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Ischaemic preconditioning improves microvascular perfusion and oxygenation following reperfusion injury of the intestine

✍ Scribed by I. H. Mallick; W. Yang; M. C. Winslet; A. M. Seifalian


Book ID
101747284
Publisher
John Wiley and Sons
Year
2005
Tongue
English
Weight
341 KB
Volume
92
Category
Article
ISSN
0007-1323

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✦ Synopsis


Abstract

Background

Ischaemia–reperfusion (IR) injury of the intestine occurs commonly during abdominal surgery. Ischaemic preconditioning (IPC) provides a way of protecting the organ from damage inflicted by IR. This study was designed to evaluate the beneficial effect of IPC, focusing on the intestinal microcirculation and oxygenation in intestinal IR injury.

Methods

Rats were allocated to three groups. Animals in the IR and IPC groups underwent 30 min of intestinal ischaemia followed by 2 h of reperfusion. In the IPC group this was preceded by 10 min of ischaemia and 10 min of reperfusion. Animals in the third group underwent laparotomy but no vascular occlusion. Intestinal microvascular perfusion, oxygenation and portal venous blood flow (PVF) were monitored continuously. At the end of the reperfusion period, blood samples were obtained for measurement of lactate dehydrogenase (LDH) and biopsies of ileum for histological evaluation.

Results

IPC improved intestinal microvascular perfusion and tissue oxygenation significantly at the end of the reperfusion period (P < 0·001). PVF improved significantly in the IPC compared with the IR group (P = 0·005). The serum LDH concentration was significantly lower in the IPC than the IR group (mean(s.e.m.) 667·1(86·8) versus 1973·8(306·5) U/l; P < 0·001) Histological examination showed that ileal mucosa was significantly less injured in the IPC group.

Conclusions

This study demonstrated that IPC improves intestinal microvascular perfusion and oxygenation.


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## Abstract This work was performed to elucidate further the main cellular events underlying the protective effect of ischaemic preconditioning in an __in vivo__ rat liver model of 90 min ischaemia followed by 30 min reperfusion. A significant attenuation of the various aspects of post‐ischaemic in