Clinic for Horses, University of Veterinary Medicine Hannover, Hannover, Germany.
Institute for Physiology and Cell Biology, University of Veterinary Medicine Hannover, Hannover, Germany.
Equine Vet J. 2022 Mar;54(2):427-437. doi: 10.1111/evj.13450. Epub 2021 May 18.
Ischaemic postconditioning (IPoC) has been shown to ameliorate ischaemia reperfusion injury in different species and tissues.
To assess the feasibility of IPoC in equine small intestinal ischaemia and to assess its effect on histomorphology, electrophysiology and paracellular permeability.
Randomised in vivo experiment.
Experimental jejunal ischaemia was induced for 90 min in horses under general anaesthesia. In the control group (C; n = 7), the jejunum was reperfused without further intervention. In the postconditioning group (IPoC; n = 7), reocclusion was implemented following release of ischaemia by clamping the mesenteric vessels in three cycles of 30 seconds. This was followed by 120 minutes of reperfusion in both groups. Intestinal microperfusion and oxygenation was measured during IPoC using spectrophotometry and Doppler flowmetry. Histomorphology and histomorphometry of the intestinal mucosa were assessed. Furthermore, electrophysiological variables and unidirectional flux rates of H-mannitol were determined in Ussing chambers. Western blot analysis was performed to determine the tight junction protein levels of claudin-1, claudin-2 and occludin in the intestinal mucosa. Comparisons between the groups and time points were performed using a two-way repeated measures analysis of variance (ANOVA) or non-parametric statistical tests for the ordinal and not normally distributed data (significance P < .05).
IPoC significantly reduced intestinal microperfusion during all clamping cycles yet affected oxygen saturation only during the first cycle. After reperfusion, Group IPoC showed significantly less mucosal villus denudation (mean difference 21.5%, P = .02) and decreased mucosal-to-serosal flux rates (mean difference 15.2 nM/cm /h, P = .007) compared to Group C. There were no significant differences between the groups for the other tested variables.
Small sample size, long-term effects were not investigated.
Following IPoC, the intestinal mucosa demonstrated significantly less villus denudation and paracellular permeability compared to the untreated control group, possibly indicating a protective effect of IPoC on ischaemia reperfusion injury.
缺血后处理(IPoC)已被证明可改善不同物种和组织的缺血再灌注损伤。
评估 IPoC 在马小肠缺血中的可行性,并评估其对组织形态学、电生理学和细胞旁通透性的影响。
随机体内实验。
在全身麻醉下,对马进行实验性空肠缺血 90 分钟。在对照组(C;n=7)中,在不进行进一步干预的情况下再灌注空肠。在缺血后处理组(IPoC;n=7)中,在夹闭肠系膜血管的三个 30 秒循环后重新闭塞。两组均再灌注 120 分钟。使用分光光度法和多普勒血流仪在 IPoC 期间测量肠道微灌注和氧合。评估肠道黏膜的组织形态学和组织形态计量学。此外,在 Ussing 室中测定单向 H-甘露醇通量率和电生理学变量。进行 Western blot 分析以确定肠道黏膜中紧密连接蛋白 claudin-1、claudin-2 和 occludin 的水平。使用双向重复测量方差分析(ANOVA)或非参数统计检验(对于有序和非正态分布数据)对组间和时间点进行比较(显著性 P <.05)。
IPoC 在所有夹闭循环中均显著降低肠道微灌注,但仅在第一循环中影响氧饱和度。再灌注后,与 C 组相比,IPoC 组黏膜绒毛脱落明显减少(平均差异 21.5%,P =.02),黏膜-浆膜通量率降低(平均差异 15.2 nM/cm/h,P =.007)。组间其他测试变量无显著差异。
样本量小,未研究长期效果。
与未处理的对照组相比,IPoC 后肠道黏膜的绒毛脱落和细胞旁通透性明显减少,这可能表明 IPoC 对缺血再灌注损伤具有保护作用。