scholarly journals EFFECTS OF ACUTE ETHANOL ON THE Ca2+ RESPONSE TO AMPA IN CULTURED RAT CORTICAL GABAergic NONPYRAMIDAL NEURONS

2003 ◽  
Vol 38 (5) ◽  
pp. 394-399 ◽  
Author(s):  
W. Fischer ◽  
H. Franke ◽  
P. Illes
2010 ◽  
Vol 39 (3) ◽  
pp. 343-349 ◽  
Author(s):  
Dong-Chun Jin ◽  
Seung-Wook Jeong ◽  
Pyoung-Sim Park

2010 ◽  
Vol 68 ◽  
pp. e422-e423
Author(s):  
Keisuke Mizuo ◽  
Yoko Nishitani ◽  
Ryuichi Katada ◽  
Shunichiro Okazaki ◽  
Kenji Tateda ◽  
...  

2007 ◽  
Vol 223 (3) ◽  
pp. 225-233 ◽  
Author(s):  
Hu-Quan Yin ◽  
Mingoo Kim ◽  
Ju-Han Kim ◽  
Gu Kong ◽  
Kyung-Sun Kang ◽  
...  

2017 ◽  
Vol 6 ◽  
Author(s):  
Ryusei Uchio ◽  
Yohei Higashi ◽  
Yusuke Kohama ◽  
Kengo Kawasaki ◽  
Takashi Hirao ◽  
...  

AbstractTurmeric (Curcuma longa) is a widely used spice that has various biological effects, and aqueous extracts of turmeric exhibit potent antioxidant activity and anti-inflammatory activity. Bisacurone, a component of turmeric extract, is known to have similar effects. Oxidative stress and inflammatory cytokines play an important role in ethanol-induced liver injury. This study was performed to evaluate the influence of a hot water extract of C. longa (WEC) or bisacurone on acute ethanol-induced liver injury. C57BL/6 mice were orally administered WEC (20 mg/kg body weight; BW) or bisacurone (60 µg/kg BW) at 30 min before a single dose of ethanol was given by oral administration (3·0 g/kg BW). Plasma levels of aspartate aminotransferase and alanine aminotransferase were markedly increased in ethanol-treated mice, while the increase of these enzymes was significantly suppressed by prior administration of WEC. The increase of alanine aminotransferase was also significantly suppressed by pretreatment with bisacurone. Compared with control mice, animals given WEC had higher hepatic tissue levels of superoxide dismutase and glutathione, as well as lower hepatic tissue levels of thiobarbituric acid-reactive substances, TNF-α protein and IL-6 mRNA. These results suggest that oral administration of WEC may have a protective effect against ethanol-induced liver injury by suppressing hepatic oxidation and inflammation, at least partly through the effects of bisacurone.


2016 ◽  
Vol 118 ◽  
pp. 139
Author(s):  
Akio Horibe ◽  
Nabil Eid ◽  
Yuko Ito ◽  
Yoshihisa Tanaka ◽  
Yoshinori Otsuki ◽  
...  
Keyword(s):  

2010 ◽  
Vol 38 (1) ◽  
pp. 172-176 ◽  
Author(s):  
Jeff W. Barclay ◽  
Margaret E. Graham ◽  
Mark R. Edwards ◽  
James R. Johnson ◽  
Alan Morgan ◽  
...  

Acute exposure to ethanol is known to modulate signalling within the nervous system. Physiologically these effects are both presynaptic and postsynaptic in origin; however, considerably more research has focused primarily on postsynaptic targets. Recent research using the model organism Caenorhabditis elegans has determined a role for specific proteins (Munc18-1 and Rab3) and processes (synaptic vesicle recruitment and fusion) in transducing the presynaptic effects of ethanol. In the present paper, we review these results, identifying the proteins and protein interactions involved in ethanol sensitivity and discuss their links with mammalian studies of alcohol abuse.


1980 ◽  
Vol 186 (3) ◽  
pp. 755-761 ◽  
Author(s):  
A A B Badawy ◽  
B M Snape ◽  
M Evans

1. Acute ethanol administration causes a biphasic change in rat liver tyrosine aminotransferase activity. 2. The initial decrease is significant with a 200 mg/kg dose of ethanol, is prevented by adrenoceptor-blocking agnets and by reserpine, but not by inhibitors of ethanol metabolism, and exhibits many of the characteristics of the inhibition caused by noradrenaline. 3. The subsequent enhancement of the enzyme activity by ethanol is not associated with stabilization of the enzyme, but is sensitive to actinomycin D and cycloheximide. 4. It is suggested that the initial decrease in aminotransferase activity is caused by the release of catecholamines, whereas the subsequent enhancement may be related to the release of glucocorticoids.


2007 ◽  
Vol 41 (2) ◽  
pp. 79-84 ◽  
Author(s):  
Willy Aasebø ◽  
Willy Aasebø ◽  
Jan Erikssen ◽  
Jørgen Jonsbu ◽  
Knut Stavem

Sign in / Sign up

Export Citation Format

Share Document