1.Effect of alpha-lipoic acid on cardiomyocyte apoptosis following renal ischemia-reperfusion injury in rats
Yan LIU ; Leiqiang LI ; Yunlu LI ; Chenlu DU ; Yuntao SHAO ; Xinchun ZHENG ; Cuiying ZHANG
Chinese Journal of Anesthesiology 2011;31(11):1374-1376
ObjectiveTo evaluate the effect of alpha-lipoic acid (ALA) on cardiomyocyte apoptosis following renal ischemia-reperfusion injury(RIRI) in rats.MethodsThirty-six male SD rats weighing 250-280 g were randomly divided into 3 groups ( n =12 each): group sham operation (group S) ; group I/R and group I/R + ALA ( group L).The model of RIRI was produced by occlusion of renal artery and vein for 45 min followed by 24 h reperfusion,in group S the renal pedicles were exposed but not occluded.In group L ALA infusion (30 mg/kg) was given via tail vein at 20 mln before ischemia and at 20 min before reperfusion,while in group I/R the equal volume of solution (35% polyethylene glycol + 60% physiological saline + 5% ethanol) was infused instead of ALA.The animals were saerificed at the end of 24 h of reperfusion,blood samples were taken for detecting concentrations of serum creatinine (Cr) and malondialdehyde (MDA).Then the hearts were immediately removed for determination of SOD activity,MDA content,cardiomyocyte apoptosis (flow cytometry) and Bcl-2/Bax ratio (immunohistology).ResultsSerum Cr concentration,serum and myocardium MDA levels and cardiomyocyte apoptosis were significantly increased after RIRI in groups I/R and L as compared with group S ( P < 0.05).ALA treatment significantly decreased serum Cr concentration,serum and myocardium MDA levels,cardiomyocyte apoptosis and increased SOD activity and Bcl-2/Bax ratio ( P < 0.05).ConclusionALA can attenuate myocardium injury by inhibiting cardiomyocyte apoptosis following RIRI in rats.
2.Down-regulation of pannexin 2 channel enhances cisplatin-induced apoptosis in testicular cancer I-10 cells.
Yanxue YAO ; Shuying DONG ; Chenlu ZHU ; Miao HU ; Baolong DU ; Xuhui TONG
Journal of Southern Medical University 2020;40(8):1090-1096
OBJECTIVE:
To investigate the effect of down-regulation of pannexin 2 (Panx-2) channels on cisplatin-induced apoptosis in I-10 cells.
METHODS:
The expression of Panx-2 protein in testicular cancer cells was detected with Western blotting. The testicular cancer cell line I-10 was transfected with two short hairpin RNA (shRNA1 and shRNA2) Lipofectamine, the empty vector (NC group) or Lipofectamine2000 (blank control group), and the changes in the expression of Panx-2 was detected with Western blotting. The effects of transfection with a Panx-2 inhibitor on surviving fraction of the cells treated with cisplatin (16 μmol/L) for 24 h, 48 h and 72 h was assessed with MTT assay, and the clonogenic capacity of the cells was evaluated with colony-forming assay. At 8 h after incubation with 16 μmol/L cisplatin, AnnexinV/PI double staining was used to detect the early apoptosis of the cells. After 24 h of treatment with 16 μmol/L cisplatin, the cells were examined for expressions of caspase-3, Bcl-2 and Bax using Western blotting.
RESULTS:
The expression of Panx-2 was significantly increased in cisplatin-resistant I-10/DDP ( < 0.001) cells and Tcam-2/DDP ( < 0.01) cells as compared with I-10 cells and Tcam-2 cells. Transfection of I-10 cells with shRNA1 and shRNA2 resulted in significantly decreased Panx-2 expression ( < 0.05) and significantly reduced cell surviving fraction ( < 0.001). In the presence of cisplatin, the cells in NC group showed a higher clonogenic efficiency than those in shRNA1 and shRNA2 groups ( < 0.001). The early-stage apoptosis rate of the cells in shRNA1 and shRNA2 groups were significantly higher than that in NC group ( < 0.01). Panx-2 knockdown in I-10 cells significantly increased caspase-3 and Bax expressions ( < 0.05) and significantly decreased the expression of Bcl-2 ( < 0.01).
CONCLUSIONS
Down-regulation of Panx-2 channel enhances cisplatin-induced apoptosis in cultured testicular cancer cells.
Antineoplastic Agents
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Apoptosis
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Cell Line, Tumor
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Cell Proliferation
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Cisplatin
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Connexins
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Down-Regulation
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Drug Resistance, Neoplasm
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Humans
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Male
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Testicular Neoplasms
3.Cytosolic delivery of the immunological adjuvant Poly I:C and cytotoxic drug crystals
Xiaoqing DU ; Yuqi HOU ; Jia HUANG ; Yan PANG ; Chenlu RUAN ; Wei WU ; Chenjie XU ; Hongwei ZHANG ; Lifang YIN ; Wei HE
Acta Pharmaceutica Sinica B 2021;11(10):3272-3285
Co-delivery of chemotherapeutics and immunostimulant or chemoimmunotherapy is an emerging strategy in cancer therapy. The precise control of the targeting and release of agents is critical in this methodology. This article proposes the asynchronous release of the chemotherapeutic agents and immunostimulants to realize the synergistic effect between chemotherapy and immunotherapy. To obtain a proof-of-concept, a co-delivery system was prepared
4.Analysis on the imported Coronavirus Disease 2019 related cluster epidemic in rural areas of Chengdu.
Yong YUE ; Heng CHEN ; Liang WANG ; XunBo DU ; XuFang GAO ; Jun LIAO ; Rong ZHOU ; ZhenHua CHEN ; YueZhu CHEN ; WeiWei HUANG ; XiaoFang HUANG ; Min HU ; ChenLu ZHAO ; ChangHui DU ; LiLiang DENG ; Xian LIANG ; Zhu LIU
Chinese Journal of Preventive Medicine 2021;55(10):1240-1244
An epidemiological investigation was carried out on a local cluster of outbreak caused by imported cases of Coronavirus Disease 2019 (COVID-19) in rural areas of Chengdu in December 2020, to find out the source of infection and the chain of transmission. According to
COVID-19
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Disease Outbreaks
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Epidemics
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Humans
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Quarantine
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SARS-CoV-2