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在一种新型血脂异常大鼠模型中,使用[铟]铟 - DANBIRT通过LFA - 1的SPECT/CT成像识别炎症性动脉粥样硬化斑块。

Inflammatory atherosclerotic plaque identification by SPECT/CT imaging of LFA-1 using [In] In-DANBIRT in a novel dyslipidemic rat model.

作者信息

Liu Zeyu, Daniels Tamara, Campen Matthew J, Alvidrez Roberto Ivan Mota

机构信息

Trauma and Transfusion Medicine Research Center, Department of Surgery, University of Pittsburgh Medical Center, Pittsburgh, PA, 15213, USA.

Department of Radiopharmaceutical Sciences, University of New Mexico College of Pharmacy, Albuquerque, NM, 87131, USA.

出版信息

Ann Nucl Med. 2023 Nov;37(11):635-643. doi: 10.1007/s12149-023-01868-3. Epub 2023 Sep 24.

Abstract

INTRODUCTION

Atherosclerosis is prevalent globally, closely associated with dyslipidemia and other metabolic dysfunction. Early diagnosis of atherosclerosis is challenging due to limited diagnostic capabilities that need to be expanded with animal models with enhanced vascular biology like rats. Our previous research showed [111In] In-DANBIRT has potential as a diagnostic tool for detecting atherosclerosis in mice. The primary aim of the present study is to evaluate [111In] In-DANBIRT in a novel atherosclerotic rat with early- and late-stage atherosclerosis and metabolic disease.

METHODS

We characterized metabolic and body composition differences in these novel dyslipidemic rats under different diets using serum chemistry and dual-energy X-ray absorptiometry (DEXA) scan, respectively. We performed 1-h post-injection in vivo molecular imaging of ApoE knockout, lean Zucker (LZ) male rats at baseline and followed them into 10 weeks of either normal or high-fat/cholesterol diet implementation (22 weeks of age).

RESULTS

We identified significant differences in body composition and metabolic changes in ApoE knockout rats compared to ApoE wildtype rats. Our findings indicate an increased uptake of [111In] In-DANBIRT in ApoE knockout, lean Zucker (LZ) rats, particularly in the descending aorta, a location where early-stage atherosclerosis is commonly found. Our findings, however, also revealed that the ApoE knockout, Zucker diabetic fatty (ZDF) model has high mortality rate, which may be attributed to alterations of critical enzymes involved in regulating metabolism and liver function.

CONCLUSION

Our results are highly encouraging as they demonstrated the potential of [111In] In-DANBIRT to detect early-stage atherosclerosis in rats that might otherwise go unnoticed by other methods, showcasing the high sensitivity of [111In] In-DANBIRT. Our future studies will aim to establish a viable T2D atherosclerosis model in rats with more advanced stages of the disease to further demonstrate the reliability of [111In] In-DANBIRT as a diagnostic tool for patients in all stages of atherosclerosis.

摘要

引言

动脉粥样硬化在全球范围内普遍存在,与血脂异常及其他代谢功能障碍密切相关。由于诊断能力有限,动脉粥样硬化的早期诊断具有挑战性,需要借助具有增强血管生物学特性的动物模型(如大鼠)来拓展诊断方法。我们之前的研究表明,[111In]In-DANBIRT有潜力作为检测小鼠动脉粥样硬化的诊断工具。本研究的主要目的是在一种患有早期和晚期动脉粥样硬化及代谢疾病的新型动脉粥样硬化大鼠中评估[111In]In-DANBIRT。

方法

我们分别使用血清化学检测和双能X射线吸收法(DEXA)扫描,对这些新型血脂异常大鼠在不同饮食条件下的代谢和身体成分差异进行了表征。我们在注射后1小时对载脂蛋白E基因敲除的瘦型 Zucker(LZ)雄性大鼠进行了体内分子成像,记录其基线情况,并在随后的10周内给予正常饮食或高脂/高胆固醇饮食(22周龄)。

结果

我们发现,与载脂蛋白E野生型大鼠相比,载脂蛋白E基因敲除大鼠在身体成分和代谢变化方面存在显著差异。我们的研究结果表明,[111In]In-DANBIRT在载脂蛋白E基因敲除的瘦型 Zucker(LZ)大鼠中的摄取增加,尤其是在降主动脉,这是早期动脉粥样硬化常见的部位。然而,我们的研究结果还显示,载脂蛋白E基因敲除的 Zucker 糖尿病脂肪(ZDF)模型死亡率很高,这可能归因于参与调节代谢和肝功能的关键酶的改变。

结论

我们的结果非常令人鼓舞,因为它们证明了[111In]In-DANBIRT在检测大鼠早期动脉粥样硬化方面的潜力,而这些早期病变可能会被其他方法忽视,这展示了[111In]In-DANBIRT的高灵敏度。我们未来的研究旨在建立一种患有更晚期疾病的大鼠2型糖尿病动脉粥样硬化模型,以进一步证明[111In]In-DANBIRT作为动脉粥样硬化各阶段患者诊断工具的可靠性。

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