Division of Cardiology, Pulmonology and Vascular Medicine, Medical Faculty and University Hospital, Heinrich Heine University, 40225 Düsseldorf, Germany.
Cardiovascular Research Institute Düsseldorf (CARID), Medical Faculty, Heinrich Heine University, 40225 Düsseldorf, Germany.
Cells. 2024 Sep 30;13(19):1633. doi: 10.3390/cells13191633.
Determination of infarct and scar size following myocardial infarction (MI) is commonly used to evaluate the efficacy of potential cardioprotective treatments in animal models. However, histological methods to determine morphological features in the infarcted heart have barely improved since implementation while still consuming large parts of the tissue and offering little options for parallel analyses. We aim to develop a new fluorescence technology for determining infarct area and area at risk that is comparable to 2,3,5-triphenyltetrazolium chloride (TTC) staining but allows for multiple analyses on the same heart tissue. For early and late time points following MI, we compared classical histochemical approaches with fluorescence staining methods. Reperfused MI was induced in male mice, the hearts were extracted 24 h, 7-, 21-, or 28-days later and fluorescently stained by combining Hoechst and phalloidin. This approach allowed for clear visualization of the infarct area, the area at ischemic risk and the remote area not affected by MI. The combined fluorescence staining correlated with the classic TTC/Evans Blue staining 24 h after MI (r = 0.8334). In later phases (>7 d) post-MI, wheat germ agglutinin (WGA) is equally accurate as classical Sirius Red (r = 0.9752), Masson's (r = 0.9920) and Gomori's Trichrome (r = 0.8082) staining for determination of scar size. Additionally, feasibility to co-localize fluorescence-stained immune cells in specific regions of the infarcted myocardium was demonstrated with this protocol. In conclusion, this new procedure for determination of post-MI infarct size is not inferior to classical TTC staining, yet provides substantial benefits, including the option for unbiased software-assisted analysis while sparing ample residual tissue for additional analyses. Overall, this enhances the data quality and reduces the required animal numbers consistent with the 3R concept of animal experimentation.
确定心肌梗死(MI)后的梗塞和疤痕大小通常用于评估潜在的心脏保护治疗在动物模型中的疗效。然而,用于确定梗塞心脏形态特征的组织学方法自实施以来几乎没有改进,仍然消耗大量组织,并且几乎没有提供并行分析的选择。我们旨在开发一种新的荧光技术,用于确定梗塞面积和危险区面积,该技术可与 2,3,5-三苯基氯化四氮唑(TTC)染色相媲美,但允许在同一心脏组织上进行多次分析。对于 MI 后的早期和晚期时间点,我们将经典组织化学方法与荧光染色方法进行了比较。在雄性小鼠中诱导再灌注性 MI,在 24 小时、7 天、21 天或 28 天后提取心脏,并通过结合 Hoechst 和鬼笔环肽进行荧光染色。这种方法允许清晰地观察梗塞面积、缺血危险区和不受 MI 影响的远区。联合荧光染色与 MI 后 24 小时的经典 TTC/Evans Blue 染色相关性良好(r = 0.8334)。在 MI 后>7 天的后期阶段,小麦胚凝集素(WGA)与经典的 Sirius Red(r = 0.9752)、Masson's(r = 0.9920)和 Gomori's Trichrome(r = 0.8082)染色一样准确,用于确定疤痕大小。此外,通过该方案还证明了在梗塞心肌的特定区域中荧光染色免疫细胞的共定位的可行性。总之,这种用于确定 MI 后梗塞面积的新程序并不逊于经典的 TTC 染色,但具有实质性的优势,包括具有选择软件辅助分析的选项,同时节省了大量剩余组织以供进行额外分析。总体而言,这提高了数据质量,并根据动物实验的 3R 概念减少了所需的动物数量。