Abstract

Noninvasive imaging of the kidney vasculature in preclinical murine models is important for the assessment of renal development, studying diseases and evaluating new therapies but is challenging to achieve using existing imaging modalities. Photoacoustic imaging is a promising new technique that is particularly well suited to visualizing the vasculature and could provide an alternative to existing preclinical imaging methods for studying renal vascular anatomy and function. To investigate this, an all-optical Fabry-Perot-based photoacoustic scanner was used to image the abdominal region of mice. High-resolution three-dimensional, noninvasive, label-free photoacoustic images of the mouse kidney and renal vasculature were acquired in vivo. The scanner was also used to visualize and quantify differences in the vascular architecture of the kidney in vivo due to polycystic kidney disease. This study suggests that photoacoustic imaging could be utilized as a novel preclinical imaging tool for studying the biology of renal disease.

Highlights

  • The kidney is a highly vascular organ that receives over 10% of the cardiac output

  • Horizontal (x–y) and vertical (x–z) maximum intensity projections (MIPs) of the 3D image data set acquired for one position of the mouse are shown in Fig. 2, A and B, respectively

  • This image is shown as a horizontal projection in the same plane as the x–y MIP in Fig. 2A but viewed from the underside

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Summary

Introduction

The kidney is a highly vascular organ that receives over 10% of the cardiac output. Within the kidney there is a vast microvasculature consisting of the glomerular capillary network, peritubular capillaries, and vasa rectae, which are critical for blood filtration and electrolyte control. New insights into disease progression and therapeutic response may be possible through the use of in vivo imaging techniques, which can provide serial longitudinal three-dimensional (3D) information about the vasculature. Magnetic resonance imaging (MRI) [14], ultrasound [19], and high-resolution micro X-ray computed tomography (micro-CT) [10] have been used to study renal structure and function in mice. With these imaging modalities, the relatively low intrinsic contrast from the microvasculature often necessitates the use of exogenous contrast agents introducing additional procedural complexity. High-resolution micro-CT [24] requires high X-ray doses limiting the number of repeat measurements in longitudinal studies

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