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Exercise prevents cardiometabolic alterations induced by chronic use of glucocorticoids
Chronically, glucocorticoids induce adverse cardiometabolic alterations including insulin resistance, diabetes, dyslipidemia, liver steatosis and arterial hypertension. To evaluate the effect of regular practice of aerobic exercise on cardiometabolic alterations induced by chronic administration of...
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Published in: | Arquivos brasileiros de cardiologia 2009-10, Vol.93 (4), p.400 |
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creator | Pinheiro, Carlos Hermano da Justa Sousa Filho, Wilson Martins de Oliveira Neto, Joselito de Marinho, Maria de Jesus Ferreira Motta Neto, Renato Smith, Manuela Maria Ramos Lima Silva, Carlos Antônio Bruno da |
description | Chronically, glucocorticoids induce adverse cardiometabolic alterations including insulin resistance, diabetes, dyslipidemia, liver steatosis and arterial hypertension.
To evaluate the effect of regular practice of aerobic exercise on cardiometabolic alterations induced by chronic administration of dexamethasone (Dex - 0.5 mg/kg/day ip) in rats.
Male Wistar rats (n = 24) were divided in four groups: Control group; Trained group; Treated with Dex group and Treated with Dex and trained group. The exercise training (initiated 72 hours after the first dose of Dex) was carried out three times a week until the end of the treatment. At the end of this period, the following biochemical assessments were performed: fasting glycemia, oral glucose tolerance test and analysis of the blood lipid profile that included total cholesterol (TC), LDL-c, HDL-c, VLDL-c and triglycerides (TG). The weight of the gastrocnemius muscle, the histopathological analysis of the liver and cardiometabolic indices (TC/HDL-c, LDL-c/HDL-c and TG/HDL-c) were also performed.
Hyperglycemia, lower glucose tolerance, increased TC, LDL-c, VLDL-c, TG, CT/HDL-c, LDL-c/HDL-c and TG/HDL-c, decreased HDL-c, presence of liver steatosis and muscular hypotrophy were observed in the animals treated with Dex. The exercise training reduced hyperglycemia, improved glucose tolerance, decreased dyslipidemia and prevented liver steatosis, muscular hypotrophy and reduced CT/HDL-c, LDL-c/HDL-c and TG/HDL-c ratios. However, there was no significant effect on HDL-c.
The aerobic exercise training have a protective effect against the cardiometabolic alterations induced by the chronic use of glucocorticoids. |
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To evaluate the effect of regular practice of aerobic exercise on cardiometabolic alterations induced by chronic administration of dexamethasone (Dex - 0.5 mg/kg/day ip) in rats.
Male Wistar rats (n = 24) were divided in four groups: Control group; Trained group; Treated with Dex group and Treated with Dex and trained group. The exercise training (initiated 72 hours after the first dose of Dex) was carried out three times a week until the end of the treatment. At the end of this period, the following biochemical assessments were performed: fasting glycemia, oral glucose tolerance test and analysis of the blood lipid profile that included total cholesterol (TC), LDL-c, HDL-c, VLDL-c and triglycerides (TG). The weight of the gastrocnemius muscle, the histopathological analysis of the liver and cardiometabolic indices (TC/HDL-c, LDL-c/HDL-c and TG/HDL-c) were also performed.
Hyperglycemia, lower glucose tolerance, increased TC, LDL-c, VLDL-c, TG, CT/HDL-c, LDL-c/HDL-c and TG/HDL-c, decreased HDL-c, presence of liver steatosis and muscular hypotrophy were observed in the animals treated with Dex. The exercise training reduced hyperglycemia, improved glucose tolerance, decreased dyslipidemia and prevented liver steatosis, muscular hypotrophy and reduced CT/HDL-c, LDL-c/HDL-c and TG/HDL-c ratios. However, there was no significant effect on HDL-c.
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To evaluate the effect of regular practice of aerobic exercise on cardiometabolic alterations induced by chronic administration of dexamethasone (Dex - 0.5 mg/kg/day ip) in rats.
