• 文献检索
  • 文档翻译
  • 深度研究
  • 学术资讯
  • Suppr Zotero 插件Zotero 插件
  • 邀请有礼
  • 套餐&价格
  • 历史记录
应用&插件
Suppr Zotero 插件Zotero 插件浏览器插件Mac 客户端Windows 客户端微信小程序
定价
高级版会员购买积分包购买API积分包
服务
文献检索文档翻译深度研究API 文档MCP 服务
关于我们
关于 Suppr公司介绍联系我们用户协议隐私条款
关注我们

Suppr 超能文献

核心技术专利:CN118964589B侵权必究
粤ICP备2023148730 号-1Suppr @ 2026

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验

肝移植患者再灌注时采集的血浆的体外负性肌力作用。

In vitro negative inotropic effect of plasma collected at the time of reperfusion in humans undergoing liver transplantation.

作者信息

Chemla D, Jayais P, Ecoffey C, Declere A D, Lecarpentier Y

机构信息

Département d'Anesthésiologie et de Physiologie Cardiorespiratoire, Université Paris Sud, Hôpital de Bicêtre, France.

出版信息

Anesthesiology. 1997 Aug;87(2):378-86. doi: 10.1097/00000542-199708000-00026.

DOI:10.1097/00000542-199708000-00026
PMID:9286903
Abstract

BACKGROUND

During orthotopic liver transplantation (OLT), acute depression of myocardial contractility has been suspected at the time of the graft reperfusion.

METHODS

The authors tested the hypothesis that plasma collected at the time of reperfusion in OLT patients exerted a negative inotropic effect on isolated rat myocardium. Plasma from 13 OLT patients was collected either before surgical incision (group 1, n = 8) or 3-5 min after vena cava and portal vein unclamping (group 2, n = 9). Six patients had their pre- and postincision plasma analyzed. A postreperfusion syndrome was observed in 3 of 13 patients. Left ventricular rat papillary muscles were studied at baseline (T0), 30 min after the addition of plasma (T30), and 60 min after the addition of plasma (T60). The authors recorded contraction parameters (maximum unloaded shortening velocity [Vmax], peak extent of systolic shortening at preload [deltaL], maximum active isometric tension [AFi], positive peak tension derivative [+dFi/dt], time-to-peak shortening [TPS], and time-to-peak force [TPF]) and relaxation parameters (maximum lengthening velocity at preload [VI], negative peak tension derivative [-dFi/dt], index of load sensitivity of relaxation [tRi]).

RESULTS

In group 1, contraction parameters remained unchanged, with the exception of a decreased Vmax at T30 and AFi at T60 (each P < 0.05). In group 2, all contraction parameters were significantly decreased at T30 and at T60, with the exception of AFi at T60. Both types of plasma decreased V1 and altered tRi at T30 and T60, whereas only reperfusion plasma decreased -dFi/dt at T30 and T60. At T30, deltaL, -dFi/dt, and tRi were significantly more impaired in group 2 than in group 1. There was no relationship between inotropic changes and mean arterial pressure decrease at the time of reperfusion.

CONCLUSION

Plasma collected at the time of graft reperfusion in OLT patients exerted negative effects on contraction and relaxation performance in isolated rat left ventricular papillary muscle.

摘要

背景

在原位肝移植(OLT)过程中,人们怀疑在移植物再灌注时心肌收缩力会急性下降。

方法

作者检验了以下假设,即OLT患者再灌注时采集的血浆对离体大鼠心肌具有负性变力作用。从13例OLT患者中采集血浆,其中8例在手术切口前采集(第1组),9例在腔静脉和门静脉夹闭后3 - 5分钟采集(第2组)。对6例患者的切口前后血浆进行了分析。13例患者中有3例观察到再灌注综合征。对大鼠左心室乳头肌在基线(T0)、添加血浆后30分钟(T30)和添加血浆后60分钟(T60)进行研究。作者记录了收缩参数(最大无负荷缩短速度[Vmax]、前负荷下收缩期缩短的峰值程度[δL]、最大主动等长张力[AFi]、正性峰值张力导数[+dFi/dt]、达到峰值缩短的时间[TPS]和达到峰值力的时间[TPF])以及舒张参数(前负荷下最大延长速度[VI]、负性峰值张力导数[-dFi/dt]、舒张负荷敏感性指数[tRi])。

