Regional and temporal changes in cardiovascular responses to norepinephrine and vasopressin during continuous infusion of lipopolysaccharide in conscious rats

被引:18
作者
Bennett, T
Mahajan, RP
March, JE
Kemp, PA
Gardiner, SM [1 ]
机构
[1] Univ Nottingham, Queens Med Ctr, Sch Med & Surg Sci, Nottingham NG7 2UH, England
[2] Univ Nottingham, Queens Med Ctr, Ctr Integrated Syst Biol & Med, Sch Biomed Sci, Nottingham NG7 2UH, England
关键词
blood; regional haemodynamics; complications; endotoxaemia; model; rat; sympathetic nervous system; norepinephrine; ornithine-8-vasopressin;
D O I
10.1093/bja/aeh214
中图分类号
R614 [麻醉学];
学科分类号
100217 ;
摘要
Background. Reduced pressor responsiveness to norepinephrine (NE) in sepsis is well documented but the associated regional haemodynamic changes are less well characterized, and there are varying reports of changes in haemodynamic responses to arginine vasopressin (AVP). We compared changes in regional haemodynamic responsiveness to AVP and NE during a 24 h continuous infusion of lipopolysaccharide (LPS) in conscious rats. Methods. Conscious, male Sprague-Dawley rats were infused with saline (0.4 ml h(-1)) or LPS (150 mug kg(-1) h(-1)). Renal, mesenteric, and hindquarter haemodynamic responses to 3 min infusions of AVP (0.25, 0.625, and 1.25 ng kg(-1) min(-1)) or NE (75, 250, and 750 ng kg(-1) min(-1)) were assessed 2, 6, and 24 h after the onset of LPS or saline. Results. Two and six hours after the onset of LPS, all haemodynamic effects of NE were markedly reduced, but by 24 h, there was some recovery in the vasoconstrictor actions of NE although the pressor and bradycardic effects were still depressed. Two hours after the onset of LPS, the cardiovascular effects of AVP were depressed but there was some recovery in vascular responsiveness at 6 h. By 24 h, only the mesenteric vasoconstrictor effect of AVP was consistently reduced. Conclusions. During low dose LPS infusion, there are differential changes in haemodynamic responsiveness to AVP and NE, which show different temporal and regional profiles of recovery with time. Furthermore, reduced pressor responsiveness to NE is not necessarily accompanied by a reduced capacity of vessels for vasoconstriction.
引用
收藏
页码:400 / 407
页数:8
相关论文
共 33 条
[11]   ENDOGENOUS VASOPRESSIN AND BAROREFLEX MECHANISMS [J].
GARDINER, SM ;
BENNETT, T .
BRAIN RESEARCH REVIEWS, 1986, 11 (04) :317-334
[12]   Temporal differences between the involvement of angiotensin II and endothelin in the cardiovascular responses to endotoxaemia in conscious rats [J].
Gardiner, SM ;
Kemp, PA ;
March, JE ;
Bennett, T .
BRITISH JOURNAL OF PHARMACOLOGY, 1996, 119 (08) :1619-1627
[13]   CARDIAC AND REGIONAL HEMODYNAMICS, INDUCIBLE NITRIC-OXIDE SYNTHASE (NOS) ACTIVITY, AND THE EFFECTS OF NOS INHIBITORS IN CONSCIOUS, ENDOTOXAEMIC RATS [J].
GARDINER, SM ;
KEMP, PA ;
MARCH, JE ;
BENNETT, T .
BRITISH JOURNAL OF PHARMACOLOGY, 1995, 116 (03) :2005-2016
[14]   Vasopressin vs. norepinephrine in endotoxic shock: systemic, renal, and splanchnic hemodynamic and oxygen transport effects [J].
Guzman, JA ;
Rosado, AE ;
Kruse, JA .
JOURNAL OF APPLIED PHYSIOLOGY, 2003, 95 (02) :803-809
[15]   Physiology of vasopressin relevant to management of septic shock [J].
Holmes, CL ;
Patel, BM ;
Russell, JA ;
Walley, KR .
CHEST, 2001, 120 (03) :989-1002
[16]   High-dose vasopressin is not superior to norepinephrine in septic shock [J].
Klinzing, S ;
Simon, M ;
Reinhart, K ;
Bredle, DL ;
Meier-Hellmann, A .
CRITICAL CARE MEDICINE, 2003, 31 (11) :2646-2650
[17]  
Landry DW, 1997, CIRCULATION, V95, P1122
[18]   Mechanisms of disease: The pathogenesis of vasodilatory shock [J].
Landry, DW ;
Oliver, JA .
NEW ENGLAND JOURNAL OF MEDICINE, 2001, 345 (08) :588-595
[19]   Vasopressin pressor hypersensitivity in vasodilatory septic shock [J].
Landy, DW ;
Levin, HR ;
Gallant, EM ;
Seo, S ;
DAlessandro, D ;
Oz, MC ;
Oliver, JA .
CRITICAL CARE MEDICINE, 1997, 25 (08) :1279-1282
[20]  
MARCH JE, P BRIT PHARM SOC