Male Wistar rats (n = 24) were divided in four groups: Control group; Trained group; Treated with Dex group and Treated with Dex and trained group. The exercise training (initiated 72 hours after the first dose of Dex) was carried out three times a week until the end of the treatment. At the end of this period, the following biochemical assessments were performed: fasting glycemia, oral glucose tolerance test and analysis of the blood lipid profile that included total cholesterol (TC), LDL-c, HDL-c, VLDL-c and triglycerides (TG). The weight of the gastrocnemius muscle, the histopathological analysis of the liver and cardiometabolic indices (TC/HDL-c, LDL-c/HDL-c and TG/HDL-c) were also performed.
Hyperglycemia, lower glucose tolerance, increased TC, LDL-c, VLDL-c, TG, CT/HDL-c, LDL-c/HDL-c and TG/HDL-c, decreased HDL-c, presence of liver steatosis and muscular hypotrophy were observed in the animals treated with Dex. The exercise training reduced hyperglycemia, improved glucose tolerance, decreased dyslipidemia and prevented liver steatosis, muscular hypotrophy and reduced CT/HDL-c, LDL-c/HDL-c and TG/HDL-c ratios. However, there was no significant effect on HDL-c.
The aerobic exercise training have a protective effect against the cardiometabolic alterations induced by the chronic use of glucocorticoids.</description><subject>Animals</subject><subject>Cardiovascular Diseases - chemically induced</subject><subject>Cardiovascular Diseases - metabolism</subject><subject>Cardiovascular Diseases - prevention & control</subject><subject>Dexamethasone - administration & dosage</subject><subject>Dexamethasone - adverse effects</subject><subject>Glucocorticoids - administration & dosage</subject><subject>Glucocorticoids - adverse effects</subject><subject>Male</subject><subject>Metabolic Syndrome - chemically induced</subject><subject>Metabolic Syndrome - metabolism</subject><subject>Metabolic Syndrome - prevention & control</subject><subject>Physical Conditioning, Animal - methods</subject><subject>Random Allocation</subject><subject>Rats</subject><subject>Rats, Wistar</subject><issn>1678-4170</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2009</creationdate><recordtype>article</recordtype><recordid>eNo1j8tKAzEYRoMgtlZfQfICA7lNMrOUUi9Q6EZxWZI_fzQyMxmSjNi3t6CuvsXhHPguyJpr0zWKG7Yi16V8MiaEke0VWfG-l1ppviZvu2_MEAvSOeMXTrVQsNnHNGK1Lg0RqB0qZltjmgqNk18APXUnCh85TWe8nN0U6PuwQIKUa4QUfbkhl8EOBW__dkNeH3Yv26dmf3h83t7vm5krXhuHXBirHRNWs9DKgL2XAEpKo4UQ3lrdmbZVEJRCGcD1newNU6rVIaDQckPufrvz4kb0xznH0ebT8f-h_AH28k3A</recordid><startdate>200910</startdate><enddate>200910</enddate><creator>Pinheiro, Carlos Hermano da Justa</creator><creator>Sousa Filho, Wilson Martins de</creator><creator>Oliveira Neto, Joselito de</creator><creator>Marinho, Maria de Jesus Ferreira</creator><creator>Motta Neto, Renato</creator><creator>Smith, Manuela Maria Ramos Lima</creator><creator>Silva, Carlos Antônio Bruno da</creator><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope></search><sort><creationdate>200910</creationdate><title>Exercise prevents cardiometabolic alterations induced by chronic use of glucocorticoids</title><author>Pinheiro, Carlos Hermano da Justa ; Sousa Filho, Wilson Martins de ; Oliveira Neto, Joselito de ; Marinho, Maria de Jesus Ferreira ; Motta Neto, Renato ; Smith, Manuela Maria Ramos Lima ; Silva, Carlos Antônio Bruno da</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-p141t-be127a6b02a60f53fe9d3cc43376222daa687554cf44e3fcb9839704456ffe263</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng ; por</language><creationdate>2009</creationdate><topic>Animals</topic><topic>Cardiovascular Diseases - chemically induced</topic><topic>Cardiovascular Diseases - metabolism</topic><topic>Cardiovascular Diseases - prevention & control</topic><topic>Dexamethasone - administration & dosage</topic><topic>Dexamethasone - adverse effects</topic><topic>Glucocorticoids - administration & dosage</topic><topic>Glucocorticoids - adverse effects</topic><topic>Male</topic><topic>Metabolic Syndrome - chemically