scholarly journals Responses of heat shock protein 70 and caspase-3/7 to dietary selenomethionine in juvenile white sturgeon

2016 ◽  
Vol 2 (1) ◽  
pp. 45-50 ◽  
Author(s):  
Weifang Wang ◽  
Seunghyung Lee ◽  
Silas S.O. Hung ◽  
Dong-Fang Deng
2013 ◽  
Vol 75 (2) ◽  
pp. 164-169 ◽  
Author(s):  
Weifang Wang ◽  
Dong-Fang Deng ◽  
Nicola De Riu ◽  
Giuseppe Moniello ◽  
Silas S. O. Hung

2004 ◽  
Vol 96 (5) ◽  
pp. 1776-1781 ◽  
Author(s):  
Toshio Mikami ◽  
Satoshi Sumida ◽  
Yoshitomo Ishibashi ◽  
Shigeo Ohta

A single bout of exercise increases production of heat shock protein 70 (HSP70), which protects cells against various stresses. In this study, we investigated whether endurance exercise training enhances liver level of HSP70 and, if so, whether HSP70 contributes to hepatic protection against stress in vivo. Mice of an exercise-training group performed 60 min of treadmill running 5 days/wk for 4 wk. The resting level of liver HSP70 was 4.5 times higher in the trained than in sedentary mice. After 4 wk of exercise training, both groups of mice were exposed to the following stresses: 1) heat stress, 2) cold stress, 3) oxidative stress, 4) ethanol stress, and 5) exercise stress by compelling the mice to run on a treadmill until exhausted. After exposure to the stresses, the liver was immediately isolated. Elevation of liver HSP70 in the trained mice was evident, whereas no elevation was found in the sedentary mice. On exposure to heat, diethyldithiocarbamate and ethanol, activities of glutanic oxalacetic transaminase in plasma, and liver caspase-3, a key enzyme of apoptotic processing, were elevated in the sedentary mice but not in the trained mice. These results suggest that exercise training enhanced the resting level of liver HSP70 and hepatic protection against various stresses, at least partly attributing to the suppression of caspase-3 activity by the increase in HSP70.


2000 ◽  
Vol 275 (33) ◽  
pp. 25665-25671 ◽  
Author(s):  
Chun-Ying Li ◽  
Jae-Seon Lee ◽  
Young-Gyu Ko ◽  
Jong-Il Kim ◽  
Jeong-Sun Seo

PLoS ONE ◽  
2014 ◽  
Vol 9 (6) ◽  
pp. e98886 ◽  
Author(s):  
Arvind Kumar Shukla ◽  
Prakash Pragya ◽  
Hitesh Singh Chaouhan ◽  
Anand Krishna Tiwari ◽  
Devendra Kumar Patel ◽  
...  

2020 ◽  
Vol 10 (1) ◽  
Author(s):  
Mohammad Ghasem Golmohammadi ◽  
Shokofeh Banaei ◽  
Kazem Nejati ◽  
Mir Mehdi Chinifroush-Asl

AbstractKidney ischemia reperfusion (IR) contributes to the development of acute kidney injury. The hypoxic conditions in ischemic damage lead to oxidative stress and apoptotic cell death. We investigated the effects of vitamin D3 (Vit D) and erythropoietin (EPO) on microRNA-21(miR-21) expression in renal IR. Wistar rats were divided into five groups including the control, vehicle + IR, Vit D + IR, EPO + IR, and Vit D + EPO + IR groups. The animals were unilaterally nephrectomized and subjected to 45 min of renal pedicle occlusion followed by 24 h reperfusion. Vitamin D3 and EPO were administered prior to ischemia. After 24 h reperfusion, the kidney samples were collected for the detection of miR-21, heat shock protein 70 (hsp70) and caspase-3 expression levels. Kidney IR significantly increased the expression of miR-21, hsp70 and capase-3 and blood urea nitrogen (BUN)-Cr levels. Treatment with vitamin D3 and EPO significantly decreased the BUN-Cr levels and hsp70 and caspase-3 expression. Also, the co-administration of two drugs significantly increased miR-21 expression. It seems that vitamin D3 or EPO administration could protect the kidney against IR injury. However, vitamin D3 and EPO co-treatment was the most effective compared with the other treatment groups.


Toxicon ◽  
2004 ◽  
Vol 43 (1) ◽  
pp. 93-100 ◽  
Author(s):  
Abdel-Raheim M.A Meki ◽  
Emade El-Dein F Esmail ◽  
Ahmed A Hussein ◽  
Hamdy M Hassanein

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