Abstract | OBJECTIVE: METHODS: RESULTS: Compared with the normal group, there were physiological changes associated with hepatic steatosis and inflammation in liver tissues in the untreated group as observed by oil red O staining and HE staining. The TG, FFA, malony1-CoA, FAS, and ACCase concentrations in liver tissues in the untreated group were elevated significantly. While the contents of ADP in serum and AdipoR2, CPT-1 and AMPK in liver tissues in the untreated group were decreased markedly. The pathological damages in each QSHYD-treated group were significantly less than those in the untreated group. The TG and FFA contents in liver tissues in each QSHYD-treated group were significantly decreased. The FAS, ACCase and malonyl-CoA concentrations in liver tissues of the high QSHYD-treated group were reduced markedly as compared with the untreated group. High- and medium-dose of QSHYD could significantly increase ADP content in serum and AMPK, CPT-1 and AdipoR2 contents in liver tissues. CONCLUSION: QSHYD can affect the ADP-FFA pathway by increasing the content of serum ADP, which may be one of its important mechanisms in preventing and treating NAFLD in rats.
|
Authors | Hong-Shan Li, Qin Feng, Li-Li Xu, Shao-Dong Chen, Xue-Mei Li, Yi-Yang Hu |
Journal | Zhong xi yi jie he xue bao = Journal of Chinese integrative medicine
(Zhong Xi Yi Jie He Xue Bao)
Vol. 7
Issue 6
Pg. 546-51
(Jun 2009)
ISSN: 1672-1977 [Print] China |
PMID | 19583937
(Publication Type: English Abstract, Journal Article, Research Support, Non-U.S. Gov't)
|
Chemical References |
- Adiponectin
- Drugs, Chinese Herbal
- Fatty Acids, Nonesterified
- Receptors, Adiponectin
- adiponectin receptor 2, rat
- qushi huayu
- Carbon Tetrachloride
|
Topics |
- Adiponectin
(blood)
- Animals
- Carbon Tetrachloride
- Carbon Tetrachloride Poisoning
- Disease Models, Animal
- Drugs, Chinese Herbal
(therapeutic use)
- Fatty Acids, Nonesterified
(metabolism)
- Fatty Liver
(chemically induced, drug therapy, prevention & control)
- Male
- Phytotherapy
- Random Allocation
- Rats
- Rats, Wistar
- Receptors, Adiponectin
(metabolism)
|