1.Ethical Analysis on Iatrogenic Factors for Current Tense Doctor-patient Relationship
Chunfeng WEN ; Hongying LI ; Yuan WANG ; Enchang LI ; Xinying HE ; Xinqing ZHANG ; Huaqi CHAI
Chinese Medical Ethics 2015;(1):15-18
Objective:To investigate the reasons of the tension of doctor-patient relationship and the medical violence from the perspective of the doctors, in order to provide a reference for finding a viable solution. Methods:Questionnaires survey were conducted about doctors' working conditions in 45 hospitals of 9 provinces. Results:On-ly 3. 6% medical staff had a harmonious doctor-patient relationship, the causes for the tense doctor-patient rela-tionship were poor communication with patients (75%), medical limitations (46. 2%);From the patients perspec-tive, the patients 'unpleasant caused by overtreatment due to complex illness accounted for 54. 2%;Institutional health-related reasons accounted for 82 . 6%. Conclusions:In the past five years after the new health care re-form, the tense doctor-patient relationship has not been released. So, should focus on training to enhance the com-munication skills of medical personnel and medical humanities education while the implementation of the national health care reform, in order to reduce iatrogenic conflicts.
2.Chuju total flavonoids control the SFRP4 expression in Wnt pathway in rheumatoid arthritis model rats
Chenggui MIAO ; Jian LIU ; Yonghe ZHANG ; Min GAO ; Qingyu CHEN ; Huaqi HE
Journal of Central South University(Medical Sciences) 2013;38(7):715-721
Objective:To determine the effect of Chuju total flavonoids (CJTF) on the secreted frizzled-related protein 4 (SFRP4) expression in Wnt pathway in rheumatoid arthritis (AR) model rats. Methods:hTe role of CJTF in the treatment of AR model rats was evaluated by rat arthritis score and paw edema score. The expression regulation of the SFRP4,β-catenin and C-myc in Wnt pathway in AR model rats was detected by RT-PCR and Western blot atfer CJTF gavage treatment. Results:Atfer CJTF treatment, the rat arthritis score and paw edema score in AR model rats were signiifcantly decreased when the AR model rats were treated with CJTF, the SFRP4 expression was signiifcantly up-regulated, while theβ-catenin and C-myc gene expression were signiifcantly down-regulated in AR model rat synovial tissues. Conclusion:CJTF has significant therapeutic effect and inhibitory effect on Wnt pathway activation by targeting SFRP4 in AR model rat synovium.
3.Pulchinenoside inhibits the fibroblast-like synoviocytes apoptosis in adjuvant arthritis rats.
Chenggui MIAO ; Guoliang ZHOU ; Meisong QIN ; Jianzhong CHEN ; Chengfeng LI ; Huaqi HE
Journal of Central South University(Medical Sciences) 2015;40(2):144-149
OBJECTIVE:
To explore the eff ect of pulchinenoside (PULC) on fi broblast-like synoviocytes (FLS) apoptosis in adjuvant arthritis (AA) rats.
METHODS:
A total of 60 SD rats were randomly divided into 8 groups: A normal control group, an AA group, a low PULC group (50 mg/kg), a middle PULC group (100 mg/kg) or a high PULC group (150 mg/kg) and an ibuprofen (8 mg/kg) group (n=10 per group). FLS from the AA rats was cultured. The expression of Bcl-2, Bax, caspase-3 and the FLS proliferation were detected by the real time qPCR and MTT, respectively. The expression of IL-6 and IL-8 in culture medium was detected by ELISA.
RESULTS:
Compared with the AA group, the Bcl-2 expression was down-regulated (all P<0.05), the Bax and caspase-3 expression was up-regulated (all P<0.05), and the FLS proliferation was inhibited (all P<0.05). The IL-6 and IL-8 expression was suppressed in the FLS in the PULC groups at different dosages (all P<0.05) as well as in the ibuprofen group (P<0.05).
CONCLUSION
PULC may inhibit the FLS proliferation in AA rats by increase in FLS apoptosis.
Animals
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Apoptosis
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drug effects
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Arthritis, Experimental
;
Caspase 3
;
metabolism
;
Fibroblasts
;
cytology
;
drug effects
;
Interleukin-6
;
metabolism
;
Interleukin-8
;
metabolism
;
Proto-Oncogene Proteins c-bcl-2
;
metabolism
;
Pulsatilla
;
chemistry
;
Rats
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Rats, Sprague-Dawley
;
Synovial Membrane
;
cytology
;
bcl-2-Associated X Protein
;
metabolism