Literature DB >> 15514600

Superiority of early relative to late ischemic preconditioning in spinal cord protection after descending thoracic aortic occlusion.

Ioannis K Toumpoulis1, John C Papakostas, Miltiadis I Matsagas, Vassiliki D Malamou-Mitsi, Lina S Pappa, George E Drossos, Joseph J Derose, Constantine E Anagnostopoulos.   

Abstract

OBJECTIVE: We previously showed that ischemic preconditioning significantly reduced spinal cord injury caused by 35-minute aortic occlusion. In this study we investigated the effect of ischemic preconditioning on spinal cord injury after 45-minute aortic occlusion.
METHODS: Thirty-two pigs were divided as follows: group 1 (n = 6) underwent sham operation, group 2 (n = 6) underwent 20 minutes of aortic occlusion, group 3 (n = 6) underwent 45 minutes of occlusion, group 4 (n = 6) underwent 20 minutes of occlusion and 48 hours later underwent an additional 45 minutes, and group 5 (n = 8) underwent 20 minutes of occlusion and 80 minutes later underwent an additional 45 minutes. Aortic occlusion was accomplished with two balloon occlusion catheters placed fluoroscopically after the origin of the left subclavian artery and at the aortic bifurcation. Neurologic evaluation was by Tarlov score. The lower thoracic and lumbar spinal cords were harvested at 120 hours and examined histologically with hematoxylin-eosin staining. The number of neurons was counted, and the inflammation was scored (0-4). Statistical analysis was by Kruskal-Wallis and 1-way analysis of variance tests.
RESULTS: Group 5 (early ischemic preconditioning) had better Tarlov scores than group 3 ( P < .001) and group 4 (late ischemic preconditioning, P < .001). The histologic changes were proportional to the Tarlov scores, with the least histologic damage in the animals of group 5 relative to group 3 (number of neurons P < .001, inflammation P = .004) and group 4 (number of neurons P < .001, inflammation P = .006).
CONCLUSION: Early ischemic preconditioning is superior to late ischemic preconditioning in reducing spinal cord injury caused by the extreme ischemia of 45 minutes of descending thoracic aortic occlusion.

Entities:  

Mesh:

Year:  2004        PMID: 15514600     DOI: 10.1016/j.jtcvs.2004.06.031

Source DB:  PubMed          Journal:  J Thorac Cardiovasc Surg        ISSN: 0022-5223            Impact factor:   5.209


  3 in total

1.  Postconditioning, a series of brief interruptions of early reperfusion, prevents neurologic injury after spinal cord ischemia.

Authors:  Xiaojing Jiang; Enyi Shi; Yoshiki Nakajima; Shigehito Sato
Journal:  Ann Surg       Date:  2006-07       Impact factor: 12.969

2.  The selective poly(ADP)ribose-polymerase 1 inhibitor INO1001 reduces spinal cord injury during porcine aortic cross-clamping-induced ischemia/reperfusion injury.

Authors:  Christian Maier; Angelika Scheuerle; Balázs Hauser; Hubert Schelzig; Csaba Szabó; Peter Radermacher; Jochen Kick
Journal:  Intensive Care Med       Date:  2007-03-15       Impact factor: 17.440

3.  Effects of D‑Ala2, D‑Leu5‑Enkephalin pre‑ and post‑conditioning in a rabbit model of spinal cord ischemia and reperfusion injury.

Authors:  Danyun Fu; Haitong Liu; Hua Liu; Junyan Yao
Journal:  Mol Med Rep       Date:  2019-10-07       Impact factor: 2.952

  3 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.