A nanoprobe for nonprotein thiols based on assembling of QDs and 4-amino-2,2,6,6-tetramethylpiperidine oxide

2011 ◽  
Vol 26 (11) ◽  
pp. 4632-4636 ◽  
Author(s):  
Kehua Xu ◽  
Huachao Chen ◽  
Huixia Wang ◽  
Jiangwei Tian ◽  
Jing Li ◽  
...  
Keyword(s):  
1998 ◽  
Vol 275 (5) ◽  
pp. R1468-R1477 ◽  
Author(s):  
Scott K. Powers ◽  
Haydar A. Demirel ◽  
Heather K. Vincent ◽  
Jeff S. Coombes ◽  
Hisashi Naito ◽  
...  

Experimental studies examining the effects of regular exercise on cardiac responses to ischemia and reperfusion (I/R) are limited. Therefore, these experiments examined the effects of endurance exercise training on myocardial biochemical and physiological responses during in vivo I/R. Female Sprague-Dawley rats (4 mo old) were randomly assigned to either a sedentary control group or to an exercise training group. After a 10-wk endurance exercise training program, animals were anesthetized and mechanically ventilated, and the chest was opened by thoracotomy. Coronary occlusion was achieved by a ligature around the left coronary artery; occlusion was maintained for 20 min, followed by a 10-min period of reperfusion. Compared with untrained, exercise-trained animals maintained higher ( P < 0.05) peak systolic blood pressure throughout I/R. Training resulted in a significant ( P < 0.05) increase in ventricular nonprotein thiols, heat shock protein (HSP) 72, and the activities of superoxide dismutase (SOD), phosphofructokinase (PFK), and lactate dehydrogenase. Furthermore, compared with untrained controls, left ventricles from trained animals exhibited lower levels ( P < 0.05) of lipid peroxidation after I/R. These data demonstrate that endurance exercise training improves myocardial contractile performance and reduces lipid peroxidation during I/R in the rat in vivo. It appears likely that the improvement in the myocardial responses to I/R was related to training-induced increases in nonprotein thiols, HSP72, and the activities of SOD and PFK in the myocardium.


1988 ◽  
Vol 255 (5) ◽  
pp. F874-F884
Author(s):  
J. M. Messana ◽  
D. A. Cieslinski ◽  
R. P. O'Connor ◽  
H. D. Humes

Glutathione, comprising a major portion of cellular nonprotein thiols, plays a central role in a diverse group of cell metabolic functions. Glutathione and related enzyme systems have been shown to protect against both toxin and oxidant-induced injury in several organ systems. The role of glutathione in protecting renal epithelia against oxidant stress has not been investigated previously. We report here the response of enriched, isolated rabbit renal proximal tubule segments to oxidant stress induced by tert-butyl hydroperoxide. In addition, the effects of glutathione depletion by various biochemical means and of exogenous glutathione supplementation on the response of tubule segments to tert-butyl hydroperoxide exposure are described. Depletion of cell glutathione by several distinct methods potentiates oxidant-induced injury. Augmentation of cellular glutathione affords significant protection against exogenous oxidant stress. The protective effect of glutathione may reside in its ability, in conjunction with glutathione peroxidase, to arrest the propagation of lipid peroxidation and, therefore, to minimize alterations in plasma membrane permeability. The results of this study do not exclude the possibility that glutathione prevents tert-butyl hydroperoxide induced oxidation of critical sulfhydryl groups of catalytic or structural proteins associated with control of cell cation homeostasis. These results confirm the important role of glutathione in protecting renal tubular epithelia against oxidant stress.


2014 ◽  
Vol 2014 ◽  
pp. 1-9 ◽  
Author(s):  
Neelam Chandra ◽  
Nalini Pandey

Black gram (Vigna mungo L. var. DPU-88-31), an edible legume, was grown at 1, 2, 4, 6, and 8 meq S L−1 to study the effect of deficient and excess level of sulfur on oxidative metabolism. Plants supplied by 4 meq S L−1 showed optimum yield. Sulfur deficient plants (1 and 2 meq S L−1) showed reduction in growth and chlorosis of young leaves. Tissue sulfur and cysteine concentration was increased with increasing sulfur supply. The thresholds for critical concentration of sulfur deficiency and toxicity were 0.315% and 0.434% dry weight. Biomass and photoassimilatory pigments were decreased and carbohydrates (sugar and starch) were accumulated in leaves of sulfur deficient and excess plants. Accumulation of hydrogen peroxide and thiobarbituric acid reactive substances in sulfur deficient and excess plants caused oxidative damage in plants which was also evident by the increase in the activity of superoxide dismutase, catalase, peroxidase, ascorbate peroxidase, glutathione reductase, and concentration of ascorbate and nonprotein thiols.


1986 ◽  
Vol 34 (9) ◽  
pp. 3823-3829 ◽  
Author(s):  
HIDEO TAKAHATA ◽  
RIFA CHOH ◽  
JUNKO MATSUMOTO ◽  
TOSHIAKI NISHIHATA ◽  
MASARU YAMAZAKI ◽  
...  

Cytometry ◽  
1988 ◽  
Vol 9 (6) ◽  
pp. 529-532 ◽  
Author(s):  
Jose Enrique O'Connor ◽  
Bruce F. Kimler ◽  
Michael C. Morgan ◽  
Kathryn J. Tempas

2012 ◽  
Vol 64 (2) ◽  
pp. 243-252 ◽  
Author(s):  
Jianyun Sun ◽  
Jin Cui ◽  
Chunling Luo ◽  
Lu Gao ◽  
Yahua Chen ◽  
...  

1986 ◽  
Vol 154 (1) ◽  
pp. 186-193 ◽  
Author(s):  
Frank C. Ayers ◽  
Garvin L. Warner ◽  
Kathy L. Smith ◽  
David A. Lawrence
Keyword(s):  

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