Synthesis of nitroxyl (aminoxyl) labeled probes for studies of intracellular environment by EPR and MRI

1989 ◽  
Vol 54 (15) ◽  
pp. 3667-3674 ◽  
Author(s):  
George Sosnovsky ◽  
Nuti Uma Maheswara Rao ◽  
Shu Wen Li ◽  
Harold M. Swartz
Keyword(s):  
Intracellular Environment

Ubiquinone-BODIPY nanoparticles for tumor redox-responsive fluorescence imaging and photodynamic activity

2021 ◽  
Author(s):  
Byunghee Hwang ◽  
Tae-Il Kim ◽  
Hyunjin Kim ◽  
Sungjin Jeon ◽  
Yongdoo Choi ◽  
...  
Keyword(s):  
Fluorescence Imaging ◽  
Selective Activation ◽  
Turn On ◽  
Intracellular Environment ◽  
Redox Responsive ◽  
Photodynamic Activity

A ubiquinone-BODIPY photosensitizer self-assembles into nanoparticles (PS-Q-NPs) and undergoes selective activation within the highly reductive intracellular environment of tumors, resulting in “turn-on” fluorescence and photosensitizing activities.

Manipulating the intracellular environment of hippocampal slices: pH and high-energy phosphates

1989 ◽  
Vol 28 (1-2) ◽  
pp. 83-91 ◽  
Author(s):  
Tim S. Whittingham ◽  
Eduardo Warman ◽  
Hussein Assaf ◽  
Thomas J. Sick ◽  
Joseph C. LaManna
Keyword(s):  
Hippocampal Slices ◽  
High Energy ◽  
High Energy Phosphates ◽  
Intracellular Environment

Nuclear Magnetic Resonance Methods for Observing the Intracellular Environment of Mammalian Cells

1990 ◽  
Vol 589 (1 Biochemical E) ◽  
pp. 458-475 ◽  
Author(s):  
ERIK J. FERNANDEZ ◽  
ANTHONY MANCUSO ◽  
MARILEE K. MURPHY ◽  
HARVEY W. BLANCH ◽  
DOUGLAS S. CLARK
Keyword(s):  
Nuclear Magnetic Resonance ◽  
Magnetic Resonance ◽  
Mammalian Cells ◽  
Intracellular Environment ◽  
Nuclear Magnetic

scholarly journals A phosphorus-31 nuclear magnetic resonance investigation of intracellular environment in human normal and sickle cell blood

Blood ◽  
1979 ◽  
Vol 54 (1) ◽  
pp. 196-209 ◽  
Author(s):  
YF Lam ◽  
AK Lin ◽  
C Ho
Keyword(s):  
Nuclear Magnetic Resonance ◽  
Magnetic Resonance ◽  
Magnetic Resonance Spectroscopy ◽  
Nuclear Magnetic Resonance Spectroscopy ◽  
Intracellular Ph ◽  
Sickle Cell ◽  
Resonance Spectroscopy ◽  
Blood Samples ◽  
Intracellular Environment ◽  
Nuclear Magnetic

Abstract Intracellular pH and 2,3-diphosphoglycerate concentration in sickle cell amenia and normal human blood samples were measured by means of phosphorus-31 nuclear magnetic resonance spectroscopy. To monitor the concentrations of various internal phosphorylated metabolites of intact red blood cells, heparinized blood samples were used and were incubated at 37 degrees C with 5.6% C92, 25% O2, and 69.4% N2. The 31P chemical shifts of phosphorylated compounds, such as 2,3-diphosphoglycerate, adenosine 5′-triphosp-ate, and inorganic phosphate, depend on pH, and by using an appropriate calibration curve, the intracellular pH of intact erythrocytes can be obtained. The intracellular pH values in fresh sickl cell blood and normal blood were found to be 7.14 and 7.29, respectively. However, the whole-blood pH, as measured by a standard pH meter, was found to be 7.54 for both types of blood. The initial concentration of 2,3-diphosphoglycerate in sickle cell blood was about 30% higher, but it was depleted much faster during incubation than that in normal blood. The difference in intracellular pH between these two types of blood samples remained constant during incubation, even after depletion of 2,3-diphosphoglycerate. These results suggest that there are differences in intracellular environment between normal and sickle cell blood. Thus, 31P nuclear magnetic resonance spectroscopy provides a fast, direct, continuous, and noninvasive way to monitor the intracellular environment of intact erythrocytes.

scholarly journals Modulation of membrane currents by cyclic AMP in cleavage-arrested Drosophila neurons.

1996 ◽  
Vol 199 (3) ◽  
pp. 537-548
Author(s):  
W B Alshuaib ◽  
L Byerly
Keyword(s):  
Cyclic Amp ◽  
Membrane Currents ◽  
K Channel ◽  
Neuronal Membrane ◽  
Patch Clamp Technique ◽  
Large Variability ◽  
Whole Cell ◽  
Intracellular Environment ◽  
K Current ◽  
Channel Currents

A number of Drosophila learning mutants have defective intracellular second-messenger systems. In an effort to develop techniques that will allow direct measurement of the effects of these mutations on whole-cell neuronal membrane currents, the perforated-patch whole-cell (PPWC) technique has been applied to cleavage-arrested cultured embryonic Drosophila neurons. This technique permits the measurement of membrane currents without disturbing the intracellular environment. As a result of the maintenance of the intracellular environment, Drosophila neuron currents are found to be much more stable than when measured using the conventional whole-cell (CWC) patch-clamp technique. Ca2+ channel currents, which typically 'wash out' within a few minutes of the beginning of CWC recording, are stable for the duration of the seal (tens of minutes) when measured using the PPWC technique. Since the learning mutations dunce and rutabaga disrupt cyclic AMP signalling, the action of externally applied dibutyryl cyclic AMP (db-cAMP) and theophylline on Ca2+ and K+ channel currents were studied. db-cAMP and theophylline enhanced the Ba2+ current, carried by Ca2+ channels, but had no effect on the K+ current in the cleavage-arrested neurons. However, the large variability and reduction in density of Ba2+ and K+ currents raise questions about the suitability of using these cleavage-arrested cells as models for Drosophila neurons.

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