1.Radical resection of rectal carcinoma by laparoscopic versus open approach
Hongxu JIN ; Xuefeng ZHANG ; Jin LI ; Yongshuang LI ; Guoqiang WU ; Xize WANG ; Huayuan QU ; Xiukun ZONG
Chinese Journal of General Surgery 1997;0(04):-
Objective To study the feasibility and curative effect of laparoscopic radical resection of rectal carcinoma. Methods Sixty-two cases were enrolled in this study between Feb 2003 and Mar 2005, including 32 cases undergoing laparoscopic radical resection (19 Dixon and 13 Miles) , and 30 cases undergoing open radical resection (22 Dixons and 8 Miles). Results The mean operation time of laparoscopic group was 195 min, and open group was 156 min (P 0. 05 ). The GI and urination function of laparoscopic group recovered faster than open group ( evacuated was 2. 7 days vs. 3. 7 days, P
2.Relationship between expression of Mycobacteriumtuberculosis Hsp16.3 and apoptosis of infected mouse alveolar macrophages
Qingzhang TUO ; Jiangtao DONG ; Xize TIAN ; Yunxia LIU ; Weijie DONG ; Danxia LIU ; Wei LI ; Fang WU ; Le ZHANG ; Wanjiang ZHANG
Journal of Xi'an Jiaotong University(Medical Sciences) 2014;(3):300-305
Objective To study the relationship between the expression of Mycobacterium tuberculosis small heat shock protein Hsp16.3 and the apoptosis of infected mouse alveolar macrophages.Methods The laboratory mice were infected with bacterial suspension of the international standard virulent strain of Mycobacterium tuberculosis H37Rv strains (H37Rv),Hsp16.3 gene deletion mutants of the international standard virulent of Mycobacterium tuberculosis H37Rv strains(△H37Rv),or sterile saline solution (normal control)by the tail vein. After successful replication of mouse infection model in each group,we cleaved the alveolus of each group of mice and collected lavage fluid to obtain alveolar macrophages of the infected mice at days 1 ,3 ,5 ,7 ,9 ,1 1 ,1 3 and 1 5 .Then the infection status of macrophages was observed with confocal laser scanning microscopy;flow cytometry was used to detect the apoptosis rate of alveolar macrophages of the infected mice;Caspase-3 and Bcl-2 expressions were examined by Western blot.Results The apoptosis rate of Hsp16.3 gene was higher in deletion strain (△H37Rv)group and H37Rv strains (H37Rv)group than in control group.The apoptosis rate of alveolar macrophages in △ H37Rv group gradually increased,peaked at day 7 ,and then gradually decreased.It was significantly higher in H3 7 Rv group than in H3 7 Rv strain group from day 1 to 7 and from day 1 3 to 1 5 (P<0 .0 5 ).Caspase-3 and Bcl-2 protein expressions in the macrophages of△H37Rv group and H37Rv group were higher than those of control group.Caspase-3 expression in the microphages of △H3 7 Rv group and H3 7 Rv group gradually increased from day 1 to 7 and peaked at day 7;it peaked again at day 13 in H37Rv group.However,Caspase-3 expression remained significantly higher in△H37Rv group than in H3 7 Rv group (P<0 .0 5 ).Bcl-2 expression in △H3 7 Rv group did not change much at the early stage of infection (P<0 .0 5 ),but gradually increased after day 9 .Bcl-2 expression in H3 7 Rv group did did not change much from day 1 to 7 (P<0.05),but gradually increased after day 7.However,it remained lower in△H37Rv group than in H37Rv group,especially after 7 days(P<0.05).Conclusion Mycobacterium tuberculosis small heat shock protein Hsp16.3 can inhibit the apoptosis of macrophages during the early and late stages of infection,and this inhibition may be achieved by inhibiting the expression of apoptotic protease Caspase-3 and promoting the expression of Bcl-2 protein.
