ACUTE EFFECTS OF TUMOR-NECROSIS-FACTOR ON THE MICROCIRCULATION IN RAT CREMASTER MUSCLE

被引:52
作者
VICAUT, E
HOU, X
PAYEN, D
BOUSSEAU, A
TEDGUI, A
机构
[1] HOP LARIBOISIERE, INSERM, U141, F-75475 PARIS 10, FRANCE
[2] HOP LARIBOISIERE, DEPT ANESTHESIE, F-75475 PARIS 10, FRANCE
[3] RHONE POULENC SANTE, CTR RECH, Vitry Sur Seine, FRANCE
关键词
TUMOR NECROSIS FACTOR; SEPSIS; MICROCIRCULATION;
D O I
10.1172/JCI115165
中图分类号
R-3 [医学研究方法]; R3 [基础医学];
学科分类号
1001 ;
摘要
The acute effects of TNF on the microcirculation were studied by in vivo microscopy in rat cremaster muscle. The changes in arteriolar diameter after topical administration of recombinant TNF (rTNF; 10(-4)-10(4) ng/ml) were studied in second-, third-, and fourth-order arterioles (A2-A4) whose mean diameters under control conditions were 64.3, 30.7, and 14.8-mu-m, respectively. rTNF induced a concentration-dependent vasodilation whose amplitude was largest for the smallest arterioles. At the highest concentration tested, arteriolar diameter increased by 21, 29, and 41% of control diameter for the A2, A3, and A4 arterioles, respectively. Indomethacin or mefenamic acid, two structurally different prostaglandin synthesis inhibitors, markedly inhibited the degree of vasodilation induced by rTNF in the three arteriolar orders. As regards the effect of rTNF on vasoconstriction in response to norepinephrine, vasoconstriction was greatest for the smallest arterioles, and did not change 10 min after rTNF administration for any of the three arteriolar orders. We conclude that (a) rTNF has a direct vasodilatory effect which is greatest in the smallest arterioles, (b) this vasodilation is at least partly mediated by prostaglandins, and (c) administration of rTNF in itself does not acutely alter the response of the arterioles to vasopressive drugs.
引用
收藏
页码:1537 / 1540
页数:4
相关论文
共 28 条
[1]  
[Anonymous], 1971, STAT PRINCIPLES EXPT
[2]   OPEN CREMASTER MUSCLE PREPARATION FOR STUDY OF BLOOD-VESSELS BY IN-VIVO MICROSCOPY [J].
BAEZ, S .
MICROVASCULAR RESEARCH, 1973, 5 (03) :384-394
[3]   TUMOR-NECROSIS-FACTOR MEDIATES ENDOTOXIC EFFECTS IN MICE [J].
BAUSS, F ;
DROGE, W ;
MANNEL, DN .
INFECTION AND IMMUNITY, 1987, 55 (07) :1622-1625
[4]   PASSIVE-IMMUNIZATION AGAINST CACHECTIN TUMOR NECROSIS FACTOR PROTECTS MICE FROM LETHAL EFFECT OF ENDOTOXIN [J].
BEUTLER, B ;
MILSARK, IW ;
CERAMI, AC .
SCIENCE, 1985, 229 (4716) :869-871
[5]  
BEUTLER BA, 1985, J IMMUNOL, V135, P3972
[6]  
CRYER HM, 1987, ARCH SURG-CHICAGO, V122, P86
[7]   ROLE OF MUSCLE MICROVASCULATURE DURING HYPERDYNAMIC AND HYPODYNAMIC PHASES OF ENDOTOXIN-SHOCK IN DECEREBRATE RATS [J].
CRYER, HM ;
GARRISON, RN ;
HARRIS, PD .
JOURNAL OF TRAUMA-INJURY INFECTION AND CRITICAL CARE, 1988, 28 (03) :312-318
[8]   THE EFFECTS OF TUMOR NECROSIS FACTOR AND THEIR SELECTIVE-INHIBITION BY IBUPROFEN [J].
EVANS, DA ;
JACOBS, DO ;
REVHAUG, A ;
WILMORE, DW .
ANNALS OF SURGERY, 1989, 209 (03) :312-321
[9]  
FLETCHER JR, 1982, SCAND J INFECT DIS, P55
[10]   TUMOR-NECROSIS-FACTOR TYPE-ALPHA, A POTENT INHIBITOR OF ENDOTHELIAL-CELL GROWTH-INVITRO, IS ANGIOGENIC INVIVO [J].
FRATERSCHRODER, M ;
RISAU, W ;
HALLMANN, R ;
GAUTSCHI, P ;
BOHLEN, P .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1987, 84 (15) :5277-5281