Effects of chronic caffeine intake and low‐intensity exercise on skeletal muscle of Wistar rats

Caffeine can affect muscle cell physiology and the inflammatory response during exercise. The purpose of this study was to analyse muscle damage markers and inflammatory cell infiltration into the soleus muscle of sedentary and exercised animals submitted to chronic caffeine intake. Thirty‐two male...

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Veröffentlicht in:Experimental physiology 2011-11, Vol.96 (11), p.1228-1238
Hauptverfasser: da Costa Santos, Vanessa Batista, Ruiz, Roberto José, Vettorato, Evandro Doite, Nakamura, Fabio Yuzo, Juliani, Luiz Carlos, Polito, Marcos Doederlein, Siqueira, Claudia Patricia Cardoso Martins, de Paula Ramos, Solange
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container_end_page 1238
container_issue 11
container_start_page 1228
container_title Experimental physiology
container_volume 96
creator da Costa Santos, Vanessa Batista
Ruiz, Roberto José
Vettorato, Evandro Doite
Nakamura, Fabio Yuzo
Juliani, Luiz Carlos
Polito, Marcos Doederlein
Siqueira, Claudia Patricia Cardoso Martins
de Paula Ramos, Solange
description Caffeine can affect muscle cell physiology and the inflammatory response during exercise. The purpose of this study was to analyse muscle damage markers and inflammatory cell infiltration into the soleus muscle of sedentary and exercised animals submitted to chronic caffeine intake. Thirty‐two male Wistar rats were divided into the following four groups (n= 8 per group): sedentary control (SCO); sedentary + caffeine (SCAF); trained control (TCO); and trained + caffeine (TCAF). The animals were housed in individual cages and received tap water or caffeine (1 mg ml−1); they were maintained at rest or submitted to swimming for up to 40 min day−1 with a 4% load, five times per week for 30 days. Blood samples were collected for analysis of serum lactate, creatine kinase and calcium. The right soleus muscle and the epididymal fat depot were weighed, and the muscle was submitted to histological analysis. Training and caffeine did not change body or muscle weight, food and liquid intake or serum calcium levels among groups. Decreased fat tissue (P < 0.05) was observed in the SCAF (4.05 ± 1.03 g), TCO (4.14 ± 0.78 g) and TCAF groups (4.02 ± 1.02 g) compared with the SCO group (5.31 ± 1.06 g). Serum creatine kinase activity was significantly reduced in the SCAF (787.3 ± 230.3 U l−1), TCO (775.3 ± 232.3 U l−1) and TCAF groups (379.5 ± 110.5 U l−1) compared with the SCO group (1610.2 ± 276.5 U l−1). Few damaged muscle fibres (P < 0.05) were found in SCAF (16.7 ± 12.8%) and TCAF groups (17.3 ± 11.7%) compared with the SCO group (53.6 ± 13.9%). The SCAF group presented fewer fields with inflammatory cells (7.6 ± 8.7 fields) compared with the SCO group (123 ± 146 fields). The results suggest that the chronic intake of caffeine, as well as chronic low‐intensity exercise, decreased muscle damage and inflammatory infiltration into skeletal muscle.
doi_str_mv 10.1113/expphysiol.2011.060483
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The purpose of this study was to analyse muscle damage markers and inflammatory cell infiltration into the soleus muscle of sedentary and exercised animals submitted to chronic caffeine intake. Thirty‐two male Wistar rats were divided into the following four groups (n= 8 per group): sedentary control (SCO); sedentary + caffeine (SCAF); trained control (TCO); and trained + caffeine (TCAF). The animals were housed in individual cages and received tap water or caffeine (1 mg ml−1); they were maintained at rest or submitted to swimming for up to 40 min day−1 with a 4% load, five times per week for 30 days. Blood samples were collected for analysis of serum lactate, creatine kinase and calcium. The right soleus muscle and the epididymal fat depot were weighed, and the muscle was submitted to histological analysis. Training and caffeine did not change body or muscle weight, food and liquid intake or serum calcium levels among groups. Decreased fat tissue (P &lt; 0.05) was observed in the SCAF (4.05 ± 1.03 g), TCO (4.14 ± 0.78 g) and TCAF groups (4.02 ± 1.02 g) compared with the SCO group (5.31 ± 1.06 g). Serum creatine kinase activity was significantly reduced in the SCAF (787.3 ± 230.3 U l−1), TCO (775.3 ± 232.3 U l−1) and TCAF groups (379.5 ± 110.5 U l−1) compared with the SCO group (1610.2 ± 276.5 U l−1). Few damaged muscle fibres (P &lt; 0.05) were found in SCAF (16.7 ± 12.8%) and TCAF groups (17.3 ± 11.7%) compared with the SCO group (53.6 ± 13.9%). The SCAF group presented fewer fields with inflammatory cells (7.6 ± 8.7 fields) compared with the SCO group (123 ± 146 fields). 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The purpose of this study was to analyse muscle damage markers and inflammatory cell infiltration into the soleus muscle of sedentary and exercised animals submitted to chronic caffeine intake. Thirty‐two male Wistar rats were divided into the following four groups (n= 8 per group): sedentary control (SCO); sedentary + caffeine (SCAF); trained control (TCO); and trained + caffeine (TCAF). The animals were housed in individual cages and received tap water or caffeine (1 mg ml−1); they were maintained at rest or submitted to swimming for up to 40 min day−1 with a 4% load, five times per week for 30 days. Blood samples were collected for analysis of serum lactate, creatine kinase and calcium. The right soleus muscle and the epididymal fat depot were weighed, and the muscle was submitted to histological analysis. Training and caffeine did not change body or muscle weight, food and liquid intake or serum calcium levels among groups. Decreased fat tissue (P &lt; 0.05) was observed in the SCAF (4.05 ± 1.03 g), TCO (4.14 ± 0.78 g) and TCAF groups (4.02 ± 1.02 g) compared with the SCO group (5.31 ± 1.06 g). Serum creatine kinase activity was significantly reduced in the SCAF (787.3 ± 230.3 U l−1), TCO (775.3 ± 232.3 U l−1) and TCAF groups (379.5 ± 110.5 U l−1) compared with the SCO group (1610.2 ± 276.5 U l−1). Few damaged muscle fibres (P &lt; 0.05) were found in SCAF (16.7 ± 12.8%) and TCAF groups (17.3 ± 11.7%) compared with the SCO group (53.6 ± 13.9%). The SCAF group presented fewer fields with inflammatory cells (7.6 ± 8.7 fields) compared with the SCO group (123 ± 146 fields). The results suggest that the chronic intake of caffeine, as well as chronic low‐intensity exercise, decreased muscle damage and inflammatory infiltration into skeletal muscle.</abstract><cop>Oxford, UK</cop><pub>Blackwell Publishing Ltd</pub><pmid>21890517</pmid><doi>10.1113/expphysiol.2011.060483</doi><tpages>11</tpages><oa>free_for_read</oa></addata></record>
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subjects Adipose Tissue - drug effects
Animals
Caffeine - pharmacology
Calcium - blood
Creatine Kinase - blood
Inflammation - physiopathology
Lactic Acid - blood
Macrophages - physiology
Male
Muscle, Skeletal - drug effects
Muscle, Skeletal - metabolism
Muscle, Skeletal - pathology
Neutrophil Infiltration
Physical Conditioning, Animal - physiology
Rats
Rats, Wistar
Swimming
title Effects of chronic caffeine intake and low‐intensity exercise on skeletal muscle of Wistar rats
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