3.Didangtang: A Review
Xize WU ; Jian KANG ; Yue LI ; Jiaxiang PAN
Chinese Journal of Experimental Traditional Medical Formulae 2023;29(20):230-238
As one of the classic prescriptions of traditional Chinese medicine, Didangtang is an effective prescription for breaking and expelling blood stasis. It was considered that Didangtang damage the healthy qi and contained toxic Chinese medicinal materials such as leeches and gadflies, and thus it was rarely used. However, as the attention to classic prescriptions increases, Didangtang has been widely used in clinical practice and demonstrated definite efficacy in treating diabetes mellitus and its complications, malignant tumors, Alzheimer's disease, stroke, renal diseases, cardiovascular diseases, peripheral vascular diseases, gynecological disease, and male diseases according to the disease location, pathogenesis, symptoms, and pharmacological effects. Didangtang has the effects of mitigating insulin resistance, improving microvascular and peripheral vascular circulation, delaying diabetic macrovascular lesions, preventing vascular fibrosis, improving immunity, inhibiting tumor growth, protecting the brain tissue, nerve cells, vascular endothelial function, and kidney, reducing inflammation, and delaying aging. This paper summarizes the clinical application of Didangtang and initially explores the underlying mechanism.
4.Hepatocyte steatosis activates macrophage inflammatory response accelerating atherosclerosis development.
Yue LI ; Xize WU ; Jiaxiang PAN ; Lihong GONG ; Dongyu MIN
Journal of Zhejiang University. Medical sciences 2023;52(6):751-765
OBJECTIVES:
To investigate the mechanism of comorbidity between non-alcoholic fatty liver disease (NAFLD) and atherosclerosis (AS) based on metabolomics and network pharmacology.
METHODS:
Six ApoE-/- mice were fed with a high-fat diet for 16 weeks as a comorbid model of NAFLD and AS (model group). Normal diet was given to 6 wildtype C57BL/6J mice (control group). Serum samples were taken from both groups for a non-targeted metabolomics assay to identify differential metabolites. Network pharmacology was applied to explore the possible mechanistic effects of differential metabolites on AS and NAFLD. An in vitro comorbid cell model was constructed using NCTC1469 cells and RAW264.7 macrophage. Cellular lipid accumulation, cell viability, morphology and function of mitochondria were detected with oil red O staining, CCK-8 assay, transmission electron microscopy and JC-1 staining, respectively.
RESULTS:
A total of 85 differential metabolites associated with comorbidity of NAFLD and AS were identified. The top 20 differential metabolites were subjected to network pharmacology analysis, which showed that the core targets of differential metabolites related to AS and NAFLD were STAT3, EGFR, MAPK14, PPARG, NFKB1, PTGS2, ESR1, PPARA, PTPN1 and SCD. The Kyoto Encyclopedia of Genes and Genomes showed the top 10 signaling pathways were PPAR signaling pathway, AGE-RAGE signaling pathway in diabetic complications, alcoholic liver disease, prolactin signaling pathway, insulin resistance, TNF signaling pathway, hepatitis B, the relax in signaling pathway, IL-17 signaling pathway and NAFLD. Experimental validation showed that lipid metabolism-related genes PPARG, PPARA, PTPN1, and SCD were significantly changed in hepatocyte models, and steatotic hepatocytes affected the expression of macrophage inflammation-related genes STAT3, NFKB1 and PTGS2; steatotic hepatocytes promoted the formation of foam cells and exacerbated the accumulation of lipids in foam cells; the disrupted morphology, impaired function, and increased reactive oxygen species production were observed in steatotic hepatocyte mitochondria, while the formation of foam cells aggravated mitochondrial damage.
CONCLUSIONS
Abnormal lipid metabolism and inflammatory response are distinctive features of comorbid AS and NAFLD. Hepatocyte steatosis causes mitochondrial damage, which leads to mitochondrial dysfunction, increased reactive oxygen species and activation of macrophage inflammatory response, resulting in the acceleration of AS development.
Animals
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Mice
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Non-alcoholic Fatty Liver Disease/metabolism*
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Cyclooxygenase 2/metabolism*
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PPAR gamma/metabolism*
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Reactive Oxygen Species/metabolism*
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Mice, Inbred C57BL
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Hepatocytes
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Macrophages/metabolism*
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Liver