Epidural Analgesia Prevents Endotoxin-Induced Gut Mucosal Injury in Rabbits
Epidural Analgesia Prevents Endotoxin-Induced Gut Mucosal Injury in Rabbits
复制标题
硬膜外镇痛可预防兔子内毒素引起的肠道粘膜损伤
DOI:
10.1213/01.ane.0000153863.95598.08
复制
发表时间:
2005
影响因子:
5.7
通讯作者:
J. Takeda
中科院分区:
文献类型:
--
作者:
Shizuko Kosugi;H. Morisaki;T. Satoh;K. Ai;Michiko Yamamoto;J. Soejima;R. Serita;Y. Kotake;A. Ishizaka;J. Takeda
In the present study, we evaluated the effect of epidural analgesia on the alterations of gut barrier function elicited by endotoxin in rabbits. After the placement of an epidural catheter, 28 male rabbits were randomized into either 0.5% lidocaine (group E) or saline (group C) group. The solutions (0.4 mL/kg) were epidurally injected, followed by continuous infusion (0.1 mL · kg−1 · h−1) throughout the study period. Under a continuous infusion of lipopolysaccharide (15 &mgr;g · kg−1 · h−1), mean arterial blood pressure, intramucosal pH, and plasma thrombomodulin concentrations were measured. At 4 h, mean arterial blood pressure was lower (P < 0.05), intramucosal pH was higher (P < 0.01), and the progression of hemodilution more profound (P < 0.05) in group E versus group C, whereas plasma thrombomodulin levels were increased to a similar extent between the groups. With less wet-to-dry weight ratio of ileum, histopathological injury scores of gut mucosa were significantly less in group E versus group C (P < 0.01). In a separate series of experiments (n = 10 each group), mucosal permeability in group E was significantly less compared with group C (P < 0.05). Collectively, these studies showed that despite a significant decrease of perfusion pressure and arterial oxygen content, epidural analgesia minimized endotoxin-induced functional and structural injury of gut mucosa possibly through endothelium-independent mechanisms.
DOI:
10.1001/archsurg.1989.01410060065013
发表时间:
1989
期刊:
Archives of surgery (Chicago, Ill. : 1960)
影响因子:
--
作者:
Deitch,EA
通讯作者:
Deitch,EA
影响因子:
2.2
作者:
Wang, WY;Smail, N;Chaudry, IH
通讯作者:
Chaudry, IH
影响因子:
2.2
作者:
Kajikawa,O;Goodman,RB;Johnson2nd,MC;Konishi,K;Martin,TR
通讯作者:
Martin,TR