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J Exp Med. 1965 Dec 1;122(6):1063-73. doi: 10.1084/jem.122.6.1063.
2
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6
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Prevention of the toxicity of erythromycin estolate in the perfused rat liver by endotoxin.内毒素对灌注大鼠肝脏中依托红霉素毒性的预防作用。
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Antimicrob Agents Chemother. 2008 Mar;52(3):1046-51. doi: 10.1128/AAC.01210-07. Epub 2007 Dec 26.
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Essential role for estrogen in protection against Vibrio vulnificus-induced endotoxic shock.雌激素在预防创伤弧菌诱导的内毒素休克中起关键作用。
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3
Effect of a bacterial lipopolysaccharide on biliary excretion of a beta-lactam antibiotic, cefoperazone, in rats.一种细菌脂多糖对大鼠体内β-内酰胺类抗生素头孢哌酮胆汁排泄的影响。
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Jpn J Surg. 1984 Jan;14(1):52-60. doi: 10.1007/BF02469604.
5
Hepatic circulation: potential for therapeutic intervention.肝循环:治疗干预的潜力。
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本文引用的文献

1
The dominant role of the liver in plasma protein synthesis; a direct study of the isolated perfused rat liver with the aid of lysine-epsilon-C14.肝脏在血浆蛋白合成中的主导作用;借助赖氨酸-ε-C14对离体灌注大鼠肝脏进行的直接研究。
J Exp Med. 1951 Nov;94(5):431-53. doi: 10.1084/jem.94.5.431.
2
VASOACTIVE MEDIATORS AS THE "TRIGGER MECHANISM" OF ENDOTOXIN SHOCK.血管活性介质作为内毒素休克的“触发机制” 。
J Clin Invest. 1964 May;43(5):1000-13. doi: 10.1172/JCI104963.
3
EFFECT OF SEROTONIN ON GLYCOGEN METABOLISM IN ISOLATED RAT LIVER.血清素对离体大鼠肝脏糖原代谢的影响。
J Clin Invest. 1964 May;43(5):797-809. doi: 10.1172/JCI104966.
4
BEHAVIOR OF MICROORGANISMS AND ENDOTOXIN PERFUSED THROUGH THE ISOLATED RAT LIVER.通过离体大鼠肝脏灌注的微生物和内毒素的行为
Proc Soc Exp Biol Med. 1964 Jan;115:222-5. doi: 10.3181/00379727-115-28875.
5
INFLUENCE OF ROUTE OF ADMINISTRATION ON HEMODYNAMIC EFFECTS OF ENDOTOXIN.给药途径对内毒素血流动力学效应的影响
Am J Physiol. 1963 Oct;205:799-802. doi: 10.1152/ajplegacy.1963.205.4.799.
6
Effect of endotoxin on simultaneously determined cardiac output and hepatic blood flow in rabbits.内毒素对兔心输出量和肝血流量同步测定的影响。
J Lab Clin Med. 1963 Mar;61:483-93.
7
Vascular changes associated with development of irreversible endotoxin shock.与不可逆性内毒素休克发展相关的血管变化。
Am J Physiol. 1962 Jan;202:103-10. doi: 10.1152/ajplegacy.1962.202.1.103.
8
Serotonin release by bacterial endotoxin.细菌内毒素释放血清素。
Proc Soc Exp Biol Med. 1961 Dec;108:774-6. doi: 10.3181/00379727-108-27063.
9
Mechanisms of the hemodynamic effects of endotoxin.内毒素血流动力学效应的机制。
Physiol Rev. 1960 Apr;40:245-79. doi: 10.1152/physrev.1960.40.2.245.
10
Species differences in effect of gram-negative endotoxin on circulation.革兰氏阴性内毒素对循环系统作用的种属差异。
Am J Physiol. 1961 Jun;200:1197-202. doi: 10.1152/ajplegacy.1961.200.6.1197.

大鼠离体肝脏的血管反应。I. 内毒素的直接作用。

Vascular response in the isolated rat liver. I. Endotoxin, direct effects.

作者信息

Nolan J P, O'Connell C J

出版信息

J Exp Med. 1965 Dec 1;122(6):1063-73. doi: 10.1084/jem.122.6.1063.

DOI:10.1084/jem.122.6.1063
PMID:5334541
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC2138104/
Abstract

Sublethal doses of E. coli endotoxin were shown to cause direct slowing of blood flow in the isolated perfused rat liver. Concentrations as low as SO ng per ml elicited this vasoconstrictive response. The decrease in flow after the initial lipopolysaccharide injection was immediate and lasted from. 5 to 15 minutes before recovering to baseline values. Succeeding injections of the same concentration, however, had little or no circulatory effects, and this tachyphylaxis persisted through 5 hours of perfusion. The replacement of the perfusate with fresh whole blood after several hours partially restored the ability of the hepatic vasculature to respond to the lipopolysaccharide. However, the presence of plasma or formed blood elements was not essential to the response, as brisk decreases occurred after endotoxin when a modified Ringer's solution was the sole perfusate. Catecholamines or serotonin did not appear to be key mediators in the primary vascular effect of endotoxin as phentolamine and methysergide administration did not appreciably modify the response. On the other hand, hydrocortisone when given in large doses with the endotoxin or in smaller doses 15 to 45 minutes prior to the lipopolysaccharide completely blocked vasoconstriction. The isolated preparation seems to be an excellent model for the study of direct circulatory effects of various substances in the liver.

摘要

已表明,亚致死剂量的大肠杆菌内毒素可导致离体灌注大鼠肝脏的血流直接减缓。低至每毫升50纳克的浓度即可引发这种血管收缩反应。初次注射脂多糖后血流立即减少,持续0.5至15分钟,然后恢复到基线值。然而,后续注射相同浓度的脂多糖几乎没有或没有循环效应,这种快速耐受性在5小时的灌注过程中持续存在。数小时后用新鲜全血替换灌注液可部分恢复肝血管系统对脂多糖的反应能力。然而,血浆或血液有形成分的存在对该反应并非必不可少,因为当改良林格氏液作为唯一灌注液时,内毒素注射后血流会迅速减少。儿茶酚胺或5-羟色胺似乎不是内毒素主要血管效应的关键介质,因为给予酚妥拉明和麦角新碱并未明显改变该反应。另一方面,在内毒素注射时大剂量给予氢化可的松或在内毒素注射前15至45分钟小剂量给予氢化可的松可完全阻断血管收缩。离体标本似乎是研究各种物质在肝脏中的直接循环效应的极佳模型。