intensity interval training (HIIT), and their combination on the transcription factors and enzymes of the DNL pathway in male Sprague‒Dawley rats fed a high-fructose diet (HFrD).
Forty male rats were assigned to 5 groups (n = 8): CS (the control group had a standard diet); CF (the control group had HFrD (10% (w/v) fructose solution in tap water)); and FT (HFrD + HIIT: 10 bouts of 4 min of high-intensity running, corresponding to 85-90% of the maximal speed with 2 min active rest periods of 50% maximal speed, 5 days per week); FD (HFrD + intervention of intraperitoneal injection of 10000 IU/kg/week VDS); FTD (HFrD + HIIT + VDS) that were maintained for 12 weeks. ELISA, the GOD-POD assay, folch, western blotting, and oil red O staining were used to determine insulin, fasting blood glucose (FBG), hepatic triglyceride (TG) and cholesterol levels; SREBP1c, ChREBP-β, ACC1, FASN, p-ACC1, AMPK, p-AMPK, and PKA protein expression; and IHL content, respectively.
Both HIIT and VDS led to significant increases in the levels of PKA, AMPK, p-AMPK, and p-ACC1, as well as significant decreases in the levels of SREBP1c, ChREBP-β, ACC1, FASN, insulin, FBG, liver TG, liver cholesterol, and IHL. HIIT exhibited superior efficacy over VDS in reducing ChREBP-β, ACC1, insulin, FBG, liver TG and cholesterol, as well as increasing p-ACC1 and PKA. Notably, the combined intervention of HIIT and VDS yielded the most substantial improvements across all the parameters.
HFrD causes IHL accumulation and the onset of diabetes, whereas VDS and HIIT, along with their combined effects, prevent the consequences of HFrD.</description><subject>AMP-Activated Protein Kinases - metabolism</subject><subject>Animals</subject><subject>Basic Helix-Loop-Helix Leucine Zipper Transcription Factors - metabolism</subject><subject>Cholecalciferol - pharmacology</subject><subject>Dietary Supplements</subject><subject>Fructose</subject><subject>High-Intensity Interval Training</subject><subject>Lipid Metabolism - drug effects</subject><subject>Lipogenesis - drug effects</subject><subject>Liver - drug effects</subject><subject>Liver - metabolism</subject><subject>Male</subject><subject>Physical Conditioning, Animal</subject><subject>Rats</subject><subject>Rats, Sprague-Dawley</subject><subject>Sterol Regulatory Element Binding Protein 1 - genetics</subject><subject>Sterol Regulatory Element Binding Protein 1 - metabolism</subject><subject>Triglycerides - metabolism</subject><issn>1476-511X</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2024</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqFTztOw0AQXSEhEj4XoEBzAcOu7dikRAREDwVdNLHHzqDd9Wo_Qe44Az2X4yQ4CtQUoxm9z-g9IS6VvFbqtroJKl-WZSbz_RRlnY1HYq7KusoWSr3OxGkIb1Lmsq6qEzErlgupiryai687Q5oHj5EHC0MHnU9NHAJlbNvUUAtbchPZgGbHLWDTJJP0Qb4ZYccRDVtYQQEhOafJkI0HGu3k5n47vYpkA8cR9pffoYbokS3bfkLAoCZ4dh77RN8fnyt81zTCFCmci-MOdaCL330mrh4fXu6fMpc2htq182zQj-u_PsW_gh_9UGC8</recordid><startdate>20241105</startdate><enddate>20241105</enddate><creator>Shokri, Behnaz</creator><creator>Mohebbi, Hamid</creator><creator>Mehrabani, Javad</creator><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope></search><sort><creationdate>20241105</creationdate><title>Amelioration of fructose-induced hepatic lipid accumulation by vitamin D 3 supplementation and high-intensity interval training in male Sprague‒Dawley rats</title><author>Shokri, Behnaz ; Mohebbi, Hamid ; Mehrabani, Javad</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-pubmed_primary_395013263</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2024</creationdate><topic>AMP-Activated Protein Kinases - metabolism</topic><topic>Animals</topic><topic>Basic Helix-Loop-Helix Leucine Zipper Transcription Factors - metabolism</topic><topic>Cholecalciferol - pharmacology</topic><topic>Dietary Supplements</topic><topic>Fructose</topic><topic>High-Intensity Interval Training</topic><topic>Lipid Metabolism - drug effects</topic><topic>Lipogenesis - drug effects</topic><topic>Liver - drug effects</topic><topic>Liver - metabolism</topic><topic>Male</topic><topic>Physical Conditioning, Animal</topic><topic>Rats</topic><topic>Rats, Sprague-Dawley</topic><topic>Sterol Regulatory Element Binding Protein 1 - genetics</topic><topic>Sterol Regulatory Element Binding Protein 1 - metabolism</topic><topic>Triglycerides - metabolism</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Shokri, Behnaz</creatorcontrib><creatorcontrib>Mohebbi, Hamid</creatorcontrib><creatorcontrib>Mehrabani, Javad</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><jtitle>Lipids in health and disease</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Shokri, Behnaz</au><au>Mohebbi, Hamid</au><au>Mehrabani, Javad</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Amelioration of fructose-induced hepatic lipid accumulation by vitamin D 3 supplementation and high-intensity interval training in male Sprague‒Dawley rats</atitle><jtitle>Lipids in health and disease</jtitle><addtitle>Lipids Health Dis</addtitle><date>2024-11-05</date><risdate>2024</risdate><volume>23</volume><issue>1</issue><spage>362</spage><pages>362-</pages><eissn>1476-511X</eissn><abstract>Intrahepatic lipid accumulation (IHL), a hallmark of metabolic disorders, is closely associated with de novo lipogenesis (DNL). Notably, fructose feeding increased the DNL. Lifestyle modifications resulting from dietary changes and increased physical activity/exercise can decrease the IHL content. We examined the effects of vitamin D
supplementation (VDS), high-intensity interval training (HIIT), and their combination on the transcription factors and enzymes of the DNL pathway in male Sprague‒Dawley rats fed a high-fructose diet (HFrD).
Forty male rats were assigned to 5 groups (n = 8): CS (the control group had a standard diet); CF (the control group had HFrD (10% (w/v) fructose solution in tap water)); and FT (HFrD + HIIT: 10 bouts of 4 min of high-intensity running, corresponding to 85-90% of the maximal speed with 2 min active rest periods of 50% maximal speed, 5 days per week); FD (HFrD + intervention of intraperitoneal injection of 10000 IU/kg/week VDS); FTD (HFrD + HIIT + VDS) that were maintained for 12 weeks. ELISA, the GOD-POD assay, folch, western blotting, and oil red O staining were used to determine insulin, fasting blood glucose (FBG), hepatic triglyceride (TG) and cholesterol levels; SREBP1c, ChREBP-β, ACC1, FASN, p-ACC1, AMPK, p-AMPK, and PKA protein expression; and IHL content, respectively.
Both HIIT and VDS led to significant increases in the levels of PKA, AMPK, p-AMPK, and p-ACC1, as well as significant decreases in the levels of SREBP1c, ChREBP-β, ACC1, FASN, insulin, FBG, liver TG, liver cholesterol, and IHL. HIIT exhibited superior efficacy over VDS in reducing ChREBP-β, ACC1, insulin, FBG, liver TG and cholesterol, as well as increasing p-ACC1 and PKA. Notably, the combined intervention of HIIT and VDS yielded the most substantial improvements across all the parameters.
HFrD causes IHL accumulation and the onset of diabetes, whereas VDS and HIIT, along with their combined effects, prevent the consequences of HFrD.</abstract><cop>England</cop><pmid>39501326</pmid><doi>10.1186/s12944-024-02347-y</doi></addata></record> |
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subjects | AMP-Activated Protein Kinases - metabolism Animals Basic Helix-Loop-Helix Leucine Zipper Transcription Factors - metabolism Cholecalciferol - pharmacology Dietary Supplements Fructose High-Intensity Interval Training Lipid Metabolism - drug effects Lipogenesis - drug effects Liver - drug effects Liver - metabolism Male Physical Conditioning, Animal Rats Rats, Sprague-Dawley Sterol Regulatory Element Binding Protein 1 - genetics Sterol Regulatory Element Binding Protein 1 - metabolism Triglycerides - metabolism |
title | Amelioration of fructose-induced hepatic lipid accumulation by vitamin D 3 supplementation and high-intensity interval training in male Sprague‒Dawley rats |
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