A scanning phosphorescence quenching microscopy technique, designed to prevent accumulated O(2) consumption by the method, was applied to Po(2) measurements in mesenteric tissue. In an attempt to further increase the accuracy of the measurements, albumin-bound probe was topically applied to the tissue and an objective-mounted pressurized bag was used to reduce the oxygen transport bypass through the thin layer of fluid over the mesentery. Po(2) was measured at multiple sites perpendicular to the blood/wall interface in the vicinity of 84 mesenteric arterioles (7-39 microm in diameter) at distances of 5, 15, 30, 60, 120, and 180 microm in seven anesthetized Sprague-Dawley rats, thereby creating Po(2) profiles. Interstitial Po(2) above and immediately beside arterioles was found to agree with known intravascular values. No significant difference in Po(2) profiles was found between small and large arterioles, indicating a small longitudinal Po(2) gradient in the precapillary mesenteric microvasculature. In addition, the Po(2) profiles were used to calculate oxygen consumption in the mesenteric tissue (56-65 nl O(2) x cm(-3) x s(-1)). Correction of these values for contamination with ambient oxygen yielded an oxygen consumption rate of 60-68 nl O(2) x cm(-3) x s(-1), the maximal limit for consumption in the mesentery. The results were compared with measurements made by other workers in regard to the employed techniques.
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http://dx.doi.org/10.1152/ajpheart.00077.2007 | DOI Listing |
Adv Exp Med Biol
October 2024
Julius-Bernstein-Institute of Physiology, University of Halle, Halle, Germany.
Immunotargets Ther
September 2024
Department of Internal Medicine, Section of Hematology and Medical Oncology, King Hussein Cancer Center, Amman, Jordan.
Background: Cyclin-dependent kinase (CDK) 4/6 inhibitors have revolutionized the treatment landscape of hormone receptor-positive (HR+) and human epidermal growth factor receptor 2-negative (HER2 -) metastatic breast cancer (MBC). Here, we present the real-world clinical outcomes and toxicity data of patients treated at a single cancer center.
Methods: A retrospective analysis was conducted on patients with HR+/HER2- MBC treated with ribociclib plus endocrine therapy (ET).
mSystems
October 2024
Department of Food and Nutrition, University of Helsinki, Helsinki, Finland.
Unlabelled: () DSM 20271 is a bacterium known for its ability to thrive in diverse environments and to produce vitamin B12. Despite its anaerobic preference, recent studies have elucidated its ability to prosper in the presence of oxygen, prompting a deeper exploration of its physiology under aerobic conditions. Here, we investigated the response of DSM 20271 to aerobic growth by employing comparative transcriptomic and surfaceome analyses alongside metabolite profiling.
View Article and Find Full Text PDFEnergy Fuels
August 2024
Sustainable Energy Technology, SINTEF, P.O. Box 124, NO-0314 Oslo, Norway.
The understanding and development of stable redox materials based on cheap and abundant elements, forming Ca-Mn-Ti-Fe-O-based perovskites, have been in focus for applications in renewable technologies such as chemical looping combustion and thermal energy storage. The present research focuses on developing stable materials to be utilized up to 1050 °C in a CLC process and has shown that the structure stability and oxygen transfer capacity can be achieved by tuning the content of different elements on B-sites of the perovskites. Various experiments, such as redox cycling under various fuels, temperatures, and O, were carried out to evaluate the oxygen transfer capacity, reaction rates under various fuels, etc.
View Article and Find Full Text PDFJ Appl Physiol (1985)
October 2024
Department of Bioengineering, University of California, San Diego, California, United States.
Unfortunately, during pathological conditions resulting in chronic hemolysis cell-free hemoglobin (Hb) is released into the circulation that releases free heme, resulting in several complications. One approach to prevent these toxicities is the administration of supplemental scavenger proteins, haptoglobin (Hp) and hemopexin (Hpx). The goal of this body of work is to objectively measure the levels of vascular reactivity and inflammatory profiles after an infusion of acellular hemoglobin in animals that were given a coadministration of PEGylated human apohemoglobin (PEG-apoHb), a hemopexin (Hpx)-mimetic that can scavenge free heme from hemoglobin, together with human plasma-derived Hp that can scavenge dimerized Hb.
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