结果

在第1组中,收缩参数保持不变,但T30时Vmax降低,T60时AFi降低(均P < 0.05)。在第2组中,除T60时的AFi外,所有收缩参数在T30和T60时均显著降低。两种血浆在T30和T60时均降低了VI并改变了tRi,而只有再灌注血浆在T30和T60时降低了 -dFi/dt。在T30时,第2组的δL、 -dFi/dt和tRi受损程度明显高于第1组。变力变化与再灌注时平均动脉压降低之间无相关性。

结论

OLT患者移植物再灌注时采集的血浆对离体大鼠左心室乳头肌的收缩和舒张性能产生负面影响。

相似文献

1
In vitro negative inotropic effect of plasma collected at the time of reperfusion in humans undergoing liver transplantation.肝移植患者再灌注时采集的血浆的体外负性肌力作用。
Anesthesiology. 1997 Aug;87(2):378-86. doi: 10.1097/00000542-199708000-00026.
2
Preconditioning prevents the negative inotropic action of phenylephrine in rat isolated stunned papillary muscle.
Gen Pharmacol. 1999 May;32(5):591-5. doi: 10.1016/s0306-3623(98)00278-x.
3
Preload does not affect relaxation rate in normal, hypoxic, or hypertrophic myocardium.
Am J Physiol. 1990 Jan;258(1 Pt 2):H191-7. doi: 10.1152/ajpheart.1990.258.1.H191.
4
Dependence of peak dP/dt and mean ejection rate on load and effect of inotropic agents on the relationship between peak dP/dt and left ventricular developed pressure--assessed in the isolated working rat heart and cardiac muscles.
Int J Cardiol. 1992 Jun;35(3):333-41. doi: 10.1016/0167-5273(92)90231-q.
5
Modulation of myocardial function by pyruvate.丙酮酸对心肌功能的调节作用。
Rev Port Cardiol. 2002 Apr;21(4):437-45.
6
4-Aminopyridine induces positive lusitropic effects and prevents the negative inotropic action of phenylephrine in the rat cardiac tissue subjected to ischaemia.4-氨基吡啶可诱导正性变力效应,并预防去氧肾上腺素对缺血大鼠心脏组织的负性变力作用。
J Physiol Pharmacol. 1999 Sep;50(3):381-9.
7
Effects of isoproterenol on myocardial relaxation rate: influence of the level of load.异丙肾上腺素对心肌舒张速率的影响:负荷水平的作用
Am J Physiol. 1993 Nov;265(5 Pt 2):H1645-53. doi: 10.1152/ajpheart.1993.265.5.H1645.
8
The effects of potassium channel modulators on the simulated ischaemia-induced changes in contractility and responsiveness to phenylephrine of rat-isolated papillary muscle.钾通道调节剂对模拟缺血诱导的大鼠离体乳头肌收缩性及对去氧肾上腺素反应性变化的影响。
Pharmacol Res. 1998 Sep;38(3):183-9. doi: 10.1006/phrs.1998.0351.
9
The influence of the neuropeptide galanin on the contractility and the effective refractory period of guinea-pig heart papillary muscle under normoxic and hypoxic conditions.神经肽甘丙肽在常氧和低氧条件下对豚鼠心脏乳头肌收缩性和有效不应期的影响。
J Pharm Pharmacol. 1998 Dec;50(12):1361-4. doi: 10.1111/j.2042-7158.1998.tb03360.x.
10
The influence of experimental hyperlipidemia on the time course of contractility during simulated ischaemia and reperfusion and responsiveness to phenylephrine of rat heart papillary muscle.实验性高脂血症对大鼠心脏乳头肌在模拟缺血和再灌注期间收缩力的时程以及对去氧肾上腺素反应性的影响。
J Physiol Pharmacol. 1998 Sep;49(3):353-65.

引用本文的文献

1
Donor hepatic function: a factor in postreperfusion syndrome.供体肝功能:再灌注综合征的一个因素。
J Gastrointest Surg. 2002 Mar-Apr;6(2):248-54. doi: 10.1016/s1091-255x(01)00065-8.