Tumour necrosis factor-α, but not septic plasma depresses cardiac myofilament contraction

被引:11
作者
Gu, M
Bose, R
Bose, D
Yang, J
Li, X
Light, RB
Jacobs, H
Mink, SN
机构
[1] Univ Manitoba, Dept Med, Winnipeg, MB, Canada
[2] Univ Manitoba, Dept Anesthesiol, Winnipeg, MB, Canada
[3] Univ Manitoba, Dept Pharmacol & Therapeut, Winnipeg, MB, Canada
[4] Univ Manitoba, Dept Biochem & Mol Biol, Winnipeg, MB, Canada
来源
CANADIAN JOURNAL OF ANAESTHESIA-JOURNAL CANADIEN D ANESTHESIE | 1998年 / 45卷 / 04期
关键词
D O I
10.1007/BF03012028
中图分类号
R614 [麻醉学];
学科分类号
100217 ;
摘要
Purpose: In sepsis, myocardial depression may be caused by mediators released as part of the inflammatory reaction. Tumour necrosis factor alpha (TNF-alpha) is one mediator that may contribute to this depression. In the present study we contrasted the effects of TNF-alpha and septic plasma fraction (SP) obtained from an E. coli model on contractile tension in intact and skinned canine ventricular trabecular (VT) preparations. The objectives were to determine whether SP or TNF-alpha could impair contractile tension at the level of the myofilaments, and to determine the extent to which TNF-alpha may account for myocardial depression found in E. coli sepsis. Methods: Measurements of isometric tensions were made after TNF-alpha and SP (10,000 to 30,000 MW fraction) were added to respective intact or skinned canine VT preparations. In the skinned preparation, trabeculae were chemically skinned with Triton X-100. Results: Septic plasma caused a decrease in contraction in the intact preparation compared with preseptic plasma(50 +/- 7 vs 33 +/- 7%, P < 0.05), but had no effect in the skinned preparation. On the other hand, TNF-alpha (30 ng . ml(-1)) caused an approximately 50% reduction in tension (29 +/- 2 mg vs 16 +/-: 5 mg) in the skinned preparation (P < 0.05), but had no effect in the intact preparation. Conclusion: These results suggest that TNF-alpha and SP act through different mechanisms. While SP requires an intact membrane, TNF-alpha impairs function by a direct effect on the myofilaments.
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页码:352 / 359
页数:8
相关论文
共 36 条
[1]  
ADAMSON GM, 1994, J PHARMACOL EXP THER, V269, P367
[2]  
BEUTLER B, 1987, NEW ENGL J MED, V316, P379
[3]  
BEUTLER BA, 1985, J IMMUNOL, V135, P3972
[4]   INJECTION OF GUANOSINE 5'-CYCLIC MONOPHOSPHATE INTO HEART-CELLS BLOCKS CALCIUM SLOW CHANNELS [J].
BKAILY, G ;
SPERELAKIS, N .
AMERICAN JOURNAL OF PHYSIOLOGY, 1985, 248 (05) :H745-H749
[5]   NITRIC-OXIDE PRODUCTION WITHIN CARDIAC MYOCYTES REDUCES THEIR CONTRACTILITY IN ENDOTOXEMIA [J].
BRADY, AJB ;
POOLEWILSON, PA ;
HARDING, SE ;
WARREN, JB .
AMERICAN JOURNAL OF PHYSIOLOGY, 1992, 263 (06) :H1963-H1966
[6]   FURTHER CHARACTERIZATION OF A MYOCARDIAL DEPRESSANT FACTOR PRESENT IN HEMORRHAGIC SHOCK [J].
BRAND, ED ;
COWGILL, R ;
LEFER, AM .
JOURNAL OF TRAUMA, 1969, 9 (03) :216-&
[7]  
CUNNION RE, 1989, CRIT CARE CLIN, V5, P99
[8]   THE PROINFLAMMATORY CYTOKINES INTERLEUKIN-1 AND TUMOR-NECROSIS-FACTOR AND TREATMENT OF THE SEPTIC SHOCK SYNDROME [J].
DINARELLO, CA .
JOURNAL OF INFECTIOUS DISEASES, 1991, 163 (06) :1177-1184
[9]  
DRAPIER JC, 1988, J IMMUNOL, V140, P2829
[10]   TUMOR-NECROSIS-FACTOR CHALLENGES IN CANINES - PATTERNS OF CARDIOVASCULAR DYSFUNCTION [J].
EICHENHOLZ, PW ;
EICHACKER, PQ ;
HOFFMAN, WD ;
BANKS, SM ;
PARRILLO, JE ;
DANNER, RL ;
NATANSON, C .
AMERICAN JOURNAL OF PHYSIOLOGY, 1992, 263 (03) :H668-H675