The effect of preventive use of alanyl-glutamine on diaphragm muscle function in cecal ligation and puncture-induced sepsis model

被引:12
作者
Doruk, N
Buyukakilli, B
Atici, S
Cinel, I
Cinel, L
Tamer, L
Avlan, D
Bilgin, E
Oral, U
机构
[1] Mersin Univ, Sch Med, Dept Anesthesiol & Reanimat, Mersin, Turkey
[2] Mersin Univ, Sch Med, Dept Biophys, Mersin, Turkey
[3] Mersin Univ, Sch Med, Dept Biochem, Mersin, Turkey
[4] Mersin Univ, Sch Med, Dept Pediat Surg, Mersin, Turkey
关键词
D O I
10.1177/014860710502900136
中图分类号
R15 [营养卫生、食品卫生]; TS201 [基础科学];
学科分类号
100403 ;
摘要
Background: Low muscle glutamine levels during sepsis are associated with reduced protein synthesis and elevated protein breakdown, in particular myofibrillar protein breakdown. Thus, in a cecal ligation and puncture (CLP)-induced sepsis model in the rat, we hypothesized that glutamine pretreatment would protect the diaphragm muscle function. Methods: Eighty-four male Wistar rats weighing between 180 g and 200 g received standard amino acid solution 1.2 g kg(-1) per day intraperitoneally (IP) or standard amino acid solution 1.2 g kg(-1) per day plus alanyl-glutamine (GLN) 0.25 g kg(-1) per day (IP) during the first 6 days of the experiment. On the seventh day, CLP or sham procedures were applied. The sham and CLP groups were equally divided into 3 subgroups according to the termination of the experiment, which took place at either the 24(th) hour, 48(th) hour, or 72(nd) hour. After the compound muscle action potentials (CMAP) were recorded from the diaphragms of the rats at these selected times, they were decapitated under ketamine/xylazine anesthesia, and diaphragms were harvested for biochemical and histopathological examination. Results: The mean area and amplitude of CMAP were significantly larger in sham+GLN groups when compared with CLP and CLP+GLN groups at all times (p < .05). Diaphragm Ca+2-ATPase levels were found to be significantly decreased in CLP group at all times compared to sham groups (p < .05). Diaphragm reduced glutathione levels were significantly higher in sham+GLN groups when compared with CLP and CLP+GLN groups at all times (p < .05). In histopathologic assessment, moderate neutrophil infiltration, which was observed in CLP48, was significantly reduced with alanyl-glutamine supplementation in CLP+GLN48 group (p < .05). Conclusions: This study showed that glutamine pretreatment did not improve diaphragm muscle function, but prevented the biochemical and histopathological changes in diaphragmatic muscle in CLP-induced sepsis. However, further studies are needed to clarify whether a higher dose of glutamine supplementation might protect the diaphragmatic muscle functions.
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页码:36 / 43
页数:8
相关论文
共 36 条
[1]  
ACKER BAC, 2000, AM J CLIN NUTR, V72, P790
[2]  
AMINOFF MJ, 1998, ELECTROMYOGRAPHY CLI, P525
[3]  
Aubier M, 1998, EUR RESPIR J, V11, P758
[4]  
BAKER CC, 1985, SURG FORUM, V36, P68
[5]   Glutamine alimentation in catabolic state [J].
Boelens, PG ;
Nijveldt, RJ ;
Houdijk, APJ ;
Meijer, S ;
van Leeuwen, PAM .
JOURNAL OF NUTRITION, 2001, 131 (09) :2569S-2577S
[6]   Hydrogen peroxide disrupts Ca2+ release from the sarcoplasmic reticulum of rat skeletal muscle fibers [J].
Brotto, MAP ;
Nosek, TM .
JOURNAL OF APPLIED PHYSIOLOGY, 1996, 81 (02) :731-737
[7]   IS MUSCLE PROTEIN-TURNOVER REGULATED BY INTRACELLULAR GLUTAMINE DURING SEPSIS [J].
FANG, CH ;
JAMES, JH ;
FISCHER, JE ;
HASSELGREN, PO .
JOURNAL OF PARENTERAL AND ENTERAL NUTRITION, 1995, 19 (04) :279-285
[8]   HYDROGEN-PEROXIDE STIMULATES THE CA2+ RELEASE CHANNEL FROM SKELETAL-MUSCLE SARCOPLASMIC-RETICULUM [J].
FAVERO, TG ;
ZABLE, AC ;
ABRAMSON, JJ .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1995, 270 (43) :25557-25563
[9]   Effect of free radical scavengers on diaphragmatic contractility in septic peritonitis [J].
Fujimura, N ;
Sumita, S ;
Aimono, M ;
Masuda, Y ;
Shichinohe, Y ;
Narimatsu, E ;
Namiki, A .
AMERICAN JOURNAL OF RESPIRATORY AND CRITICAL CARE MEDICINE, 2000, 162 (06) :2159-2165
[10]   Parenteral L-alanyl-L-glutamine improves 6-month outcome in critically ill patients [J].
Goeters, C ;
Wenn, A ;
Mertes, N ;
Wempe, C ;
Van Aken, H ;
Stehle, P ;
Bone, HG .
CRITICAL CARE MEDICINE, 2002, 30 (09) :2032-2037