Abstract | BACKGROUND:
Hydrogen sulfide (H2S) is known to exert anti-inflammatory properties. Apoptosis and autophagy play important roles in concanavalin A (Con A)-induced acute hepatitis. The purpose of this study was to explore both the effect and mechanism of H2S on Con A-induced acute hepatitis. METHODS: BALB/c mice were randomized into sham group, Con A-injection group, and 14 μmol/kg of sodium hydrosulfide ( NaHS, an H2S donor) pretreatment group. RESULTS: CONCLUSION: H2S attenuates Con A-induced acute hepatitis by inhibiting apoptosis and autophagy, in part, through activation of the PtdIns3K-AKT1 signaling pathway.
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Authors | Ping Cheng, Kan Chen, Yujing Xia, Weiqi Dai, Fan Wang, Miao Shen, Chengfen Wang, Jing Yang, Rong Zhu, Huawei Zhang, Jingjing Li, Yuanyuan Zheng, Junshan Wang, Yan Zhang, Jie Lu, Yingqun Zhou, Chuanyong Guo |
Journal | Drug design, development and therapy
(Drug Des Devel Ther)
Vol. 8
Pg. 1277-86
( 2014)
ISSN: 1177-8881 [Electronic] New Zealand |
PMID | 25246769
(Publication Type: Journal Article, Research Support, Non-U.S. Gov't)
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Chemical References |
- Concanavalin A
- Phosphatidylinositol 3-Kinases
- Proto-Oncogene Proteins c-akt
- Hydrogen Sulfide
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Topics |
- Acute Disease
- Animals
- Apoptosis
(drug effects)
- Autophagy
(drug effects)
- Concanavalin A
(administration & dosage, antagonists & inhibitors, pharmacology)
- Dose-Response Relationship, Drug
- Hepatitis
(drug therapy, metabolism, pathology)
- Hydrogen Sulfide
(administration & dosage, pharmacology, therapeutic use)
- Injections, Intravenous
- Male
- Mice
- Mice, Inbred BALB C
- Phosphatidylinositol 3-Kinases
(metabolism)
- Proto-Oncogene Proteins c-akt
(metabolism)
- Signal Transduction
(drug effects)
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