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Pogue, B. W.

Publications and source records attributed to Pogue, B. W..

2 recordsLinked to original sources

Lymphatic dynamics visualized by native transient hypoxia imaging in areas of tissue damage, edema and in sentinel lymph nodes.

Imaging lymphatic compartments and their function has always been challenging, yet this capability is key to understanding the dynamics of immune response and lymph dysfunction in disease states. This study reports the first ever visualization of murine lymphatic pumping and function imaged from the inherent transient hypoxia that occurs within the lymph ducts and nodes. The lymphatic system appears as one of the few naturally hypoxic areas in vivo. Hypoxia in lymphatics is detected via delayed fluorescence (DF) of endogenous protoporphyrin IX (PpIX), enabling real-time imaging. Lymph nodes and their function were localized by hypoxia transcutaneous imaging and in surgically exposed nodes, followed by correlation of localization to indocyanine green (ICG) local injection. The lymphatic pumping frequency was altered through progressive damage from mild, moderate, and severe wound injuries, and hypoxia appeared readily in the sentinel lymph nodes near tumor regions. Cyclical pumping was observed at sites of edema and in nodes near tumors. Control data from uninjured anesthetized mice showed little lymphatic contrast, whereas awake mice exhibited hypoxia localized to lymph nodes. Unlike contrast injection-based regional lymph node imaging by ICG or MRI, DF hypoxia imaging appears to provide a natural whole-body contrast mechanism, highlighting its potential for visualizing lymphatic function and associated hypoxia dynamics. The value for localization of sentinel lymph nodes and for allowing for visualization of damaged lymph has very practical potential applications.

bioengineering↗

Anesthetic oxygen use and sex are critical factors in the FLASH sparing effect

IntroductionUltra-high dose-rate (UHDR) radiation has been reported to spare normal tissue compared to conventional dose-rate (CDR) radiation. However, reproducibility of the FLASH effect remains challenging due to varying dose ranges, radiation beam structure, and in-vivo endpoints. A better understanding of these inconsistencies may shed light on the mechanism of FLASH sparing. Here, we evaluate whether sex and/or use of 100% oxygen as carrier gas during irradiation contribute to the variability of the FLASH effect. MethodsC57BL/6 mice (24 male, 24 female) were anesthetized using isoflurane mixed with either room air or 100% oxygen. Subsequently, the mice received 27 Gy of either 9 MeV electron UHDR or CDR to a 1.6 cm2 diameter area of the right leg skin using the Mobetron linear accelerator. The primary post-radiation endpoint was time to full thickness skin ulceration. In a separate cohort of mice (4 male, 4 female) skin oxygenation was measured using PdG4 Oxyphor under identical anesthesia conditions. ResultsIn the UHDR group, time to ulceration was significantly shorter in mice that received 100% oxygen compared to room air, and amongst them female mice ulcerated sooner compared to males. However, no significant difference was observed between male and female UHDR mice that received room air. Oxygen measurements showed significantly higher tissue oxygenation using 100% oxygen as the anesthesia carrier gas compared to room air, and female mice showed higher levels of tissue oxygenation compared to males under 100% oxygen. ConclusionThe FLASH sparing effect is significantly reduced using oxygen during anesthesia compared to room air. The FLASH sparing was significantly lower in female mice compared to males. Both tissue oxygenation and sex are likely sources of variability in UHDR studies. These results suggest an oxygen-based mechanism for FLASH, as well as a key role for sex in the FLASH skin sparing effect.

cancer biology↗