induced</topic><topic>Metabolic Syndrome - metabolism</topic><topic>Metabolic Syndrome - prevention & control</topic><topic>Physical Conditioning, Animal - methods</topic><topic>Random Allocation</topic><topic>Rats</topic><topic>Rats, Wistar</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Pinheiro, Carlos Hermano da Justa</creatorcontrib><creatorcontrib>Sousa Filho, Wilson Martins de</creatorcontrib><creatorcontrib>Oliveira Neto, Joselito de</creatorcontrib><creatorcontrib>Marinho, Maria de Jesus Ferreira</creatorcontrib><creatorcontrib>Motta Neto, Renato</creatorcontrib><creatorcontrib>Smith, Manuela Maria Ramos Lima</creatorcontrib><creatorcontrib>Silva, Carlos Antônio Bruno da</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><jtitle>Arquivos brasileiros de cardiologia</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Pinheiro, Carlos Hermano da Justa</au><au>Sousa Filho, Wilson Martins de</au><au>Oliveira Neto, Joselito de</au><au>Marinho, Maria de Jesus Ferreira</au><au>Motta Neto, Renato</au><au>Smith, Manuela Maria Ramos Lima</au><au>Silva, Carlos Antônio Bruno da</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Exercise prevents cardiometabolic alterations induced by chronic use of glucocorticoids</atitle><jtitle>Arquivos brasileiros de cardiologia</jtitle><addtitle>Arq Bras Cardiol</addtitle><date>2009-10</date><risdate>2009</risdate><volume>93</volume><issue>4</issue><spage>400</spage><pages>400-</pages><eissn>1678-4170</eissn><abstract>Chronically, glucocorticoids induce adverse cardiometabolic alterations including insulin resistance, diabetes, dyslipidemia, liver steatosis and arterial hypertension.
To evaluate the effect of regular practice of aerobic exercise on cardiometabolic alterations induced by chronic administration of dexamethasone (Dex - 0.5 mg/kg/day ip) in rats.
Male Wistar rats (n = 24) were divided in four groups: Control group; Trained group; Treated with Dex group and Treated with Dex and trained group. The exercise training (initiated 72 hours after the first dose of Dex) was carried out three times a week until the end of the treatment. At the end of this period, the following biochemical assessments were performed: fasting glycemia, oral glucose tolerance test and analysis of the blood lipid profile that included total cholesterol (TC), LDL-c, HDL-c, VLDL-c and triglycerides (TG). The weight of the gastrocnemius muscle, the histopathological analysis of the liver and cardiometabolic indices (TC/HDL-c, LDL-c/HDL-c and TG/HDL-c) were also performed.
Hyperglycemia, lower glucose tolerance, increased TC, LDL-c, VLDL-c, TG, CT/HDL-c, LDL-c/HDL-c and TG/HDL-c, decreased HDL-c, presence of liver steatosis and muscular hypotrophy were observed in the animals treated with Dex. The exercise training reduced hyperglycemia, improved glucose tolerance, decreased dyslipidemia and prevented liver steatosis, muscular hypotrophy and reduced CT/HDL-c, LDL-c/HDL-c and TG/HDL-c ratios. However, there was no significant effect on HDL-c.
The aerobic exercise training have a protective effect against the cardiometabolic alterations induced by the chronic use of glucocorticoids.</abstract><cop>Brazil</cop><pmid>19936461</pmid><oa>free_for_read</oa></addata></record> |
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language | eng ; por |
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source | SciELO Brazil |
subjects | Animals Cardiovascular Diseases - chemically induced Cardiovascular Diseases - metabolism Cardiovascular Diseases - prevention & control Dexamethasone - administration & dosage Dexamethasone - adverse effects Glucocorticoids - administration & dosage Glucocorticoids - adverse effects Male Metabolic Syndrome - chemically induced Metabolic Syndrome - metabolism Metabolic Syndrome - prevention & control Physical Conditioning, Animal - methods Random Allocation Rats Rats, Wistar |
title | Exercise prevents cardiometabolic alterations induced by chronic use of glucocorticoids |
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