scholarly journals Suppressive effects of mead acid supplementation on acute liver damage model in rats

2020 ◽  
Vol 29 (2) ◽  
pp. 114
Author(s):  
Akiko Takenouchi ◽  
Yuichi Kinoshita ◽  
Yukari Hirayama ◽  
Yumiko Shinke ◽  
Kei Hamazaki ◽  
...  
2021 ◽  
Vol 30 (1) ◽  
pp. 60-72
Author(s):  
Yuichi Kinoshita ◽  
Akiko Takenouchi ◽  
Momoka Chatani ◽  
Masahiro Yoshioka ◽  
Yuko Emoto ◽  
...  

2014 ◽  
Vol 2 (1) ◽  
pp. 21-25
Author(s):  
Ali Asghar Yoonesi ◽  
Durdi Qujeq ◽  
Mohsen Esmaili ◽  
Farideh Feizi ◽  
◽  
...  

1989 ◽  
Vol 107 (1) ◽  
pp. 38-41
Author(s):  
D. Adzharov ◽  
N. Donchev ◽  
M. Kerimova ◽  
E. Naidenova ◽  
B. Borov ◽  
...  

2008 ◽  
Vol 31 (9) ◽  
pp. 1160-1165 ◽  
Author(s):  
Hee Seung Lee ◽  
Kyung-Hee Jung ◽  
Sang-Won Hong ◽  
In-Suh Park ◽  
Chongmu Lee ◽  
...  

2022 ◽  
Author(s):  
Urmila Jagtap ◽  
Sandeep Basu ◽  
Lavanya Lokhande ◽  
Nikhil Bharti ◽  
Chetana Sachidanandan

The use of many essential drugs is restricted due to their deleterious effects on the liver. Molecules that can prevent or protect the liver from drug induced liver injury (DILI) would be valuable in such situations. We used hepatocyte-specific expression of bacterial nitroreductase in zebrafish to cause temporally controlled liver damage. This transgenic line was used to run a whole organism based chemical screen in zebrafish larvae. In this screen we identified BML-257, a potent small molecule AKT inhibitor, that protected the liver against metronidazole-induced liver injury. BML-257 also showed potent prophylactic and pro-regenerative activity in this liver damage model. BML-257 also showed remarkable protective action in two independent toxicological models of liver injury caused by acetaminophen and Isoniazid. This suggests that BML-257 may have the potential to protect against multiple kinds of drug induced liver injury.


1995 ◽  
Vol 23 (03n04) ◽  
pp. 243-254 ◽  
Author(s):  
Song-Chow Li ◽  
Chun-Ching Lin ◽  
Yun-Ho Lin ◽  
S. Supriyatna ◽  
Chao-Wei Teng

Curcuma xanthorrhiza Roxb. (Zingiberaceae family, commonly known as temu lawak or Javanese turmeric in Indonesia), which is found both wild and cultivated in Indonesia, has been traditionally used for medicinal purposes. C. xanthorrhiza is also used as a tonic in Indonesia. The aim of the present study is to clarify whether C. xanthorrhiza treatment may prevent acute liver damage induced by acetaminophen and carbon tetrachloride in mice. The results clearly indicated that extract of C. xanthorrhiza could reduce significantly the acute elevation of serum transaminases levels induced by the two kinds of hepatotoxins, and alleviated the degree of liver damage at 24 hours after the intraperitoneal administration of two hepatotoxins. It may be concluded that C. xanthorrhiza can protect the liver from various hepatotoxins, hence C. xanthorrhiza could be useful in the treatment of liver injuries and has promise as a kind of broad spectrum hepatoprotective agent.


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