| Literature DB >> 34045095 |
Wei Zhang1, Matthew R Lowerison2, Zhijie Dong2, Rita J Miller2, Krista A Keller3, Pengfei Song4.
Abstract
Ultrasound localization microscopy can image microvasculature in vivo without sacrificing imaging penetration depth. However, the reliance on super-resolution inference limits the applicability of the technique because subpixel tissue motion can corrupt microvascular reconstruction. Consequently, the majority of previous pre-clinical research on this super-resolution procedure has been restricted to low-motion experimental models with ample motion correction or data rejection, which precludes the imaging of organ sites that exhibit a high degree of respiratory and other motion. In this article, we present a novel anesthesia protocol in rabbits that induces safe, controllable periods of apnea to enable the long image-acquisition times required for ultrasound localization microscopy. We apply this protocol to a VX2 liver tumor model undergoing sorafenib therapy and compare the results to super-resolution images from conventional high-dose isoflurane anesthesia. We find that the apneic protocol was necessary to correctly identify the poorly vascularized tumor cores, as verified by immunohistochemistry, and to reveal the tumoral microvascular architecture.Entities:
Keywords: Animal model; Cancer; Contrast agents; Liver; Microbubbles; Microvessels; Rabbit; Super-resolution; Ultrasound localization microscopy; VX2
Mesh:
Year: 2021 PMID: 34045095 PMCID: PMC8278629 DOI: 10.1016/j.ultrasmedbio.2021.04.012
Source DB: PubMed Journal: Ultrasound Med Biol ISSN: 0301-5629 Impact factor: 3.694