Hillenbrand Hanns B, Becker Lewis C, Kharrazian Reza, Hu Kai, Rochitte Carlos E, Kim Raymond J, Chen Enn L, Ertl Georg, Hruban Ralph H, Lima João A C
Johns Hopkins University School of Medicine, Baltimore, MD 21287, USA.
Magn Reson Med. 2005 Apr;53(4):843-50. doi: 10.1002/mrm.20417.
Although (23)Na MRI has been shown to delineate acute myocardial infarction (MI), the time course of in vivo (23)Na MRI during infarct healing remains unknown. In this study (23)Na MRI was combined with contrast-enhanced (CE) (1)H MRI to noninvasively characterize infarct healing in vivo. Serial in vivo 3D (23)Na MRI and (1)H MRI were performed for up to 9 weeks postinfarction in 10 dogs. Radioactive microspheres were used to measure myocardial perfusion, and Hematoxylin-Eosin (H&E) and Masson's trichrome (MT) staining were used to assess interstitial cell infiltrate and collagen content. In vivo (23)Na MRI accurately delineated infarct size up to day 5 postinfarction in comparison with (1)H MRI (8.9% +/- 8.1% vs. 8.6% +/- 7.9% on day 1 postinfarction, P = NS; and 6.3% +/- 6.2% vs. 6.2% +/- 6.2% on days 4/5 postinfarction, P = NS). The in vivo (23)Na MRI signal intensity, expressed as the signal intensity ratio of infarcted tissue vs. noninfarcted tissue (MI/R) peaked on day 1 of infarction (2.04 +/- 0.23) but decreased significantly to 1.27 at 9 weeks postinfarction (P < 0.05) due to granulation tissue infiltrate and collagen deposition. To confirm the MI/R decrease during scar formation ex vivo, we performed (23)Na MRI in 12 rats on day 3 post-MI (N = 5) and after 6 weeks (N = 7). H&E and Picrosirius Red staining confirmed granulation tissue infiltrate on day 3 and scar formation after 6 weeks. MI/R decreased significantly from 1.91 +/- 0.45 on day 3 post-MI to 1.3 +/- 0.09 after 6 weeks. Thus, in vivo (23)Na MRI accurately delineates infarct size up to day 5 postinfarction. In vivo (23)Na MRI signal intensity decreases during infarct healing as a result of the underlying infarct healing process.
尽管已证实(23)Na磁共振成像(MRI)能够清晰显示急性心肌梗死(MI),但梗死愈合过程中活体(23)Na MRI的时间进程仍不清楚。在本研究中,将(23)Na MRI与对比增强(CE)(1)H MRI相结合,以在活体中对梗死愈合进行无创性特征描述。对10只犬在心肌梗死后长达9周的时间内进行了系列活体三维(23)Na MRI和(1)H MRI检查。使用放射性微球测量心肌灌注,并采用苏木精-伊红(H&E)染色和马松三色(MT)染色评估间质细胞浸润和胶原含量。与(1)H MRI相比,活体(23)Na MRI在心肌梗死后第5天之前能够准确描绘梗死大小(心肌梗死后第1天,8.9%±8.1%对8.6%±7.9%,P=无显著性差异;心肌梗死后第4/5天,6.3%±6.2%对6.2%±6.2%,P=无显著性差异)。活体(23)Na MRI信号强度,以梗死组织与非梗死组织的信号强度比(MI/R)表示,在梗死第1天达到峰值(2.04±0.23),但在心肌梗死后9周时显著下降至1.27(P<0.05),这是由于肉芽组织浸润和胶原沉积所致。为了在体外证实瘢痕形成过程中MI/R的降低,我们在心肌梗死后第3天(n=5)和6周后(n=7)对12只大鼠进行了(23)Na MRI检查。H&E染色和天狼星红苦味酸染色证实了第3天的肉芽组织浸润和6周后的瘢痕形成。MI/R从心肌梗死后第3天的1.91±0.45显著降低至6周后的1.3±0.09。因此,活体(23)Na MRI在心肌梗死后第5天之前能够准确描绘梗死大小。由于潜在的梗死愈合过程,活体(23)Na MRI信号强度在梗死愈合过程中降低。