Résumé
Objective:To explore the chain mediating effect of adult attachment and psychological capital on the relationship between parenting style and mental health of university students.Methods:The short-form egna minnen av barndoms uppfostran (s-EMBU), experiences in close relationship inventory (ECR), positive psycap questionnaire (PPQ) and mental health scale for residents (MHSR) were adopted to test 1 415 students from 23 universities in Beijing.Pearson correlation analysis and regression analysis were performed by SPSS 24.0 software, the structural equation model was built by Mplus 8.0 software, and mediating effect analysis was conducted by Bootstrap method.Results:Mental health of university students (241.48±30.19) was positively correlated ( r=0.40-0.84, all P<0.01) with positive parenting style (father emotional warmth (2.97±0.67), mother emotional warmth (3.10±0.62)) and psychological capital (4.91±0.84). And the mental health of university students was negatively correlated ( r=-0.36--0.18, all P<0.01) with negative parenting style (father rejection (1.42±0.53), mother rejection (1.42±0.51), father overprotection (2.06±0.53), mother overprotection (2.18±0.55)) and adult attachment (attachment avoidance (3.31±0.88), attachment anxiety (3.66±0.97). Adult attachment was the mediation between parenting style (rejection, emotional warmth, over protection) and mental health ( β=-0.04, 0.04, -0.04, 95% CI=-0.08--0.01, 0.02-0.07, -0.07--0.02), while psychological capital was the mediation between parental emotional warmth and mental health ( β=0.21, 95% CI=0.14-0.26), both of which played a chain mediating role between parenting style and mental health ( β=-0.15, 0.11, -0.12, 95% CI=-0.21--0.10, 0.07-0.16, -0.18--0.07). Conclusion:Parenting style can not only directly affect mental health, but also indirectly affect mental health through the mediating role of adult attachment and the chain mediating role of adult attachment and psychological capital.
Résumé
Background & objectives: Selective cyclooxygenase-2 (COX-2) inhibitor is a form of non steroidal anti-inflammatory drug (NSAID) and is commonly used in autoimmune and rheumatic diseases to control inflammation and alleviate pain. Tumour necrosis factor-alpha (TNF-α) production and an imbalance of T helper 1 (Th1)/Th2 contribute to the pathogenesis of autoimmune and also anti-tumour activity. Dipyrone is a NSAID used to treat pain worldwide. The celecoxib analogue, 2,5-dimethylcelecoxib (DMC), lacks COX-2 inhibitory activity but exhibits anti-tumour properties. However, the effects and the mechanisms of dipyrone and 2,5-dimethylcelecoxib on tumour necrosis factor (TNF)-α and Th1- and Th2-related chemokines in monocytes remain poorly defined. This study was carried out to investigate the effects of dipyrone and 2,5-dimethylcelecoxib on the expression of Th1 (IP-10) and Th2 (I-309 and MDC) and TNF-α in human monocytes and the associated intracellular mechanism. methods: THP-1 cells and peripheral blood mononuclear cells (PBMCs) were pre-treated with dipyrone (10-9 – 10-4 M) and 2,5-dimethylcelecoxib (10-9 – 10-5 M) 2 h before lipopolysaccharide (LPS) stimulation. Cell supernatant was collected 24 h after LPS stimulation. TNF-α, I-309, MDC and IP-10 concentrations of cell supernatants were determined using ELISA. Intracellular signaling was evaluated by western blot. results: Dipyrone and 2,5-dimethylcelecoxib downregulated LPS-induced Th2-related chemokine I-309 and macrophage derived chemokine (MDC) production. Only high dose of 2,5-dimethylcelecoxib (10-5 M), but not dipyrone downregulated LPS-induced IP-10. Only very high dose of 2,5-dimethylcelecoxib had effect on LPS-induced TNF-α expression in PBMCs. Dipyrone and 2,5-dimethylcelecoxib suppressed LPS-induced p65 and JNK MAPK (C-Jun N-terminal kinase mitogen activated protein kinase). expression. Interpretation & conclusions: Dipyrone and 2,5-dimethylcelecoxib downregulated LPS-induced Th2-related chemokine I-309 and MDC in THP-1 cells. The suppressive effect on Th2-related