The Kinetics of the Production of Reactive Oxygen Species by Neutrophils after Incubation in a Hypomagnetic Field

BIOPHYSICS ◽  
2021 ◽  
Vol 66 (3) ◽  
pp. 434-437
Author(s):  
V. V. Novikov ◽  
E. V. Yablokova ◽  
I. A. Shaev ◽  
E. E. Fesenko
2015 ◽  
Vol 7 (6) ◽  
pp. 13 ◽  
Author(s):  
Kh. P. Tiras ◽  
S. V. Gudkov ◽  
V. I. Emelyanenko ◽  
K. B. Aslanidi

<p class="1Body">Reactive oxygen species (ROS) are directly involved in cell proliferation, differentiation and apoptosis in a variety of organisms. We studied kinetics of own luminescence induced by changes of ROS in early stages of planarian regeneration. Kinetics of chemiluminescence were measured in intact planarians and the same individuals after decapitation within 15 hours. We analyzed the traumatic fluorescent signal obtained as the difference between kinetics of intact and decapitated planarians. It was found that regeneration is accompanied by changes in the content of ROS correlated with the energy-intensive process in regenerating planarians. Oxidative stress was caused by damage to cell membranes in the dissection of the planarian and it was accompanied by a drop in the intensity of luminescence with a time constant of about 3.6 hours. Phagocytosis of dying cells by neoblasts was accompanied by an increase of the luminescence intensity after 2 - 3 hours after decapitation. Neoblast mitosis was described by two maximums of luminescence over 5.1 hours and 8.3 hours after decapitation. For the first time we demonstrated the opportunity of registering the physiological state of pluripotent stem cells at the level of the organism <em>in vivo</em>.</p>


2013 ◽  
Vol 30 (6) ◽  
pp. 2653-2658 ◽  
Author(s):  
SHINGO TERASHIMA ◽  
YOICHIRO HOSOKAWA ◽  
HIRONORI YOSHINO ◽  
MASARU YAMAGUCHI ◽  
TOSHIYA NAKAMURA

2013 ◽  
Vol 4 (8) ◽  
pp. 2475 ◽  
Author(s):  
R. Pynaert ◽  
J. Buguet ◽  
C. Croutxé-Barghorn ◽  
P. Moireau ◽  
X. Allonas

2013 ◽  
Vol 82 (4) ◽  
pp. 435-439 ◽  
Author(s):  
Leonardo Gomez ◽  
Raul Cortes ◽  
Ariel Valenzuela ◽  
Carlos Smith

Reactive oxygen species contribute to kill of microorganisms. Their activity is usually measured by their capacity to reduce nitroblue tetrazolium into formazan. The incubation time to allow nitroblue tetrazolium reduction by reactive oxygen species usually ranges from 30 to 60 min. The aim of our study was to determine the kinetics of formazan formation, to determine the shortest incubation time possible, and to find if astaxanthin negatively affects the availability of reactive oxygen species (and defense mechanisms of fish). The blood/nitroblue tetrazolium method is based on nitroblue tetrazolium reduction into formazan by reactive oxygen species present in blood. Formazan can be spectrophotometrically measured, allowing quantification of reactive oxygen species. Reactive oxygen species were measured in blood samples from 30 trout intramuscularly injected with astaxanthin (0.3 mg/100 g of fish) (experimental group) and 30 non-injected trout (controls). Results indicated that in trout non-treated with astaxanthin, the plateau of formazan production was reached after 20 min of incubation. Trout intramuscularly injected with astaxanthin showed the following: on Day 1 after astaxanthin injection, the kinetics were slower but finally reached a plateau similar to astaxanthin-free trouts, and by Day 11 the plateau was significantly higher after 60 min incubation. In conclusion, the kinetics curves here reported allow reducing incubation time of the method to only 20 min in antioxidant-free trout and, on the other hand, our results also revealed that astaxanthin can be used to improve flesh colour in salmonids without affecting reactive oxygen species availability and therefore the defense mechanisms of trout.


ASAIO Journal ◽  
1998 ◽  
Vol 44 (5) ◽  
pp. M423-M432 ◽  
Author(s):  
Stefano Biasioli ◽  
Renzo Schiavon ◽  
Luigi Petrosino ◽  
Lucia Cavallini ◽  
Gaetano Cavalcanti ◽  
...  

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