Abstract | OBJECTIVE: To investigate the effect of salidroside on hypoxia-induced apoptosis of corpus cavernosum smooth muscle cells (CCSMCs) in rats. METHODS: Rat CCSMCs were cultured in vitro by the enzyme digestion method and identified by immunofluorescent staining of anti-alpha-SMA and anti- Desmin. The non-toxic dose of salidroside was determined by MTT assay. Low- oxygen mixed gas (1% O2, 5% CO2, and 94% N2) was piped into a modular incubator chamber to induce hypoxia. The CCSMCs were divided into a normal, a hypoxia, and a 32 microg/mL salidroside intervention group. The apoptosis of the CCSMCs was detected by flow cytometry and the expression of the caspase-3 protein determined by Western blot. RESULTS: The majority of the CCSMCs were positive for alpha-SMA and Desmin at immunofluorescent staining. Salidroside at < 32 microg/ml produced no obvious toxicity to CCSMCs. Compared with the normal control group, the rates of early and late apoptosis of CCSMCs were both increased significantly in the hypoxia group ([12.77 +/-1.41]% vs [18.69 +/- 1.29]%, P < 0.01 and [14.63 +/- 2.00]% vs [21.03 +/- 1.530]% , P < 0.05). Western blot showed a markedly increased expression of cleaved caspase-3 (P < 0.01). Intervention with 32 microg/ml salidroside significantly reduced hypoxia-induced early apoptosis of CCSMCs ([13.46% +/- 1.87]%, P < 0.01) and decreased the expression of cleaved caspase-3 (P < 0.01). CONCLUSION:
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Authors | Jian-Feng Zhao, Hui-Ying Fu, Fan Yang, Xiao-Jun Huang, Gang Chen, Bo-Dong Lü |
Journal | Zhonghua nan ke xue = National journal of andrology
(Zhonghua Nan Ke Xue)
Vol. 20
Issue 4
Pg. 309-14
(Apr 2014)
ISSN: 1009-3591 [Print] China |
PMID | 24873155
(Publication Type: Journal Article, Research Support, Non-U.S. Gov't)
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Chemical References |
- Glucosides
- Phenols
- Caspase 3
- rhodioloside
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Topics |
- Animals
- Apoptosis
(drug effects, physiology)
- Caspase 3
(metabolism)
- Cell Hypoxia
(physiology)
- Cells, Cultured
- Glucosides
(pharmacology)
- Humans
- Male
- Myocytes, Smooth Muscle
(cytology, drug effects, enzymology)
- Penis
(cytology, drug effects)
- Phenols
(pharmacology)
- Rats
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