Impaired Muscle Regeneration in Ob/ob and Db/db Mice
In obesity and type 2 diabetes, efficient skeletal muscle repair following injury may be required, not only for restoring muscle structure and function, but also for maintaining exercise capacity and insulin sensitivity. The hypothesis of this study was that muscle regeneration would be impaired in...
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2011-01-01
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Series: | The Scientific World Journal |
Online Access: | http://dx.doi.org/10.1100/tsw.2011.137 |
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author | Mai-Huong Nguyen Ming Cheng Timothy J. Koh |
author_facet | Mai-Huong Nguyen Ming Cheng Timothy J. Koh |
author_sort | Mai-Huong Nguyen |
collection | DOAJ |
description | In obesity and type 2 diabetes, efficient skeletal muscle repair following injury may be required, not only for restoring muscle structure and function, but also for maintaining exercise capacity and insulin sensitivity. The hypothesis of this study was that muscle regeneration would be impaired in ob/ob and db/db mice, which are common mouse models of obesity and type 2 diabetes. Muscle injury was produced by cardiotoxin injection, and regeneration was assessed by morphological and immunostaining techniques. Muscle regeneration was delayed in ob/ob and db/db mice, but not in a less severe model of insulin resistance – feeding a high-fat diet to wild-type mice. Angiogenesis, cell proliferation, and myoblast accumulation were also impaired in ob/ob and db/db mice, but not the high-fat diet mice. The impairments in muscle regeneration were associated with impaired macrophage accumulation; macrophages have been shown previously to be required for efficient muscle regeneration. Impaired regeneration in ob/ob and db/db mice could be due partly to the lack of leptin signaling, since leptin is expressed both in damaged muscle and in cultured muscle cells. In summary, impaired muscle regeneration in ob/ob and db/db mice was associated with reduced macrophage accumulation, angiogenesis, and myoblast activity, and could have implications for insulin sensitivity in the skeletal muscle of obese and type 2 diabetic patients. |
format | Article |
id | doaj-art-6880218303874c60866f36fb61e26b63 |
institution | Kabale University |
issn | 1537-744X |
language | English |
publishDate | 2011-01-01 |
publisher | Wiley |
record_format | Article |
series | The Scientific World Journal |
spelling | doaj-art-6880218303874c60866f36fb61e26b632025-02-03T01:32:49ZengWileyThe Scientific World Journal1537-744X2011-01-01111525153510.1100/tsw.2011.137Impaired Muscle Regeneration in Ob/ob and Db/db MiceMai-Huong Nguyen0Ming Cheng1Timothy J. Koh2Department of Kinesiology and Nutrition, University of Illinois at Chicago, USADepartment of Kinesiology and Nutrition, University of Illinois at Chicago, USADepartment of Kinesiology and Nutrition, University of Illinois at Chicago, USAIn obesity and type 2 diabetes, efficient skeletal muscle repair following injury may be required, not only for restoring muscle structure and function, but also for maintaining exercise capacity and insulin sensitivity. The hypothesis of this study was that muscle regeneration would be impaired in ob/ob and db/db mice, which are common mouse models of obesity and type 2 diabetes. Muscle injury was produced by cardiotoxin injection, and regeneration was assessed by morphological and immunostaining techniques. Muscle regeneration was delayed in ob/ob and db/db mice, but not in a less severe model of insulin resistance – feeding a high-fat diet to wild-type mice. Angiogenesis, cell proliferation, and myoblast accumulation were also impaired in ob/ob and db/db mice, but not the high-fat diet mice. The impairments in muscle regeneration were associated with impaired macrophage accumulation; macrophages have been shown previously to be required for efficient muscle regeneration. Impaired regeneration in ob/ob and db/db mice could be due partly to the lack of leptin signaling, since leptin is expressed both in damaged muscle and in cultured muscle cells. In summary, impaired muscle regeneration in ob/ob and db/db mice was associated with reduced macrophage accumulation, angiogenesis, and myoblast activity, and could have implications for insulin sensitivity in the skeletal muscle of obese and type 2 diabetic patients.http://dx.doi.org/10.1100/tsw.2011.137 |
spellingShingle | Mai-Huong Nguyen Ming Cheng Timothy J. Koh Impaired Muscle Regeneration in Ob/ob and Db/db Mice The Scientific World Journal |
title | Impaired Muscle Regeneration in Ob/ob and Db/db Mice |
title_full | Impaired Muscle Regeneration in Ob/ob and Db/db Mice |
title_fullStr | Impaired Muscle Regeneration in Ob/ob and Db/db Mice |
title_full_unstemmed | Impaired Muscle Regeneration in Ob/ob and Db/db Mice |
title_short | Impaired Muscle Regeneration in Ob/ob and Db/db Mice |
title_sort | impaired muscle regeneration in ob ob and db db mice |
url | http://dx.doi.org/10.1100/tsw.2011.137 |
work_keys_str_mv | AT maihuongnguyen impairedmuscleregenerationinobobanddbdbmice AT mingcheng impairedmuscleregenerationinobobanddbdbmice AT timothyjkoh impairedmuscleregenerationinobobanddbdbmice |